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Published in: Clinical and Translational Oncology 11/2014

01-11-2014 | Research Article

TGF-beta induced RBL2 expression in renal cancer cells by down-regulating miR-93

Authors: J. Shi, Y. Zhuang, X. K. Liu, Y. X. Zhang, Y. Zhang

Published in: Clinical and Translational Oncology | Issue 11/2014

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Abstract

Purpose

TGF-beta can induce G1 arrest via many mechanisms including up-regulating p21, p27, and Rb. However, as the member of Rb family, whether RBL2 is induced by TGF-beta treatment remains exclusive.

Methods

The expression of RBL2 and miR-93 after TGF-beta treatment was determined by quantitative real-time PCR and western blot. The growth of renal cancer cells was determined by CCK-8 assays and cell cycle was determined by PI staining. The binding of miR-93 on RBL2 3′-UTR was determined by double luciferase system.

Results

In renal cancer cells, TGF-beta treatment induced expression of RBL2 in a time- and concentration-dependent manner, and RBL2 mediated TGF-beta induced growth inhibition and cell cycle arrest in renal cancer cells. Furthermore, we found that miR-93 directly targeted RBL2 by binding to its 3′-UTR in renal cancer cells. Over-expression of miR-93 significantly reduced the expression of RBL2, whereas knock down of miR-93 up-regulated the expression of RBL2. More importantly, TGF-beta treatment inhibited miR-93 expression, which resulted in up-regulation of RBL2 after TGF-beta treatment.

Conclusion

TGF-beta induced RBL2 expression through down-regulating miR-93 in renal cancer cells. The newly identified TGF-beta/miR-93/RBL2 signal pathway reveals a new mechanism of TGF-beta induced growth arrest in renal cancer.
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Metadata
Title
TGF-beta induced RBL2 expression in renal cancer cells by down-regulating miR-93
Authors
J. Shi
Y. Zhuang
X. K. Liu
Y. X. Zhang
Y. Zhang
Publication date
01-11-2014
Publisher
Springer Milan
Published in
Clinical and Translational Oncology / Issue 11/2014
Print ISSN: 1699-048X
Electronic ISSN: 1699-3055
DOI
https://doi.org/10.1007/s12094-014-1185-7

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