PMID- 23404111 OWN - NLM STAT- MEDLINE DCOM- 20140725 LR - 20211203 IS - 1791-3004 (Electronic) IS - 1791-2997 (Linking) VI - 7 IP - 4 DP - 2013 Apr TI - Hcrcn81 is upregulated by rapamycin treatment in human colorectal adenocarcinoma cells. PG - 1257-60 LID - 10.3892/mmr.2013.1317 [doi] AB - The aim of the present study was to determine the role of hcrcn81 in the regulation of the mammalian target of rapamycin (mTOR) pathway in human colorectal adenocarcinoma cells. The effect of rapamycin treatment on hcrcn81 expression was evaluated by examining the mRNA and protein expression of hcrcn81 in rapamycin‑treated human colon carcinoma cell lines, SW480 and LoVo, using real‑time PCR and western blot analysis, respectively. The results demonstrated that mRNA and protein levels of hcrcn81 were elevated following rapamycin treatment in these cell lines, indicating that hcrcn81 expression is upregulated by rapamycin treatment in human colorectal adenocarcinoma cells. Observations of the current study indicate that hcrcn81 may play a role in tumorigenesis by regulating the mTOR signaling pathway. FAU - Wen, Xiaoxia AU - Wen X AD - Department of Anatomy, Basic Medical and Forensic Medical Institute, Sichuan University, Chengdu, Sichuan 610041, P.R. China. FAU - Dong, Lei AU - Dong L FAU - Zhu, Jianjun AU - Zhu J FAU - Chen, Yao AU - Chen Y LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20130208 PL - Greece TA - Mol Med Rep JT - Molecular medicine reports JID - 101475259 RN - 0 (HCRCN81 protein, human) RN - 0 (Neoplasm Proteins) RN - EC 2.7.1.1 (MTOR protein, human) RN - EC 2.7.11.1 (TOR Serine-Threonine Kinases) RN - W36ZG6FT64 (Sirolimus) SB - IM MH - Adenocarcinoma/*genetics/pathology MH - *Carcinogenesis MH - Cell Line, Tumor MH - Colorectal Neoplasms/*genetics/pathology MH - Gene Expression Regulation, Neoplastic/drug effects MH - Humans MH - Neoplasm Proteins/*biosynthesis/genetics MH - Signal Transduction/genetics MH - Sirolimus/pharmacology MH - TOR Serine-Threonine Kinases/genetics EDAT- 2013/02/14 06:00 MHDA- 2014/07/26 06:00 CRDT- 2013/02/14 06:00 PHST- 2012/10/31 00:00 [received] PHST- 2013/02/01 00:00 [accepted] PHST- 2013/02/14 06:00 [entrez] PHST- 2013/02/14 06:00 [pubmed] PHST- 2014/07/26 06:00 [medline] AID - 10.3892/mmr.2013.1317 [doi] PST - ppublish SO - Mol Med Rep. 2013 Apr;7(4):1257-60. doi: 10.3892/mmr.2013.1317. Epub 2013 Feb 8.