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  2. CDK7-YAP-LDHD axis promotes D-lactate elimination and ferroptosis defense to support cancer stem cell-like properties

CDK7-YAP-LDHD axis promotes D-lactate elimination and ferroptosis defense to support cancer stem cell-like properties

  • Signal Transduct Target Ther. 2023 Aug 16;8(1):302. doi: 10.1038/s41392-023-01555-9.
Mengzhu Lv # 1 Ying Gong # 1 2 Xuesong Liu # 1 Yan Wang 1 3 Qingnan Wu 1 3 Jie Chen 1 3 Qingjie Min 1 Dongyu Zhao 4 Xianfeng Li 1 Dongshao Chen 1 Di Yang 1 Danna Yeerken 1 Rui Liu 1 Jinting Li 1 Weimin Zhang 5 6 7 8 Qimin Zhan 9 10 11 12 13
Affiliations

Affiliations

  • 1 Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Molecular Oncology, Peking University Cancer Hospital and Institute, Beijing, 100142, China.
  • 2 Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Breast Oncology, Peking University Cancer Hospital and Institute, Beijing, 100142, China.
  • 3 Research Unit of Molecular Cancer Research, Chinese Academy of Medical Sciences, Beijing, 100021, China.
  • 4 Peking University International Cancer Institute, Beijing, 100191, China.
  • 5 Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Molecular Oncology, Peking University Cancer Hospital and Institute, Beijing, 100142, China. zhangweimin@bjmu.edu.cn.
  • 6 Research Unit of Molecular Cancer Research, Chinese Academy of Medical Sciences, Beijing, 100021, China. zhangweimin@bjmu.edu.cn.
  • 7 Institute of Cancer Research, Shenzhen Bay Laboratory, Shenzhen, 518107, China. zhangweimin@bjmu.edu.cn.
  • 8 Department of Oncology, Cancer Institute, Peking University Shenzhen Hospital, Shenzhen Peking University-Hong Kong University of Science and Technology (PKU-HKUST) Medical Center, Shenzhen, 518036, China. zhangweimin@bjmu.edu.cn.
  • 9 Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Molecular Oncology, Peking University Cancer Hospital and Institute, Beijing, 100142, China. zhanqimin@bjmu.edu.cn.
  • 10 Research Unit of Molecular Cancer Research, Chinese Academy of Medical Sciences, Beijing, 100021, China. zhanqimin@bjmu.edu.cn.
  • 11 Peking University International Cancer Institute, Beijing, 100191, China. zhanqimin@bjmu.edu.cn.
  • 12 Institute of Cancer Research, Shenzhen Bay Laboratory, Shenzhen, 518107, China. zhanqimin@bjmu.edu.cn.
  • 13 Soochow University Cancer Institute, Suzhou, 215127, China. zhanqimin@bjmu.edu.cn.
  • # Contributed equally.
Abstract

Reprogrammed cellular metabolism is essential for maintaining Cancer Stem Cells (CSCs) state. Here, we report that mitochondrial D-lactate catabolism is a necessary initiating oncogenic event during tumorigenesis of esophageal squamous cell carcinoma (ESCC). We discover that cyclin-dependent kinase 7 (CDK7) phosphorylates nuclear Yes-associated protein 1 (YAP) at S127 and S397 sites and enhances its transcription function, which promotes D-lactate dehydrogenase (LDHD) protein expression. Moreover, LDHD is enriched significantly in ESCC-CSCs rather than differentiated tumor cells and high LDHD status is connected with poor prognosis in ESCC patients. Mechanistically, the CDK7-YAP-LDHD axis helps ESCC-CSCs escape from Ferroptosis induced by D-lactate and generates pyruvate to satisfy energetic demands for their elevated self-renewal potential. Hence, we conclude that esophageal CSCs adopt a D-lactate elimination and pyruvate accumulation mode dependent on CDK7-YAP-LDHD axis, which drives stemness-associated hallmarks of ESCC-CSCs. Reasonably, targeting metabolic checkpoints may serve as an effective strategy for ESCC therapy.

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