Cancer Center Archives - Page 2 of 10 - Sanford Burnham Prebys
Institute News

Raising awareness of breast cancer research at Sanford Burnham Prebys

AuthorGreg Calhoun
Date

October 31, 2024

The October Science Connect Series event was themed around Breast Cancer Awareness Month and featured two cancer research experts.

The Sanford Burnham Prebys Wellness Ambassadors hosted a Science Connect event on Wednesday, October 30, 2024, featuring two faculty experts discussing their breast cancer research and its implications.

The Science Connect Series provides a forum for Sanford Burnham Prebys principal investigators to share their research with administrative personnel. Faculty members gain experience in communicating their science to a lay audience, and administrators gain a better understanding of research conducted at the institute so they can become better advocates and ambassadors of the shared mission to translate science into health.

Kelly Kersten, PhD, an assistant professor in the Cancer Metabolism and Microenvironment Program, opened the event by focusing on the importance of finding new treatments —such as immunotherapies — for the one-third of breast cancer patients that are diagnosed after the early stages of the disease when surgery is less effective.

The immune system is one of the main defenses of the human body to fend off harmful pathogens and invasive cells, such as cancer. Among all white blood cells, a particular cell type, called a T cell, can directly kill cancer cells and therefore plays an essential role in building anti-tumor immune responses.

Many types of cancer are confronted and infiltrated by T cells, only to be suppressed by the local tumor environment.

“While immunotherapies that boost the immune system have revolutionized the way we treat cancer, many patients do not respond to the treatments, and the mechanisms of resistance remain largely unclear,” said Kersten.

Kersten’s goal is to understand why T cells enter a state known as exhaustion and lose their tumor-killing capacity. This knowledge will help her team find potential future therapies that could prevent T-cell exhaustion and improve immunotherapies for cancer patients.

Kevin Tharp, PhD, also an assistant professor in the Cancer Metabolism and Microenvironment Program, shared that his lab’s focus is on how cancer cells adapt their metabolism to generate the energy needed to spread to other tissues through metastasis. He presented his team’s work with the Kersten lab on another aspect of potential resistance to immunotherapy in breast cancer.

Tharp and Kersten are studying the hypothesis that part of the reason why these therapies fail is due to tumor-associated fibrosis, the creation of a thick layer of fibrous collagen (like scar tissue) that acts as a barrier against the anti-tumor immune response. They published a paper on June 3, 2024, in Nature Cancer,  discussing how tumor-associated macrophages, a type of immune cell found abundantly in the tumor microenvironment, respond to the physical properties of fibrosis.

By synthesizing injury-associated collagens that facilitate wound closure, TAMs experience metabolic changes and generate metabolic byproducts that suppress the anti-tumor function of immune cells.

“The metabolic changes in the microenvironment present more of a challenge to anti-tumor responses than the physical barrier,” said Tharp. “Our study provides an alternative explanation for why anti-tumor immunity is impaired in fibrotic solid tumors.”

To follow up on these results, Tharp is collaborating with Sarah Blair, MD, a professor of surgery at the University of California San Diego, to fund and initiate a clinical trial testing the potential of dietary supplements to counteract the suppressive effects of TAM metabolic byproducts as an adjunct therapy to surgery.

Institute News

A Conversation About Aging and Cancer at Sanford Burnham Prebys 

AuthorGreg Calhoun
Date

October 24, 2024

Event recording now available for panel discussion with scientists held on October 9, 2024

David A. Brenner, MD, president and CEO of Sanford Burnham Prebys, welcomed attendees to the launch of a new community engagement program called “A Conversation About” in the institute’s Victor E. LaFave III Memorial Auditorium on October 9, 2024.

The initial panel discussion in the A Conversation About series focused on the connection between aging and cancer and included information about a current breast cancer research collaboration. A recording of the event is available online.

Reena Horowitz, the founder of Group of 12 and Friends at Sanford Burnham Prebys, provided introductory remarks. Brooke Emerling, PhD, director of the Cancer Metabolism and Microenvironment Program, moderated the discussion among three featured panelists:

  • Peter Adams, PhD, director of the Cancer Genome and Epigenetics Program, Sanford Burnham Prebys
  • Xiao Tian, PhD, assistant professor in the Degenerative Diseases Program, Sanford Burnham Prebys
  • Kay Yeung, MD, PhD, associate clinical professor in the Division of Hematology-Oncology, University of California San Diego Health

By bringing together community collaborators and clinicians with Sanford Burnham Prebys researchers, A Conversation About offers a unique perspective on how clinical research and practice can be used to inform fundamental and translational science.

