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通过导入谷胱甘肽S-转移酶π基因对人肺癌细胞系化学放射敏感性的修饰

Modification of chemo-radiosensitivity of a human lung cancer cell line by introduction of the glutathione S-transferase pi gene.

作者信息

Miyara H, Hida T, Nishida K, Takahashi T, Sugiura T, Ariyoshi Y, Morishita M, Takahashi T, Ueda R

机构信息

Laboratory of Chemotherapy, Aichi Cancer Center Research Institute, Nagoya.

出版信息

Jpn J Clin Oncol. 1996 Feb;26(1):1-5. doi: 10.1093/oxfordjournals.jjco.a023171.

Abstract

Recent studies have suggested that glutathione S-transferase pi (GST-pi) may play a role in determining tumor sensitivities to cytotoxic drugs. In order to better understand the role of this enzyme in chemo- and/or radioresistance of lung cancer cells, we examined whether introduction of GST-pi cDNA into a chemo- and radiosensitive lung cancer cell line altered its sensitivities to various chemotherapeutic agents and/or ionizing radiation, which are often used in the management of lung cancers. Modestly increased resistance of the GST-pi transfectants preferentially to sublethal damage caused by ionizing radiation as well as to adriamycin (ADM) was observed. In contrast, resistances to cisplatin (CDDP), etoposide (VP-16), irinotecan hydrochloride (CPT-11) and paclitaxel were virtually unaltered. These results suggest that GST-pi may not play a major role in chemo- and radioresistance of lung cancers, although it could afford selective and limited protection against ADM- and ionizing radiation-induced damage.

摘要

近期研究表明,谷胱甘肽S-转移酶π(GST-π)可能在决定肿瘤对细胞毒性药物的敏感性方面发挥作用。为了更好地理解该酶在肺癌细胞化疗和/或放射抗性中的作用,我们检测了将GST-π cDNA导入化疗和放射敏感的肺癌细胞系后,其对常用于肺癌治疗的各种化疗药物和/或电离辐射的敏感性是否发生改变。观察到GST-π转染子对电离辐射以及阿霉素(ADM)所致亚致死损伤的抗性适度增加。相比之下,对顺铂(CDDP)、依托泊苷(VP-16)、盐酸伊立替康(CPT-11)和紫杉醇的抗性几乎未改变。这些结果表明,GST-π可能在肺癌的化疗和放射抗性中不发挥主要作用,尽管它可以对ADM和电离辐射诱导的损伤提供选择性和有限的保护。

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