2. Academic Validation
  3. 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. [email protected].
  • 6 Research Unit of Molecular Cancer Research, Chinese Academy of Medical Sciences, Beijing, 100021, China. [email protected].
  • 7 Institute of Cancer Research, Shenzhen Bay Laboratory, Shenzhen, 518107, China. [email protected].
  • 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. [email protected].
  • 9 Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Molecular Oncology, Peking University Cancer Hospital and Institute, Beijing, 100142, China. [email protected].
  • 10 Research Unit of Molecular Cancer Research, Chinese Academy of Medical Sciences, Beijing, 100021, China. [email protected].
  • 11 Peking University International Cancer Institute, Beijing, 100191, China. [email protected].
  • 12 Institute of Cancer Research, Shenzhen Bay Laboratory, Shenzhen, 518107, China. [email protected].
  • 13 Soochow University Cancer Institute, Suzhou, 215127, China. [email protected].
  • # Contributed equally.
PMID: 37582812 DOI: 10.1038/s41392-023-01555-9
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.

Figures
Products
Inhibitors & Agonists
Other Products