Regulation of HMGA1 expression by MicroRNA-296 affects prostate cancer growth and invasion

Jian Jun Wei, Xinyu Wu, Yi Peng, Guizhi Shi, Basturk Olca, Ximing Yang, Garrett Daniels, Iman Osman, Jiangyong Ouyang, Eva Hernando, Angel Pellicer, Johng S. Rhim, Jonathan Melamed, Peng Lee*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

41 Scopus citations


Purpose: High-motility group AT-hook gene 1 (HMGA1) is a non-histone nuclear binding protein that is developmentally regulated. HMGA1 is significantly overexpressed in and associated with high grade and advance stage of prostate cancer (PC). The oncogenic role of HMGA1 is at least mediated through chromosomal instability and structural aberrations. However, regulation of HMGA1 expression is not well understood. Identification of microRNA-mediated HMGA1 regulation will provide a promising therapeutic target in treating PC. Experimental Design: In this study, we examined the functional relation between miR-296 and HMGA1 expression in several PC cell lines and a large PC cohort. We further examined the oncogenic property of HMGA1 regulated by miR-296. Results: Here we report that miR-296, a microRNA predicted to target HMGA1, specifically represses HMGA1 expression by promoting degradation and inhibiting HMGA1translation. Repression of HMGA1 by miR-296 is direct and sequence specific. Importantly, ectopic miR-296 expression significantly reduced PC cell proliferation and invasion, in part through the downregulation of HMGA1. Examining PC patient samples, we found an inverse correlation between HMGA1 and miR-296 expression: high levels of HMGA1 were associated with low miR-296 expression and strongly linked to more advanced tumor grade and stage. Conclusions: Our results indicate that miR-296 regulates HMGA1 expression and is associated with PC growth and invasion.

Original languageEnglish (US)
Pages (from-to)1297-1305
Number of pages9
JournalClinical Cancer Research
Issue number6
StatePublished - Mar 15 2011

ASJC Scopus subject areas

  • Oncology
  • Cancer Research


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