Retracted: Long Non‐coding RNA Linc‐ ITGB 1 Knockdown Inhibits Cell Migration and Invasion in GBC ‐ SD /M and GBC ‐ SD Gallbladder Cancer Cell Lines

Gallbladder cancer is a highly aggressive malignancy with a low 5‐year survival rate. Despite advances in the molecular understanding of the initiation and progression in gallbladder cancer, treatment modalities such as surgery, radiotherapy, or chemotherapy in advanced cases did not yield promising...

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Veröffentlicht in:Chemical biology & drug design 2015-11, Vol.86 (5), p.1064-1071
Hauptverfasser: Wang, Lei, Zhang, Yunjiao, Lv, Wenjie, Lu, Jianhua, Mu, Jiasheng, Liu, Yingbin, Dong, Ping
Format: Artikel
Sprache:eng
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Zusammenfassung:Gallbladder cancer is a highly aggressive malignancy with a low 5‐year survival rate. Despite advances in the molecular understanding of the initiation and progression in gallbladder cancer, treatment modalities such as surgery, radiotherapy, or chemotherapy in advanced cases did not yield promising outcomes. Therefore, it is of great importance to uncover new mechanism underlying gallbladder cancer growth and metastasis. In this study, we identified a differentially expressed long intergenic non‐coding RNA , linc‐ ITGB 1, in a pair of higher and lower metastatic gallbladder cancer cell sublines. Then, the potential role of linc‐ ITGB 1 in gallbladder cancer cell proliferation, migration, and invasion was explored using a lentivirus‐mediated RNA interference system. Functional analysis showed that knockdown of linc‐ ITGB 1 significantly inhibited gallbladder cancer cell proliferation. Moreover, cell migration and invasion were reduced by over twofold in linc‐ ITGB 1 knockdown cells probably due to upregulation of β ‐catenin and downregulation of vimentin, slug, and TCF 8. In conclusion, linc‐ ITGB 1 potentially promoted gallbladder cancer invasion and metastasis by accelerating the process of epithelial‐to‐mesenchymal transition, and the application of RNA interference targeting linc‐ ITGB 1 might be a potential form of gallbladder cancer treatment in advanced cases.
ISSN:1747-0277
1747-0285
DOI:10.1111/cbdd.12573