K
Kavya Ramkumar
Researcher at University of Texas MD Anderson Cancer Center
Publications - 11
Citations - 564
Kavya Ramkumar is an academic researcher from University of Texas MD Anderson Cancer Center. The author has contributed to research in topics: Cancer & Population. The author has an hindex of 5, co-authored 11 publications receiving 170 citations.
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Journal ArticleDOI
Patterns of transcription factor programs and immune pathway activation define four major subtypes of SCLC with distinct therapeutic vulnerabilities
C. Allison Stewart,Elizabeth M. Park,Lixia Diao,Sarah M. Groves,Simon Heeke,Barzin Y. Nabet,Junya Fujimoto,Luisa M. Solis,Wei Lu,Yuanxin Xi,Robert J. Cardnell,Qi Wang,Giulia Fabbri,Kasey R. Cargill,Natalie I. Vokes,Kavya Ramkumar,Bingnan Zhang,Carminia Maria Della Corte,Paul Robson,Stephen G. Swisher,Jack A. Roth,Bonnie S. Glisson,David S. Shames,Ignacio I. Wistuba,Jing Wang,Vito Quaranta,John D. Minna,John V. Heymach,Lauren Averett Byers +28 more
TL;DR: In this paper, the authors used tumor expression data and non-negative matrix factorization to identify four SCLC subtypes defined largely by differential expression of transcription factors ASCL1, NEUROD1, and POU2F3 or low expression of all three transcription factor signatures accompanied by an Inflamed gene signature.
Journal ArticleDOI
STING Pathway Expression Identifies NSCLC With an Immune-Responsive Phenotype
Carminia Maria Della Corte,Carminia Maria Della Corte,Triparna Sen,Triparna Sen,Kavya Ramkumar,Lixia Diao,Robert J. Cardnell,Bertha Leticia Rodriguez,C. Allison Stewart,Vassiliki A. Papadimitrakopoulou,Laura A. Gibson,Jared J. Fradette,Qi Wang,Youhong Fan,David H. Peng,Marcelo V. Negrao,Ignacio I. Wistuba,Junya Fujimoto,Luisa M. Solis Soto,Carmen Behrens,Ferdinandos Skoulidis,John V. Heymach,Jing Wang,Don L. Gibbons,Lauren Averett Byers +24 more
TL;DR: STING pathway activation in NSCLC predicts features of immunotherapy response and is enhanced by cisplatin treatment, suggesting a possible predictive biomarker, and mechanism, for improved response to chemo-immunotherapy combinations.
Journal ArticleDOI
Combination Treatment of the Oral CHK1 Inhibitor, SRA737, and Low-Dose Gemcitabine Enhances the Effect of Programmed Death Ligand 1 Blockade by Modulating the Immune Microenvironment in SCLC
Triparna Sen,Carminia Maria Della Corte,Snezana Milutinovic,Robert J. Cardnell,Lixia Diao,Kavya Ramkumar,C. Allison Stewart,Youhong Fan,Li Shen,Ryan J. Hansen,Bryan Strouse,Michael P Hedrick,Christian A. Hassig,John V. Heymach,Jing Wang,Lauren Averett Byers +15 more
TL;DR: It is shown that combined treatment of SRA737, an oral CHK1 inhibitor, and anti-PD-(L)1 leads to an anti-tumor response in multiple cancer models, including SCLC.
Journal ArticleDOI
Lung Cancer Models Reveal Severe Acute Respiratory Syndrome Coronavirus 2-Induced Epithelial-to-Mesenchymal Transition Contributes to Coronavirus Disease 2019 Pathophysiology.
C. Allison Stewart,Kavya Ramkumar,Kasey R. Cargill,Robert J. Cardnell,Monique B. Nilsson,Simon Heeke,Elizabeth M. Park,Samrat T. Kundu,Lixia Diao,Qi Wang,Li Shen,Yuanxin Xi,Bingnan Zhang,Carminia Maria Della Corte,Youhong Fan,Kiran Kundu,Boning Gao,Kimberley Avila,Curtis R. Pickering,Faye M. Johnson,Jianjun Zhang,Humam Kadara,John D. Minna,Don L. Gibbons,Jing Wang,John V. Heymach,Lauren Averett Byers +26 more
TL;DR: In this article, the expression and regulation of ACE2 and TMPRSS2 were investigated using a variety of normal and malignant models and tissues from the aerodigestive and respiratory tracts, and they found that ACE2 expression is restricted to a select population of epithelial cells.
Posted ContentDOI
SARS-CoV-2 infection induces EMT-like molecular changes, including ZEB1-mediated repression of the viral receptor ACE2, in lung cancer models
C. Allison Stewart,Kavya Ramkumar,Kasey R. Cargill,Robert J. Cardnell,Monique B. Nilsson,Simon Heeke,Elizabeth M. Park,Samrat T. Kundu,Lixia Diao,Qi Wang,Li Shen,Yuanxin Xi,Carminia Maria Della Corte,Youhong Fan,Kiran Kundu,Curtis R. Pickering,Faye M. Johnson,Jianjun Zhang,Humam Kadara,John D. Minna,Don L. Gibbons,Jing Wang,John V. Heymach,Lauren Averett Byers +23 more
TL;DR: A novel model of SARS-CoV-2 pathogenesis is suggested in which infected cells shift toward an increasingly mesenchymal state and lose ACE2 expression, along with its acute respiratory distress syndrome-protective effect, in a ZEB1-dependent manner.