通过循环系统中某些物质的混合物抑制培养物和小鼠体内小鼠和各种人类肿瘤细胞系的生长

G Kulcsár
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引用次数: 12

摘要

有充分的证据表明,尽管艾滋病和其他免疫缺陷疾病或免疫抑制患者的免疫系统普遍异常,但只有少数几种肿瘤的发病率增加,并且免疫抑制的程度似乎不是这些肿瘤发展的关键因素。尽管已知的免疫系统对大多数肿瘤无效,但大多数人在其一生中都不会发生肿瘤,这一事实只能通过假设生命系统对肿瘤有额外的防御机制来解释。根据文献资料,可以假设这种防御机制的有效代理人是循环系统的某些物质。我们通过能够从71种被测试的化合物中选择13种循环系统物质来证明这一假设,以协同肿瘤细胞杀伤作用为标准。在控制条件良好的情况下,含有L-色氨酸、L-酪氨酸、L-蛋氨酸、L(-)-苹果酸盐、L-抗坏血酸盐、L-精氨酸、L-苯丙氨酸、L-组氨酸、2-脱氧d-核糖、d-生物素、吡醇、腺嘌呤和核黄素13种物质的混合物对Sp2/0-Ag14小鼠和K562、HEp-2、HeLa和Caco-2人肿瘤细胞株具有细胞毒性,但对Vero正常细胞株无细胞毒性。上述物质的混合可显著提高注射Sp2/0-Ag14小鼠骨髓瘤细胞的存活时间(T/C% 148.1),杀死超过2 log(99%)的细胞。处理结束后,对照和处理动物腹水中Sp2/0-Ag14细胞的死亡数量大致相同,为2 log。上述合剂明显减缓HeLa实体瘤的生长(T/C%,最小值35.7)。对照组和治疗组在治疗期间体重下降无显著差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inhibition of the growth of a murine and various human tumor cell lines in culture and in mice by mixture of certain substances of the circulatory system.

It is well documented that despite global abnormalities of the immune system in AIDS and other immune deficiency diseases or in immunosuppressed patients, the incidence of only a few kinds of tumor increases, and that the degree of immunosuppression seems not to be a critical factor in the development of even these tumors. The fact that tumors do not develop in the majority of population during their lifetime, despite the ineffectiveness of the known immune system against the majority of tumors, can only be explained by hypothesizing that the living system has an additional defense mechanism against tumors. On the bases of literary data, it can be assumed that the effective agents of this defense mechanism are certain substances of the circulatory system. We proved this hypothesis by being able to select thirteen substances of the circulatory system from 71 compounds tested, using the synergistic tumor cell-killing effect as criteria. The mixture containing the thirteen substances (L-tryptophan, L-tyrosine, L-methionine, L(-)-malate, L-ascorbate, L-arginine, L-phenylalanine, L-histidine, 2-deoxy-D-ribose, d-biotin, pyridoxine, adenine and riboflavin) had a cytotoxic effect against Sp2/0-Ag14 mouse and K562, HEp-2, HeLa and Caco-2 human tumor cell lines in well-controlled conditions, but it was not cytotoxic against Vero normal cell line. The mixture of the above substances increased significantly the survival time of mice (T/C% 148.1) injected i.p. with Sp2/0-Ag14 mouse myeloma cells by killing more than 2 logs (99%) of the cells. Approximately the same 2 logs cell kill was found counting the Sp2/0-Ag14 cells in the ascitic fluid of control and treated animals after finishing treatment. The above mixture slowed down the growth of HeLa solid tumor significantly (T/C%, the least value 35.7). The weight loss of control and treated group during treatment did not differ significantly.

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