Aging and Regeneration Archives - Sanford Burnham Prebys
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Top Sanford Burnham Prebys research stories of 2021

AuthorSusan Gammon
Date

December 14, 2021

This year’s most popular research stories include scientific breakthroughs in COVID-19, cancer, schizophrenia and more.

As we bid farewell to 2021, let’s celebrate our most newsworthy research breakthroughs. Despite the continuing challenges brought on by COVID-19, Sanford Burnham Prebys achieved important milestones on the frontiers of biomedical science.

The following 10 research-related stories received top views on Newswise—the press release distribution service for journalists seeking health and science news.
 

  1. COVID-19: Scientists identify human genes that fight infection


    A research team was able to pinpoint specific human genes that control viral infection. The information sheds new light on factors that lead to severe disease and guides therapeutic options.
     
  2. Tumor marker may help overcome endocrine treatment-resistant breast cancer


    The study discovered a new approach to select breast cancer patients for HER2 therapy and could help individuals avoid disease relapse or progression of endocrine-sensitive disease.
     
  3. Scientists identify potential drug candidates for deadly pediatric leukemia


    Two existing drugs—JAK inhibitors and Mepron—show promise for a subtype of acute myeloid leukemia (AML) that is more common in children. The drugs are proven safe in humans, which could accelerate clinical studies.
     
  4. Leprosy drug holds promise as at-home treatment for COVID-19


    Scientists found that the leprosy drug clofazimine, which is FDA approved and on the World Health Organization’s List of Essential Medicines, exhibits potent antiviral activities against SARS-CoV-2, and could become an important weapon against future pandemics.
     
  5. Researchers dig deeper into how cells transport their waste for recycling


    Research describing how the “trash bags” in a cell—called autophagosomes—are tagged for recycling opened new paths to understand age-related diseases such as cancer and neurological disorders.
     
  6. New drug combination shows promise as powerful treatment for AML


    Researchers identified two drugs that are potent against acute myeloid leukemia (AML) when combined, but only weakly effective when used alone. The study provides a scientific rationale for advancing clinical studies of the drug combination.
     
  7. Biomarker could help diagnose schizophrenia at an early age


    A study described how elevated levels of a protein called CRMP2—found in the brain and blood—could become a format for a rapid, minimally invasive blood test to support the diagnosis of schizophrenia.
     
  8. Scientists identify “immune cop” that detects SARS-CoV-2


    Researchers discovered the sensor in human lungs that detects SARS-CoV-2 and signals that it’s time to mount an antiviral attack. The sensor activates interferon, the body’s own frontline defender against viral invasion.
     
  9. Study finds promising therapeutic target for colitis


    Scientists identified an enzyme in the gut that triggers an inflammatory cascade leading to colitis. Therapeutically targeting the enzyme may be a viable approach to help the millions of people worldwide affected by the disorder.
     
  10. Scientists shrink pancreatic tumors by starving their cellular “neighbors”


    For the first time, blocking “cell drinking,” or micropinocytosis in the thick tissue surrounding a pancreatic tumor, was shown to slow tumor growth—providing more evidence that micropinocytosis is an important therapeutic target.
Institute News

SBP Collaborates with NIH’s Translational Science Center on pancreatic cancer

Authorsgammon
Date

October 13, 2015

The National Center for Advancing Translational Sciences (NCATS) has initiated a novel collaborative study with Pamela Itkin-Ansari, PhD., to screen for drugs that reprogram pancreatic cancer cells back to a normal, non-threatening phenotype. The collaboration is based on Itkin-Ansari’s research and development of a screening platform to find drugs that induce the overexpression of E47, a protein that binds to specific DNA sequences, causing cells to differentiate to acinar cells—cells with normal pancreatic cell traits and characteristics.

Continue reading “SBP Collaborates with NIH’s Translational Science Center on pancreatic cancer”

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Unraveling the mystery of muscle regeneration could lead to effective treatment for muscular dystrophies

Authorsgammon
Date

September 22, 2015

By shedding light on the distinct functions of a protein complex that controls the formation of skeletal muscle tissue, SBP researchers could pave the way for the development of novel therapies for neuromuscular diseases.

Continue reading “Unraveling the mystery of muscle regeneration could lead to effective treatment for muscular dystrophies”

Institute News

Q&A with MS patient advocate Denise Boucher

Authorrbruni
Date

May 21, 2015

Denise Boucher is a vibrant, gregarious, and engaging individual, with an easy smile and a quick wit. When you meet her the for the first time and feel her infectious energy, it’s hard to imagine that she has endured a nearly 20-year long battle with multiple sclerosis (MS) that has taken most of her sight and her ability walk.

