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高分化和低分化人结肠癌及细胞系中pp60c-src活性的差异

Differential pp60c-src activity in well and poorly differentiated human colon carcinomas and cell lines.

作者信息

Weber T K, Steele G, Summerhayes I C

机构信息

Department of Surgery, New England Deaconess Hospital, Boston, Massachusetts 02115.

出版信息

J Clin Invest. 1992 Sep;90(3):815-21. doi: 10.1172/JCI115956.

Abstract

The results presented in this report demonstrate increased pp60c-src kinase activity associated with moderate to well differentiated colon tumors, corroborating previous observations by other groups. Extension of this analysis to include a small number of poorly differentiated colon carcinomas revealed src kinase activity comparable to that observed in normal colonic mucosa, considerably less than that observed in moderate/well differentiated lesions. Correlations of src kinase activity with differentiation was confirmed within a panel of colon cell lines where increased activity, associated with moderate/well differentiated lines, was accompanied by increased expression of pp60c-src protein. Use of an antiphosphotyrosine antibody in immunoprecipitation revealed the presence of novel phosphotyrosyl cellular substrates in human colon cell lines displaying elevated pp60c-src kinase activity. These observations suggest a role for the src protooncogene in colonic differentiation pathways.

摘要

本报告中呈现的结果表明,中分化至高分化结肠肿瘤中pp60c-src激酶活性增加,这证实了其他研究小组先前的观察结果。将该分析扩展至少数低分化结肠癌后发现,src激酶活性与正常结肠黏膜中观察到的相当,远低于中分化/高分化病变中观察到的活性。在一组结肠细胞系中,src激酶活性与分化之间的相关性得到了证实,其中与中分化/高分化细胞系相关的活性增加伴随着pp60c-src蛋白表达的增加。在免疫沉淀中使用抗磷酸酪氨酸抗体,发现在显示pp60c-src激酶活性升高的人结肠细胞系中存在新的磷酸酪氨酸细胞底物。这些观察结果表明src原癌基因在结肠分化途径中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a3fe/329935/bc42e97610da/jcinvest00488-0140-a.jpg

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