Dong Peixin, Xiong Ying, Konno Yosuke, Ihira Kei, Xu Daozhi, Kobayashi Noriko, Yue Junming, Watari Hidemichi
Department of Obstetrics and Gynecology, Hokkaido University School of Medicine, Hokkaido University, Sapporo, Japan.
State Key Laboratory of Oncology in South China, Department of Gynecology, Sun Yat-sen University Cancer Center, Guangzhou, China.
Front Cell Dev Biol. 2021 Feb 26;9:656993. doi: 10.3389/fcell.2021.656993. eCollection 2021.
P-element-induced wimpy testis (PIWI)-interacting RNAs (piRNAs) are a class of small non-coding RNA molecules that are 24-31 nucleotides in length. PiRNAs are thought to bind to PIWI proteins (PIWL1-4, a subfamily of Argonaute proteins), forming piRNA/PIWI complexes that influence gene expression at the transcriptional or post-transcriptional levels. However, it has been recently reported that the interaction of PIWI proteins with piRNAs does not encompass the entire function of PIWI proteins in human tumor cells. PIWIL1 (also called HIWI) is specifically expressed in the testis but not in other normal tissues. In tumor tissues, PIWIL1 is frequently overexpressed in tumor tissues compared with normal tissues. Its high expression is closely correlated with adverse clinicopathological features and shorter patient survival. Upregulation of PIWIL1 drastically induces tumor cell proliferation, epithelial-mesenchymal transition (EMT), invasion, cancer stem-like properties, tumorigenesis, metastasis and chemoresistance, probably via piRNA-independent mechanisms. In this article, we summarize the current existing literature on PIWIL1 in human tumors, including its expression, biological functions and regulatory mechanisms, providing new insights into how the dysregulation of PIWIL1 contributes to tumor initiation, development and chemoresistance through diverse signaling pathways. We also discuss the most recent findings on the potential clinical applications of PIWIL1 in cancer diagnosis and treatment.
P 元件诱导的弱精睾丸(PIWI)相互作用 RNA(piRNA)是一类长度为 24 - 31 个核苷酸的小型非编码 RNA 分子。PiRNA 被认为与 PIWI 蛋白(PIWL1 - 4,AGO 蛋白亚家族)结合,形成 piRNA/PIWI 复合物,该复合物在转录或转录后水平影响基因表达。然而,最近有报道称,PIWI 蛋白与 piRNA 的相互作用并不涵盖 PIWI 蛋白在人类肿瘤细胞中的全部功能。PIWIL1(也称为 HIWI)在睾丸中特异性表达,而在其他正常组织中不表达。在肿瘤组织中,与正常组织相比,PIWIL1 在肿瘤组织中经常过度表达。其高表达与不良的临床病理特征和患者较短的生存期密切相关。PIWIL1 的上调可能通过不依赖 piRNA 的机制显著诱导肿瘤细胞增殖、上皮 - 间质转化(EMT)、侵袭、癌症干细胞样特性、肿瘤发生、转移和化疗耐药性。在本文中,我们总结了目前关于人类肿瘤中 PIWIL1 的现有文献,包括其表达、生物学功能和调控机制,为 PIWIL1 的失调如何通过多种信号通路促进肿瘤起始、发展和化疗耐药性提供了新的见解。我们还讨论了关于 PIWIL1 在癌症诊断和治疗中的潜在临床应用的最新发现。