Watch Event Recording

Institute News

Two Sanford Burnham Prebys scientists selected for American Cancer Society postdoctoral fellowships

AuthorGreg Calhoun
Date

October 18, 2024

Funds will support Alicia Llorente Lope and Ambroise Manceau who study breast and pancreatic cancer

Alicia Llorente Lope, PhD, and Ambroise Manceau, PhD, were awarded 2024 Postdoctoral Fellowships from the American Cancer Society (ACS). These prestigious awards provide more than $65,000 per year for up to three years to support early career scientists studying cancer.

“I was so excited when I heard the news,” said Llorente. “It is a privilege to have this award, and it feels very validating to know that someone saw enough potential in my research to deem it worthy of funding.”

Tackling treatment-resistant breast cancer

Llorente joined the lab of Brooke Emerling, PhD, director of the Cancer Metabolism and Microenvironment Program at Sanford Burnham Prebys, nearly three years ago after beginning her breast cancer research career as a doctoral student.

“I was first interested in breast cancer because my grandmother died of the disease, and I wanted to contribute to finding new therapeutic opportunities for cancer patients,” said Llorente. Llorente’s ACS-funded research project focuses on HER2-positive (HER2+) breast cancer.

Roughly one in five breast cancer tumors have elevated levels of the HER2 protein. While these tumors tend to grow quickly, drugs targeting the HER2 protein are usually effective at first. However, HER2+ tumors often are able to adapt and develop resistance to these drugs over time, leaving patients with few if any remaining treatments options.

Llorente has found evidence that a form of the protein phosphatidylinositol-5-phosphate 4-kinase (PI5P4K) plays a role in breast cancer tumors becoming resistant to HER2 drugs.

Brooke Emerling

Brooke Emerling, PhD

“We’ve revealed a strong connection between elevated levels of PI5P4K gamma and reduced survival rates in patients with HER2+ breast cancer,” explained Llorente. “I plan to explore whether targeting both HER2 and PI5P4K gamma in breast cancer cells may provide a path to overcoming treatment resistance.” Llorente also will study the functions of PI5P4K gamma in breast cancer cells to see why these cells cease to respond to HER2-targeting drugs.

“I am incredibly proud of Alicia for spearheading this groundbreaking project targeting the lipid kinase PI5P4K gamma,” said Emerling. “Her insightful analysis of breast cancer datasets, which uncovered a correlation between elevated expression of PI5P4K gamma and worse outcomes in HER2+ patients, has set the stage for vital research aimed at overcoming the significant challenge of resistance to targeted therapies in HER2+ tumors.”

Cosimo Commisso headshot

Cosimo Commisso, PhD

Powering down pancreatic cancer

Manceau is in the second year of his postdoctoral training in the lab of Cosimo Commisso, PhD, interim director and deputy director of the institute’s NCI-Designated Cancer Center. During his doctoral program, Manceau studied how abnormal cells die in a programmed series of steps called apoptosis, a process known to go awry in cancer and neurodegenerative diseases.

“It began as a basic science project about the molecular processes around cell death, and over time it led to possible therapeutic implications,” said Manceau. “I learned that I like to study fundamental biology and then try to find an application for it, and I saw in the Commisso lab an opportunity to do just that in pancreatic cancer.”

Manceau’s fellowship project focuses on pancreatic ductal adenocarcinoma (PDAC) — the most common form of pancreatic cancer with only a 13% five-year survival rate — and its ravenous pursuit of energy. Because of PDAC cells’ constant need for fuel to sustain their rampant growth, they adapt by reshaping the surface of their cells to snatch extra nutrients from the jelly-like substance between cells.

Commisso and others have shown that cutting off the extra power supplied by this process — known as macropinocytosis — reduces tumor growth. Manceau has studied the contents taken by contorted pancreatic cell surfaces in pockets called macropinosomes. By analyzing every single protein in this scooped goop, he found that calcium transporter proteins present in macropinosomes also are required for macropinocytosis.

“During the fellowship, I will work to understand how these transporter proteins affect macropinocytosis,” said Manceau. “These proteins have never been targeted before in pancreatic cancer, so our long-term goal is to use this strategy to cut the nutrient supply to tumors and see if we can inhibit tumor growth.”

“By disrupting the cancer cells’ ability to feed themselves through macropinocytosis, we can potentially starve tumors and inhibit their growth,” added Commisso. “Ambroise’s research aims to target key proteins involved in this process, opening up new possibilities for treatments that could significantly improve outcomes for patients battling pancreatic cancer.”

Institute News

Mammalian Genome Engineering Group holds 2024 symposium in San Diego

AuthorGreg Calhoun
Date

September 25, 2024

The four-day event included talks from experts from across North America and opportunities to discuss improving experimental methods and approaches to analyzing the resulting data.

Researchers convened at Sanford Burnham Prebys in La Jolla from September 12-15 to hear presentations from their peers and confer about the latest developments in modifying the genomes of mammalian animal models to advance biomedical research.

