|dc.contributor.author||Y R Jung||-|
|dc.contributor.author||J J Park||-|
|dc.contributor.author||Yeung Bae Jin||-|
|dc.contributor.author||Y J Cao||-|
|dc.contributor.author||M J Park||-|
|dc.contributor.author||E J Kim||-|
|dc.description.abstract||Aberrant sialylation has long been correlated with human cancer. Increased ST6 Gal I (β-galactoside α 2, 6 sialyltransferase) and consequently higher levels of cell-surface α 2, 6 sialylation has been associated with human colorectal cancer (CRC) metastasis. We have extensive circumstantial data that sialylation is connected to cancer metastasis, but we do not understand in detail how sialylation can switch on/off multiple steps in cancer metastasis. To investigate the molecular mechanism underlying the ST6Gal I-mediated metastasis of CRC, we silenced the ST6Gal I gene in a metastatic SW620 CRC cell line (SW620-shST6Gal I) and examined the metastatic behavior of the cells. We found that various hallmarks of metastatic ability were considerably enhanced in ST6Gal 1-depleted SW620 clones, as assessed both in vitro and in vivo. In particular, the metastasis suppressor, KAI1, was down-regulated in ST6Gal I-deficient SW620 clones. This reflected the increased exosome-mediated exportation of KAI1, and was associated with a decrease in the KAI1-mediated inhibition of integrin. These findings indicate that gene silencing of ST6Gal I could enhance metastasis of CRC by down-regulating KAI1 activity and rescuing its negative effects on integrin signaling.||-|
|dc.publisher||Oxford Univ Press||-|
|dc.title||Silencing of ST6Gal I enhances colorectal cancer metastasis by down-regulating KAI1 via exosome-mediated exportation and thereby rescues integrin signaling||-|
|dc.title.alternative||Silencing of ST6Gal I enhances colorectal cancer metastasis by down-regulating KAI1 via exosome-mediated exportation and thereby rescues integrin signaling||-|
|dc.contributor.affiliatedAuthor||Yeung Bae Jin||-|
|dc.identifier.bibliographicCitation||Carcinogenesis, vol. 37, no. 11, pp. 1089-1097||-|
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