Valentina Hoyos, M.D.
Associate Professor
Positions
- Associate Professor
-
Center for Cell and Gene Therapy
Lester and Sue Smith Breast Center
Baylor College of Medicine
Education
- MD from Javeriana University
- 12/2006 - Bogota, Colombia
- Postdoctoral Fellowship at Baylor College of Medicine
- 06/2009 - Houston, Texas, United States
- Residency at Baylor College of Medicine/Internal Medicine/MeRIT scholar
- 06/2014 - Houston, Texas, United States
- Clinical Fellowship at Johns Hopkins University/Oncology
- 06/2017 - Baltimore, Maryland, United States
Certifications
- Board certified internal medicine
- American Board of Internal Medicine
- Board certified medical oncology
- American Board of Internal Medicine
Professional Statement
I am a physician-scientist involved in research focused on improving cellular immunotherapies for the treatment of cancer. During my research training, I acquired the skills necessary to design viral vectors to genetically manipulate cells for the generation of novel cancer treatments. My clinical interests lie in treating patients with breast cancer, and my current research goal is to develop effective T cell therapies against new tumor specific targets and incorporate strategies to overcome the hostile breast tumor microenvironment. My long-term goal is to translate these therapies into the clinic to give breast cancer patients the opportunity to benefit from them.
Selected Publications
-
Nalawade SA, Shafer P, Bajgain P, McKenna MK, Ali A, Kelly L, Joubert J, Gottschalk S, Watanabe N, Leen A, Parihar R, Vera Valdes JF, Hoyos V.. " Selectively targeting myeloid-derived suppressor cells through TRAIL receptor 2 to enhance the efficacy of CAR T cell therapy for treatment of breast cancer " Journal for Immunotherapy of cancer. 2021 Nov 9; 11
Pubmed PMID: 34815355. -
Shafer P, Leung WK, Woods M, Choi JM, Rodriguez-Plata CM, Maknojia A, Mosquera A, Somes LK, Joubert J, Manliguez A, Ranjan R, Burt B, Lee HS, Zhang B, Fuqua S, Rooney C, Leen AM, Hoyos V.. " Incongruity between T cell receptor recognition of breast cancer hotspot mutations ESR1 Y537S and D538G following exogenous peptide loading versus endogenous antigen processing. " Cytotherapy. 2024 Mar ; 26 (3) : 266-275.
Pubmed PMID: 38231165. -
Savage SR, Yi X, Lei JT, Wen B, Zhao H, Liao Y, Jaehnig EJ, Somes LK, Shafer PW, Lee TD, Fu Z, Dou Y, Shi Z, Gao D, Hoyos V, Gao Q, Zhang B. " Pan-cancer proteogenomics expands the landscape of therapeutic targets. " Cell. 2024 Aug ; 187 (16) : 4389-4407.
Pubmed PMID: 38917788. -
Chamorro DF, Somes LK, Hoyos V.. " Engineered Adoptive T-Cell Therapies for Breast Cancer: Current Progress, Challenges, and Potential. " Cancers. 2023 Dec ; 26 (16)
Pubmed PMID: 38201551.
Funding
-
CPRIT Scholar
- (10/01/2017 - 10/01/2022)
- Cancer Prevention and Research Institute of Texas
-
ESTROGEN RECEPTOR 1 MUTATION (ESR1M) SPECIFIC T CELLS FOR THE TREATMENT OF HORMONE RECEPTOR POSITIVE METASTATIC BREAST CANCER
- (11/01/2019 - 11/01/2022)
- Grant funding from Susan G. Komen Career Catalyst Research Grant
Languages
Spanish
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