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靶向PI3K/mTOR:一种针对透明细胞卵巢癌的潜在治疗策略。

Targeting on the PI3K/mTOR: a potential treatment strategy for clear cell ovarian carcinoma.

作者信息

Zheng Kewei, Jin Guanqin, Cao Rui, Gao Yi, Xu Jing, Chai Ranran, Kang Yu

机构信息

Department of Obstetrics and Gynecology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, 200011, China.

Department of Gynecology, Dalian Obstetrics and Gynecology Hospital, Dalian, 116033, China.

出版信息

Cancer Chemother Pharmacol. 2025 Jan 10;95(1):21. doi: 10.1007/s00280-024-04748-3.

Abstract

PURPOSE

Ovarian clear cell carcinoma is a highly malignant gynecological tumor characterized by a high rate of chemotherapy resistance and poor prognosis. The PI3K/AKT/mTOR pathway is well-known to be closely related to the progression of various malignancies, and recent studies have indicated that this pathway may play a critical role in the progression and worsening of OCCC.

METHODS

In this study, we investigated the combined effects of WX390, a dual inhibitor of PI3K/mTOR, and cisplatin on OCCC through both in vitro and in vivo experiments to further elucidate their therapeutic effects.

RESULTS

WX390 significantly inhibited the proliferation of human OCCC cell lines ES2 and OVISE, while promoting apoptosis. Furthermore, the combination of WX390 with CDDP exhibited a synergistic effect, markedly increasing the sensitivity of OCCC cells to chemotherapeutic agents and significantly suppressing tumor growth in PDX models. Western blot and RNA-seq analyses revealed that WX390 robustly inhibited the PI3K/AKT/mTOR pathway, interrupt autophagy, altered cell cycle dynamics, and induced apoptosis.

CONCLUSION

This study comprehensively assessed the efficacy of WX390 across multiple models of OCCC, laying a solid foundation for the development of new therapeutic strategies for this challenging malignancy.

摘要

目的

卵巢透明细胞癌是一种高度恶性的妇科肿瘤,其特点是化疗耐药率高且预后差。众所周知,PI3K/AKT/mTOR通路与各种恶性肿瘤的进展密切相关,最近的研究表明该通路可能在卵巢透明细胞癌的进展和恶化中起关键作用。

方法

在本研究中,我们通过体外和体内实验研究了PI3K/mTOR双重抑制剂WX390和顺铂对卵巢透明细胞癌的联合作用,以进一步阐明它们的治疗效果。

结果

WX390显著抑制人卵巢透明细胞癌细胞系ES2和OVISE的增殖,同时促进细胞凋亡。此外,WX390与顺铂联合使用表现出协同效应,显著提高卵巢透明细胞癌细胞对化疗药物的敏感性,并在人源肿瘤异种移植模型中显著抑制肿瘤生长。蛋白质免疫印迹法和RNA测序分析显示,WX390强烈抑制PI3K/AKT/mTOR通路,中断自噬,改变细胞周期动力学,并诱导细胞凋亡。

结论

本研究全面评估了WX390在多种卵巢透明细胞癌模型中的疗效,为开发针对这种具有挑战性的恶性肿瘤的新治疗策略奠定了坚实基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/972f/11723846/eaeb1b78bb52/280_2024_4748_Fig1_HTML.jpg

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