Anindya Bagchi, PhD, associate professor in the Institute’s Cancer Genome and Epigenetics Program, planned the 4th Mammalian Genome Engineering Symposium, which included 26 presentations from experts across the United States and Canada. Attendees asked many questions throughout, and numerous speakers commented on how valuable the conversation at the meeting was for refining planned experiments and considering new ideas and approaches.

“It was a truly enjoyable and thought-provoking meeting,” said Angela Liou, MD, an instructor in the Cancer Genome and Epigenetics Program at Sanford Burnham Prebys and pediatric oncologist and hematologist at Rady Children’s Hospital-San Diego. “It also was incredibly helpful in informing the next steps of my research project.”

“I’m so grateful for the invitation to attend this symposium,” said Praveen Raju, MD, PhD, the Nathan Gordon Chair in Neuro-Oncology and medical director of the Pediatric Neuro-Oncology Program at Rady Children’s Hospital-San Diego and director of the Pediatric Neuro-Oncology Program at the University of California San Diego School of Medicine.

Anindya Bagchi, PhD, headshot

Anindya Bagchi, PhD, is an associate professor in the Cancer Genome and Epigenetics Program.

“The presenters and attendees were welcoming and collaborative, and I certainly learned a lot.”

The symposium brings together the Mammalian Genome Engineering Group, which was formed by a small group of genome engineering enthusiasts including Bagchi, Nada Jabado, MD, PhD, professor of Pediatrics and Human Genetics at McGill University and a hematologist and oncologist at Montreal Children’s Hospital; David Largaespada, PhD, a professor of Pediatrics, Genetics, Cell Biology and Development at the University of Minnesota Medical School and the associate director for Basic Research in the Masonic Cancer Center; and Michael Taylor, MD, PhD, The Cyvia and Melvyn Wolff Chair of Pediatric Neuro-Oncology at Texas Children’s Cancer and Hematology Center and professor of Pediatrics (Hematology-Oncology) at Baylor College of Medicine.

The group is interested in developing functional models of genomic and epigenetic mutations associated with human diseases—especially cancers—that are difficult to recreate in animal models. The group’s first symposium was coordinated by Taylor in Napa, Calif., in 2014, followed by the 2nd symposium that was organized by Jabado in Montreal in 2015. After a hiatus, the group was revived in 2023 with the 3rd symposium hosted again by Taylor in Houston.

“We believe this symposium will, in the coming years, become a leading forum for discussing cutting-edge genomic and epigenomic approaches to tackle challenging genetic and epigenetic mutations,” said Bagchi. “These approaches are likely to become standard practice in the near future.”

The Sanford Burnham Prebys scientists that presented at the 4th Mammalian Genome Engineering Symposium were:

  • Bagchi, “Why are MYC-driven cancers so lethal?” 
  • Liou, “Investigating the deposition of H3.3K27M oncohistone and its effect on retrotransposon reactivation in H3K27M pediatric diffuse midline glioma” 
  • Ani Deshpande, PhD, associate professor in the Cancer Genome and Epigenetics Program and associate director of Diversity, Equity and Inclusion in the NCI-Designated Cancer Center, “Functional genomic approaches to identify selective dependencies in synovial sarcoma” 
  • Peter D. Adams, PhD, the director of the Cancer Genome and Epigenetics Program, “The role of aging in cancer” 
  • Lukas Chavez, PhD, associate professor in the Cancer Genome and Epigenetics Program, “Circular extrachromosomal DNA promotes tumor heterogeneity and enhancer rewiring” 
  • Jerold Chun, MD, PhD, professor in the Degenerative Diseases Program, “Genetic mosaicism and somatic gene recombination in the brain” 
  • Adarsh Rajesh, graduate student, Sanford Burnham Prebys, “CCND1-CDK6 complex inhibits DNA damage repair and promotes inflammation in senescence and the aged liver”

Additional speakers included:

