| Literature DB >> 28632999 |
Kaiming Wu1, Zhenxian Zhao2, Kuanzhi Liu3, Jian Zhang4, Guanghua Li4, Liang Wang4.
Abstract
Long non-coding RNAs (LncRNAs) have been recently regarded as systemic regulators in multiple biologic processes including tumorigenesis. In this study, we observed the expression of lncRNA lnc-sox5 was significantly increased in colorectal cancer (CRC). Despite the CRC cell growth, cell cycle and cell apoptosis was not affected by lnc-sox5 knock-down, lnc-sox5 knock-down suppressed CRC cell migration and invasion. In addition, xenograft animal model suggested that lnc-sox5 knock-down significantly suppressed the CRC tumorigenesis. Our results also showed that the expression of indoleamine 2,3-dioxygenase 1 (IDO1) was significantly reduced by lnc-sox5 knock-down and therefore modulated the infiltration and cytotoxicity of CD3+CD8+T cells. Taken together, these results suggested that lnc-sox5 unbalances tumor microenvironment to regulate colorectal cancer progression.Entities:
Keywords: Indoleamine 2,3-dioxygenase 1 (IDO1); Tregs; colorectal cancer (CRC); lnc-sox5; long non-coding RNA; tumor microenvironment
Mesh:
Substances:
Year: 2017 PMID: 28632999 PMCID: PMC5531622 DOI: 10.1080/15384101.2017.1317416
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534