首页> 外文期刊>Urologic oncology >(Z)-1,1-Dichloro-2-(4-methoxyphenyl)-3-phenylcyclopropane induces concentration-dependent growth inhibition, apoptosis, and coordinates regulation of apoptotic genes in TRAMP cells.
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(Z)-1,1-Dichloro-2-(4-methoxyphenyl)-3-phenylcyclopropane induces concentration-dependent growth inhibition, apoptosis, and coordinates regulation of apoptotic genes in TRAMP cells.

机译:(Z)-1,1-二氯-2-(4-甲氧基苯基)-3-苯基环丙烷诱导TRAMP细胞中浓度依赖性的生长抑制,细胞凋亡并协调凋亡基因的调控。

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摘要

(Z)-1-1-Dichloro-2,3-diphenylcyclopropane (A(II)) and (Z)-1,1-dichloro-2-(4-methoxyphenyl)-3-phenylcyclopropane [2-(4-methoxyphenyl)-A(II)] inhibit tubulin polymerization, PSA production, and the proliferation of human prostate cancer cells. The actions of the agents were studied in three transgenic adenocarcinomas of the mouse prostate (TRAMP) cell lines. Antiproliferative potencies were determined and cells treated with the more potent 2-(4-methoxyphenyl)-A(II) were examined for induction of apoptosis. Microarray analyses were conducted to determine the apoptosis-related genes up- and down-regulated by the agent. 2-(4-Methoxyphenyl)-A(II) concentration-dependently inhibited growth of all three cell lines. Fifty percent and 100% growth inhibitory and 50% lethal concentrations were determined to be 0.3, 1.5, and 5 muM, respectively. Minimum detectable apoptosis-inducing concentrations by ELISA were 0.10 to 0.14 muM. PARP cleavage and two-color flow cytometry assays verified apoptosis induction. Microarray analyses showed Bok and Siva-pending to be up-regulated and that Birc, Dad1, and Atf5 were down-regulated. 2-(4-methoxyphenyl)-A(II) inhibits proliferation and induces apoptosis in the in vivo-adaptable TRAMP cells, suggesting the compound should be further examined in preclinical models.
机译:(Z)-1-1-二氯-2,3-二苯基环丙烷(A(II))和(Z)-1,1-二氯-2-(4-甲氧基苯基)-3-苯基环丙烷[2-(4-甲氧基苯基) )-A(II)]抑制微管蛋白聚合,PSA产生和人前列腺癌细胞的增殖。在小鼠前列腺(TRAMP)细胞系的三种转基因腺癌​​中研究了这些试剂的作用。测定抗增殖能力,并检查用更有效的2-(4-甲氧基苯基)-A(II)处理的细胞的凋亡诱导。进行微阵列分析以确定由药剂上调和下调的凋亡相关基因。 2-(4-甲氧基苯基)-A(II)浓度依赖性抑制所有三个细胞系的生长。 50%和100%的生长抑制浓度和50%的致死浓度分别确定为0.3、1.5和5μM。通过ELISA检测的最小诱导凋亡浓度为0.10至0.14μM。 PARP裂解和两色流式细胞仪检测证实了凋亡诱导。基因芯片分析显示Bok和Siva-pending被上调,而Birc,Dad1和Atf5被下调。 2-(4-甲氧基苯基)-A(II)在体内可适应的TRAMP细胞中抑制增殖并诱导凋亡,这表明该化合物应在临床前模型中进一步检查。

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