Research Papers:

Comparative RNA-seq analysis reveals dys-regulation of major canonical pathways in ERG-inducible LNCaP cell progression model of prostate cancer

Parameet Kumar _, Joyeeta Chakraborty, Gauthaman Sukumar, Clifton Dalgard, Raghunath Chatterjee and Roopa Biswas _

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Oncotarget. 2019; 10:4290-4306. https://doi.org/10.18632/oncotarget.27019

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Parameet Kumar1, Joyeeta Chakraborty2, Gauthaman Sukumar1,3, Clifton Dalgard1,4, Raghunath Chatterjee2 and Roopa Biswas1

1 Department of Anatomy, Physiology and Genetics, Uniformed Services University of the Health Sciences, Bethesda, MD, USA

2 Human Genetics Unit, Indian Statistical Institute, Kolkata, India

3 Collaborative Health Initiative Research Program, Henry Jackson Foundation, Bethesda, MD, USA

4 The American Genome Center, Uniformed Service University of the Health Sciences, Bethesda, MD, USA

Correspondence to:

Roopa Biswas,email: [email protected]
Parameet Kumar,email: [email protected]

Keywords: RNAseq; prostate cancer; LNCaP cells; ERG; mRNA

Received: December 29, 2018     Accepted: May 30, 2019     Published: July 02, 2019


Prostate Cancer (CaP) is the second leading cause of cancer related death in USA. In human CaP, gene fusion between androgen responsive regulatory elements at the 5'-untranslated region of TMPRSS2 and ETS-related genes (ERG) is present in at least 50% of prostate tumors. Here we have investigated the unique cellular transcriptome associated with over-expression of ERG in ERG-inducible LNCaP cell model system of human CaP. Comprehensive transcriptome analyses reveal a distinct signature that distinguishes ERG dependent and independent CaP in LNCaP cells. Our data highlight a significant heterogeneity among the transcripts. Out of the 526 statistically significant differentially expressed genes, 232 genes are up-regulated and 294 genes are down-regulated in response to ERG. These ERG-associated genes are linked to several major cellular pathways, cell cycle regulation being the most significant. Consistently our data indicate that ERG plays a key role in modulating the expression of genes required for G1 to S phase transition, particularly those that affect cell cycle arrest at G1 phase. Moreover, cell cycle arrest in response to ERG appears to be promoted by induction of p21 in a p53 independent manner. These findings may provide new insights into mechanisms that promote growth and progression of CaP.

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