| Literature DB >> 30473216 |
Yueqiong Lao1, Qian Li2, Nanshan Li2, Hong Liu2, Kuiliang Liu2, Guojun Jiang2, Nan Wei2, Canghai Wang2, Yadan Wang2, Jing Wu3.
Abstract
DNA mismatch repair-proficient colon cancer is the most common type of colon cancer, but its initiation and progression are still unknown. Our previous study has revealed that a long noncoding RNA (lncRNA) ENST00000455974 was significantly associated with TNM stage and distant metastasis in patients with DNA mismatch repair-proficient (pMMR) colon cancer (CC). Here, firstly, we observed that ENST00000455974 was gradual increased across colon normal-adenoma-carcinoma-metastasis sequence by quantitative real-time PCR. Secondly, ENST00000455974 showed a better sensitivity and specificity than CEA and CA19-9 in the diagnosis of pMMR CC by drawing the receiver operating characteristic (ROC) curve. Thirdly, a higher level of ENST00000455974 was associated with a poorer patient survival. Furthermore, Knockdown of ENST00000455974 led to reduced proliferation and migration of colon cancer cells. Mechanistically, ENST00000455974 was mainly located in the nucleus of colon cancer cells and it promoted the growth and metastasis of pMMR CC cells through up-regulating JAG2.Entities:
Keywords: Colon cancer; Migration; Proficient DNA mismatch repair; Proliferation; lncRNA
Mesh:
Substances:
Year: 2018 PMID: 30473216 DOI: 10.1016/j.bbrc.2018.11.088
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575