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舒林酸硫化物改变HT-29结肠腺癌细胞中细胞周期蛋白的表达。

Sulindac sulfide alters the expression of cyclin proteins in HT-29 colon adenocarcinoma cells.

作者信息

Qiao L, Shiff S J, Rigas B

机构信息

Department of Medicine, New York Methodist Hospital, Brooklyn, USA.

出版信息

Int J Cancer. 1998 Mar 30;76(1):99-104. doi: 10.1002/(sici)1097-0215(19980330)76:1<99::aid-ijc16>3.0.co;2-b.

Abstract

Sulindac sulfide (SS), the active metabolite of the colon cancer chemopreventive compound sulindac, inhibits the proliferation of HT-29 colon cancer cells mainly by inducing cell quiescence. We determined by bivariate flow-cytometric analysis both the DNA and cyclin protein content of individual cells. Thus, we assessed in detail the expression of several cyclins during the cell-cycle phases and demonstrated that SS (i) decreases the expression of cyclins B1 and E and (ii) increases the expression of cyclins D1, D2 and D3, particularly in the G1 phase of the cell cycle. SS-induced apoptotic cells expressed both E- and D-type cyclins but not cyclin B1. The changes in cyclin expression combined with reduced catalytic activity of cyclin-dependent kinases could explain in molecular terms the anti-proliferative effect of SS on HT-29 colon cancer cells. These changes may contribute to the chemopreventive effect of sulindac.

摘要

舒林酸硫化物(SS)是结肠癌化学预防化合物舒林酸的活性代谢产物,主要通过诱导细胞静止来抑制HT - 29结肠癌细胞的增殖。我们通过双变量流式细胞术分析了单个细胞的DNA和细胞周期蛋白含量。因此,我们详细评估了细胞周期各阶段几种细胞周期蛋白的表达,并证明SS(i)降低细胞周期蛋白B1和E的表达,(ii)增加细胞周期蛋白D1、D2和D3的表达,特别是在细胞周期的G1期。SS诱导的凋亡细胞同时表达E型和D型细胞周期蛋白,但不表达细胞周期蛋白B1。细胞周期蛋白表达的变化与细胞周期蛋白依赖性激酶催化活性的降低相结合,可以从分子角度解释SS对HT - 29结肠癌细胞的抗增殖作用。这些变化可能有助于舒林酸的化学预防作用。

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