Stabilization of beta-catenin by genetic defects in melanoma cell lines

被引:1120
作者
Rubinfeld, B
Robbins, P
ElGamil, M
Albert, I
Porfiri, E
Polakis, P
机构
[1] ONYX PHARMACEUT,RICHMOND,CA 94806
[2] NCI,SURG BRANCH,NIH,BETHESDA,MD 20892
关键词
D O I
10.1126/science.275.5307.1790
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Signal transduction by beta-catenin involves its posttranslational stabilization and downstream coupling to the Lef and Tcf transcription factors, Abnormally high amounts of beta-catenin were detected in 7 of 26 human melanoma cell lines, Unusual messenger RNA splicing and missense mutations in the beta-catenin gene (CTNNB1) that result in stabilization of the protein were identified in six of the lines, and the adenomatous polyposis coli tumor suppressor protein (APC) was altered or missing in two others, In the APC-deficient cells, ectopic expression of wild-type APC eliminated the excess beta-catenin, Cells with stabilized beta-catenin contained a constitutive beta-catenin-Lef-1 complex, Thus, genetic defects that result in up-regulation of beta-catenin may play a role in melanoma progression.
引用
收藏
页码:1790 / 1792
页数:3
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