Helicobacter pylori plus N-Methyl-N′-nitro-N-nitrosoguanidine: DNA damage and repair: Malignant transformation of human esophageal epithelial cells

恶性转化 DNA损伤 癌变 甲基亚硝基胍 彗星试验 癌症研究 细胞生长 分子生物学 生物 幽门螺杆菌 DNA修复 细胞 细胞周期 癌细胞 致癌物 癌症 化学 DNA 生物化学 遗传学 基因 突变
作者
Siyao Li,Yusong Guo,Xiaomin Liu,Yan Chen
出处
期刊:Mutation Research [Elsevier BV]
卷期号:888: 503636-503636 被引量:2
标识
DOI:10.1016/j.mrgentox.2023.503636
摘要

N-Methyl-N'-nitro-N-nitrosoguanidine (MNNG), found in pickled foods and in chlorinated water, has been used to induce malignant transformation and gastrointestinal cancer in rats. Helicobacter pylori (HP) is implicated in human gastric cancer and possibly also in esophageal cancer. These two agents - one chemical and the other biological - might act together to induce esophageal cancer. In this study, human esophageal epithelial cells (HEECs) were divided into four groups: HP, MNNG, HP + MNNG, and control. The HP-to-HEEC ratio was 100:1. Cells were exposed for 6 h and then passaged until malignant transformation. HEEC at early, intermediate, and late stages of malignant transformation were used for proliferation, cell-cycle, and invasion assays. The alkaline comet assay was performed and expression of proteins, including γ-H2AX and PAXX, was studied by western blotting, to explore DNA damage and repair processes. Measurements of cell morphology, soft-agar clone formation, and invasiveness, and a nude mouse xenograft model, were used to examine malignancy. The effect of HP was stronger than that of MNNG. The combination HP + MNNG exerted a stronger malignant transformation effect than either HP or MNNG alone. Mechanisms of this combined carcinogenesis may include promotion of cell proliferation, perturbation of the cell cycle, promotion of invasiveness, DNA double-strand break induction, or PAXX inhibition.
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