Promotion of colorectal cancer growth and metastasis by the LIM and SH3 domain protein 1

BackgroundLIM and SH3 protein 1 (LASP-1), initially identified from a cDNA library of metastatic axillary lymph nodes of breast cancer patients, is a specific focal adhesion protein involved in numerous biological and pathological processes. The overexpression of LASP-1 has been described in several...

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Veröffentlicht in:Gut 2010-09, Vol.59 (9), p.1226-1235
Hauptverfasser: Zhao, Liang, Wang, Hui, Liu, Chao, Liu, Yawei, Wang, Xiaoyan, Wang, Shuang, Sun, Xuegang, Li, Jianming, Deng, Yongjian, Jiang, Yong, Ding, Yanqing
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Sprache:eng
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Zusammenfassung:BackgroundLIM and SH3 protein 1 (LASP-1), initially identified from a cDNA library of metastatic axillary lymph nodes of breast cancer patients, is a specific focal adhesion protein involved in numerous biological and pathological processes. The overexpression of LASP-1 has been described in several types of cancers, but the role of LASP-1 in colorectal cancer (CRC) is unknown. In a previous study, comparative proteomic analysis was performed and LASP-1 was identified as a CRC-associated protein in those patients with CRC.MethodsUsing immunohistochemistry, we analysed LASP-1 protein expression in 126 clinicopathologically characterised CRC cases. Using gene transfection and RNA interference, we investigated the effects of LASP-1 overexpression and depletion on tumor cellular behavior in vitro and in vivo. Using 2-D DIGE, we analysed the effect of the presence and absence of LASP-1 gene on protein expression profiles of CRC cells.ResultsOverexpression of LASP-1 was found in metastatic CRC tissues (p=0.002), and its expression level was closely correlated with overall survival of patients with CRC (p=0.002). RNA interference-mediated silencing of the LASP-1 gene in SW620 CRC cells inhibited cell proliferation and migration significantly. However, gene transfection-mediated overexpression of LASP-1 in SW480 CRC cells resulted in aggressive phenotypes of cancer cells and promoted cancer growth and metastasis. Furthermore, both overexpression and silencing of the LASP-1 gene caused a very similar protein expression pattern in different CRC cell lines. The identified LASP-1-modulated proteins, including some key cellular molecules, were involved in various biological processes.ConclusionsThe results show that LASP-1 might be a promising target in the treatment of patients with CRC with growth and metastasis of CRC.
ISSN:0017-5749
1468-3288
DOI:10.1136/gut.2009.202739