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Mutational Hotspots in the Mitochondrial D-Loop Region of Cancerous and Precancerous Colorectal Lesions in Egyptian Patients

机译:埃及患者癌前期和结直肠前病变线粒体D环区域的突变热点

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摘要

Mutations in the mitochondrial genome (mtDNA) are associated with different types of cancer, specifically colorectal cancer (CRC). However, few studies have been performed on precancerous lesions, such as ulcerative colitis (UC) lesions and adenomatous polyps (AP). The aim of this study was to identify mtDNA mutations in the cancerous and precancerous lesions of Egyptian patients. An analysis of the mutations found in six regions of the mtDNA genome (ND1, ND5, COI, tRNAser, D-loop 1, and 2) in 80 Egyptian patients (40 CRC, 20 UC, and 20 AP) was performed using polymerase chain reaction–single-strand conformational polymorphism techniques and followed up by direct sequencing. The overall incidence of mutations was 25%, 25%, and 35% in CRC, UC, and AP cases, respectively. Although there was no common mutation pattern within each group, a large number of mutations were detected in the D-loop region in all of the groups. Some mutations (e.g., T414G) were detected repeatedly in precancerous (UC and AP) and cancerous lesions. Mutations detected in patients with CRC were predominantly found in the ND1 gene (40%). Our preliminary study suggests that Egyptian patients with CRC have a large number of mtDNA mutations, especially in the D-loop region, which have not been previously reported. Mutations in the mtDNA of precancerous lesions (i.e., AP and UC) may contribute to transformation events that lead to CRC.
机译:线粒体基因组(mtDNA)中的突变与不同类型的癌症相关,特别是结直肠癌(CRC)。但是,针对癌前病变,如溃疡性结肠炎(UC)病变和腺瘤性息肉(AP)的研究很少。本研究的目的是鉴定埃及患者癌变和癌前病变中的mtDNA突变。使用聚合酶链分析对80名埃及患者(40 CRC,20 UC和20 AP)的mtDNA基因组六个区域(ND1,ND5,COI,tRNAser,D-loop 1和2)中发现的突变进行了分析。反应-单链构象多态性技术,然后进行直接测序。在CRC,UC和AP病例中,突变的总发生率分别为25%,25%和35%。尽管每个组中没有常见的突变模式,但是在所有组的D环区域中都检测到大量突变。在癌前病变(UC和AP)和癌性病变中反复检测到某些突变(例如T414G)。在CRC患者中检测到的突变主要在ND1基因中发现(40%)。我们的初步研究表明,埃及CRC患者有大量mtDNA突变,尤其是在D环区域,以前没有报道。癌前病变(即AP和UC)的mtDNA突变可能会导致导致CRC的转化事件。

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