Leibovici J, Klorin G, Klein O, Michowitz M
Department of Pathology, Sackler Faculty of Medicine, Tel-Aviv University, Israel.
Cancer Biother. 1995 Spring;10(1):53-60. doi: 10.1089/cbr.1995.10.53.
The tumor progression process has been found to be accompanied by various cell membrane modifications. This cell organelle may therefore be considered as a target for drugs directed against tumor cells of advanced cancer. Hyperthermia acts on tumor cells largely, although not only, via an effect on the cell membrane. In the present study, the in vitro effect of hyperthermia on the tumorigenicity of cells derived from two AKR lymphoma variants of malignancy, TAU-39 of low (LM) and TAU-38 of high-malignancy (HM), was compared. The cells of the HM variant were markedly more sensitive to hyperthermic treatment than those of the LM one. Pretreatment of cells at 41 degrees C or 43 degrees C resulted in a more marked delay in tumor appearance in mice injected with the HM than in those inoculated with the LM variant. Moreover, in mice inoculated with cells pretreated at 45 degrees C, long term survivors were found only in those inoculated with the HM variant. These results corroborate our previous data regarding the effect of hyperthermia on metastatic and primary tumor cells of AKR lymphoma as well as the F1 and F10 variants of B16 melanoma.
已发现肿瘤进展过程伴随着各种细胞膜修饰。因此,这种细胞器可被视为针对晚期癌症肿瘤细胞的药物靶点。热疗对肿瘤细胞的作用很大程度上(尽管不仅如此)是通过对细胞膜的影响来实现的。在本研究中,比较了热疗对源自两种恶性程度不同的AKR淋巴瘤变体(低恶性的TAU - 39和高恶性的TAU - 38)的细胞致瘤性的体外作用。高恶性变体的细胞比低恶性变体的细胞对热疗明显更敏感。在41℃或43℃对细胞进行预处理,导致注射高恶性变体细胞的小鼠比注射低恶性变体细胞的小鼠肿瘤出现延迟更明显。此外,在接种了45℃预处理细胞的小鼠中,仅在接种高恶性变体细胞的小鼠中发现了长期存活者。这些结果证实了我们之前关于热疗对AKR淋巴瘤转移瘤和原发瘤细胞以及B16黑色素瘤F1和F10变体作用的数据。