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钙离子通道阻滞剂维拉帕米可增强B16小鼠黑色素瘤的黑色素生成,而不改变其转移潜能。

The Ca2+ channel blocker verapamil enhances melanogenesis without altering metastatic potential in the B16 murine melanoma.

作者信息

Parker C, Sherbet G V

机构信息

Cancer Research Unit, Medical School, University of Newcastle upon Tyne, UK.

出版信息

Melanoma Res. 1993 Oct;3(5):347-50. doi: 10.1097/00008390-199310000-00008.

Abstract

The relationship between the processes of melanogenesis and metastasis were investigated using metastatic variants of the B16 murine melanoma. alpha-Melanocyte stimulating hormone (MSH) enhanced lung colonization by the low metastasis variant F1 as well as inducing melanogenesis. The Ca2+ channel blocker verapamil had no effect on lung colonization by the F1 and ML8 variants but markedly enhanced melanogenesis in both these cell lines. We previously showed that the expression of the dominant metastasis associated gene mts1 was up-regulated by MSH but down-regulated by verapamil. These findings may demonstrate that the processes of melanogenesis and metastasis can be uncoupled at both genetic and phenotypic levels, and that the mechanisms involved in the regulation of metastatic behaviour and melanogenesis are different.

摘要

利用B16小鼠黑色素瘤的转移变体研究了黑色素生成过程与转移之间的关系。α-黑素细胞刺激素(MSH)增强了低转移变体F1的肺定植,并诱导了黑色素生成。钙离子通道阻滞剂维拉帕米对F1和ML8变体的肺定植没有影响,但显著增强了这两种细胞系中的黑色素生成。我们之前表明,优势转移相关基因mts1的表达受MSH上调,但受维拉帕米下调。这些发现可能表明,黑色素生成和转移过程在基因和表型水平上都可以解偶联,并且参与调节转移行为和黑色素生成的机制是不同的。

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