  • Taylor, “Why does medulloblastoma love to be tetraploid and other nonsense”
  • Jabado, “Co-opting 3D structures to fuel tumorigenesis”
  • Tannishtha Reya, PhD, Herbert and Florence Irving Professor of Basic Science Research in Physiology and Cellular Biophysics, Columbia University, “New genetically engineered models to understand cancer heterogeneity and therapy resistance in pancreatic cancer”
  • Simona Dalin, PhD, postdoctoral fellow, Broad Institute of the Massachusetts Institute of Technology and Harvard University, “Contributions of perfect and imperfect homology to rearrangement formation in human and cancer genomes”
  • Alison M. Taylor, PhD, assistant professor of Pathology and Cell Biology, Columbia University, “Functional and computational approaches to uncover the consequences of chromosome arm aneuploidy in cancer”
  • Sean Eagan, PhD, senior scientist in the Cell Biology program at The Hospital for Sick Children, professor of Molecular Genetics, University of Toronto, “An update on Genetic analysis of 16q-syntenic block deletion in the mouse mammary gland – a tumor suppressor arm”
  • Claudia Kleinman, PhD, associate professor of Human Genetics, McGill University, investigator at the Lady Davis Institute for Medical Research, Jewish General Hospital, “Lineage programs and the 3D genome in pediatric brain tumors”
  • Branden Moriarity, PhD, associate professor of Pediatrics (Hematology and Oncology), University of Minnesota Medical School, “Next generation engineered immune effector cells for immunotherapy”
  • Beau Webber, PhD, associate professor of Pediatrics (Hematology and Oncology), University of Minnesota Medical School, “Building cancer in a dish: Sarcoma modeling using human pluripotent stem cells”
  • Sameer Agnihotri, PhD, associate professor of Neurological Surgery and director of the Brain Tumor Biology and Therapy Lab, University of Pittsburgh Medical Center Children’s Hospital of Pittsburgh, “Identifying genetic vulnerabilities by modeling Chromosome 9p loss”
  • Largaespada, “Loss of the polycomb repressor complex 2 (PRC2) alters the super-enhancer landscape, genome/epigenome stability, and therapeutic sensitivities of malignant peripheral nerve sheath tumors”
  • Teresa Davoli, PhD, assistant professor of Biochemistry and Molecular Pharmacology, New York University Langone Health, “Engineering chromosome specific aneuploidy by targeting human centromeres”
  • Rameen Beroukhim, MD, PhD, associate professor of Medicine, Dana-Farber Cancer Institute and Harvard Medical School, associate member of the Broad Institute of MIT and Harvard, “Detecting rearrangement signatures—naturally”
  • Quang Trinh, PhD, scientist, Ontario Institute for Cancer Research, “Perspectives and Challenges in PFA Integrative Analysis”
  • Taylor Gatesman, graduate student, University of Pittsburgh, “Genome Engineering: DREaming of and vCREating new models”
  • Joseph Skeate, PhD, postdoctoral fellow, University of Minnesota Medical School, “Targeted CAR integration and multiplex base editing in a single-step manufacturing process for enhanced cancer immunotherapies”
Institute News

Michael Alcaraz awarded Melvin and Phyllis McCardle Clause Scholarship

AuthorGreg Calhoun
Date

September 18, 2024

The scholarship program for graduate students was created by the Clause family’s generous donation to Sanford Burnham Prebys.

Michael Alcaraz, a fourth-year graduate student in the Sanford Burnham Prebys Graduate School of Biomedical Sciences, was selected as the 2024 recipient of the Melvin and Phyllis McCardle Clause Scholarship.

“I am very excited about being chosen for this scholarship,” said Alcaraz. “I’ll be gaining mentorship opportunities from researchers in neuroscience that complement my lab’s focus on aging.

“This funding will make a big difference as my research moves forward. The scholarship also provides support for professional development, which will allow me to attend conferences to share what I’m studying and grow my network.”

The McCardle Clause Scholarship was established in honor of Phyllis McCardle Clause after her long struggle with Alzheimer’s disease (AD). The award supports graduate student education in age-related neurodegeneration within the Institute’s graduate school.

Alcaraz conducts research in the laboratory of Peter D. Adams, PhD, the director of the Cancer Genome and Epigenetics Program, with a focus on the mechanisms of aging.

With support from the scholarship, Alcaraz will be investigating the fundamental connections between aging and the increased risk of AD, the most common cause of dementia. His project is focused on the role of nicotinamide adenine dinucleotide (NAD+), an essential metabolite and building block for enzymes.

NAD+ levels decrease with age in several tissues, including in the brains of humans and mouse models of AD. The decline of this important metabolite is associated with insufficient energy metabolism that is a major hallmark of AD.

“In collaboration with the Conrad Prebys Center for Chemical Genomics, we will test a potential drug to promote production of NAD+ in the brain by activating a key enzyme involved in NAD+ biosynthesis,” said Alcaraz.  The compound was developed by the Conrad Prebys Center for Chemical Genomics led by Michael Jackson, PhD, senior vice president of Drug Discovery and Development.

“The goal of my project is to raise the levels of NAD+ in mice suffering from an analogous condition to AD and test its effects on improving brain metabolism, function and behavior,” added Alcaraz.

“The objective is to build the preclinical foundation for one day achieving benefits for patients. We all know how devastating AD is for patients and families, and the need for new treatments grows greater every single day.

“This project will require a lot of collaboration between experts in aging, drug discovery, neuroscience and behavioral analysis. We have all this expertise available across the Institute, and I’m looking forward to working with an interdisciplinary team on this effort thanks to the generosity of the Clause family.”

