Demidem A, Broquet C, Menciahuerta J, Salahuddin S, Lam T, Khan R, Braquet P, Levine A, Bonavida B
UNIV CALIF LOS ANGELES, SCH MED, DEPT MICROBIOL & IMMUNOL, 10833 LE CONTE AVE, LOS ANGELES, CA 90024 USA. UNIV CALIF LOS ANGELES, JONSSON COMPREHENS CANC CTR, LOS ANGELES, CA 90024 USA. INST HENRI BEAUFOUR, F-92350 LE PLESSIS ROBINSON, FRANCE. HUNTINGTON MEM HOSP, INST MOLEC MED & TECHNOL, PASADENA, CA 91105 USA. UNIV SO CALIF, SCH MED, DEPT MED, LOS ANGELES, CA 90033 USA.
Int J Oncol. 1994 Jun;4(6):1203-9. doi: 10.3892/ijo.4.6.1203.
Non-Hodgkin's lymphoma B cells (NHL-B) often become refractory to conventional chemotherapeutic drugs. The present study investigated the sensitivity of three AIDS-derived NHL-B cell lines to newly synthesized azaalkyllysophospholipids (AALP) and podophyllotoxin derivatives. All three cell lines were sensitive to 5 AALP derivatives and toxicity was detectable at 24 h of culture and was increased at 48 and 72 h of incubation. Toxicity was concentration-dependent and die extent of cytotoxicity varied slightly from one cell line to another. These cell lines were less sensitive to the podophyllotoxin derivatives VP-16, BDPTN and BEPT than to die AALP. This was shown by the extent of cytotoxicity calculated on a molar basis and by the delayed kinetics of lysis. Pretreatment of the tumor cells with IFN-gamma stimulated cell proliferation. IFN-gamma treated tumor cells were also tested for their sensitivity to the various cytotoxic agents. In all cases, the sensitivity of the IFN-gamma pretreated cell lines to the podophyllotoxin derivatives and AALP was significantly enhanced. These findings demonstrate that drug resistant NHL-B cells are sensitive to a new family of AALP and podophyllotoxin derivatives. Further, the sensitivity of the tumor cells was enhanced by treatment with IFN-gamma. The potential clinical use of these new cytotoxic agents to overcome resistance of AIDS-related cell lymphomas is discussed.
非霍奇金淋巴瘤B细胞(NHL - B)常常对传统化疗药物产生耐药性。本研究调查了三种源自艾滋病患者的NHL - B细胞系对新合成的氮杂烷基溶血磷脂(AALP)和鬼臼毒素衍生物的敏感性。所有三种细胞系对5种AALP衍生物均敏感,在培养24小时时可检测到毒性,且在孵育48小时和72小时时毒性增加。毒性呈浓度依赖性,不同细胞系的细胞毒性程度略有差异。这些细胞系对鬼臼毒素衍生物VP - 16、BDPTN和BEPT的敏感性低于对AALP的敏感性。这通过基于摩尔计算的细胞毒性程度以及延迟的裂解动力学得以体现。用γ干扰素预处理肿瘤细胞可刺激细胞增殖。还测试了经γ干扰素处理的肿瘤细胞对各种细胞毒性药物的敏感性。在所有情况下,经γ干扰素预处理的细胞系对鬼臼毒素衍生物和AALP的敏感性均显著增强。这些发现表明,耐药的NHL - B细胞对新的AALP家族和鬼臼毒素衍生物敏感。此外,用γ干扰素处理可增强肿瘤细胞的敏感性。本文还讨论了这些新型细胞毒性药物在克服艾滋病相关细胞淋巴瘤耐药性方面的潜在临床应用。