Anbarasu Kumaraswamy
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PROX1 is an early driver of lineage plasticity in prostate cancer
Abstract Lineage plasticity is recognized as a critical determinant of lethality and resistance to AR pathway inhibitors in prostate cancer. Lineage plasticity is a continuum, ranging from AR activity-low tumors, AR-null tumors that do not express a neuroendocrine prostate cancer (NEPC) program (i.e., double-negative prostate cancer [DNPC]), and AR-null NEPC tumors. Factors upregulated early in lineage plasticity are not well-characterized.
LSD1 promotes prostate cancer cell reprogramming by repressing TP53 signaling independently of its demethylase function
ResearchIn-Press PreviewOncology Open Access | 10.1172/jci.insight.167440 JCI Insight. https://doi.org/10.1172/jci.insight.167440. Copyright © 2023, Kumaraswamy et al. This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. View PDF Abstract Lysine-specific demethylase 1 (LSD1) is a histone demethylase that promotes stemness and cancer cell survival, including in prostate cancer.
Recent Advances in Epigenetic Biomarkers and Epigenetic Targeting in Prostate Cancer
Ferlay J. Colombet M. Soerjomataram I. et al. Estimating the global cancer incidence and mortality in 2018: GLOBOCAN sources and methods. Int J Cancer. 2019; 144: 1941-1953 Montgomery R.B. Mostaghel E.A. Vessella R. et al. Maintenance of intratumoral androgens in metastatic prostate cancer: a mechanism for castration-resistant tumor growth. Cancer Res. 2008; 68: 4447-4454 Cancer Genome Atlas Research N The molecular taxonomy of primary prostate cancer. Cell. 2015; 163: 1011-1025 Robinson D.
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