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Identify the role of RNA-binding protein in activating anti-tumor immunity by directly decaying PD-L1-3'UTR

Research Project

Project/Area Number 23KJ1296
Research Category

Grant-in-Aid for JSPS Fellows

Allocation TypeMulti-year Fund
Section国内
Review Section Basic Section 49070:Immunology-related
Research InstitutionKyoto University

Principal Investigator

RONG XINGYU  京都大学, 医学研究科, 特別研究員(DC2)

Project Period (FY) 2023-04-25 – 2025-03-31
Project Status Granted (Fiscal Year 2023)
Budget Amount *help
¥2,000,000 (Direct Cost: ¥2,000,000)
Fiscal Year 2024: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 2023: ¥1,000,000 (Direct Cost: ¥1,000,000)
Outline of Research at the Start

In this study we carried out a well-designed CRISPR screening in which we transduced the cells with PD-L1-3’UTR. In this case, we can find out the RNA-binding proteins which can directly decay PD-L1 mRNA, which so far remains elusive. We will investigate the underlying mechanism of how the candidate RBP delays PD-L1 mRNA, and provide new insights into regulation of RBPs in anti-tumor immunity. So far, clinical research has proven that only few strategies may be efficient in reducing PD-L1.We will provide a novel therapeutic strategyto promote the efficacy of immunotherapy to tumor patients.

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Published: 2023-04-26   Modified: 2023-07-24  

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