Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8322120 | The International Journal of Biochemistry & Cell Biology | 2018 | 18 Pages |
Abstract
Steroid receptor co-activator3 (SRC3) has been known to severe as an androgen receptor (AR) coactivator and is involved in the prostate cancer progression. Non-coding RNA (ncRNA) plays an important role in the cancer progression. However, the mechanism underlying the relationship between ncRNA and AR coactivators is still unclear. Here, we found a ncRNA, Nuclear Enriched Abundant Transcript 1 (NEAT1), was able to interact with SRC3 in the prostate cancer cell lines. NEAT1 can upregulate the AKT phosphorylation via a SRC3/IGF1R pathway. In function, NEAT1 promoted the prostate cancer cell growth through IGF1R/AKT signaling pathway. The NEAT1, SRC3, and IGF1R were highly expressed in the patients' samples of prostate cancer. Therefore, we found a novel SRC3 binding ncRNA that can promote the prostate cancer cell growth through SRC3/IGF1R/AKT pathway.
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Authors
Wei Xiong, Changkun Huang, Huanghao Deng, Chengzhu Jian, Cong Zen, Kun Ye, Zhaohui Zhong, Xiaokun Zhao, Liang Zhu,