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Effects of folate deficiency on gene expression in the apoptosis and cancer pathways in colon cancer cells

机译:叶酸缺乏对结肠癌细胞凋亡和癌细胞通路中基因表达的影响

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摘要

Folate is a B vitamin, deficiency of which appears to increase the risk of developing several malignancies including colorectal cancer. In contrast to the cancer-promoting effect of folate deficiency in normal tissues, several lines of evidence indicate that folate depletion suppresses the progression of existing neoplasms and enhance the sensitivity of cancer cells to chemotherapy. Folate mediates the transfer of one-carbon necessary for the de novo biosynthesis of purines and thymidylate, and hence is an essential factor for DNA synthesis and repair, and the maintenance of DNA integrity and stability. Folate deficiency induces DNA strand breaks, increases uracil misincorporation into DNA, impairs DNA repair and appears to induce apoptosis. Although the effects of folate depletion on DNA integrity and apoptosis and on subsequent cancer development, progression and treatment in colonic epithelial cells have been well characterized, it is largely unknown at present how folate depletion modulates specific upstream genes in apoptosis and cancer pathways that regulate these processes. We therefore investigated the effects of folate depletion on expression of genes involved in apoptosis and cancer pathways in four human colon adenocarcinoma cell lines in an in vitro model of folate deficiency. Apoptosis and cancer pathway-specific mini-microarray were used to screen for differentially expressed genes in response to folate deficiency, and the expression of seven most notably and consistently affected genes was confirmed by real time RT–PCR. Our data suggest that folate deficiency affects the expression of key genes that are related to cell cycle control, DNA repair, apoptosis and angiogenesis in a cell-specific manner. Cell-specificity in gene expression changes in response to folate deficiency is likely due to significant differences in molecular and phenotypic characteristics, growth rates and intracellular folate concentrations among the four cell lines.
机译:叶酸是一种B族维生素,缺乏维生素B会增加罹患包括结肠直肠癌在内的多种恶性肿瘤的风险。与正常组织中叶酸缺乏的促癌作用相反,几条证据表明叶酸耗竭抑制了现有肿瘤的进展并增强了癌细胞对化学疗法的敏感性。叶酸介导嘌呤和胸苷酸从头进行生物合成所需的一碳转移,因此是DNA合成和修复以及DNA完整性和稳定性维持的重要因素。叶酸缺乏会诱导DNA链断裂,增加尿嘧啶误掺入DNA,损害DNA修复,并似乎诱导凋亡。尽管已经充分表征了叶酸耗竭对DNA完整性和细胞凋亡以及随后的癌症发展,结肠上皮细胞的进展和治疗的影响,但目前在很大程度上尚不清楚叶酸耗竭如何调节细胞凋亡和调节这些基因的癌症途径中的特定上游基因。流程。因此,我们在叶酸缺乏的体外模型中研究了叶酸耗竭对参与凋亡的基因表达和四种人结肠腺癌细胞系中癌症途径的影响。细胞凋亡和特定于癌症途径的微型芯片用于筛选对叶酸缺乏反应的差异表达基因,实时RT-PCR证实了七个最显着且持续受影响的基因的表达。我们的数据表明,叶酸缺乏会以细胞特异性方式影响与细胞周期控制,DNA修复,凋亡和血管生成有关的关键基因的表达。应对叶酸缺乏的基因表达变化的细胞特异性可能是由于四种细胞系之间分子和表型特征,生长速率和细胞内叶酸浓度的显着差异。

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  • 来源
    《Carcinogenesis》 |2006年第5期|916-924|共9页
  • 作者单位

    Institute of Medical Science;

    Department of Nutritional Sciences and;

    Department of Medicine University of Toronto Toronto Ontario Canada M5S 1A8 and;

    Division of Gastroenterology St Michael's Hospital Toronto Ontario Canada M5B 1W8;

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