Institute News

Sanford Burnham Prebys event explores the science behind addiction

AuthorGreg Calhoun
Date

August 2, 2024

Scientists and clinicians from three local research institutions converged July 31 to discuss new ways to treat multiple addictions at Sanford Burnham Prebys open house

The  NCI-designated Cancer Center at Sanford Burnham Prebys welcomed San Diego community members to the institute’s campus on July 31, 2024 for an open house focused on addiction research.  The Cancer Center team developed the event in partnership with scientists from Scripps Research and the University of California San Diego School of Medicine.

Ze’ev Ronai, PhD, director of the Sanford Burnham Prebys Cancer Center, formally opened the event and welcomed attendees before introducing David A. Brenner, MD, president and CEO of Sanford Burnham Prebys.

William Gerhart, chair of the Sanford Burnham Prebys board of trustees

William Gerhart, chair of the Sanford Burnham Prebys board of trustees, delivered welcoming remarks focused on the potential benefits to families of improving the treatment and prevention of addiction and addiction-associated cancers.

“As I have learned more about the research being presented here, I am impressed by just how much of a powerhouse we have on this mesa regarding both cancer and addiction science,” said Brenner.

William Gerhart, chair of the Sanford Burnham Prebys board of trustees; Nicholas Cosford, PhD, co-director of the Cancer Molecular Therapeutics Program; and Michael Jackson, PhD, senior vice president of Drug Discovery and Development at the Conrad Prebys Center for Chemical Genomics (Prebys Center), also provided opening remarks emphasizing the collaborative nature of the featured research as well as the potential benefits to families of improving the treatment and prevention of addiction and addiction-associated cancers.

Attendees had the opportunity to learn from and interact with the following scientists at stations featuring posters describing research underway at all three represented institutions:

In addition to his welcoming comments, Cosford also presented an overview of the many links between addiction and cancer.

  • Douglas Sheffler, PhD, is an associate professor in the Center for Therapeutics Discovery at Sanford Burnham Prebys. Sheffler discussed a drug discovery effort focused on treating nicotine addiction.
  • Benjamin Mckenna, PhD, is an assistant clinical professor of psychiatry at UC San Diego School of Medicine and staff psychologist at Veterans Affairs San Diego Healthcare System. Mckenna presented on the same drug as Sheffler with an update on phase I clinical trial results regarding safety, optimal dosage and efficacy.
  • Steven Olson, PhD, executive director of Medicinal Chemistry at the Prebys Center, presented on work being conducted at the center in collaboration with Jackson. Olson described a drug being studied as an alternative to opioids that has shown promising benefits for reducing pain and addiction-related behavior.
  • Kokila Shankar, PhD, is a postdoctoral associate at Sanford Burnham Prebys working in the Cosford lab. Shankar detailed efforts to find new drugs to treat alcohol use disorder, which is estimated to cause approximately one of every 25 cancer diagnoses.
  • Bryan Cruz, PhD, is a postdoctoral fellow at Scripps Research working in the lab of Marisa Roberto, PhD, vice chair and Paul and Cleo Schimmel Endowed Chair in the Department of Molecular Medicine. Cruz discussed his research to uncover new ways of treating alcohol use disorder rooted in posttraumatic stress disorder, and thereby reduce cancer cases associated with excessive alcohol consumption.
  • Valentina Vozella, PhD, is a postdoctoral researcher in the Department of Molecular Medicine at Scripps Research. She also is a member of the Roberto lab. Vozella presented on studies regarding the effect of social isolation on the development of alcohol use disorder during adolescence, as well as on potential methods of treatment and prevention.

Participants were able to tour the Prebys Center, which is the institute’s comprehensive center for drug discovery and chemical biology. Visitors were able to see how the center’s researchers can quickly test the potential effectiveness of hundreds of thousands of compounds to find new prospective treatments. Many scientists at Sanford Burnham Prebys partner with the Prebys Center to conduct drug discovery searches based on new research findings, including several of the event’s poster presenters.

The open house featured a reception with remarks from Robert Anthenelli, MD, a professor in the Department of Psychiatry at UC San Diego School of Medicine. Anthenelli’s research focuses on developing new or improved treatments for cancer-causing tobacco and alcohol use disorders. He shared insights he has gained as a physician-scientist working in this area over the past 30 years.

The reception also included concluding remarks from Helen Eckmann, EdD, an NCI-designated Cancer Center Community Advisory Board member. The board hosts the center’s open house events. Its members strive to bridge the gap between biomedical science and the people who need it most: patients and the families and friends who love and support them.

Institute News

Using machines to personalize patient care

AuthorGreg Calhoun
Date

July 30, 2024

Artificial intelligence (AI) and other computational techniques are aiding scientists and physicians in their quest to create treatments for individuals rather than populations

The Human Genome Project captured the public’s imagination with its global quest to better understand the genetic blueprint stored on the DNA within our cells. The project succeeded in delivering the first-ever sequence of the human genome while foreshadowing a future for medicine once considered to be science fiction. The project presaged the possibility that health care could be personalized based on clues within a patient’s unique genetic code.

