General Directorate of Education, Basra, Iraq.
Department of Biology, College of Education in Qurna, University of Basra, Basra, Iraq.
Arch Razi Inst. 2023 Feb 28;78(1):185-193. doi: 10.22092/ARI.2022.358486.2227. eCollection 2023 Feb.
Endometrial and ovarian tumours are almost mechanistically affected by reproductive hormones. Ovarian cancer may be explained as metastatic or synchronous primary ovarian cancer, and the specific diagnosis is a challenge. This study aimed to investigate the mutations in fat mass and obesity-associated () genes and investigated the association of these mutations with the risk of endometrial and ovarian cancers as well as with cancer grade and stage. Blood samples were collected from 48 endometrial and ovarian cancer cases and 48 healthy women. Genomic DNA was extracted, and PCR was done to amplify exons 4-9. Sanger sequencing identified 6 different novel mutations submitted to DDBJ: p.W278G and p.G284G in exon 4, p.S318I and p.A324G in exon 5 and two mutations in intron 4. Other mutations were also detected in gene sequencing results, rs112997407 in intron 3, rs62033438, rs62033439, rs8048254 and rs8046502 in intron 4. The novel p.W278G, p.S318I and p.A324G mutations were predicted to be damaging. We did not find a significant association for all variables with cancer risk or clinical stage and grade except for rs62033438 variants, which showed a significant association with cancer grade, especially AA genotype (OR= 15, 95% CI:1.32 -169.88, = 0.03). In conclusion, the statistical analysis did not clarify whether mutations are implicated in cancer. Further studies with more samples are recommended to provide a more accurate picture of the correlation between mutations and endometrial and ovarian cancer susceptibility.
子宫内膜癌和卵巢癌几乎都是由生殖激素引起的。卵巢癌可以解释为转移性或同步性原发性卵巢癌,具体诊断具有挑战性。本研究旨在研究脂肪量和肥胖相关(FTO)基因的突变,并研究这些突变与子宫内膜癌和卵巢癌的风险以及与癌症分级和分期的关系。采集了 48 例子宫内膜癌和卵巢癌患者和 48 例健康女性的血液样本。提取基因组 DNA,进行 PCR 扩增外显子 4-9。Sanger 测序鉴定出 6 种不同的新突变,提交给 DDBJ:外显子 4 中的 p.W278G 和 p.G284G,外显子 5 中的 p.S318I 和 p.A324G 以及内含子 4 中的两个突变。在基因测序结果中还检测到其他突变,外显子 3 中的 rs112997407,内含子 4 中的 rs62033438、rs62033439、rs8048254 和 rs8046502。新发现的 p.W278G、p.S318I 和 p.A324G 突变被预测为有害。我们没有发现所有变量与癌症风险或临床分期和分级之间存在显著关联,除了 rs62033438 变异,其与癌症分级,特别是 AA 基因型(OR=15,95%CI:1.32-169.88,=0.03)之间存在显著关联。总之,统计分析没有阐明 FTO 基因突变是否与癌症有关。建议进行更多样本的进一步研究,以更准确地了解 FTO 基因突变与子宫内膜癌和卵巢癌易感性之间的相关性。