TRPV4 drives the progression of leiomyosarcoma by promoting ECM1 generation and co-activating the FAK/PI3K/AKT/GSK3β pathway

Our findings provide a novel mechanism by which TRPV4 directly activates Ca<sup>2+</sup>/FAK/PI3K/AKT/GSK3β pathway and further indirectly enhances the FAK/PI3K/AKT/GSK3β pathway through the promotion and secretion of ECM1 to promote LMS malignant progression. Targeting the TRPV4/FAK axis might be a promising potential strategy for prognosis and treatment of LMS.

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Publication Details

Journal
Cellular Oncology
Published
2024-11-29
DOI
https://doi.org/10.1007/s13402-024-01008-7
Citations
4
Primary Topic
Ion Channels and Receptors
Type
article
Field-Weighted Citation Impact
1.44

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article

TRPV4 drives the progression of leiomyosarcoma by promoting ECM1 generation and co-activating the FAK/PI3K/AKT/GSK3β pathway

Yingying Zhao, Yingyong Hou, Yuhong Zhou, Xi Guo et al.
4 citations
Cellular Oncology
Ion Channels and Receptors
1.44
article

TRPV4 drives the progression of leiomyosarcoma by promoting ECM1 generation and co-activating the FAK/PI3K/AKT/GSK3β pathway

Yingying Zhao, Yingyong Hou, Yuhong Zhou, Xi Guo, Zhiming Wang, Rongkui Luo, Zhengqing Song, Qiwen Zhou, You Yang, Jiefeng Cui, Shuxiu Xiao, Yong Zhang, Wei Li, Jiali Qian, Chenlu Zhang, Long‐Sheng Lu, Chuxin Huang, Weiqi Lu, Hanxing Tong
article en
4 citations

Abstract

Our findings provide a novel mechanism by which TRPV4 directly activates Ca<sup>2+</sup>/FAK/PI3K/AKT/GSK3β pathway and further indirectly enhances the FAK/PI3K/AKT/GSK3β pathway through the promotion and secretion of ECM1 to promote LMS malignant progression. Targeting the TRPV4/FAK axis might be a promising potential strategy for prognosis and treatment of LMS.

Cellular OncologyVol. 48(2)
Sun Yat-sen University (CN), Fudan University (CN), Suzhou Municipal Hospital (CN), Zhongshan Hospital (CN), The First Affiliated Hospital, Sun Yat-sen University (CN), Xiamen Chang Gung Hospital (CN), Huashan Hospital (CN)
Wu Jieping Medical Foundation
Openalex Percentile: Top 19%
Ion Channels and Receptors
1.44
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