Kawashima Atsunari, Takayama Hitoshi, Tsujimura Akira
The Department of Urology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita City, Osaka 565-0871, Japan.
Adv Urol. 2012;2012:812398. doi: 10.1155/2012/812398. Epub 2011 Oct 26.
The excision repair cross-complementing group 1 (ERCC1) gene performs a critical incision step in DNA repair and is reported to be correlated with carcinogenesis and resistance to drug or ionizing radiation therapy. We reviewed the correlation between ERCC1 and bladder cancer. In carcinogenesis, several reports discussed the relation between ERCC1 single nucleotide polymorphisms and carcinogenesis in bladder cancer only in case-control studies. Regarding the relation between ERCC1 and resistance to chemoradiotherapy, in vitro and clinical studies indicate that ERCC1 might be related to resistance to radiation therapy rather than cisplatin therapy. It is controversial whether ERCC1 predicts prognosis of bladder cancer treated with cisplatin-based chemotherapy. Tyrosine kinase receptors or endothelial-mesenchymal transition are reported to regulate the expression of ERCC1, and further study is needed to clarify the mechanism of ERCC1 expression and resistance to chemoradiotherapy in vitro and to discover novel therapies for advanced and metastatic bladder cancer.
切除修复交叉互补基因1(ERCC1)在DNA修复过程中执行关键的切割步骤,据报道,它与癌症发生以及对药物或电离辐射治疗的抗性相关。我们回顾了ERCC1与膀胱癌之间的相关性。在癌症发生方面,仅有几项病例对照研究讨论了ERCC1单核苷酸多态性与膀胱癌发生之间的关系。关于ERCC1与放化疗抗性之间的关系,体外研究和临床研究表明,ERCC1可能与放射治疗抗性相关,而非顺铂治疗抗性。ERCC1是否能预测基于顺铂的化疗治疗膀胱癌的预后仍存在争议。据报道,酪氨酸激酶受体或内皮-间充质转化可调节ERCC1的表达,需要进一步研究以阐明ERCC1表达的机制以及体外对放化疗的抗性,并发现针对晚期和转移性膀胱癌的新疗法。