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Completed TRAINING, INDIVIDUAL NIH (US)

Contributions of SETD2 mutations in clear cell renal cell carcinoma (ccRCC)

$191.5K USD

Funder NATIONAL CANCER INSTITUTE
Recipient Organization Ut Southwestern Medical Center
Country United States
Start Date Apr 16, 2021
End Date Aug 31, 2024
Duration 1,233 days
Number of Grantees 1
Roles Principal Investigator
Data Source NIH (US)
Grant ID 10812323
Grant Description

Project Summary Cancer epigenetics has driven a surge of research in recent years as several chromatin- associated factors have been identified in the process of tumorigenesis. A critical chromatin- modifying protein involved in active transcription, SETD2, has been found to be mutated in approximately 15% of clear cell renal cell carcinomas (ccRCCs). ccRCC patients have shown

resistance to both chemotherapy and conventional radiation therapies, and although major therapeutic advances have been made, only a fraction of patients shows durable clinical responses and long-term remission; thus, there is an urgent need for novel therapies in the field. Typically, SETD2 mutations are grouped as functionally identical; however, they can be

grouped according to their structural or enzymatic characteristics. This project seeks to answer the question of how the loss of SETD2 protein is molecularly distinct from loss of its enzymatic activities. The first aim will use ChIP-seq and biochemical studies to determine the relationship between SETD2 mutation and differential chromatin dysregulation and to elucidate the particular

mechanism in which another protein or peptide fragment acts aberrantly in the absence of SETD2. The second aim will use ChIP-seq and cellular studies to determine how distinct molecular mechanisms of SETD2 mutations in the context of ccRCC results in differential ccRCC development and progression. The multi-disciplinary environment in the Banaszynski laboratory fosters collaboration

amongst diverse scientists and trainees benefit from the guidance of Dr. Banaszynski and established scientists in the Green Center for Reproductive Biology. By the end of this training fellowship period, I will accomplish four goals, I will : 1) become a disciplined experimentalist, 2) gain ownership of my data, 3) grasp a thorough understanding of the foundational and current

literature that shapes the field of cancer biology, and 4) be an effective scientific communicator and leader.

All Grantees

Ut Southwestern Medical Center

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