Chavez lab

The Chavez Lab

While many more people have undergone genetic testing through consumer genealogy and health services such as 23andMe and Ancestry than through health care systems, genomic sequencing has influenced clinical care in some specialties. Personalized medicine—also known as precision medicine or genomic medicine—has been especially helpful for people suffering from rare diseases that historically have been difficult to diagnose and treat.

Scientists at Sanford Burnham Prebys are employing new technologies and expertise to test ways to improve diagnoses and customize treatments for many diseases based on unique characteristics within tumors, blood samples and other biopsies.

AI and other computational techniques are enabling patient samples to be rapidly analyzed and compared to data from vast numbers of individuals who have been treated for the same condition. Physicians can use AI and other tools to identify subtypes of cancers and other conditions, as well as improve selection of eligible candidates for clinical trials.

“I think we’ve gotten a lot better at precision diagnostics,” says Lukas Chavez, PhD, an assistant professor in the Cancer Genome and Epigenetics Program at Sanford Burnham Prebys. “In my work at Rady Children’s Hospital in cancer, we can characterize a tumor based on mutations, including predicting how quickly different tumors will spread. What we too often lack, however, are better treatment approaches or medicines. That will be the next generation of precision medicine.”

Sanju Sinha, PhD, an assistant professor in the Cancer Molecular Therapeutics Program at Sanford Burnham Prebys, is developing projects to help bridge the gap between precision diagnostics and treatment. He is partnering with the National Cancer Institute on a first-of-its-kind computational tool to systematically predict patient response to cancer drugs at single-cell resolution.

A study published in the journal  Nature Cancer discussed how the tool, called PERCEPTION, was successfully validated by predicting the response to individual therapies and combination treatments in three independent published clinical trials for multiple myeloma, breast and lung cancer.

Lukas Chavez, PhD

Lukas Chavez, PhD, is an assistant professor in the Cancer Genome and Epigenetics Program at Sanford Burnham Prebys.

In each case, PERCEPTION correctly stratified patients into responder and non-responder categories. In lung cancer, it even captured the development of drug resistance as the disease progressed, a notable discovery with great potential.

Sanju Sinha, PhD

Sanju Sinha, PhD, is an assistant professor in the Cancer Molecular
Therapeutics Program at Sanford Burnham Prebys.

“The ability to monitor the emergence of resistance is the most exciting part for me,” says Sinha. “It has the potential to allow us to adapt to the evolution of cancer cells and even modify our treatment strategy.”

While PERCEPTION is not yet ready for clinics, Sinha hopes that widespread adoption of this technology will generate more data, which can be used to further develop and refine the technology for use by health care providers.

In another project, Sinha is focused on patients being treated for potential cancers that may never progress into dangerous conditions warranting treatment and its accompanying side effects.

“Many women who are diagnosed with precancerous changes in the breast seek early treatment,” says Sinha. “Most precancerous cells never lead to cancer, so it may be that as many as eight of 10 women with this diagnosis are being overtreated, which is a huge issue.”

To try and counter this phenomenon, Sinha is training AI models on images of biopsied samples in conjunction with multi-omics sequencing data. His team’s goal is to develop a tool capable of predicting which patients’ cancers would progress based on the imaged samples alone.

“In the field of precancer, insurance does not cover the cost of computing this omics data,” says Sinha. “Health care systems do routinely generate histopathological slides from patient biopsies, so we feel that a tool leveraging these images could be a scalable and accessible solution.”

If Sinha’s team is successful, an AI tool integrated into clinics would predict whether precancerous cells would progress within the next 10 years to guide treatment decisions and how patients are monitored.

“With precision medicine, our hope is not to just treat patients with better drugs, but also to make sure that patients are not unnecessarily treated and made to bear needless costs and side effects that disrupt their quality of life.”


Programming in a Petri Dish, an 8-part series

How artificial intelligence, machine learning and emerging computational technologies are changing biomedical research and the future of health care

