Students Summer in Oncology at Anderson Research (SOAR) 2025
 

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Description

In pursuit of identifying new potential targets for immunotherapy, there has been renewed focus on Oxidative Phosphorylation (OxPhos) metabolism that cancers rely on for growth and, to some degree, immune suppression. Previous research has shown selective deletion of the mitochondrial Complex I (CI) subunits Ndufs4 and Ndufs6 increases the efficacy of immunotherapy through induction of genes related to MHC class-I expression leading to improved tumor antigen presentation. Based on these studies, we hypothesize that selectively targeting CI subunits differentially expressed in tumor cells versus immune effector cells will significantly hinder tumor cell viability and growth without compromising anti-tumor immunity.

Program Affiliation

Med Student SOAR Program

Publication Date

8-2025

Publisher

The University of Texas MD Anderson Cancer Center

Keywords

immunology, cancer immunotherapy, cancer biology and cancer research

Differential Inhibition of Tumor Oxidative Metabolism while Sparing T Cells through a Novel Genetic Approach

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