Gomi A, Shinoda S, Sakai R, Hirai H, Ozawa K, Masuzawa T
Department of Surgical Neurology, Jichi Medical School, Tochigi, Japan.
Biochem Biophys Res Commun. 1996 Oct 14;227(2):558-63. doi: 10.1006/bbrc.1996.1545.
We investigated the expression of DNA polymerase beta (beta-pol) and O6-methylguanine-DNA methyltransferase (MGMT) in human glioma cells with acquired resistance to 1-(4-amino-2-methyl-5-pyrimidinyl)-methyl-3-(2-chloroethyl)-3-nitrosoure a (ACNU) and in the parent cells. ACNU-resistant T430 (T430R) and A172 (A172R) glioma cell lines were established following repeated exposure to ACNU. The level of MGMT mRNA expression was elevated in T430R, but not in A172R. In contrast, the level of beta-pol mRNA expression and the level of beta-pol protein were elevated in A172R, compared with the parent cells. While the mechanism of MGMT repair has been considered to be important in the drug resistance of human brain tumors to ACNU, our present results demonstrate that beta-pol may also play an important role in the acquisition of tumor cell resistance to ACNU in human gliomas.
我们研究了对1-(4-氨基-2-甲基-5-嘧啶基)甲基-3-(2-氯乙基)-3-亚硝基脲(ACNU)产生获得性耐药的人胶质瘤细胞及其亲本细胞中DNA聚合酶β(beta-pol)和O6-甲基鸟嘌呤-DNA甲基转移酶(MGMT)的表达情况。通过反复暴露于ACNU建立了ACNU耐药的T430 (T430R)和A172 (A172R)胶质瘤细胞系。T430R中MGMT mRNA表达水平升高,但A172R中未升高。相反,与亲本细胞相比,A172R中beta-pol mRNA表达水平和beta-pol蛋白水平升高。虽然MGMT修复机制被认为在人脑肿瘤对ACNU的耐药性中起重要作用,但我们目前的结果表明,beta-pol在人胶质瘤肿瘤细胞对ACNU耐药性的获得中也可能起重要作用。