Inna Smalley

Inna Smalley

Department of Cancer Physiology, H. Lee Moffitt Cancer Center & Research Institute

Affiliated withH. Lee Moffitt Cancer Center & Research InstituteUniversity of South Florida, H. Lee Moffitt Cancer Center & Research Institute

Research Area

Biography

With over 12 years of experience studying melanoma biology, my research has largely focused on developing novel therapeutic rationales for treating BRAF- and NRAS-mutant melanoma, with an emphasis on the role of the tumor microenvironment in drug resistance. My previous work was dedicated to delineating the mechanisms of drug resistance in BRAF-mutant melanoma that rely on extracellular matrix remodeling and fibroblast activation. My most recent efforts are focused on exploring how intra-tumoral heterogeneity facilitates tumor growth, drug resistance and dissemination, with a special focus on single cell analysis techniques and metabolism-associated signaling. I would like to elucidate what drives tumor cells to certain metastatic sites, including the brain and leptomeninges, as well as the mechanism supporting their survival in different microenvironments. I believe that the future treatment of melanoma lies in personalized, rational drug combinations that will turn a terminal disease into a manageable chronic illness. My career goal is to develop efficacious treatment strategies for patients with CNS metastasis and late-stage disease.

JoVE Journal Publications

ArticleTotal : 2
Year
A Murine Ommaya Xenograft Model to Study Direct-Targeted Therapy of Leptomeningeal Disease
Publication title

Cited by 10

2021
2024

Other Publications

Article
Year
Noncanonical EphA2 Signaling Is a Driver of Tumor-Endothelial Cell Interactions and Metastatic Dissemination in BRAF Inhibitor‒Resistant Melanoma.

The Journal of investigative dermatology| PubMed ID: 32890629

2020
Single-Cell Characterization of the Immune Microenvironment of Melanoma Brain and Leptomeningeal Metastases.

Clinical cancer research : an official journal of the American Association for Cancer Research| PubMed ID: 34035069

2021