TRANSCRIPTOMIC DIFFERENCES IN MONOZYGOTIC TWINS WITH OVARIAN CANCER

Gözde Kuru Türkcan, Demet Akdeniz Ödemiş, B. Kurt, Ş. Tuncer, Seda Kilic Erciyas, Özge Şükrüoğlu Erdoğan, H. Yazici
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Abstract

Objectives : The most significant barrier to treating epithelial ovarian cancer(EOC), is the late diagnosis and the emergence of chemotherapy resistance in the early stages.The ineffectiveness of standard treatment protocols in advanced-stage cases highlights the value of individualized EOC treatment.Even monozygotic(MZ) twins, with almost the same genotype in nature, can develop different phenotypic characteristics throughout life. Materials-Methods : In this context, the peripheral blood and ovarian tissues of monozygotic twins who are discordant in terms of ovarian cancer and the other healthy sibling who is a BRCA1 mutation carrier were compared in the study to analyze all RNA molecules transcribed at the genome level using next-generation sequencing technology.Through analyzing the molecules transcribed in the whole genome,the genetic variations underlying the development of ovarian cancer in a high-risk family bearing the BRCA1 mutation but only one of whom was found to have ovarian cancer were examined. Results : As a result of the transcriptomic analysis of the total RNA of 6 samples obtained from the ovarian tissues and peripheral blood samples of MZ twins with ovarian cancer and healthy sibling, the protein-encoding protein that shows expression changes in tissue and blood compared to healthy people genes,lncRNAs,precursor-miRNAs and fusion-transcripts have been identified.Filtering procedures and expression change coefficients(log2Fc) were calculated based on the expression data of identified ovarian cancer tumor markers CA125 and CA15-3. Conclusions : According to our study the expression levels of 66 protein-coding genes,23 novel lncRNAs,9 miRNAs and,2 fusion transcripts were found to vary in three groups and,these molecules are thought to be candidate molecules associated with epithelial ovarian cancer.
同卵双胞胎卵巢癌的转录组差异
目的:上皮性卵巢癌(EOC)治疗的最大障碍是晚期诊断和早期化疗耐药的出现。标准治疗方案在晚期病例中的无效突出了个体化EOC治疗的价值。即使是天生基因型几乎相同的同卵双胞胎,也可能在一生中发展出不同的表型特征。材料-方法:在此背景下,本研究比较了卵巢癌不一致的同卵双胞胎和另一个携带BRCA1突变的健康兄弟姐妹的外周血和卵巢组织,利用下一代测序技术分析了基因组水平上转录的所有RNA分子。通过分析整个基因组中转录的分子,研究了一个携带BRCA1突变的高风险家族中卵巢癌发生的遗传变异,但只有一个家族被发现患有卵巢癌。结果:通过对患有卵巢癌的MZ双胞胎和健康同胞的卵巢组织和外周血样本的6个样本的总RNA转录组学分析,确定了与健康人基因、lncRNAs、前体mirnas和融合转录物相比,在组织和血液中表达变化的蛋白编码蛋白。根据鉴定出的卵巢癌肿瘤标志物CA125和CA15-3的表达数据计算筛选程序和表达变化系数(log2Fc)。结论:根据我们的研究,我们发现了66个蛋白编码基因,23个新的lncrna,9个mirna和2个融合转录物在三组中表达水平不同,这些分子被认为是与上皮性卵巢癌相关的候选分子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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