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Illuminating the immunological landscape: mitochondrial gene defects in pancreatic cancer through a multiomics lens.
Chi, Hao; Su, Lanqian; Yan, Yalan; Gu, Xiang; Su, Ke; Li, Han; Yu, Lili; Liu, Jie; Wang, Jue; Wu, Qibiao; Yang, Guanhu.
Affiliation
  • Chi H; Faculty of Chinese Medicine, and State Key Laboratory of Quality Research in Chinese Medicine, and University Hospital, Macau University of Science and Technology, Macau, Macao SAR, China.
  • Su L; Clinical Medical College, Southwest Medical University, Luzhou, China.
  • Yan Y; Clinical Medical College, Southwest Medical University, Luzhou, China.
  • Gu X; Clinical Medical College, Southwest Medical University, Luzhou, China.
  • Su K; Biology Department, Southern Methodist University, Dallas, TX, United States.
  • Li H; Department of Radiation Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
  • Yu L; Clinical Medical College, Southwest Medical University, Luzhou, China.
  • Liu J; Faculty of Chinese Medicine, and State Key Laboratory of Quality Research in Chinese Medicine, and University Hospital, Macau University of Science and Technology, Macau, Macao SAR, China.
  • Wang J; Department of General Surgery, Dazhou Central Hospital, Dazhou, China.
  • Wu Q; Faculty of Chinese Medicine, and State Key Laboratory of Quality Research in Chinese Medicine, and University Hospital, Macau University of Science and Technology, Macau, Macao SAR, China.
  • Yang G; Faculty of Chinese Medicine, and State Key Laboratory of Quality Research in Chinese Medicine, and University Hospital, Macau University of Science and Technology, Macau, Macao SAR, China.
Front Immunol ; 15: 1375143, 2024.
Article in En | MEDLINE | ID: mdl-38510247
ABSTRACT
This comprehensive review delves into the complex interplay between mitochondrial gene defects and pancreatic cancer pathogenesis through a multiomics approach. By amalgamating data from genomic, transcriptomic, proteomic, and metabolomic studies, we dissected the mechanisms by which mitochondrial genetic variations dictate cancer progression. Emphasis has been placed on the roles of these genes in altering cellular metabolic processes, signal transduction pathways, and immune system interactions. We further explored how these findings could refine therapeutic interventions, with a particular focus on precision medicine applications. This analysis not only fills pivotal knowledge gaps about mitochondrial anomalies in pancreatic cancer but also paves the way for future investigations into personalized therapy options. This finding underscores the crucial nexus between mitochondrial genetics and oncological immunology, opening new avenues for targeted cancer treatment strategies.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pancreatic Neoplasms / Proteomics Limits: Humans Language: En Journal: Front Immunol Year: 2024 Document type: Article Affiliation country: China Country of publication: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pancreatic Neoplasms / Proteomics Limits: Humans Language: En Journal: Front Immunol Year: 2024 Document type: Article Affiliation country: China Country of publication: Switzerland