Fibach E, Yamasaki H, Weinstein I B, Marks P A, Rifkind R A
Cancer Res. 1978 Nov;38(11 Pt 1):3685-8.
Spontaneous and induced differentiation of murine erythroleukemia cells (strain 745A DS19 ) is reversibly inhibited by 12-O-tetradecanoylphorbol-13-acetate (TPA), a potent promoter of mouse skin carcinogenesis, and by other tumor-promoting macrocyclic plant diterpenes, but it is not by nonpromoting diterpenes. Twelve clones randomly isolated from this strain vary in their response to TPA. All clones are induced to differentiate by several compounds, the most potent of which is hexamethylene bisacetamide. In six clones TPA (100 ng/ml) caused greater than 90% inhibition of differentiation, as measured by the appearance of benzidine-reactive cells. In two clones cell differentiation was not inhibited by TPA even at concentrations as high as 1 microgram/ml. In four clones, differentiation was only partially inhibited (16 to 47%) by TPA. Clones resistant to TPA inhibition of differentiation were also resistant to structurally related tumor-promoting agents. The isolation of variant cell lines, sensitive and resistant to TPA, provides a tool for elucidating the mechanism of tumor promoter-mediated inhibition of cell differentiation.
小鼠红白血病细胞(745A DS19株)的自发分化和诱导分化可被12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA,一种强效的小鼠皮肤癌发生促进剂)以及其他促肿瘤大环植物二萜类化合物可逆性抑制,但不会被非促肿瘤二萜类化合物抑制。从该菌株中随机分离出的12个克隆对TPA的反应各不相同。所有克隆都能被几种化合物诱导分化,其中最有效的是六亚甲基双乙酰胺。在6个克隆中,通过联苯胺反应性细胞的出现来衡量,TPA(100纳克/毫升)导致超过90%的分化抑制。在2个克隆中,即使TPA浓度高达1微克/毫升,细胞分化也未被抑制。在4个克隆中,TPA仅部分抑制(16%至47%)分化。对TPA抑制分化具有抗性的克隆对结构相关的促肿瘤剂也具有抗性。分离出对TPA敏感和抗性的变异细胞系,为阐明肿瘤促进剂介导的细胞分化抑制机制提供了一种工具。