Wnt5a promotes VM formation by modulating the stemness and EMT progression of prostate cancer cell

IF 5 2区 医学 Q2 Medicine Translational Oncology Pub Date : 2024-11-01 DOI:10.1016/j.tranon.2024.102155
Bide Liu , Xun Li , Shuheng Wang , Hongliang Jia , Xiaoan Zhang , Qiang Dong , Jiuzhi Li
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Abstract

The incidence of prostate cancer (PCa) is increasing annually, making it the leading cause of tumor-related mortality in males. The available treatment options for metastatic PCa are limited. Vasculogenic mimicry (VM), an emerging phenomenon involving aggressive tumor cells, has a significant impact on patient survival. Misregulation of Wnt5a expression is commonly observed during cancer progression. However, there is a lack of comprehensive studies investigating the effects of Wnt5a on tumor VM formation. In this study, we demonstrate that alterations in wnt5a expression, either through gain or loss, have a significant influence on the formation of VM in tumor cells mediated by cell stemness and EMT progression. Further research has demonstrated that Wnt5a regulates the formation of VM through the PI3K/JNK signaling pathway. These experimental findings offer a novel avenue for the clinical management of prostate cancer.

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Wnt5a 通过调节前列腺癌细胞的干性和 EMT 进展促进血管瘤的形成。
前列腺癌(PCa)的发病率逐年上升,已成为男性肿瘤相关死亡的主要原因。转移性前列腺癌的现有治疗方案十分有限。血管生成模拟(VM)是一种涉及侵袭性肿瘤细胞的新兴现象,对患者的生存有重大影响。在癌症进展过程中,通常会观察到 Wnt5a 表达的失调。然而,目前还缺乏有关 Wnt5a 对肿瘤 VM 形成影响的全面研究。在这项研究中,我们证明了 Wnt5a 表达的改变,无论是增益还是缺失,都会对肿瘤细胞中由细胞干性和 EMT 进展介导的 VM 的形成产生重大影响。进一步的研究表明,Wnt5a 通过 PI3K/JNK 信号通路调控 VM 的形成。这些实验发现为前列腺癌的临床治疗提供了一条新途径。
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来源期刊
CiteScore
8.40
自引率
2.00%
发文量
314
审稿时长
54 days
期刊介绍: Translational Oncology publishes the results of novel research investigations which bridge the laboratory and clinical settings including risk assessment, cellular and molecular characterization, prevention, detection, diagnosis and treatment of human cancers with the overall goal of improving the clinical care of oncology patients. Translational Oncology will publish laboratory studies of novel therapeutic interventions as well as clinical trials which evaluate new treatment paradigms for cancer. Peer reviewed manuscript types include Original Reports, Reviews and Editorials.
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