Abstract | BACKGROUND: METHODS: DLD1 cells with WT (+/-) or KRAS G13D mutant allele were treated with different concentrations of Cetuximab (Cet) or panitumumab (Pab) to study the mechanism underlying the KRAS mutation-induced resistance to anti-EGFR antibodies. The function of AMPK in KRAS mutation-induced resistance to anti-EGFR antibodies in CRC cells, and the regulatory role of Bcl-2 family proteins in DLD1 cells with WT or mutated KRAS upon AMPK activation were investigated. In addition, xenograft tumor models with the nude mouse using DLD1 cells with WT or mutated KRAS were established to examine the effects of AMPK activation on KRAS mutation-mediated anti-EGFR antibody resistance. RESULTS: Higher levels of AMPK activity in CRC cells with wild-type KRAS treated with anti-EGFR antibody resulted in apoptosis induction. In contrast, CRC cells with mutated KRAS showed lower AMP-activated protein kinase (AMPK) activity and decreased sensitivity to the inhibitory effect of anti-EGFR antibody. CRC cells with mutated KRAS showed high levels of glycolysis and produced an excessive amount of ATP, which suppressed AMPK activation. The knockdown of AMPK expression in CRC cells with WT KRAS produced similar effects to those observed in cells with mutated KRAS and decreased their sensitivity to cetuximab. On the contrary, the activation of AMPK by metformin (Met) or 5-aminoimidazole-4-carboxamide ribonucleotide ( AICAR) could overcome the KRAS-induced resistance to the anti-EGFR antibody in vivo and in vitro. The activation of AMPK resulted in the inhibition of myeloid cell leukemia 1 (Mcl-1) translation through the suppression of the mammalian target of rapamycin (mTOR) pathway. CONCLUSION: The results established herein indicate that targeting AMPK is a potentially promising and effective CRC treatment strategy. Video abstract.
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Authors | Hua Ye, Yi Liu, Kefeng Wu, Hui Luo, Liao Cui |
Journal | Cell communication and signaling : CCS
(Cell Commun Signal)
Vol. 18
Issue 1
Pg. 115
(07 23 2020)
ISSN: 1478-811X [Electronic] England |
PMID | 32703218
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antibodies, Monoclonal
- KRAS protein, human
- MCL1 protein, human
- Myeloid Cell Leukemia Sequence 1 Protein
- ErbB Receptors
- TOR Serine-Threonine Kinases
- Adenylate Kinase
- Proto-Oncogene Proteins p21(ras)
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Topics |
- Adenylate Kinase
(metabolism)
- Animals
- Antibodies, Monoclonal
(pharmacology)
- Cell Line, Tumor
- Colorectal Neoplasms
(enzymology, genetics)
- Drug Resistance, Neoplasm
(drug effects)
- Enzyme Activation
(drug effects)
- ErbB Receptors
(metabolism)
- Female
- Glycolysis
- Humans
- Mice, Nude
- Mutation
(genetics)
- Myeloid Cell Leukemia Sequence 1 Protein
(metabolism)
- Phosphorylation
- Proto-Oncogene Proteins p21(ras)
(genetics)
- TOR Serine-Threonine Kinases
(metabolism)
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