  • Part 1 – Using machines to personalize patient care. Artificial intelligence and other computational techniques are aiding scientists and physicians in their quest to prescribe or create treatments for individuals rather than populations.
  • Part 2 – Objective omics. Although the hypothesis is a core concept in science, unbiased omics methods may reduce attachments to incorrect hypotheses that can reduce impartiality and slow progress.
  • Part 3 – Coding clinic. Rapidly evolving computational tools may unlock vast archives of untapped clinical information—and help solve complex challenges confronting health care providers.
  • Part 4 – Scripting their own futures. At Sanford Burnham Prebys Graduate School of Biomedical Sciences, students embrace computational methods to enhance their research careers.
  • Part 5 – Dodging AI and computational biology dangers. Sanford Burnham Prebys scientists say that understanding the potential pitfalls of using AI and other computational tools to guide biomedical research helps maximize benefits while minimizing concerns.
  • Part 6 – Mapping the human body to better treat disease. Scientists synthesize supersized sets of biological and clinical data to make discoveries and find promising treatments.
  • Part 7 – Simulating science or science fiction? By harnessing artificial intelligence and modern computing, scientists are simulating more complex biological, clinical and public health phenomena to accelerate discovery.
  • Part 8 – Acceleration by automation. Increases in the scale and pace of research and drug discovery are being made possible by robotic automation of time-consuming tasks that must be repeated with exhaustive exactness.
Institute News

The Science Behind Addiction

AuthorGreg Calhoun
Date

July 25, 2024

Scientists and clinicians from three local research institutions converge July 31 to discuss new ways to treat multiple addictions at Sanford Burnham Prebys Open House

The NCI-designated Cancer Center at Sanford Burnham Prebys welcomes San Diego community members to the institute’s campus for an open house focused on addiction research.  The Cancer Center team developed the event in partnership with scientists from Scripps Research and the University of California San Diego School of Medicine.

The event will take place Wednesday, July 31, 2024, at 3:30 pm at 10901 N. Torrey Pines Road in La Jolla. More information and the online registration form are located on the institute’s website.

Attendees will meet scientists working to better understand the science behind addiction. Here’s a sneak peek of presenters and topics:

  • Douglas Sheffler, PhD, is an associate professor in the Center for Therapeutics Discovery at Sanford Burnham Prebys. Sheffler will discuss a drug discovery effort focused on treating nicotine addiction.
  • Benjamin Mckenna, PhD, is an assistant clinical professor of psychiatry at UC San Diego School of Medicine and staff psychologist at Veterans Affairs San Diego Healthcare System. Mckenna will present on the same drug as Sheffler with an update on phase I clinical trial results regarding safety, optimal dosage and efficacy.
  • Michael Jackson, PhD, is senior vice president of Drug Discovery and Development at the Sanford Burnham Prebys Conrad Prebys Center for Chemical Genomics and co-director of the Cancer Molecular Therapeutics Program in the institute’s NCI-Designated Cancer Center. Jackson will talk about a drug being studied as an alternative to opioids that has shown promising benefits for reducing pain and addiction-related behavior.
  • Kokila Shankar, PhD, is a postdoctoral associate at Sanford Burnham Prebys working in the lab of Nicholas Cosford, PhD, co-director of the NCI-Designated Cancer Center’s Cancer Molecular Therapeutics Program. Shankar will detail efforts to find new drugs to treat alcohol use disorder, which is estimated to cause approximately one of every 25 cancer diagnoses.
  • Bryan Cruz, PhD, is a postdoctoral fellow at Scripps Research working in the lab of Marisa Roberto, PhD, vice chair and Paul and Cleo Schimmel Endowed Chair in the Department of Molecular Medicine. Cruz will discuss his research to uncover new ways of treating alcohol use disorder rooted in posttraumatic stress disorder, and thereby reduce cancer cases associated with excessive alcohol consumption.
  • Valentina Vozella, PhD, is a postdoctoral researcher in the Department of Molecular Medicine at Scripps Research. She also is a member of the Roberto lab. Vozella will present on studies regarding the effect of social isolation on the development of alcohol use disorder during adolescence, as well as on potential methods of treatment and prevention.
  • Robert Anthenelli, MD, is a professor in the Department of Psychiatry at UC San Diego School of Medicine. Anthenelli’s research focuses on developing new or improved treatments for cancer-causing tobacco and alcohol use disorders. He will share some of his insights as a physician-scientist working in this area over the past 30 years.

In addition to poster presentations from speakers, guests will have the opportunity to talk with  scientists, clinicians and research advocates during an informal evening reception.

The NCI-designated Cancer Center open house events are hosted by the center’s Community Advisory Board. Its members strive to bridge the gap between biomedical science and the people who need it most: patients and the families and friends who love and support them.

Institute News

How a protein component of nuclear pore complexes regulates development of blood cells and may contribute to myeloid disorders

AuthorCommunications
Date

June 5, 2024

Nuclear pore complexes (NPCs) are channels composed of multiple proteins that ferry molecules in and out of the nucleus, regulating many critical cellular functions, such as gene expression, chromatin organization and RNA processes that influence cell survival, proliferation, and differentiation.

In recent years, new studies, including work by Maximiliano D’Angelo, PhD, associate professor in the Cancer Metabolism and Microenvironment Program at Sanford Burnham Prebys, have noted that NPCs in cancer cells are different, but how these alterations contribute to malignancy and tumor development—or even how NPCs function in normal cells—is poorly understood.

