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GTI-2501是一种靶向人核糖核苷酸还原酶大亚基R1的反义药物,对多种肿瘤显示出强大的抗肿瘤活性。

GTI-2501, an antisense agent targeting R1, the large subunit of human ribonucleotide reductase, shows potent anti-tumor activity against a variety of tumors.

作者信息

Lee Yoon, Vassilakos Aikaterini, Feng Ningping, Jin Hongnan, Wang Ming, Xiong Keyong, Wright Jim, Young Aiping

机构信息

Lorus Therapeutics Inc., Ontario, M9W 4Z7, Canada.

出版信息

Int J Oncol. 2006 Feb;28(2):469-78.

Abstract

GTI-2501 is a 20-mer oligonucleotide that is complementary to a coding region in the mRNA of R1, the large subunit of ribonucleotide reductase (RNR). In vitro studies, have demonstrated that GTI-2501 decreases mRNA and protein levels of R1 in a sequence-specific and dose-dependent manner. Furthermore, GTI-2501 inhibits the growth of human lung, liver, ovary, brain, melanoma, breast and pancreatic tumor cells in colony forming assays. In vivo studies have shown that GTI-2501 significantly inhibits growth of human colon, pancreas, lung, breast, renal, ovarian, melanoma, brain glioblastoma-astrocytoma, and prostatic tumors in CD-1 nude, Balb/c nude and/or SCID mice. GTI-2501 treatment caused total regression of human breast and renal tumor xenografts in mice. These effects are not observed with a scrambled control oligonucleotide containing the same base content but not complementary to R1. GTI-2501 specifically inhibits metastasis of human melanoma cells to the lungs in CD-1 athymic nude mice and prolongs the survival of mice bearing human lymphoma. Taken together these results suggest that an antisense mechanism of action is responsible for growth inhibition in vitro and in vivo and that GTI-2501 can act as a selective and specific anti-tumor agent.

摘要

GTI-2501是一种20聚体寡核苷酸,与核糖核苷酸还原酶(RNR)的大亚基R1的mRNA中的一个编码区域互补。体外研究表明,GTI-2501以序列特异性和剂量依赖性方式降低R1的mRNA和蛋白质水平。此外,在集落形成试验中,GTI-2501抑制人肺癌、肝癌、卵巢癌、脑癌、黑色素瘤、乳腺癌和胰腺肿瘤细胞的生长。体内研究表明,GTI-2501在CD-1裸鼠、Balb/c裸鼠和/或SCID小鼠中显著抑制人结肠癌、胰腺癌、肺癌、乳腺癌、肾癌、卵巢癌、黑色素瘤、脑胶质母细胞瘤-星形细胞瘤和前列腺肿瘤的生长。GTI-2501治疗使小鼠体内的人乳腺和肾肿瘤异种移植物完全消退。用含有相同碱基含量但与R1不互补的随机对照寡核苷酸未观察到这些效果。GTI-2501在CD-1无胸腺裸鼠中特异性抑制人黑色素瘤细胞向肺部的转移,并延长荷人淋巴瘤小鼠的生存期。综上所述,这些结果表明反义作用机制在体外和体内的生长抑制中起作用,并且GTI-2501可作为一种选择性和特异性的抗肿瘤药物。

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