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Active OTHER RESEARCH-RELATED NIH (US)

Tumor-Immune Interactions and Cisplatin Resistance in Bladder Cancer

$2.11M USD

Funder NATIONAL CANCER INSTITUTE
Recipient Organization Brigham and Women'S Hospital
Country United States
Start Date Sep 01, 2024
End Date Aug 31, 2029
Duration 1,825 days
Number of Grantees 1
Roles Principal Investigator
Data Source NIH (US)
Grant ID 10985089
Grant Description

Project summary This K08 Career Development Award proposal for Dr. Filipe de Carvalho describes a research plan and career development program leading up to an academic career as an independent Urologic Oncologist surgeon- scientist investigator. Dr. De Carvalho is a urologist at Brigham and Women’s Hospital committed to an

independent research career focused on accelerating the development of therapeutic strategies to target the immune-suppressive tumor microenvironment in bladder cancer. This Career Development award will allow Dr. De Carvalho to become proficient in tumor-associated macrophage biology in bladder cancer with the ultimate

goal of developing novel macrophage-directed therapeutic strategies for bladder cancer patients. Dr. De Carvalho will be mentored by Dr. Eliezer Van Allen and co-mentors Drs. Kent Mouw and Elizabeth Mittendorf, leaders in bladder cancer genomics and cancer immunology. Dr. Van Allen is Chief of Division of Population

Sciences, Dana-Farber Cancer Institute, and has mentored over a dozen of young investigators that moved to successful independent academic positions. Dr. De Carvalho also gathered an outstanding scientific advisory committee and collaborators that excel in mouse models, statistics and cancer genomics to guide career

development and scientific progress. The research proposal focuses on tumor-associated macrophages, which are immune cells with a critical role in tumor growth and immune evasion. Recent evidence revealed a therapy-induced conversion of normally anti-tumor TAMs to a tumor-permissive phenotype. The central hypothesis is that cisplatin induces chronic

immunosuppressive IFN signaling in cancer cells leading to a TAM-infiltrated phenotype and immune evasion in treatment-resistant tumors. The central hypothesis will be tested by pursuing two specific aims: 1) Determine the mechanism and effectiveness of targeting TAMs to improve sensitivity of bladder cancer to combined cisplatin

and immune checkpoint inhibition. 2) Dissect the tumor-TAM crosstalk that mediates cisplatin resistance. These studies are expected to dissect how TAMs inhibit cytotoxic T-cells in cisplatin-resistant bladder cancer in territories of immune evasion across bladder tumors as well as position Dr. De Carvalho to submit a competitive

R01 near the completion of this Award.

All Grantees

Brigham and Women'S Hospital

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