库尔德妇女乳腺癌和线粒体DNA突变:来自伊拉克苏莱曼尼亚的病例对照研究。

Han N. Mohammed Fadhl, D. Rashid, F. Abdulkarim
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引用次数: 0

摘要

在过去的十年中,人们对癌症的分子基础进行了深入的研究。发现了许多与核相容的基因。此外,关于线粒体DNA(mtDNA)突变和线粒体单倍群决定簇(单核苷酸多态性;SNP)的研究已经探索了它们在一般癌症,特别是乳腺癌症中的潜在作用。本研究旨在确定生活在伊拉克苏莱曼尼亚的库尔德妇女中与乳腺癌相关的SNPs和mtDNA单倍群。这项病例对照研究是在苏莱曼尼亚的库尔德斯坦战略与科学研究所(KISSR)/分子实验室与韩国的一个专门实验室合作进行的。20名患有癌症的女性和20名患有良性乳腺疾病的女性被纳入研究。对40个乳腺组织标本的线粒体全基因组进行了测序。利用Haplogrep 2.0进行单倍群鉴定。使用卡方检验和Fisher精确检验进行统计分析。共鉴定了547个突变(癌症,n=344和对照,n=203),包括15个首次报告的突变。癌症样本中的HV单倍群与对照样本中的H单倍群相比(p=0.006)(比值比[OR]=28.00),是癌症发生的危险因素(p=0.002)。此外,与其他随机选择的SNP(A750G、A1438G和C7028T)相比,SNP(A8860G)是一种额外的风险(p=0.05和OR>1)。在结论中;某些mtDNA单倍群和SNPs与癌症风险的关联并不是新的。与在世界其他人群中进行的将A10398G确定为危险SNP的研究不同,我们的研究在库尔德人中确定了A8860G。人类种群之间确实存在地理和种族差异,因此在一个种群中常见的SNP在另一个种群可能要罕见得多。因此,有必要对我国癌症的分子生物学进行更多的研究,以澄清这一情况。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
BREAST CANCER AND MITOCHONDRIAL DNA MUTATIONS IN KURDISH WOMEN: A CASE-CONTROL STUDY FROM SULAYMANIYAH, IRAQ.
The molecular basis of breast cancer has been thoroughly investigated in the last decade. Many nuclear suscep tibility genes were discovered. Moreover, research about mitochondrial DNA (mtDNA) mutations and mitochondrial haplogroup determinants (single nucleotide polymorphism; SNP) has explored their potential role in cancers in general and breast cancer in particular. This study is to identify breast cancer-related SNPs and mtDNA haplogroups among Kurdish women living in Sulaymaniyah/Iraq. This case-control study was conducted in Kurdistan Institute for Strategic and Scientific Research (KISSR) / Molecular Lab in Sulaymaniyah in collaboration with a specialized lab in South Korea. Twenty women with breast cancer and 20 women with benign breast diseases were enrolled. The entire mitochondrial genome of 40 breast tissue specimens was sequenced. Haplogrep 2.0 was utilized for haplogroup identification. Statistical Analysis was performed using Chi-square and Fisher’s exact tests. A total of 547 mutations (Cancer, n=344 and Control, n=203) were identified including 15 first-reported mutations. HV haplogroup in the cancer samples was a risk factor for the development of breast cancer (p=0.002) compared to H haplogroup in the control samples (p =0.006) (Odd Ratio [OR] = 28.00). Furthermore, SNP (A8860G) was an additional risk compared to other randomly selected SNPs (A750G, A1438G, and C7028T) (p ˂0.05 and OR >1). In conclusions; the association of certain mtDNA haplogroups and SNPs with breast cancer risk is not new. Unlike studies performed in other populations of the world figuring out A10398G as the risky SNP, our study identified A8860G in the Kurds. Geographic and ethnic variations between human populations do exist, so an SNP that is common in one population group may be much rarer in another. Hence, more research on the molecular biology of breast cancer in our locality is warranted to clarify the situation.
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