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Inhibition of Colony Formation of Drug‐resistant Human Tumor Cell Lines by Combinations of Interleukin‐2‐activated Killer Cells and Antitumor Drugs

机译:白介素2激活的杀伤细胞和抗肿瘤药物联合抑制耐药性人类肿瘤细胞株的集落形成

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摘要

The cytotoxicity of interleukin‐2‐activated killer (LAK) cells with or without anticancer drugs against cell lines with acquired drug resistance was evaluated in vitro by colony assay. Human non‐small cell lung cancer cell lines, PC‐9 and PC‐14, human leukemia cell line, K‐562, and their sublines resistant to cisplatin (CDDP), PC‐9/CDDP and PC‐14/CDDP, and to adriamycin (ADM), K‐562/ADM, were used as target cells. PC‐9/CDDP demonstrated a marked increase in susceptibility to killing by both peripheral blood lymphocytes (PBL) and LAK cells, as compared to the parental cell line, PC‐9. The cytotoxicity of PBL and LAK cells against PC‐14/CDDP and K‐562/ADM was similar to that against their parental cell lines. Moreover, the combination of LAK and CDDP had a synergistic effect on PC‐14 and PC‐14/CDDP.
机译:通过集落分析在体外评估了有或没有抗癌药的白细胞介素2激活的杀伤(LAK)细胞对获得性耐药的细胞系的细胞毒性。人非小细胞肺癌细胞系PC-9和PC-14,白血病细胞系K-562及其对顺铂(CDDP),PC-9 / CDDP和PC-14 / CDDP耐药的亚系以及抗阿霉素(ADM),K‐562 / ADM用作靶细胞。与亲代细胞系PC-9相比,PC-9 / CDDP表现出对外周血淋巴细胞(PBL)和LAK细胞杀伤的敏感性显着提高。 PBL和LAK细胞对PC-14 / CDDP和K-562 / ADM的细胞毒性类似于对其亲本细胞系的细胞毒性。此外,LAK和CDDP的组合对PC-14和PC-14 / CDDP具有协同作用。

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