{"paper_id":"82d1ef9a-3304-4f4d-862b-d37d1355eae2","body_text":"Abstract\nEndometriosis is a benign gynecological disorder characterized by the abnormal presence of endometrium-like cells, referred to as ectopic tissue, located outside the uterine cavity. Beyond the abnormal proliferation of endometrium-like tissues within and beyond the pelvic cavity, compelling scientific evidence underscores the crucial involvement of the NOD-like receptor NLRP3 inflammasome and pyroptosis in the pathogenesis of EMS. Our investigation has revealed a striking upregulation of the endogenous protein GATA-binding protein 6 (GATA6) in abdominal wall EMS. Notably, the knockdown of GATA6 significantly impaired the viability and migratory potential of primary ectopic endometrial stromal cells (EESCs) while also inhibiting crucial markers of pyroptosis, such as NLRP3, the gasdermin D N-terminal fragment (GSDMD-N), and reactive oxygen species (ROS) levels within these cells. Delving deeper into the underlying mechanisms, we discovered that suppressing GATA6 mitigated the activation of the phosphatidylinositol 3-kinase (PI3K)/protein kinase B (AKT) signaling pathway in EESCs. The administration of 740 Y-P, an agonist of the PI3K/AKT pathway, mitigated the inhibitive actions of GATA6 knockdown on EESCs’ growth, migration, and pyroptosis, highlighting the intricate crosstalk between GATA6 and this intricate signaling cascade. In vivo experiments corroborated these findings, demonstrating that reduced GATA6 expression effectively restrained the growth of endometrial lesions and concurrently suppressed pyroptosis, accompanied by a dampening of PI3K/AKT signaling within these lesions. In summary, our study underscores the pivotal role of GATA6 in modulating the growth and pyroptosis of abdominal wall EMS through its regulation of the PI3K/AKT signaling pathway. Silencing GATA6 emerges as a promising approach to alleviate pyroptosis and potentially offers a novel therapeutic angle for managing abdominal wall EMS.\nSimilar content being viewed by others\nChange history\n05 September 2025\nThe article has been corrected\n05 September 2025\nA Correction to this paper has been published: https://doi.org/10.1007/s12013-025-01882-4\nReferences\nXu, Y., Liu, H., Xiong, W., Peng, Y., Li, X., Long, X., Jin, J., Liang, J., Weng, R., Liu, J., Zhang, L., & Liu, Y. (2023). A novel mechanism regulating pyroptosis-induced fibrosis in endometriosis via lnc-MALAT1/miR-141-3p/NLRP3 pathway dagger. Biology of Reproduction, 109, 156–171. https://doi.org/10.1093/biolre/ioad057.\nVercellini, P., Vigano, P., Somigliana, E., & Fedele, L. (2014). Endometriosis: Pathogenesis and treatment. Nature Reviews Endocrinology, 10, 261–275. https://doi.org/10.1038/nrendo.2013.255.\nBrichant, G., Laraki, I., Henry, L., Munaut, C., & Nisolle, M. (2021). 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Gynecological Endocrinology, 36, 436–440. https://doi.org/10.1080/09513590.2019.1680627.\nFunding\nThis study is supported by Shijiazhuang Key Research and Development Plan project (No. 221460493).\nAuthor information\nAuthors and Affiliations\nContributions\nXiufang Du, Hongjie Yang and Xiaobei Kang contributed to study conception and design. Experimentation, data collection, and analysis were performed by Xiufang Du, Hongjie Yang and Tao Yang. The manuscript was written by Xiufang Du, Changna Fu and Tao Yang. All authors have read and approved the final version of the manuscript.\nCorresponding authors\nEthics declarations\nConflict of Interest\nThe authors declare no competing interests.\nEthical Approval\nApproval for this study was granted by the ethics committee of Shijiazhuang Maternal and Child Health Care Hospital. Animal experiments were conducted following approval from the Ethical Committee of Shijiazhuang Maternal and Child Health Care Hospital.\nAdditional information\nPublisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.\nSupplementary information\nRights and permissions\nSpringer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.\nAbout this article\nCite this article\nDu, X., Yang, H., Kang, X. et al. Blocking GATA6 Alleviates Pyroptosis and Inhibits Abdominal Wall Endometriosis Lesion Growth Through Inactivating the PI3K/AKT Pathway. Cell Biochem Biophys 83, 1757–1770 (2025). https://doi.org/10.1007/s12013-024-01583-4\nPublished:\nVersion of record:\nIssue date:\nDOI: https://doi.org/10.1007/s12013-024-01583-4","source_license":"CC0","license_restricted":false}