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人胃癌细胞系中阿霉素耐药性发展早期步骤的流式细胞术分析

Flow cytometric analysis of early steps in development of adriamycin resistance in a human gastric cancer cell line.

作者信息

Tanaka S, Aizawa K, Katayanagi N, Tanaka O

机构信息

Department of Surgery I. Niigata University School of Medicine.

出版信息

Jpn J Cancer Res. 1994 Jan;85(1):86-92. doi: 10.1111/j.1349-7006.1994.tb02890.x.

Abstract

We have established a low-level adriamycin (ADM)-resistant human gastric cancer cell line (MKN45R) from the parental cell line (MKN45) by exposure to stepwise increases of ADM concentration (final concentration, 0.026 microgram/ml). The purpose of this study was to identify the early steps in the development of ADM resistance in MKN45R by flow cytometric (FCM) analysis. Comparison of the concentration required for 50% growth inhibition, determined by a tetrazolium-based colorimetric assay, showed that MKN45R was about 2.6-fold more resistant to ADM than MKN45. However, the inhibition index values were 89.5% for MKN45 and 86.4% for MKN45R, respectively, showing that ADM was judged to be "effective" against both cell lines. On the other hand, cell kinetic analysis by FCM revealed that the increase of the ratio of G2M accumulation induced by ADM treatment was significantly lower (P < 0.01) in MKN45R. Moreover, the efflux of ADM estimated by FCM analysis was significantly increased (P < 0.05) in MKN45R even though there was no significant increase of P-glycoprotein expression. These results suggest that although ADM was still effective based on a standard drug sensitivity test, the cancer cells were already acquiring resistance to ADM as judged from FCM analysis. Moreover, the mechanism of this ADM resistance is considered to be independent of P-glycoprotein expression. Thus, FCM analysis is useful for detecting the early steps in the development of drug resistance of cancer cells.

摘要

我们通过逐步提高阿霉素(ADM)浓度(终浓度为0.026微克/毫升),从亲代细胞系(MKN45)建立了一株低水平阿霉素耐药的人胃癌细胞系(MKN45R)。本研究的目的是通过流式细胞术(FCM)分析确定MKN45R中阿霉素耐药性发展的早期步骤。通过基于四氮唑的比色法测定50%生长抑制所需的浓度,比较结果显示MKN45R对阿霉素的耐药性比MKN45高约2.6倍。然而,MKN45和MKN45R的抑制指数值分别为89.5%和86.4%,表明阿霉素对这两种细胞系均被判定为“有效”。另一方面,FCM进行的细胞动力学分析显示,阿霉素处理诱导的G2M期积累比例的增加在MKN45R中显著更低(P<0.01)。此外,尽管P-糖蛋白表达没有显著增加,但FCM分析估计的MKN45R中阿霉素的外排显著增加(P<0.05)。这些结果表明,虽然基于标准药敏试验阿霉素仍然有效,但从FCM分析判断癌细胞已经在获得对阿霉素的耐药性。此外,这种阿霉素耐药的机制被认为与P-糖蛋白表达无关。因此,FCM分析对于检测癌细胞耐药性发展的早期步骤是有用的。

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