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干扰素对小细胞肺癌细胞系及其阿霉素选择的多药耐药变体中主要组织相容性复合体I类抗原表达的差异生长抑制和增强作用。

Differential growth inhibition and enhancement of major histocompatibility complex class I antigen expression by interferons in a small-cell lung cancer cell line and its doxorubicin-selected multidrug-resistant variant.

作者信息

Cole S P, Campigotto B M, Johnson J G, Elliott B E

机构信息

Department of Oncology, Queen's University, Kingston, Ontario, Canada.

出版信息

Cancer Immunol Immunother. 1991;33(4):274-7. doi: 10.1007/BF01744948.

Abstract

Expression of class I and class II major histocompatibility complex antigens on a human small-cell lung cancer cell line and its multidrug-resistant variant was examined before and after exposure to interferon alpha (IFN alpha) and IFN gamma by flow cytometry. Neither IFN alpha nor IFN gamma induced class II antigen expression on the drug-sensitive or resistant cell line. Induction of class I antigen expression along with an inhibition of proliferation was observed in both cell lines after IFN alpha treatment. On the other hand, IFN gamma treatment resulted in growth inhibition and enhancement of class I antigen expression in the sensitive cell line but not the resistant cell line. The differential response of the two cell lines to IFN gamma cannot be directly attributed to the acquisition of drug resistance but it suggests that further investigation of the possibility that drug-sensitive and resistant small-cell lung tumors may respond differently to immunotherapies that include IFN gamma is warranted.

摘要

采用流式细胞术检测了人小细胞肺癌细胞系及其多药耐药变体在暴露于α干扰素(IFNα)和γ干扰素(IFNγ)前后I类和II类主要组织相容性复合体抗原的表达情况。IFNα和IFNγ均未诱导药物敏感或耐药细胞系上II类抗原的表达。IFNα处理后,在两种细胞系中均观察到I类抗原表达的诱导以及增殖的抑制。另一方面,IFNγ处理导致敏感细胞系生长受到抑制且I类抗原表达增强,但耐药细胞系未出现此现象。这两种细胞系对IFNγ的不同反应不能直接归因于耐药性的获得,但这表明有必要进一步研究药物敏感和耐药的小细胞肺癌肿瘤对包括IFNγ在内的免疫疗法可能有不同反应的可能性。

相似文献

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Induction of MHC antigens by tumour cell lines in response to interferons.
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本文引用的文献

3
Induction of HLA class-II antigen expression on human carcinoma cell lines by IFN-Gamma.
Int J Cancer. 1985 Feb 15;35(2):245-50. doi: 10.1002/ijc.2910350217.

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