In a new paper, published June 5, 2024 in Science Advances, D’Angelo with first author Valeria Guglielmi, PhD, and co-author Davina Lam, uncover Nup358, one of roughly 30 proteins that form the NPCs, as an early player in the development of myeloid cells, blood cells that if not formed or working properly leads to myeloid disorders such as leukemias.

The researchers found that when they eliminated Nup358 in a mouse model, the animals experienced a severe loss of mature myeloid cells, a group of critical immune cells responsible for fighting pathogens that are also responsible for several human diseases including cancer. Notably, Nup358 deficient mice showed an abnormal accumulation of early progenitors of myeloid cells referred as myeloid-primed multipotent progenitors (MPPs).

“MPPs are one of the earliest precursors of blood cells,” said D’Angelo. “They are produced in the bone marrow from hematopoietic stem cells, and they differentiate to generate the different types of blood cells.

Maximiliano D’Angelo and Valeria Guglielmi

“There are different populations of MPPs that are responsible for producing specific blood cells and we found that in the absence of Nup358, the MPPs that generate myeloid cells, which include red blood cells and key components of the immune system, get stuck in the differentiation process.”

Fundamentally, said Gugliemi, Nup358 has a critical function in the early stages of myelopoiesis (the production of myeloid cells). “This is a very important finding because it provides insights into how blood cells develop, and can help to establish how alterations in Nup358 contribute to blood malignancies.”

The findings fit into D’Angelo’s ongoing research to elucidate the critical responsibilities of NPCs in healthy cells and how alterations to them contribute to immune dysfunction and the development and progression of cancer.

“Our long-term goal is to develop novel therapies targeting transport machinery like NPCs,” said D’Angelo, who recently received a two-year, $300,000 Discovery Grant from the American Cancer Society to advance his work.


This research was supported in part by a Research Scholar Grant from the American Cancer Society (RSG-17-148-01), the Department of Defense (grant W81XWH-20-1-0212) and the National Institutes of Health (AI148668).

The study’s DOI is 10.1126/sciadv.adn8963.

Institute News

Pancreatic cancer symposium celebrates 10th anniversary in San Diego

AuthorGreg Calhoun
Date

May 22, 2024

The 2024 PancWest Symposium brought more than 120 scientists to the Sanford Burnham Prebys campus in San Diego to discuss the latest advances in pancreatic cancer research.

More than 120 pancreatic cancer researchers from the West Coast traveled to San Diego from as far as Vancouver to attend the 2024 PancWest Symposium on May 17. The PancWest Symposium was founded in 2014 to regularly bring the scientific community studying pancreatic cancer together to discuss advances in the field and foster new collaborations.

The PancWest Symposium is held every two years in a different city to showcase expert scientists who are making important contributions to the field of pancreatic cancer research, including tumorigenesis, tumor progression and the discovery of novel therapeutic paradigms, such as immunomodulation and metabolic targeting.

The 2024 event was held on the Sanford Burnham Prebys campus in the Fishman Auditorium and was hosted by Cosimo Commisso, Ph.D., director of, and associate professor in, the Institute’s Cancer Metabolism and Microenvironment Program; and Pamela Itkin-Ansari, Ph.D., adjunct professor in the Institute’s Development, Aging and Regeneration Program.

“While pancreatic cancer accounts for only three percent of cancer cases, it has the highest mortality rate among major cancers and is the third leading cause of cancer-related death in the U.S.,” says Commisso.

PancWest Symposium poster presentations in Chairmen's Hall

The symposium’s events included a keynote address, 12 featured speakers, a poster session and a series of “power talks” providing attendees a chance to hear two-minute oral presentations from selected poster presenters.

“Unless we find ways to better diagnose and treat this disease, it is projected to become the second most deadly cancer in less than 20 years,” adds Itkin-Ansari. “That is why events such as PancWest are so important to enhance innovation and foster collaboration.”

Rosalie C. Sears, Ph.D., professor of Molecular and Medical Genetics, co-director of the Brenden-Colson Center for Pancreatic Care and Krista L. Lake Chair in Cancer Research at Oregon Health & Science University in Portland, gave the symposium’s keynote address.

Additional events at the symposium included 12 featured speakers, a poster session and a series of “power talks” providing attendees a chance to hear two-minute oral presentations from selected poster presenters.

“Being a part of PancWest has been a transformative experience,” shares Itkin-Ansari. “The exchange of groundbreaking research and innovative ideas among leading experts advanced our scientific understanding.”

“It also paved the way for new therapeutic strategies, ultimately offering hope and improved outcomes for patients battling pancreatic cancer,” adds Commisso.

More information about the symposium and featured speakers is available on the event’s webpage.