Investigator

Courtney A. Penn

Associate Fellowship Director, Gynecologic Oncology · Vanderbilt University Medical Center, Obstetrics and Gynecology

CAPCourtney A. Penn
Papers(2)
Current Issues in the…The Impact of …
Collaborators(10)
Dandi HuangEmanuel PetricoinErica V. CarballoJacey L. MarshallJulia A. SteeleJulia D. WulfkuhleJustin M. BalkoKatherine KleinbergPaula Gonzalez-Ericss…Rosa I. Gallagher
Institutions(4)
Vanderbilt University…Cedars Sinai Medical …George Mason Universi…Vanderbilt University

Papers

The Impact of JAK1 Pathogenic Variants and MHC-I Expression on Response to Immune Checkpoint Inhibition in Endometrial Cancer

Abstract Purpose: Immune checkpoint inhibitors (ICI) have increasing application in endometrial cancer, underscoring the need for robust biomarkers for patient selection. JAK1 pathogenic variants (PV) have previously been implicated in immune evasion. In this study, we identify biomarkers predictive of ICI response in endometrial cancer and the implications of JAK1 PVs in this context. Experimental Design: This is a translational study of tumors from 84 patients with endometrial cancer treated with ICIs. High-throughput proteomic-based profiling was used to quantify 193 phosphoprotein/protein expression levels, including key JAK/STAT signaling pathway components. Associations with clinical outcomes were assessed using multivariate regression analysis. The functional consequences of JAK1 PVs were explored through in vitro signaling assays and analyses of The Cancer Genome Atlas database. Results: MHC-I expression correlated with improved progression-free survival (P = 0.035), validated in orthogonal approaches. Notably, a subset of patients harboring JAK1 PVs demonstrated exceptional survival on ICIs. In The Cancer Genome Atlas cohort of microsatellite instability–high and DNA polymerase epsilon–mutated tumors, homozygous loss of JAK1 trended toward decreased survival, whereas heterozygous loss of JAK1 was associated with significantly improved survival (P = 0.026), suggesting partial retention of antigen presentation pathways. Among our ICI-treated microsatellite instability–high tumor samples, NK cell marker NCAM1 was associated with improved survival (P = 0.02). Conclusions: These data support MHC-I as a potential predictive biomarker for ICI response in endometrial cancer. Additionally, we show that partial retention of JAK1 signaling in JAK1 tumors with heterozygous loss is associated with improved survival, potentially attributable to enhanced NK cell activity in tumors with low MHC-I expression.

10Works
2Papers
18Collaborators
Endometrial NeoplasmsTumor EscapeOvarian NeoplasmsCarcinoma, Ovarian Epithelial

Positions

2025–

Associate Fellowship Director, Gynecologic Oncology

Vanderbilt University Medical Center · Obstetrics and Gynecology

2021–

Assistant Professor

Vanderbilt University · Obstetrics and Gynecology

Education

2021

Fellowship

Cedars-Sinai Medical Center · Gynecologic Oncology

2018

Residency

University of Michigan–Ann Arbor · Obstetrics and Gynecology

2014

MD

University of Pennsylvania · School of Medicine

2006

BA

Stanford University · American Studies and Human Biology

Links & IDs
0000-0001-7671-5895

Scopus: 57162649200