Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Rongqing Pan, Ph.D.

Title
Institution
Department
Address
Phone
Profile Picture

Biography
MD Anderson Cancer Center, HoustonPh.D.Cancer Biology
Harvard Medical School/DFCI, BostonPostdoc FellowCancer
2017
Alfred G. Knudson, Jr. Best Dissertation Award (Finalist, 2nd place)
2017
Steve Lasher and Janiece Longoria Graduate Student Research Award in Cancer Biology
2015
Presidents’ Research Scholarship
2015
AAAS/Science Program for Excellence in Science
2015
Andrew Sowell-Wade Huggins Endowed Scholarship
2015
Abstract Achievement Award
2014
Abstract Achievement Award
2014
Chinese Government Award for Outstanding Students Abroad
2015 - 2013
Graduate School GSBS Travel Award (three times, 2015, 2014, 2013)

Overview
I joined the Letai lab after completing my PhD in Cancer Biology at MD Anderson Cancer Center. My dissertation research focuses on targeting mitochondrial apoptotic pathways and overcoming cancer cell resistance. We demonstrate that targeting mitochondrial apoptosis is an effective approach to kill resistant tumor bulk cells and stem cells (Pan, et al., Cancer Discovery 2014; Pan, et al, Blood 2015). Our work demonstrates that AML cells are dependent on Bcl-2 for survival, which forms the basis for a multi-center trial of ABT-199/venetoclax in relapsed and refractory AML.

In a following project (Pan, et al., Cancer Cell 2017), We demonstrate that resistance to Bcl-2 inhibition can result from acute induction of Mcl-1 or chronic upregulation of Mcl-1, but p53 activation can effectively overcome Mcl-1-mediated resistance. Mechanistically, p53 activation regulates MAPK/GSK3 signaling to regulate Mcl-1 phosphorylation and promote its proteasomal degradation. Surprisingly, we find that p21 (highly induced upon p53 activation) triggers reversible G1-arrest to protect cancer cells from apoptosis. Nevertheless, Bcl-2 inhibition can overcome this resistance by switching the cellular outcomes of p53 activation from pro-survival G1-arrest to apoptosis. Taken together, Bcl-2 inhibition and p53 activation reciprocally overcome leukemia resistance to either strategy alone. The combinatorial strategy also has unprecedented efficacy in several mouse models of drug resistance and has been translated into a phase II trial at 19 cancer centers in US, Canada, France, and Italy. I have also gained expertise in various molecular techniques and developed a marker-recyclable method for repetitive genome editing in yeast (Pan, et al., FEMS Yeast Research, 2011).

Immune system is a powerful arsenal to fight against cancers. There are several intriguing overlaps between cancer immunotherapy and targeting mitochondrial apoptosis. Here lies my interest and I believe that combining these two emerging therapeutic approaches, that potentially complement each other, holds great promise for cancer treatment.

In my spare time, I enjoy running, cooking, good music, movies, and most importantly, playing Ping Pong!

Click HERE for my PubMed.
https://www.ncbi.nlm.nih.gov/pubmed?term=(Rongqing%20Pan)%20OR%20Rong-qing%20Pan
Click HERE for my LinkedIn.
https://www.linkedin.com/in/aaronrpan

Bibliographic
Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
Newest   |   Oldest   |   Most Cited   |   Most Discussed   |   Timeline   |   Field Summary   |   Plain Text
PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
Updating...
This operation might take several minutes to complete. Please do not close your browser.
Local representatives can answer questions about the Profiles website or help with editing a profile or issues with profile data. For assistance with this profile: HMS/HSDM faculty should contact contactcatalyst.harvard.edu. For faculty or fellow appointment updates and changes, please ask your appointing department to contact HMS. For fellow personal and demographic information, contact HMS Human Resources at human_resourceshms.harvard.edu. For faculty personal and demographic information, contact HMS Office for Faculty Affairs at facappthms.harvard.edu.
Pan's Networks
Click the
Explore
buttons for more information and interactive visualizations!
Concepts (55)
Explore
_
Co-Authors (8)
Explore
_
Similar People (60)
Explore
_
Same Department 
Explore
_
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.