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丝裂霉素C耐药结肠癌细胞系变体的建立及初步鉴定

Development and initial characterization of a mitomycin C-resistant colon cancer cell line variant.

作者信息

Perry R R, Greaves B R, Kang Y

机构信息

Department of Surgery, Eastern Virginia Medical School, Norfolk 23507-1912.

出版信息

Cancer Chemother Pharmacol. 1993;32(4):326-8. doi: 10.1007/BF00686181.

Abstract

Resistance may limit the clinical usefulness of a variety of chemotherapeutic drugs, including mitomycin C (MMC). In order to study resistance to MMC, a variant of the HT-29 human colon cell line was isolated by exposure to repeated doses of MMC. The 95% inhibitory concentration of MMC for this isolate (HT-29R13) was found to be approximately twice that for the parent line. The level of resistance did not increase with additional drug exposure, and resistance was stable for at least 6 months in the absence of drug exposure. HT-29R13 cells exhibit cross-resistance to melphalan and 5-FU but not to doxorubicin, cis-platinum, or etoposide. HT-29R13 cells are characterized by slightly decreased plating efficiency and slightly increased total protein compared with the parent line. This model of stable, low-level MMC resistance with an unusual cross-resistance pattern may prove useful for the study and characterization of MMC resistance mechanisms.

摘要

耐药性可能会限制包括丝裂霉素C(MMC)在内的多种化疗药物的临床应用。为了研究对MMC的耐药性,通过反复给予MMC剂量,分离出了HT-29人结肠癌细胞系的一个变体。发现MMC对该分离株(HT-29R13)的95%抑制浓度约为亲代细胞系的两倍。耐药水平不会随着额外的药物暴露而增加,并且在没有药物暴露的情况下,耐药性至少稳定6个月。HT-29R13细胞对美法仑和5-氟尿嘧啶表现出交叉耐药性,但对阿霉素、顺铂或依托泊苷没有交叉耐药性。与亲代细胞系相比,HT-29R13细胞的特点是接种效率略有下降,总蛋白略有增加。这种具有不寻常交叉耐药模式的稳定、低水平MMC耐药模型可能对MMC耐药机制的研究和表征有用。

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