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GTI-2040是一种针对人类核糖核苷酸还原酶小亚基成分(R2)的反义药物,对多种肿瘤显示出强大的抗肿瘤活性。

GTI-2040, an antisense agent targeting the small subunit component (R2) of human ribonucleotide reductase, shows potent antitumor activity against a variety of tumors.

作者信息

Lee Yoon, Vassilakos Aikaterini, Feng Ningping, Lam Viengthong, Xie Hongsheng, Wang Ming, Jin Hongnan, Xiong Keyong, Liu Chenyi, Wright Jim, Young Aiping

机构信息

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

出版信息

Cancer Res. 2003 Jun 1;63(11):2802-11.

Abstract

GTI-2040 is a 20-mer oligonucleotide that is complementary to a coding region in the mRNA of the R2 small subunit component of human ribonucleotide reductase. In vitro studies using a number of human tumor cell lines have demonstrated that GTI-2040 decreases mRNA and protein levels of R2 in a sequence- and target-specific manner. In vivo studies have shown that GTI-2040 significantly inhibits growth of human colon tumors (adenocarcinoma), pancreatic tumors (adenocarcinoma), liver tumors, lung tumors, breast tumors (adenocarcinoma), renal tumors, ovarian tumors (adenocarcinoma), melanoma, brain glioblastoma-astrocytoma, prostatic tumors, and cervical tumors in nude and/or severe combined immunodeficient mice. Antitumor effects were not observed with an oligonucleotide containing four mismatches to the R2 sequence or with a scrambled sequence containing the same base content but not complementary to R2. This suggests that an antisense mechanism is responsible for the in vivo observations. In addition to tumor growth assays, GTI-2040 was tested in a murine model of human lymphoma. Treatment of severe combined immunodeficient mice bearing Burkitt's lymphoma with GTI-2040, but not control oligonucleotides, greatly extended the survival of mice, and survival extended well beyond the treatment period. Finally, GTI-2040 specifically inhibits metastasis of human melanoma cells to the lungs in nude mice. Taken together, the results of these studies indicate that GTI-2040 can act as a selective and specific anticancer agent against a broad range of human tumors.

摘要

GTI-2040是一种20聚体寡核苷酸,与人核糖核苷酸还原酶R2小亚基成分的mRNA编码区互补。使用多种人类肿瘤细胞系进行的体外研究表明,GTI-2040以序列和靶点特异性方式降低R2的mRNA和蛋白质水平。体内研究表明,GTI-2040在裸鼠和/或严重联合免疫缺陷小鼠中可显著抑制人类结肠肿瘤(腺癌)、胰腺肿瘤(腺癌)、肝脏肿瘤、肺部肿瘤、乳腺肿瘤(腺癌)、肾脏肿瘤、卵巢肿瘤(腺癌)、黑色素瘤、脑胶质母细胞瘤-星形细胞瘤、前列腺肿瘤和宫颈肿瘤的生长。与R2序列有四个错配的寡核苷酸或碱基含量相同但与R2不互补的乱序序列未观察到抗肿瘤作用。这表明反义机制是体内观察结果的原因。除了肿瘤生长试验外,GTI-2040还在人类淋巴瘤的小鼠模型中进行了测试。用GTI-2040而非对照寡核苷酸治疗患有伯基特淋巴瘤的严重联合免疫缺陷小鼠,可显著延长小鼠的生存期,且生存期延长至治疗期之后。最后,GTI-2040可特异性抑制裸鼠中人类黑色素瘤细胞向肺部的转移。综上所述,这些研究结果表明,GTI-2040可作为一种针对多种人类肿瘤的选择性和特异性抗癌药物。

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