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顺铂耐药人表皮样癌细胞系A431细胞的建立与鉴定

Establishment and characterization of cisplatin-resistant human epidermoid carcinoma cell line, A431 cell.

作者信息

Mese H, Sasaki A, Alcalde R E, Nakayama S, Matsumura T

机构信息

Department of Oral and Maxillofacial Surgery II, Okayama University Dental School, Okayama, Japan.

出版信息

Chemotherapy. 1998 Nov-Dec;44(6):414-20. doi: 10.1159/000007153.

Abstract

Cisplatin, cis-diamminedichloroplatinum(II) (CDDP) is one of the most important anticancer agents, initially producing good responses in various tumors. However, resistance to this drug often develops in various tumors, and additional administration decreases its chemotherapeutic efficacy. The precise mechanism of acquisition of resistance to this drug is still uncertain. However in the present study, we established two CDDP-resistant sublines A431/CDDP1 and A431/CDDP2 from human epidermoid carcinoma cell line A431. These resistant sublines were constituted by exposing A431 cells to a gradually increasing dose of CDDP (A431/CDDP1), and by mutagenic induction with mutagen (A431/CDDP2). A431/CDDP1 and A431/CDDP2 have developed 3.1 and 2.7 times more resistance to CDDP than the original A431 cell in terms of IC50. The two CDDP-resistant sublines showed cross-resistance to the CDDP analogue, carboplatin (CBDCA), but not to other chemotherapeutic drugs such as Adriamycin (ADR) and 5-fluorouracil (5-FU). These CDDP-resistant sublines were transplanted into nude mice to demonstrate the resistance to CDDP treatment in vivo. According to the in vitro assay, the mechanism of resistance in A431/CDDP1 and A431/CDDP2 seems to be based on a reduction of intracellular accumulation of CDDP, because their platinum concentration, which is the major component of CDDP, significantly declined. The established CDDP-resistant sublines may be used in further trials to improve the understanding of the mechanisms of resistance to CDDP.

摘要

顺铂,顺二氨二氯铂(II)(CDDP)是最重要的抗癌药物之一,最初在各种肿瘤中产生良好的反应。然而,各种肿瘤中常常会出现对这种药物的耐药性,额外给药会降低其化疗效果。对这种药物产生耐药性的确切机制仍不确定。然而,在本研究中,我们从人表皮样癌细胞系A431建立了两个耐顺铂亚系A431/CDDP1和A431/CDDP2。这些耐药亚系是通过将A431细胞暴露于逐渐增加剂量的顺铂(A431/CDDP1)以及用诱变剂进行诱变诱导(A431/CDDP2)而构建的。就半数抑制浓度(IC50)而言,A431/CDDP1和A431/CDDP2对顺铂的耐药性分别比原始A431细胞高3.1倍和2.7倍。这两个耐顺铂亚系对顺铂类似物卡铂(CBDCA)表现出交叉耐药性,但对阿霉素(ADR)和5-氟尿嘧啶(5-FU)等其他化疗药物没有交叉耐药性。将这些耐顺铂亚系移植到裸鼠体内,以证明其在体内对顺铂治疗的耐药性。根据体外试验,A431/CDDP1和A431/CDDP2的耐药机制似乎是基于细胞内顺铂积累的减少,因为作为顺铂主要成分的铂浓度显著下降。所建立的耐顺铂亚系可用于进一步试验,以增进对顺铂耐药机制的了解。

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