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Vargheese M. Chennathukuzhi, Ph.D

Professional Background

I received my PhD in biochemistry from the Indian Institute of Technology, Madras, India. I completed postdoctoral training at the Indian Institute of Science, Bangalore, India and from the University of Pennsylvania Medical Center. During my post doctoral training, I received the Mellon Foundation Grant award on contraceptive drug discovery and development. After about 6 years of working in pharmaceutical drug discovery and development at Wyeth/ Pfizer, I joined the faculty of Molecular and Integrative Physiology at KUMC in 2009.

Education and Training
  • BS, Chemistry, University of Calicut, India
  • MS, Chemistry, Mahatma Gandhi University, Kottayam, India
  • PhD, Biochemistry, Indian Institute of Technology, Madras, India
  • Post Doctoral Fellowship, Reproduction, Indian Institute of Science, Bangalore, India
  • Post Doctoral Fellowship, Reproduction, University of Pennsylvania, Philadelphia, Pennsylvania
Professional Affiliations
  • Interdisciplinary Graduate Program in Biomedical Sciences, IGPBS Syllabus Committee, Member, 2023 - Present
  • Society for the Study of Reproduction, SSR Development Committee, Member, 2023 - Present
  • Society for the Study of Reproduction, SSR Virtual Education Committee, Member, 2022 - Present
  • Society for the Study of Reproduction, SSR Podcast Sub-Committee, Member, 2022 - Present
  • Institutional Biosafety Committee, IBC, Member, 2020 - Present
  • Society for the Study of Reproduction, SSR Distinguished Fellowship, Chair, 2019 - 2021
  • Society for the Study of Reproduction, Awards Committee, Chair, 2018 - 2020

Research

Overview

My research is aimed at understanding the pathophysiology of uterine fibroids and adenomyosis. My laboratory is involved in drug discovery and development for the treatment of uterine fibroids, as well as in the development of non-hormonal contraceptive drugs. We develop and characterize genetically modified rodent models of uterine pathologies as preclinical models.

Current Research and Grants
  • REST/NRSF, miRNAs, and tissue remodeling in adenomyosis pathophysiology, NIH, Multi-Principal Investigator
Publications
  • Faber, Erik., B, Sun, Luxin, Tang, Jian, Roberts, Emily, Ganeshkumar, Sornakala, Wang, Nan, Rasmussen, Damien, Majumdar, Abir, Hirsch, Laura., E, John, Kristen, Yang, An, Khalid, Hira, Hawkinson, Jon., E, Levinson, Nicholas., M, Chennathukuzhi, Vargheese., M, Harki, Daniel, Schönbrunn, Ernst, Georg, Gunda., I. 2023. Development of allosteric and selective CDK2 inhibitors for contraception with negative cooperativity to cyclin binding. Nature Communications, 14 (1), 3213-3225. https://www.nature.com/articles/s41467-023-38732-x
  • Cloud, Ashley., S, Koohestani, Faezeh, McWilliams, Michelle., M, Ganeshkumar, Sornakala, Gunewardena, Sumedha, Graham, Amanda, Nothnick, Warren, Chennathukuzhi, Vargheese., M. 2022. Loss of the repressor REST affects progesterone receptor function and promotes uterine leiomyoma pathogenesis. PNAS (Nov;119(44):e2205524119). https://www.pnas.org/doi/epdf/10.1073/pnas.2205524119
  • Cloud, Ashley, Vargheese, Aditya., M, Gunewardena, Sumedha, Shimak, Raeann, Kumaraswamy, Easwari, Jensen, Roy, Chennathukuzhi, Vargheese., M. 2022. Loss of REST in breast cancer promotes tumor progression through estrogen sensitization, MMP24 and CEMIP overexpression. . Breast Cancer Research. https://bmccancer.biomedcentral.com/articles/10.1186/s12885-022-09280-2
  • McWilliams, Michelle., M, Chennathukuzhi, Vargheese., M. 2017. Recent Advances in Uterine Fibroid Etiology. Semin Reprod Med, 35 (2), 181-189. https://www.thieme-connect.com/products/ejournals/pdf/10.1055/s-0037-1599090.pdf
  • Varghese, B., V, Koohestani, F, McWilliams, M, Colvin, A, Gunewardena, Sumedha., Senaka Abesiri, Kinsey, William., H, Nowak, R., A, Nothnick, Warren., B, Chennathukuzhi, Vargheese., Mani. 2013. Loss of the repressor REST in uterine fibroids promotes aberrant G protein-coupled receptor 10 expression and activates mammalian target of rapamycin pathway.. Proceedings of the National Academy of Sciences of the United States of America, 110 (6), 2187-92
  • Yang, J, Chennathukuzhi, Vargheese., Mani, Miki, K, O'Brien, D., A, Hecht, N., B. 2003. Mouse testis brain RNA-binding protein/translin selectively binds to the messenger RNA of the fibrous sheath protein glyceraldehyde 3-phosphate dehydrogenase-S and suppresses its translation in vitro.. Biology of reproduction, 68 (3), 853-9
  • Chennathukuzhi, Vargheese., Mani, Kurihara, Y, Bray, J., D, Yang, J, Hecht, N., B. 2001. Altering the GTP binding site of the DNA/RNA-binding protein, Translin/TB-RBP, decreases RNA binding and may create a dominant negative phenotype.. Nucleic acids research, 29 (21), 4433-40
  • Morales, C., R, Lefrancois, S, Chennathukuzhi, Vargheese., Mani, El-Alfy, M, Wu, X, Yang, J, Gerton, G., L, Hecht, N., B. 2002. A TB-RBP and Ter ATPase complex accompanies specific mRNAs from nuclei through the nuclear pores and into intercellular bridges in mouse male germ cells.. Developmental biology, 246 (2), 480-94
  • Chennathukuzhi, Vargheese., Mani, Stein, J., M, Abel, T, Donlon, S, Yang, S, Miller, J., P, Allman, D., M, Simmons, R., A, Hecht, N., B. 2003. Mice deficient for testis-brain RNA-binding protein exhibit a coordinate loss of TRAX, reduced fertility, altered gene expression in the brain, and behavioral changes.. Molecular and cellular biology, 23 (18), 6419-34
  • Chennathukuzhi, Vargheese., Mani, Morales, C., R, El-Alfy, M, Hecht, N., B. 2003. The kinesin KIF17b and RNA-binding protein TB-RBP transport specific cAMP-responsive element modulator-regulated mRNAs in male germ cells.. Proceedings of the National Academy of Sciences of the United States of America, 100 (26), 15566-71