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抑制K-Ras的异戊二烯化,而非H-Ras或N-Ras的异戊二烯化,对CAAX肽模拟物具有高度抗性,并且在人肿瘤细胞系中需要法尼基转移酶和香叶基香叶基转移酶I抑制剂两者共同作用。

Inhibition of the prenylation of K-Ras, but not H- or N-Ras, is highly resistant to CAAX peptidomimetics and requires both a farnesyltransferase and a geranylgeranyltransferase I inhibitor in human tumor cell lines.

作者信息

Lerner E C, Zhang T T, Knowles D B, Qian Y, Hamilton A D, Sebti S M

机构信息

Department of Pharmacology, University of Pittsburgh, Pennsylvania 15261, USA.

出版信息

Oncogene. 1997 Sep;15(11):1283-8. doi: 10.1038/sj.onc.1201296.

Abstract

The farnesyltransferase (FTase) inhibitor FTI-277 is highly effective at blocking oncogenic H-Ras but not K-Ras4B processing and signaling. While inhibition of processing and signaling of oncogenic K-Ras4B is more sensitive to the geranylgeranyltransferase I (GGTase I) inhibitor GGTI-286 than it is to FTI-277 in K-Ras4B-transformed NIH3T3 cells, the sensitivity of K-Ras as well as H- and N-Ras to the CAAX peptidomimetics in human tumor cell lines is not known. Here, we report that a panel of five human carcinoma cell lines from pancreatic, pulmonary, and bladder origins all express H-, N-, and K-Ras, and their respective prenylation sensitivities to the FTase and GGTase I inhibitors is variable. In all of the cell lines investigated, the prenylation of N-Ras was highly sensitive to FTI-277, and in two of the cell lines, N-Ras showed slight sensitivity to GGTI-298, an analog of GGTI-286. Although the prenylation of H-Ras was also sensitive to FTI-277, complete inhibition of H-Ras processing even at high concentrations of FTI-277 and/or GGTI-298 was never achieved. The prenylation of K-Ras, on the other hand, was highly resistant to FTI-277 and GGTI-298. Most significantly, treatment of human tumor cell lines with both inhibitors was required for inhibition of K-Ras prenylation. In one cell line, the human lung adenocarcinoma A-549, prenylation of K-Ras was highly resistant even when co-treated with both inhibitors. Furthermore, soft agar experiments demonstrated that in all the human tumor cell lines tested inhibition of K-Ras prenylation was not necessary for inhibition of anchorage-independent growth. In addition, although GGTI-298 had very little effect on soft agar growth, the combination of FTI-277 and GGTI-298 resulted in significant growth inhibition. Therefore, the results demonstrate that while FTI-277 inhibits N-Ras and H-Ras processing in the human tumor cell lines evaluated, inhibition of K-Ras processing requires both an FTase inhibitor as well as a GGTase I inhibitor, and that inhibition of human tumor growth in soft agar does not require inhibition of oncogenic K-Ras processing.

摘要

法尼基转移酶(FTase)抑制剂FTI-277在阻断致癌性H-Ras的加工和信号传导方面非常有效,但对K-Ras4B的加工和信号传导无效。在K-Ras4B转化的NIH3T3细胞中,致癌性K-Ras4B的加工和信号传导抑制对香叶基香叶基转移酶I(GGTase I)抑制剂GGTI-286比对FTI-277更敏感,而在人肿瘤细胞系中K-Ras以及H-Ras和N-Ras对CAAX拟肽的敏感性尚不清楚。在此,我们报告一组来自胰腺、肺和膀胱的五种人癌细胞系均表达H-Ras、N-Ras和K-Ras,并且它们对FTase和GGTase I抑制剂的各自异戊二烯化敏感性是可变的。在所有研究的细胞系中,N-Ras的异戊二烯化对FTI-277高度敏感,并且在其中两个细胞系中,N-Ras对GGTI-286的类似物GGTI-298表现出轻微敏感性。尽管H-Ras的异戊二烯化也对FTI-277敏感,但即使在高浓度的FTI-277和/或GGTI-298下也从未实现对H-Ras加工的完全抑制。另一方面,K-Ras的异戊二烯化对FTI-277和GGTI-298具有高度抗性。最显著的是,抑制K-Ras异戊二烯化需要用两种抑制剂处理人肿瘤细胞系。在一种细胞系,即人肺腺癌A-549中,并即使同时用两种抑制剂处理,K-Ras的异戊二烯化仍具有高度抗性。此外,软琼脂实验表明,在所有测试的人肿瘤细胞系中,抑制K-Ras异戊二烯化对于抑制非锚定依赖性生长不是必需的。此外,尽管GGTI-298对软琼脂生长几乎没有影响,但FTI-277和GGTI-298的组合导致显著的生长抑制。因此,结果表明,虽然FTI-277在评估的人肿瘤细胞系中抑制N-Ras和H-Ras的加工,但抑制K-Ras的加工需要FTase抑制剂以及GGTase I抑制剂,并且在软琼脂中抑制人肿瘤生长不需要抑制致癌性K-Ras的加工。

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