Long non-coding RNA AFAP1-AS1 facilitates tumor growth and promotes metastasis in colorectal cancer
Biol. Res; 49 (), 2016
Publication year: 2016
BACKGROUND AND OBJECTIVE:
Long non-coding RNAs can regulate tumorigenesis of various cancers. Dys-regulation of lncRNA-AFAP1-AS1 has not been studied in colorectal carcinoma (CRC). This study was to examine the function involvement of AFAP1-AS1 in tumor growth and metastasis of CRC.METHODS:
Relative expression of AFAP1-AS1 in CRC tissues and CRC cells lines was determined using quantitative real-time PCR (qRT-PCR). Functional involvement of AFAP1-AS1 in tumor proliferation and metastasis was evaluated in AFAP1-AS1-specific siRNA-treated CRC cells and in CRC cell xenograft. Expression of epithelial-mesenchymal transition (EMT)-related gene expression was determined using western blot.RESULTS:
Relative expression of AFAP1-AS1 was significantly elevated in CRC tissues and CRC HCT116 and SW480 cell lines. AFAP1-AS1 knock-down suppressed SW480 cell proliferation, colony formation, migration and invasion. Also AFAP1-AS1 knock-down inhibited tumor metastasis-associated genes expression in terms of EMT. This carcinostatic action by AFAP1-AS1 knock-down was further confirmed by suppression of tumor formation and hepatic metastasis of CRC cells in nude mice.CONCLUSION:
lncRNA-AFAP1-AS1 knock-down exhibits antitumor effect on colorectal carcinoma in respects of suppression of cell proliferation and metastasis of cancer cells.
Carcinoma/secundario, Neoplasias Colorrectales/patología, Neoplasias Hepáticas/secundario, ARN Largo no Codificante/metabolismo, Carcinoma/genética, Carcinoma/metabolismo, Carcinoma/patología, Neoplasias Colorrectales/genética, Neoplasias Colorrectales/metabolismo, Neoplasias Hepáticas/genética, ARN Largo no Codificante/análisis, Western Blotting, Movimiento Celular, Proliferación Celular, Transición Epitelial-Mesenquimal, Regulación Neoplásica de la Expresión Génica, Técnicas de Silenciamiento del Gen, Células HCT116, Ratones Endogámicos C57BL, Ratones Desnudos, Reacción en Cadena en Tiempo Real de la Polimerasa, Células Tumorales Cultivadas