Excited to share our latest preprint, a wonderful collaboration w/ Matt Freedman and Sylvan Baca’s labs. Leveraging cfChIP-seq from patient plasma functional mouse modeling, we uncover how TF subtype shapes response and resistance to tarlatamab in SCLC.
biorxiv.org/content/10.64898…
Our latest collaboration with #MattFreedman and @Oser_Lab on resistance to tarlatamab: biorxiv.org/content/10.64898…. An exciting framework for studying cancer resistance: observations from patients using epigenomic #LiquidBiopsy -> functional validation in mouse models.
It was wonderful visiting the Northwestern BMG Department today and learning about all the outstanding science going on here. Thank you @LuWangLab for the invitation!
Excited to share our new work in Dev Cell (authors.elsevier.com/a/1lg4l…), led by my highly talented postdoc Deli Hong! We find that loss of NOTCH2 creates a dependency on TRIM28, highlighting TRIM28 as a potential therapeutic target in NOTCH2-deficient or low-NOTCH2 SCLC.
Thrilled to share our new work published in Nature (rdcu.be/eBCM0). We report an exciting new potential therapeutic strategy with a fascinating mechanism of action for cancers with a compromised G1–S cell cycle checkpoint, including SCLC.
nature.com/articles/s41586-0…
This study was led by my highly talented postdoctoral fellow Shilpa Singh and was an outstanding collaboration with Circle Pharma and Deepak Nijhawan's lab at UTSW. @DanaFarberNews@DFarberThoracic.
🧩 New paper out in Nature Communications!
"Unveiling the hidden interactome of CRBN molecular glues"
Huge thanks to our incredible team and collaborators who made this possible!
📖 Read the full open-access article here: nature.com/articles/s41467-0…
This is the first year I’m riding the Pan Mass Challenge in 2 weeks! I’m riding in honor of both my parents. It will be a deeply meaningful ride for me. All proceeds go toward cancer research at Dana Farber. Please donate if you can (details/link below) profile.pmc.org/MO0250
Great talk by Dr. Shilpa Singh @Oser_Lab@DanaFarber looking at Cyclin A/B RxL Macrocyclic Inhibitors in SCLC w/ high E2F activity. Beautiful example of bridging lab to clinical research. Phase 1 trial is recruiting. #SCLC25@SclcSMASHERS
I am very excited to announce that I have started my lab at the Brigham and Women’s Hospital and Harvard Medical School in the Department of Pathology. We are seeking talented, curious, individuals and recruiting at all levels! tsailab.bwh.harvard.edu/
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Thoracic oncologist Matt Oser @Oser_Lab, and scientist @CKadoch, @kadochlab at Dana-Farber have discovered a way to stunt the function of a driver of small cell lung cancer. The finding points to a potential treatment (cont) ms.spr.ly/l/6012mpPpQ
I am excited to host Dr. Matt Oser from DFCI @Oser_Lab as our GrandRound speaker next week! Matt is a prominent physician-scientist, a colleague in thoracic oncology, a peer Damon-Runyon investigator, and a dear friend @DamonRunyon@LaurenByersMD@MDAndersonNews@EGFRResisters
Exciting to see our @kadochlab and @Oser_Lab collaborative study focused on mSWI/SNF chromatin remodeling complexes in small cell lung cancer out in @Cancer_Cell! This is one of 4 studies published/soon to be published highlighting the potential for #BAF disruption in SCLC!
Thank you @DanaFarberNews for featuring our new work, a wonderful collaborative effort with @CKadoch@kadochlab, published today in @Cancer_Cell. Congrats to Leslie Duplaquet and Kevin So who together led this study and to computational biologist Alex Ying.
A study in @Cancer_Cell, led by Matthew Oser, MD, PhD (@Oser_Lab) & Cigall Kadoch, PhD (@CKadoch) at @danafarber identify SWI/SNF inhibitors as a potential targeted treatment for POU2F3-positive small cell lung cancer, accounting for 12% of cases.
Study ▶️ ms.spr.ly/6016lRrkI
Thrilled to share our labs latest work, now online @Cancer_Cell where we used positive-selection CRISPR screening to discover that POU2F3 is regulated by the mSWI/SNF complex
cell.com/cancer-cell/fulltex… 1/
Together this study suggests that mSWI/SNF complex inhibition should be tried as a therapeutic strategy for patients with POU2F3-positive SCLC, which are the least responsive SCLC subtype to SOC chemotherapy. 6/
Lastly, thank you to all of our other collaborators as well as our reviewers and editor which greatly improved our paper during the revision process. @DamonRunyon@DanaFarberNews.