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化学预防剂姜黄素是一种有效的人类宫颈肿瘤细胞放射增敏剂,其作用机制是通过增加活性氧的产生以及丝裂原活化蛋白激酶途径的过度激活。

The chemopreventive agent curcumin is a potent radiosensitizer of human cervical tumor cells via increased reactive oxygen species production and overactivation of the mitogen-activated protein kinase pathway.

作者信息

Javvadi Prashanthi, Segan Andrew T, Tuttle Stephen W, Koumenis Constantinos

机构信息

Department of Radiation Oncology, University of Pennsylvania, 3620 Hamilton Walk, Philadelphia, PA 19104, USA.

出版信息

Mol Pharmacol. 2008 May;73(5):1491-501. doi: 10.1124/mol.107.043554. Epub 2008 Feb 5.

Abstract

Cervical cancer is the second most common malignancy among women worldwide and is highly radioresistant, often resulting in local treatment failure. For locally advanced disease, radiation is combined with low-dose chemotherapy; however, this modality often leads to severe toxicity. Curcumin, a polyphenol extracted from rhizomes of the plant Curcuma longa, is a widely studied chemopreventive agent that was shown to have a low toxicity profile in three human clinical trials. Here, we show that pretreatment of two cervical carcinoma cell lines, HeLa and SiHa, with curcumin before ionizing radiation (IR) resulted in significant dose-dependent radiosensitization of these cells. It is noteworthy that curcumin failed to radiosensitize normal human diploid fibroblasts. Although in tumor cells, curcumin did not significantly affect IR-induced activation of AKT and nuclear factor-kappaB, we found that it caused a significant increase in the production of reactive oxygen species, which further led to sustained extracellular signal-regulated kinase (ERK) 1/2 activation. The antioxidant compound N-acetylcysteine blocked the curcumin-induced increased reactive oxygen species (ROS), sustained activation of ERK1/2, and decreased survival after IR in HeLa cells, implicating a ROS-dependent mechanism for curcumin radiosensitivity. Moreover, PD98059 (2'-amino-3'-methoxyflavone)-, PD184352- [2-(2-chloro-4-iodo-phenylamino)-N-cyclopropylmethoxy-3,4-difluoro-benzamide], and U0126 [1,4-diamino-2,3-dicyano-1,4-bis(2-aminophynylthio)butadiene]-specific inhibitors of mitogen-activated protein kinase kinase 1/2 (MEK1/2) blocked curcumin-mediated radiosensitization, demonstrating that the sustained ERK1/2 activation resulting from ROS generation leads to curcumin-mediated radiosensitization. Together, these results suggest a novel mechanism for curcumin-mediated radiosensitization involving increased ROS and ERK1/2 activation and suggest that curcumin application (either systemically or topically) may be an effective radiation modifying modality in the treatment of cervical cancer.

摘要

宫颈癌是全球女性中第二常见的恶性肿瘤,且具有高度放射抗性,常导致局部治疗失败。对于局部晚期疾病,放疗联合低剂量化疗;然而,这种治疗方式常导致严重毒性。姜黄素是从姜黄属植物姜黄的根茎中提取的一种多酚,是一种经过广泛研究的化学预防剂,在三项人体临床试验中显示出低毒性特征。在此,我们表明,在电离辐射(IR)前用姜黄素预处理两种宫颈癌细胞系HeLa和SiHa,会导致这些细胞出现显著的剂量依赖性放射增敏作用。值得注意的是,姜黄素未能使正常人二倍体成纤维细胞产生放射增敏作用。虽然在肿瘤细胞中,姜黄素并未显著影响IR诱导的AKT和核因子-κB的激活,但我们发现它会导致活性氧(ROS)生成显著增加,进而导致细胞外信号调节激酶(ERK)1/2持续激活。抗氧化化合物N-乙酰半胱氨酸可阻断姜黄素诱导的HeLa细胞中ROS增加、ERK1/2持续激活以及IR后的存活率降低,这表明存在一种依赖ROS的机制介导姜黄素的放射敏感性。此外,丝裂原活化蛋白激酶激酶1/2(MEK1/2)的特异性抑制剂PD98059(2'-氨基-3'-甲氧基黄酮)、PD184352 [2-(2-氯-4-碘苯基氨基)-N-环丙基甲氧基-3,4-二氟苯甲酰胺]和U0会阻断姜黄素介导的放射增敏作用,表明由ROS生成导致的ERK1/2持续激活会引发姜黄素介导的放射增敏作用。总之,这些结果提示了一种姜黄素介导放射增敏作用的新机制,涉及ROS增加和ERK1/2激活,并表明姜黄素的应用(全身或局部)可能是宫颈癌治疗中一种有效的放疗修饰方式。

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