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Tumor regression by phenethyl isothiocyanate involves DDB2

机译:苯乙基异硫氰酸酯导致的肿瘤消退涉及DDB2

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摘要

Phenethyl isothiocyanate (PE ITC) is a promising cancer chemopreventive agent commonly found in edible cruciferous vegetables. It has been implicated also for therapy, and is in clinical trial for lung cancer. Here, we provide evidence that the tumor-suppressive effect of PE ITC is related to its ability to induce expression of Damaged DNA-binding protein 2 (DDB2), a DNA repair protein involved also in apoptosis and premature senescence. DDB2 expression is attenuated in a wide variety of cancers including the aggressive colon cancers. We show that, in colon cancer cells, reactive oxygen species, which are induced by PE ITC, augment expression of DDB2 through the p38MAP K/JNK pathway, independently of p53. PE ITC-induced expression of DDB2 is critical for inhibition of tumor progression by PE ITC. Tumors derived from DDB2- deficient colon cancer cells are refractory to PE ITC-treatments, resulting from deficiencies in apoptosis and senescence. The DDB2-proficient tumors, on the other hand, respond effectively to PE ITC. The results show that PE ITC can be used to induce expression of DDB2, and that expression of DDB2 is critical for effective response of tumors to PE ITC.
机译:异硫氰酸苯乙基酯(PE ITC)是一种有前途的癌症化学预防剂,通常在食用十字花科蔬菜中发现。它也与治疗有关,并且在肺癌的临床试验中。在这里,我们提供的证据表明,PE ITC的肿瘤抑制作用与其诱导损伤的DNA结合蛋白2(DDB2)的表达有关,DDNA2是一种也与细胞凋亡和早衰有关的DNA修复蛋白。在包括侵袭性结肠癌在内的多种癌症中,DDB2表达均减弱。我们显示,在结肠癌细胞中,由PE ITC诱导的活性氧物种通过p38MAP K / JNK途径增强了DDB2的表达,而与p53无关。 PE ITC诱导的DDB2表达对于PE ITC抑制肿瘤进展至关重要。缺乏DDB2的结肠癌细胞产生的肿瘤对PE ITC治疗无效,这是由于细胞凋亡和衰老的缺乏所致。另一方面,DDB2熟练的肿瘤对PE ITC有效。结果表明,PE ITC可用于诱导DDB2的表达,而DDB2的表达对于肿瘤对PE ITC的有效反应至关重要。

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