Entity

Time filter

Source Type


Yang M.-H.,Southern Medical University | Yang M.-H.,Key Laboratory Of Trans And Proteome For Human Major Dis Of The Min Of Educ And Guangdong Province | Hu Z.-Y.,Southern Medical University | Hu Z.-Y.,Key Laboratory Of Trans And Proteome For Human Major Dis Of The Min Of Educ And Guangdong Province | And 9 more authors.
Biochimica et Biophysica Acta - Molecular Basis of Disease | Year: 2015

Our previous studies have shown that the 3' end of metastasis associated lung adenocarcinoma transcript 1 (MALAT1) is involved in colorectal cancer (CRC) cell proliferation and migration/invasion in vitro. The role and mechanism of MALAT1 in CRC metastasis in vivo, however, remain largely unknown. In the present study, we found that MALAT1 was up-regulated in human primary CRC tissues with lymph node metastasis. Overexpression of MALAT1 via RNA activation promoted CRC cell proliferation, invasion and migration in vitro, and stimulated tumor growth and metastasis in mice in vivo. Conversely, knockdown of MALAT1 inhibited CRC tumor growth and metastasis. MALAT1 regulated at least 243 genes in CRC cells in a genome-wide expression profiling. Among these genes, PRKA kinase anchor protein 9 (AKAP-9) was significantly up-regulated at both mRNA and protein levels. AKAP-9 was highly expressed in CRC cells with metastatic potential and human primary CRC tissues with lymph node metastasis, but not in normal cells or tissues. Importantly, knockdown of AKAP-9 blocked MALAT1-mediated CRC cell proliferation, migration and invasion. These data indicate that MALAT1 may promote CRC tumor development via its target protein AKAP-9. © 2014 Elsevier B.V. Source

Discover hidden collaborations