Director NCI-designated Cancer Genome and Epigenetics Program at SBP, Co-Editor-in-Chief Aging Biology Journal, Road/Gravel/Mtn Cycling, Wolf Pack Cycling.

San Diego, CA
New road bike. S-WORKS Tarmac SL7, Campy SR wireless and disc, Campy Bora Ultra WTO wheels👍 No excuses now😧
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Peter Adams🇪🇺🇺🇳 retweeted
🔥 We’re hiring! 🔥 My lab is seeking a postdoctoral fellow for studying the role of metabolic imbalance in aging, cancer and neurodegeneration @jobRxiv @mitojobs @ScienceCareers #hiring #metabolism #massspectrometry Join us!
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Agree this is a great synthesis - and I think can likely be applied to other aging disease mechanisms in other tissues; for example, pathology caused by senescent cells, inflammation…….can also apply to interactions between multiple “hallmarks of aging”
A brilliant new @Nature synthesis of what we know about Alzheimer's disease pathogenesis, which is non-linear, with discrete phases (Figure), and notable inflection and transition points. Also helps to explain why symptoms do not correlate with underlying pathology. nature.com/articles/s41586-0…
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Peter Adams🇪🇺🇺🇳 retweeted
Tumors don’t evolve alone. 📣 New @GenomeBiology Collection on the Tumor Microenvironment: single-cell, spatial & multi-omic studies of how the TME shapes tumor evolution and therapy response. Guest eds: @IamLinghua @kchenken & me 🗓️ until 19 May 2027 link.springer.com/collection…
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Peter Adams🇪🇺🇺🇳 retweeted
🚨New preprint from the lab!🚨 LINE-1 (L1) #transposons become transcribed with #aging and #senescence, and are thought to contribute to #inflammaging. But what happens to a healthy, non-senescent human cell when #L1 turns on? biorxiv.org/content/10.64898… A 🧵, 1/7 @USCLeonardDavis
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Excellent article, Alan! The focus on mutations in cancer and the difficulty of their early detection which you discuss has contributed to the focus on advanced cancers. But there are many causes of cancer in aging, not only mutations - so more opportunities for prevention.
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Fascinating discussion with Julia Belk and my @sennetresearch colleague Nathan Zemke on age- dependent replacement of brain microglia. Consequences not clear to me though. Nathan et al seem to suggest detrimental, but Julia et al protective from Alzheimer’s. Both, perhaps?
Around age 50 your blood monocytes (Micro 2) begin a "hostile takeover" replacement of your brain microglia immune cells (Micro 1) and can promote inflammation. Two impressive studies made this remarkable discovery independently with different methods. In conversation with their lead authors, @juliabelk and Nathan Zemke erictopol.substack.com/p/two…
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This inflammatory function can be inhibited with FDA approved drugs, palbociclib and abemaciclib, suppressing frailty and improving function of old mice.
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This looks like a great meeting!
Speakers also include Sir Tony Kouzarides, Coleen Murphy, Gio Silva Garcia, @senergystic, Ali Shilatifard, @AdamsBioAging @Yael_David__ Francois Fuks, and more! #Epigenetics #Aging
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Michael Alcaraz, a very talented PhD student, led this study showing that NAMPT activation uncovers a senescence-specific vulnerability and promotes healthy aging in combination with NAM. Small molecule NAMPT activator to boost NAD+, identified at SBP. biorxiv.org/content/10.64898…
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It has been a pleasure and privilege to contribute to SenNet for the last 4 years; to participate in a true collaborative effort to build a landmark resource that is changing the way we think about cell senescence. I'm excited to read this growing collection of articles.
✨The SenNet program aims to map and characterize senescent cells across age, tissue, and species. Discover research and opinion emerging from the SenNet project in a new cross-journal collection in the Nature portfolio ✨nature.com/immersive/s43587-…
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I’m pleased to share this new study in @Nature led by Joao Passos and Helene Martini @MayoClinic “Mitochondrial metabolism and epigenetic crosstalk drive SASP”. An integration of two of the many signals reported to drive SASP. rdcu.be/fwGTf
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Interesting and inspiring…….Patrick Hsu: How Is AI Catalyzing Life Science? erictopol.substack.com/p/how…
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Peter Adams🇪🇺🇺🇳 retweeted
Tomorrow, the @HouseCommerce Subcommittee on Health will examine how the @US_FDA can maintain America's leadership in biomedical innovation and strengthen U.S. drug development. Modernizing the regulatory framework is essential if we want to accelerate innovation, maintain our competitive edge in the biomedical sector, and ensure patients have access to the next generation of treatments. A4LI has submitted a letter for the hearing record urging Congress to consider our Multi-Disease Therapeutic Designation (MDTD) proposal: a regulatory pathway designed to better support therapies that target the underlying biology of aging and reduce the burden of multiple chronic diseases. 📄 Read our MDTD proposal here: a4li.org/wp-content/uploads/… We are thrilled to see Congress continuing this important conversation about the future of biomedical innovation, and we look forward to hearing expert perspectives on how the FDA can help foster this next generation of medical breakthroughs. ▶️ The full hearing can be livestreamed here: piped.video/watch?v=sTL86njN…
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Inspirational conversation with @BriannaStubbs @BuckInstitute Basic scientists can really translate work. Raises the “heretical” idea that benefits of exercise are reverse causation and socioeconomic. @metapredict will like. I’m still not convinced, but we have to question dogma
One of the biggest challenges in longevity science isn't discovering interventions that might slow aging. It's figuring out how to prove they work in people. In Part 2 of my conversation with Dr. Brianna Stubbs, scientist at the Buck Institute for Research on Aging, we explore what may be one of the most important—and least discussed—frontiers in geroscience: building the clinical research infrastructure needed to bring aging-targeted therapies into mainstream medicine. Brianna leads an impressive portfolio of clinical studies spanning ketones, frailty, exercise, metabolism, AI-driven biomarkers, and aging measurement. We also discuss several ambitious ARPA-H initiatives aimed at creating a regulatory pathway for gerotherapeutics. Some of the topics we cover include: 🔹 How should we measure biological aging in clinical trials? 🔹 What is "intrinsic capacity," and could it become a new clinical endpoint? 🔹 Can wearables and AI improve how we assess aging? 🔹 What will it take for the FDA to approve therapies that target aging biology? 🔹 Why clinical trial design—not just drug discovery—may determine the future of longevity medicine. One of the themes that emerges throughout our discussion is that progress in longevity medicine won't come from a single breakthrough molecule. It will also require better biomarkers, smarter clinical trials, new regulatory frameworks, and collaboration between basic scientists, clinicians, data scientists, regulators, and industry. These aren't the topics that usually make headlines, but they may ultimately have the greatest impact on whether geroscience fulfills its promise. 🎥 Watch the full conversation here: piped.video/watch?v=kM6wL5dC…
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Intersection of two fascinating areas - potential benefit of p16+ cells and pathogen clearance vs tolerance……….p16High immune cells control disease tolerance as a defense and health span-extending strategy: Immunity cell.com/immunity/fulltext/S…
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