Regulation of cell proliferation and tumor suppressor roles of microRNA 329-3p of the MAP kinase pathway in cervical squamous carcinoma

Elfansu, Faria Rashid, K. Abirami, Sivakumar Krishnamoorthy, Kshitija Aherkar, R. Mythreyi, Uthamalingam Murali, Kanthesh M. Basalingappa, S. Jagannathan, E. Boojhana, M. Maghimaa
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Abstract

Cervical squamous cell carcinoma is observed as the second major cause of mortality worldwide. A highly conserved mitogen-activated protein kinase (MAPK) signaling pathway occurs in a wide range of cellular processes which includes differentiation, proliferation, migration, senescence, and apoptosis. MAPK pathway can be activated by various extracellular signals, capable of generating responses as per the cell type. Thus, alteration of the EGFR receptor in this particular pathway leads to the condition of cancer due to abnormal activation of receptor tyrosine kinases. The characteristic features of microRNA (miRNA) which are endogenous, single-stranded, small non-coding RNA for their role in RNA silencing and post-transitional regulation of gene expression have been studied over the years. The miRNA functions by base pairing with the complementary sequences within the mRNA molecule. One such miRNA, miR-329-3p has a critical tumor suppressor role in the MAPK pathway, however, is least understood. Therefore, miRNA could be considered as a potential biomarker for diagnosis, prognosis, and therapeutic purposes and brought out to its fullest use to mankind.
宫颈鳞状细胞癌中 MAP 激酶通路的 microRNA 329-3p 对细胞增殖的调控作用和肿瘤抑制作用
据观察,宫颈鳞状细胞癌是全球第二大死亡原因。高度保守的丝裂原活化蛋白激酶(MAPK)信号通路存在于多种细胞过程中,包括分化、增殖、迁移、衰老和凋亡。MAPK 通路可被各种细胞外信号激活,并能根据细胞类型产生相应的反应。因此,在这一特定途径中,表皮生长因子受体的改变会导致受体酪氨酸激酶的异常激活,从而引发癌症。微小核糖核酸(miRNA)是一种内源性、单链、小型非编码核糖核酸,多年来,人们一直在研究它们在核糖核酸沉默和基因表达过渡后调控中的作用。miRNA 通过与 mRNA 分子中的互补序列进行碱基配对来发挥作用。其中一种 miRNA,即 miR-329-3p,在 MAPK 通路中起着关键的肿瘤抑制作用,但人们对它的了解却最少。因此,miRNA 可被视为用于诊断、预后和治疗目的的潜在生物标志物,并可充分发挥其对人类的作用。
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