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一种阿霉素耐药亚系比亲代人小细胞肺癌细胞系对氯尼达明更敏感。

An adriamycin-resistant subline is more sensitive than the parent human small cell lung cancer cell line to lonidamine.

作者信息

Kiura K, Ohnoshi T, Ueoka H, Takigawa N, Tabata M, Segawa Y, Shibayama T, Kimura I

机构信息

Department of Internal Medicine, Okayama University Medical School, Japan.

出版信息

Anticancer Drug Des. 1992 Dec;7(6):463-70.

PMID:1337430
Abstract

Lonidamine, a unique new type of anticancer agent, has been shown to exert marginal activity in patients with resistant small cell lung cancer. We have assessed cytotoxic activity using seven human small cell lung cancer cell lines and the drug resistant small cell lung cancer sublines, Adriamycin-resistant SBC-3/ADM100, etoposide-resistant SBC-3/ETP and cisplatin-resistant SBC-3/CDDP. Although lonidamine had only a minimal activity in seven human small cell lung cancer cell lines, SBC-3/ADM100 cells were more sensitive to lonidamine than the parent SBC-3 cells to a 1.6-fold extent in terms of IC50. SBC-3/CDDP and SBC-3/ETP had no cross-resistance to lonidamine at all. These observations may be of potential clinical significance in treating small cell lung cancer.

摘要

氯尼达明是一种独特的新型抗癌药物,已证明其对耐药性小细胞肺癌患者的疗效有限。我们使用七种人类小细胞肺癌细胞系以及耐药性小细胞肺癌亚系,即阿霉素耐药的SBC-3/ADM100、依托泊苷耐药的SBC-3/ETP和顺铂耐药的SBC-3/CDDP,评估了氯尼达明的细胞毒性活性。尽管氯尼达明在七种人类小细胞肺癌细胞系中仅有极小的活性,但就半数抑制浓度(IC50)而言,SBC-3/ADM100细胞对氯尼达明的敏感性比亲代SBC-3细胞高1.6倍。SBC-3/CDDP和SBC-3/ETP对氯尼达明完全没有交叉耐药性。这些观察结果在治疗小细胞肺癌方面可能具有潜在的临床意义。

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