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CPT1A-mediated fatty acid oxidation promotes colorectal cancer cell metastasis by inhibiting anoikis.

Abstract
Anoikis is a critical obstacle to cancer metastasis. Colorectal cancer (CRC) exhibits a high rate of metastasis, leading to death, and the mechanisms involved in anoikis resistance are still unclear. We identified that the fatty acid oxidation (FAO) pathway was activated in detached CRC cells. Multiple genes in the FAO pathway, specifically the rate-limiting enzyme CPT1A, were upregulated in CRC cells grown in suspension. Reactive oxygen species elimination mediated by CPT1A in CRC cells was vital to anoikis resistance. In vivo experiments showed that CPT1A-suppressed CRC cells colonized the lung at a much lower rate than normal CRC cells, suggesting that CPT1A-mediated FAO activation increased metastatic capacity. In clinical tissue specimens from CRC patients, elevated expression of CPT1A was observed in metastatic sites compared with primary sites. Our results demonstrate that CPT1A-mediated FAO activation induces CRC cells to resist anoikis, suggesting that CPT1A is an attractive target for treating metastatic CRC.
AuthorsYing-Nan Wang, Zhao-Lei Zeng, Jiahuan Lu, Yun Wang, Ze-Xian Liu, Ming-Ming He, Qi Zhao, Zi-Xian Wang, Ting Li, Yun-Xin Lu, Qi-Nian Wu, Kai Yu, Feng Wang, Heng-Ying Pu, Bo Li, Wei-Hua Jia, Ming Shi, Dan Xie, Tie-Bang Kang, Peng Huang, Huai-Qiang Ju, Rui-Hua Xu
JournalOncogene (Oncogene) Vol. 37 Issue 46 Pg. 6025-6040 (11 2018) ISSN: 1476-5594 [Electronic] England
PMID29995871 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Fatty Acids
  • Reactive Oxygen Species
  • CPT1A protein, human
  • Carnitine O-Palmitoyltransferase
Topics
  • Animals
  • Anoikis (physiology)
  • Caco-2 Cells
  • Carnitine O-Palmitoyltransferase (metabolism)
  • Cell Line, Tumor
  • Colorectal Neoplasms (genetics, metabolism, pathology)
  • Fatty Acids (metabolism)
  • Gene Expression Regulation, Neoplastic (physiology)
  • HCT116 Cells
  • HT29 Cells
  • Humans
  • Lipid Metabolism (physiology)
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Nude
  • Neoplasm Metastasis (pathology)
  • Oxidation-Reduction
  • Reactive Oxygen Species (metabolism)

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