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Activity (transcription) of the genes for MLH1, MSH2 and p53 in sporadic colorectal tumours with micro-satellite instability

机译:MLH1,MSH2和p53基因在具有微卫星不稳定性的散发性结直肠肿瘤中的活性(转录)

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Micro-satellite instability (MSI) is relevant in the management of colorectal cancers (CRC) and relies on analysis of gene mutations, or production of the proteins involved in DNA mismatch repair (e.g. MLH1, MSH2). p53 mutation is also relevant in MSI, but high-level CRC (MSI-H) demonstrate fewer mutations than low-level (MSI-L) or stable (MSS) cancers. Recently, the importance of gene activity (transcription) in MSI has been identified, where rather than being mutated genes have been downregulated. In this study, 67 sporadic CRC and eight samples of normal bowel were analysed for MSI status (by SSCP) and levels of MLH1, MSH2 and p53 gene transcription (by RT–PCR and scanning densitometry). Micro-satellite instability correlated with gender and site, with more MSI-H CRC in females (PPPPPP<0.001). Although fewer mutations are reported in MSI-H than MSI-L/MSS, these results suggest that reduced p53 transcription might account for decreased tumour suppression in MSI-H. The direct correlation between MLH1 and MSH2 transcription suggests that control of these genes might be coordinated.
机译:微卫星不稳定性(MSI)与大肠癌(CRC)的治疗有关,并且依赖于基因突变的分析或涉及DNA错配修复的蛋白质的产生(例如MLH1,MSH2)。 p53突变也与MSI相关,但是高水平CRC(MSI-H)的突变少于低水平(MSI-L)或稳定(MSS)的癌症。最近,已经确定了基因活性(转录)在MSI中的重要性,在该基因中,而不是被突变的基因被下调。在这项研究中,分析了67例散发性CRC和8份正常肠的MSI状态(通过SSCP)以及MLH1,MSH2和p53基因转录水平(通过RT-PCR和扫描光密度法)。微卫星的不稳定性与性别和部位有关,女性中的MSI-H CRC更高(PPPPPP <0.001)。尽管在MSI-H中报道的突变少于MSI-L / MSS,但这些结果表明,减少的p53转录可能是MSI-H中肿瘤抑制作用降低的原因。 MLH1和MSH2转录之间的直接关系表明,这些基因的控制可能是协调的。

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