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Wnt5a:卵巢癌治疗的有希望的靶点。

Wnt5a: A promising therapeutic target in ovarian cancer.

机构信息

Department of Oncology, Wuxi People's Hospital Affiliated to Nanjing Medical University, Wuxi, 214023, China.

出版信息

Pathol Res Pract. 2021 Mar;219:153348. doi: 10.1016/j.prp.2021.153348. Epub 2021 Jan 27.

DOI:10.1016/j.prp.2021.153348
PMID:33540373
Abstract

Despite the rapid development of novel adjuvant and neoadjuvant chemotherapeutic drugs in recent years, advanced ovarian cancer still lacks effective treatment strategies and remains one of the main causes of death among women. Wnt protein family is widely expressed in a variety of human tissues, and Wnt5a is an important member of the noncanonical Wnt pathway. Wnt5a has been found to induce tumor suppression as well as to function as an oncogene depending upon the specific cancer type. In ovarian cancer, Wnt5a protein expression has been observed to be significantly upregulated and associated with poor prognosis. Researchers found that downregulating Wnt5a expression levels effectively suppresses ovarian cancer cell migration and invasion abilities. We believe that the downregulation of Wnt5a will be an attractive and promising antimetastatic therapeutic approach for the future treatment of patients with advanced ovarian cancer. The present review focuses on the mechanisms and therapeutic potential of Wnt5a as a promising novel therapeutic target for ovarian cancer.

摘要

尽管近年来新型佐剂和新辅助化疗药物发展迅速,但晚期卵巢癌仍缺乏有效治疗策略,仍是女性死亡的主要原因之一。Wnt 蛋白家族广泛表达于多种人体组织中,Wnt5a 是非经典 Wnt 通路的重要成员。Wnt5a 已被发现可根据特定癌症类型诱导肿瘤抑制或作为癌基因发挥作用。在卵巢癌中,Wnt5a 蛋白表达水平显著上调,并与不良预后相关。研究人员发现,下调 Wnt5a 表达水平可有效抑制卵巢癌细胞的迁移和侵袭能力。我们认为下调 Wnt5a 将成为未来治疗晚期卵巢癌患者有吸引力和有前途的抗转移治疗方法。本综述重点介绍了 Wnt5a 的作用机制和治疗潜力,将其作为一种有前途的新型卵巢癌治疗靶点。

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1
Wnt5a: A promising therapeutic target in ovarian cancer.Wnt5a:卵巢癌治疗的有希望的靶点。
Pathol Res Pract. 2021 Mar;219:153348. doi: 10.1016/j.prp.2021.153348. Epub 2021 Jan 27.
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Wnt5a suppresses epithelial ovarian cancer by promoting cellular senescence.Wnt5a 通过促进细胞衰老来抑制卵巢上皮性癌。
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Wnt5a promotes vasculogenic mimicry and epithelial-mesenchymal transition via protein kinase Cα in epithelial ovarian cancer.Wnt5a通过蛋白激酶Cα促进上皮性卵巢癌中的血管生成拟态和上皮-间质转化。
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Targeting the ROR1 and ROR2 receptors in epithelial ovarian cancer inhibits cell migration and invasion.靶向上皮性卵巢癌中的ROR1和ROR2受体可抑制细胞迁移和侵袭。
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Wnt5A regulates the expression of ROR2 tyrosine kinase receptor in ovarian cancer cells.Wnt5A调节卵巢癌细胞中ROR2酪氨酸激酶受体的表达。
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The non-canonical Wnt ligand, Wnt5a, is upregulated and associated with epithelial to mesenchymal transition in epithelial ovarian cancer.非经典Wnt配体Wnt5a在卵巢上皮癌中上调,并与上皮-间质转化相关。
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RSPO2 suppresses colorectal cancer metastasis by counteracting the Wnt5a/Fzd7-driven noncanonical Wnt pathway.RSPO2通过对抗Wnt5a/Fzd7驱动的非经典Wnt信号通路来抑制结直肠癌转移。
Cancer Lett. 2017 Aug 28;402:153-165. doi: 10.1016/j.canlet.2017.05.024. Epub 2017 Jun 6.

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The Cell Surface Heparan Sulfate Proteoglycan Syndecan-3 Promotes Ovarian Cancer Pathogenesis.细胞表面硫酸乙酰肝素蛋白聚糖连接蛋白-3 促进卵巢癌发病机制。
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