Cystathionine gamma-lyase-mediated hypoxia inducible factor 1-alpha expression drives clear cell ovarian cancer progression.

IF 5.6 2区 医学 Q1 ONCOLOGY
Amal M El-Naggar, Yuqin Li, Busra Turgu, Yuchen Ding, Longyijie Wei, Shary Yuting Chen, Genny Trigo-Gonzalez, Forouh Kalantari, Rodrigo Vallejos, Branden Lynch, Janine Senz, Amy Lum, J Maxwell Douglas, Clara Salamanca, Shelby Thornton, Yimei Qin, Kiran Parmar, Sandra E Spencer, Samuel Leung, Michelle Mm Woo, Paul J Yong, Hai-Feng Zhang, Christopher S Hughes, Gian Luca Negri, Yemin Wang, Gregg B Morin, Poul H Sorensen, David G Huntsman
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Abstract

Clear cell ovarian cancer (CCOC) is the second most common ovarian cancer subtype, accounting for 5%-11% of ovarian cancers in North America. Late-stage CCOC is associated with a worse prognosis compared to other ovarian cancer histotypes, a challenge that has seen limited progress in recent decades. CCOC typically originates within the toxic microenvironment of endometriotic ovarian cysts and is characterized by its intrinsic chemoresistance, a strong hypoxic signature, and abundant expression of cystathionine gamma-lyase (CTH). CTH is a key enzyme in the transsulfuration pathway and serves as a marker of ciliated cells derived from the Müllerian tract. CTH plays a pivotal role in de novo cysteine synthesis, which is essential for glutathione (GSH) production and redox homeostasis. Using an array of molecular tools and cancer models, including in vivo studies, we demonstrated that CTH expression was induced under various stress conditions, such as exposure to endometriotic cyst content and hypoxia. This induction enables cell survival and creates a differentiation state manifested by CCOC that potentiates tumor progression and metastasis. In addition to regulating redox homeostasis, CTH enhances hypoxia inducible factor 1-alpha (HIF1α) expression, independently of hydrogen sulfide (H2S) production. Re-expression of HIF1α in CTH KO cells fully restored metastatic capacity in in vivo models. Co-expression of CTH and HIF1α proteins was also observed in human CCOC samples. Importantly, targeting CTH in CCOC significantly reduced its metastatic potential in in vivo models and enhanced sensitivity to chemotherapy. These findings underscore that CTH is both a defining feature of CCOC and a promising therapeutic target, not only for CCOC patients but also for those with other CTH-expressing cancers. © 2025 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

半胱硫氨酸γ裂解酶介导的缺氧诱导因子1- α表达驱动透明细胞卵巢癌进展。
透明细胞卵巢癌(CCOC)是第二常见的卵巢癌亚型,占北美卵巢癌的5%-11%。与其他卵巢癌组织型相比,晚期CCOC与较差的预后相关,这是近几十年来进展有限的挑战。CCOC通常起源于子宫内膜异位性卵巢囊肿的毒性微环境,其特点是其内在的化疗耐药、强缺氧特征和丰富的半胱甘氨酸γ -裂解酶(CTH)表达。CTH是转硫途径的关键酶,是源自勒氏束的纤毛细胞的标记物。CTH在新生半胱氨酸合成中起着关键作用,这对于谷胱甘肽(GSH)的产生和氧化还原稳态至关重要。使用一系列分子工具和癌症模型,包括体内研究,我们证明了在各种应激条件下,如暴露于子宫内膜异位囊肿内容物和缺氧,可以诱导CTH的表达。这种诱导使细胞存活并产生分化状态,表现为CCOC,增强肿瘤进展和转移。除了调节氧化还原稳态外,CTH还能增强缺氧诱导因子1- α (HIF1α)的表达,而不依赖于硫化氢(H2S)的产生。在体内模型中,在CTH KO细胞中重新表达HIF1α完全恢复转移能力。在人CCOC样品中也观察到CTH和HIF1α蛋白的共表达。重要的是,在CCOC中靶向CTH可显著降低其在体内模型中的转移潜力,并增强对化疗的敏感性。这些发现强调,CTH既是CCOC的一个决定性特征,也是一个有希望的治疗靶点,不仅适用于CCOC患者,也适用于其他表达CTH的癌症患者。©2025作者。《病理学杂志》由John Wiley & Sons Ltd代表大不列颠和爱尔兰病理学会出版。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
The Journal of Pathology
The Journal of Pathology 医学-病理学
CiteScore
14.10
自引率
1.40%
发文量
144
审稿时长
3-8 weeks
期刊介绍: The Journal of Pathology aims to serve as a translational bridge between basic biomedical science and clinical medicine with particular emphasis on, but not restricted to, tissue based studies. The main interests of the Journal lie in publishing studies that further our understanding the pathophysiological and pathogenetic mechanisms of human disease. The Journal of Pathology welcomes investigative studies on human tissues, in vitro and in vivo experimental studies, and investigations based on animal models with a clear relevance to human disease, including transgenic systems. As well as original research papers, the Journal seeks to provide rapid publication in a variety of other formats, including editorials, review articles, commentaries and perspectives and other features, both contributed and solicited.
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