Despite these challenges, Denise does not let MS stop her from living life on her terms. She is an active, passionate MS advocate who spends her time educating others about the degenerative disease and supporting fellow survivors.

On March 24, Denise visited the Institute’s La Jolla campus for the very first time as part of the National Multiple Sclerosis Society’s (NMSS) MS Awareness Month to learn more about how our researchers are making advancements in the fight against this immune-mediated disease.

We sat down with her after her visit to hear some highlights from her time at the Institute.

Q: Tell us a little about yourself and how you became a research advocate for MS?

A: When I was 25, I moved to Arizona to continue my dream career in advertising. Suddenly, strange things began to happen, including numbness on one side of my body and later blindness in one eye.

My eyesight, which I’d never had any problems with before, was becoming an increasing issue. I later learned that this is a common early symptom for MS patients. It progressed very quickly from there and it wasn’t long before my doctors diagnosed me with MS. Shortly after, I lost most of the vision in my other eye.

It’s hard to explain what a diagnosis like that means to you when you’re 25, but I tried to keep moving forward with my life and not let it derail my career, or impact my ability stay positive and enjoy my life. After a while, my symptoms progressed and I knew that things had to change. I managed to continue working in advertising for many years, but after 21 years I ended my career to focus on my health.

It was a very difficult time, to say the least, but I made the best of it. I became an advocate along the way to help others in a similar situation and share what I’ve learned with them. It’s my way to give back, stay active, positive, and move forward with my life.

Q. When you hear about research happening at Sanford-Burnham, what does it mean to you?

A. When I was first invited to join the MS tour I was so, so excited. This was really an opportunity of a lifetime, in my opinion, to visit with scientists and learn more about what they do and the impact that they could have on potential treatments.

Just being at Sanford-Burnham and seeing what’s going on lets me know that the future will be easier for others. Seeing the dedicated scientists at Sanford-Burnham and hearing their passion for curing this disease, fills me with hope. And that means a lot.

Q. What were some of your takeaways from your visit to the Institute?

This visit meant more than I ever expected. Truthfully. You read and hear about research, but you rarely have the opportunity connect what scientists are doing to the potential end result. When you’re here on campus, talking to the scientists—who are so passionate about their work—it becomes much clearer how their research is directly correlated to future medicines.

I was also blown away by how collaborative the Institute is. I had no idea how many different departments work together with so many different specialties in order to make the discoveries that they do. The whole visit was incredibly enlightening.

Q. Why do you support early-stage research, like Dr. Ranscht’s? Dr. Ranscht is an incredible woman and her passion for curing MS is palpable. She cares and is dedicating her life to finding innovative new approaches to tackling this disease. How could I not support that?

Without people and research like hers, the next big discovery won’t be found and next-generation medicines can’t be developed. Early-stage research is imperative to our future.

 

If you would like to arrange a visit to the Institute to learn more about our research, please contact Sandy Hanna at Shanna@sanfordburnham.org, or call 858-795-5056.

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Discovery of new role of SOX2 protein sheds light on neurogenesis in the adult brain

Authorsgammon
Date

April 21, 2015

 

Newborn neurons generated from neural progenitor cells in a brain region called the hippocampus play an important role in learning and memory in adults. However, the molecular mechanisms that control this neurogenesis process have not been fully understood. Sanford-Burnham researchers recently shed new light on this question by discovering a key role of a protein called SOX2 in neuronal development. As reported online in Proceedings of the National Academy of Sciences, SOX2 promotes the activation of genes involved in differentiation, enabling neural progenitor cells to turn into mature neurons in the brains of adult mice. Continue reading “Discovery of new role of SOX2 protein sheds light on neurogenesis in the adult brain”

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New insights into how the heart forms may help identify heart defects

AuthorGuest Blogger
Date

September 29, 2014

This is a post by our guest writer Janelle Weaver, PhD

The formation of the heart during development is a highly complex process that requires precise coordination between cells and molecular signaling pathways. The fruit fly has been widely used for studying the underlying cellular and molecular mechanisms, and a great deal is known about how the fate of heart cells is controlled by signaling pathways and transcription factors—proteins that control gene activity. But beyond that, events that regulate heart formation have not been clear. Continue reading “New insights into how the heart forms may help identify heart defects”