长非编码 RNA SOX2OT rs9839776 C>T 多态性与不明原因复发性流产的相关性

Nermeen Abd Ellatif, Sara Agwa, Neveen Ashaat, Mervat Elgendy
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引用次数: 0

摘要

复发性流产(RM)是一种严重的妊娠并发症,会导致两次或两次以上的自然妊娠流产。复发性流产有几个复杂的原因。遗传学、免疫学和细胞生物学的进步将非编码 RNA(ncRNA)与复发性流产紧密联系在一起。NcRNAs 可调控胎盘滋养层细胞的过程,从而影响滋养层细胞的发育、迁移和内陷;它们还在乳腺癌和卵巢癌中发挥作用。因此,它们的异常表达可能会导致胎盘早剥。多项研究发现,RM 与调节细胞迁移的基因多态性有关。长非编码 RNA(lncRNA)SOX2OT 基因的变异与多种癌症相关疾病有关,尤其是结肠直肠癌、乳腺癌和消化道癌症。最近的一项研究发现,长非编码 SOX2OT rs9839776 CT 会增加 RM 的患病风险。在这篇综述中,我们将解释支持 LncRNA SOX2OT rs9839776 多态性与复发性流产之间关系的现有证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Correlation Between Long non-coding RNA SOX2OT rs9839776 C>T Polymorphism and Unexplained Recurrent Miscarriages
Recurrent miscarriage (RM) is a severe pregnancy complication that results in the loss of two or more spontaneous pregnancies. RM has several complex reasons. Advances in genetics, immunology, and cell biology have strongly connected non-coding RNAs (ncRNAs) to recurrent miscarriages. NcRNAs regulate placental trophoblast cell processes, which affect trophoblast development, migration, and invagination; they also have a role in breast and ovarian cancer. As a result, their abnormal expression may contribute to the progression of RM. Several investigations have found a connection between RM and genetic polymorphisms that regulate cell migration. Variations in the long non-coding RNA (lncRNA) SOX2OT gene have been associated with a variety of cancer-related illnesses, particularly colorectal cancer, breast cancer, and cancer of the digestive tract. According to a recent study, the long non-coding SOX2OT rs9839776 CT raises the risk of RM. In this review, we explain the existing evidence supporting a relationship between the LncRNA SOX2OT rs9839776 polymorphisms and recurrent miscarriages.
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