Lecture preview | professor zhou aidong: brain tumor immune microenvironment and treatment resistance

Release time:2024-04-24

academic frontiers | preview of the 22nd lecture

 

 

lecture title

"brain tumor immune microenvironment and treatment resistance"


lecture time

april 26, 2024 (friday)

15:00-16:00


lecture location

conference room 301, building 5, jinfeng laboratory


keynote speaker

professor zhou aidong


 

introduction to the keynote speakers

professor zhou aidong, professor and doctoral supervisor of the school of basic medicine of southern medical university, guangdong’s “pearl river talent” program and southern medical university’s top-level talent introduction. he has been engaged in scientific research in the neurosurgery department of md anderson cancer center for many years, mainly engaged in primary glioblastoma and research on the mechanism and translation of brain metastasis in lung cancer/breast cancer. he has published multiple research papers as the corresponding author or first author in journals such as nat cell biol, pnas, adv sci, cell reports medicine, etc., and has been cited more than 3,000 times (including science, cell, nat med and other journals). he serves as a member of the neuro-oncology branch of the chinese neurological society, a standing committee member of the neuro-oncology branch of the guangdong society of precision medicine, and a standing committee member of the metastasis branch of the society of precision medicine. he has presided over a number of research projects at the national natural and provincial and ministerial levels.

 

lecture summary

 

tumor cells use multiple mechanisms to escape immune system attack and establish a microenvironment conducive to their own survival and proliferation. the team is committed to revealing the regulatory mechanism of the immune microenvironment of brain tumors: in glioblastoma (gbm), it was found that co-amplification of the epidermal growth factor (egfr) adjacent gene sec61g can inhibit anti-tumor immune activity, leading to egfr amplification in gbm. immune escape , providing new immunotherapy targets and combination treatment strategies for gbm; in lung cancer/breast cancer brain metastases, hsp47 was found to promote microglial m2 polarization and immunosuppression by mediating collagen deposition, providing a solution for brain metastases. potential treatment avenues.



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