skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: microRNA-495 promotes bladder cancer cell growth and invasion by targeting phosphatase and tensin homolog

Journal Article · · Biochemical and Biophysical Research Communications

Accumulating evidence has linked deregulation of microRNA-495 (miR-495) to tumorigenesis; however, its function in tumor progression is controversial. This work was undertaken to explore the expression and biological roles of miR-495 in bladder cancer. The expression of miR-495 was examined in 67 pairs of bladder cancer and adjacent normal bladder tissues. The roles of miR-495 in bladder cancer cell proliferation and invasion in vitro and tumorigenesis in vivo were determined. Direct target gene(s) mediating the activity of miR-495 in bladder cancer cells was identified. It was found that miR-495 was expressed at greater levels in bladder tissues and cell lines. High expression of miR-495 was significantly associated with larger tumor size, advanced TNM stage, and lymph node metastasis. Overexpression of miR-495 significantly promoted bladder cancer cell proliferation and invasion, whereas inhibition of miR-495 suppressed cell proliferation and invasion. PTEN, a well-defined tumor suppressor was identified to be a target gene of miR-495. A significant inverse correlation between miR-495 and PTEN expression was noted in bladder cancer tissues (r = −0.3094, P = 0.0125). Overexpression of miR-495 led to reduction of PTEN expression in bladder cancer cells. Rescue experiments showed that enforced expression of PTEN impaired miR-495-mediated bladder cancer proliferation and invasion. In vivo mouse studies demonstrated that overexpression of miR-495 accelerated the growth of subcutaneous bladder cancer xenografts, which was associated with downregulation of PTEN. Overall, these findings indicate that miR-495 upregulation contributes to bladder cancer cell growth, invasion, and tumorigenesis by targeting PTEN and offer a potential therapeutic target for bladder cancer. - Highlights: • miR-495 upregulation induces aggressive phenotype in bladder cancer. • miR-495 is inversely correlated with PTEN in bladder cancer. • miR-495 promotes bladder cancer cell proliferation and invasion by targeting PTEN.

OSTI ID:
22696855
Journal Information:
Biochemical and Biophysical Research Communications, Vol. 483, Issue 2; Other Information: Copyright (c) 2017 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.; Country of input: International Atomic Energy Agency (IAEA); ISSN 0006-291X
Country of Publication:
United States
Language:
English

Similar Records

MicroRNA-187 regulates gastric cancer progression by targeting the tumor suppressor CRMP1
Journal Article · Sun Jan 22 00:00:00 EST 2017 · Biochemical and Biophysical Research Communications · OSTI ID:22696855

MicroRNA-373 functions as an oncogene and targets YOD1 gene in cervical cancer
Journal Article · Fri Apr 10 00:00:00 EDT 2015 · Biochemical and Biophysical Research Communications · OSTI ID:22696855

Long non-coding RNA FBXL19-AS1 plays oncogenic role in colorectal cancer by sponging miR-203
Journal Article · Sat Jun 17 00:00:00 EDT 2017 · Biochemical and Biophysical Research Communications · OSTI ID:22696855