Chemical Biology lab @HarvardMed and @DanaFarber. We use a multidisciplinary approach to study biological roles of epigenetic proteins & transcription factors.
Thank you, @ADurbinLab. It is fascinating to learn more cancer biology together with you and your team. We will work together to find the cures for pediatric cancers. Thanks for @curingcancer@AlexsLemonade@TheVFoundation for all the support.
It is so exciting to build the understanding of the function differences between EP300 and CBP, which can be applied to target specific therapy development.
This was a major effort between the @Adurbinlab@TheAbraLab@JunQiLab and the Ory labs. We pick up on a long-term interest of our labs: the attractive target, EP300. EP300 is a great cancer target because while many tumor cells require it, they often may not need its paralog CBP
So exciting to have this paper online @JExpMed . thanks for the wonderful collaboration with @ADurbinLab@TheAbraLab, Ory lab. Congratulations on all the team members.
@FilbinMariella, MD, PhD, studies childhood brain cancers by directly studying the tumors of the patients she treats. By understanding the biology of these cancers, she is discovering new strategies to treat them. Learn more about her work here: https://t.co/pjRseQ4vGp
A new study from @DanaFarber reports the first potent and selective compound to target IRF4 and validates degradation of IRF4 as a potential approach to the treatment of #MultipleMyeloma.
🔎 See the abstract from Drs. @JunQiLab and @IrenemGhobrial: https://t.co/XztBqvmRLt
Thrilled to share our collaborative work with @FilbinMariella, now online in Neuro-Oncology! We identify HDAC2 as a tractable target for H3K27M DMG growth in vitro and in vivo. Congrats to @JunQiLab and @FilbinMariella — excited for more to come together!
https://t.co/s7wx4fwcxR
Thrilled to share our collaborative work with @FilbinMariella, now online in Neuro-Oncology! We identify HDAC2 as a tractable target for H3K27M DMG growth in vitro and in vivo. Congrats to @JunQiLab and @FilbinMariella — excited for more to come together!
https://t.co/s7wx4fwcxR
Our study demonstrated that IRF4 can be chemically targeted. Our approach can be further developed into novel therapy for multiple myeloma.
https://t.co/oy60hATb5a
Please support our drug discovery effort for high risk tagets @JunQiLab at @DanaFarber. https://t.co/3wy9UuF0o9
Our collaborative work with @IrenemGhobrial on targeting transcription factor IRF4 is now online @nchembio. It is so exciting that we discovered an IRF4 binder & a selective IRF4 degrader that can interrupt MM cell growth. Congrats @10mM_Mike & all authors https://t.co/RJFu6wqJsU
Our collaborative study with Dr. Qiong Duan on histone acetylation regulated energy storage is now published @MolMetab. We established more understanding on how "active" acetylation vs "passive" acetylation balanced each other at different states. https://t.co/p7c8jju8vw
Hope is powerful. Research is lifesaving. 🙏
Your support helps fund groundbreaking discoveries for children battling cancer.
Read how it’s making a difference in our latest edition of Research Outcomes: https://t.co/1ZhjvSdu8A
With better understanding of proteosome machinery, hopefully, we can come up more and more cool idea to utilize the system for novel therapy development.
New research in @angew_chem by @DanaFarber’s @JunQiLab reveals a novel chemical biology approach to achieving selective targeted protein degradation using proteosome cap region proteins directly in addition to the current PROTAC strategy, which could aid in developing therapies and cancer drugs.
➡️ https://t.co/yoRfR5X0Tv
It was such a fun day to visit @PennMedicine and talk about science with @junwei_s @LilingWanLab and present our science. Thank you for having me.