Bose Bipasha, Gour Rekha R, Motiwale Leena, Rao K V K
Chemical Carcinogenesis Group, Cancer Research Institute, Advanced Centre for Treatment Research and Education in Cancer (ACTREC), Tata Memorial Centre, Kharghar, Navi Mumbai, India.
Chemotherapy. 2006;52(4):210-4. doi: 10.1159/000093038. Epub 2006 May 2.
Malachite green (MG), consisting of green crystals with a metallic lustre, is highly soluble in water, cytotoxic to various mammalian cells and also acts as a liver tumor promoter. In view of its industrial importance and possible exposure of human beings, MG poses a potential environmental health hazard. We have earlier reported the malignant transformation of Syrian hamster embryo (SHE) cells by MG.
Cell transformation assays were carried out as described in the literature. Western blotting and flow cytometry were carried out by standard methods.
In this study, we have studied the role of all three isoforms of mitogen-activated protein (MAP) kinases, i.e. extracellular regulated kinases (ERKs), Jun N-terminal kinases (JNKs) and p38 kinase in the MG-transformed SHE fibroblasts compared to controls. Our results showed that transformed cells were associated with decreased expression of ERKs and JNKs as evidenced by Western blotting studies. However, the p38 MAP kinase was found to be upregulated. Flow cytometric DNA histogram analysis indicated an increase in the expression of S phase cells in the transformed cell line as compared to their control counterparts.
The present studies indicate that decreased phosphoactive ERKs and JNKs and increased phosphoactive p38 kinase are associated with increased S phase cells during transformation of SHE cells by MG.
孔雀石绿(MG)由具有金属光泽的绿色晶体组成,高度溶于水,对各种哺乳动物细胞具有细胞毒性,并且还充当肝肿瘤促进剂。鉴于其工业重要性以及人类可能接触到它,MG对环境健康构成潜在危害。我们之前曾报道过MG可使叙利亚仓鼠胚胎(SHE)细胞发生恶性转化。
按照文献所述进行细胞转化试验。采用标准方法进行蛋白质印迹法和流式细胞术检测。
在本研究中,我们研究了丝裂原活化蛋白(MAP)激酶的三种同工型,即细胞外调节激酶(ERK)、Jun氨基末端激酶(JNK)和p38激酶在MG转化的SHE成纤维细胞中的作用,并与对照组进行比较。我们的结果表明,蛋白质印迹研究证明,转化细胞中ERK和JNK的表达降低。然而,发现p38 MAP激酶上调。流式细胞术DNA直方图分析表明,与对照细胞相比,转化细胞系中S期细胞的表达增加。
目前的研究表明,在MG转化SHE细胞的过程中,磷酸化活性ERK和JNK的降低以及磷酸化活性p38激酶的增加与S期细胞的增加有关。