Overcoming EGFR Resistance in Metastatic Colorectal Cancer Using Vitamin C: A Review

dc.contributor.authorMachmouchi, Ahmad
dc.contributor.authorChehade, Laudy
dc.contributor.authorTemraz, Sally N.
dc.contributor.authorShamseddine, Ali I.
dc.contributor.departmentInternal Medicine
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:45:47Z
dc.date.available2025-01-24T11:45:47Z
dc.date.issued2023
dc.description.abstractTargeted monoclonal antibody therapy against Epidermal Growth Factor Receptor (EGFR) is a leading treatment modality against metastatic colorectal cancer (mCRC). However, with the emergence of KRAS and BRAF mutations, resistance was inevitable. Cells harboring these mutations overexpress Glucose Transporter 1 (GLUT1) and sodium-dependent vitamin C transporter 2 (SVCT2), which enables intracellular vitamin C transport, leading to reactive oxygen species generation and finally cell death. Therefore, high dose vitamin C is proposed to overcome this resistance. A comprehensive search strategy was adopted using Pubmed and MEDLINE databases (up to 11 August 2022). There are not enough randomized clinical trials to support its use in the clinical management of mCRC, except for a subgroup analysis from a phase III study. High dose vitamin C shows a promising role in overcoming EGFR resistance in mCRC with wild KRAS mutation with resistance to anti-epidermal growth factor inhibitors and in patients with KRAS and BRAF mutations. © 2023 by the authors.
dc.identifier.doihttps://doi.org/10.3390/biomedicines11030678
dc.identifier.eid2-s2.0-85151761628
dc.identifier.urihttp://hdl.handle.net/10938/30600
dc.language.isoen
dc.publisherMDPI
dc.relation.ispartofBiomedicines
dc.sourceScopus
dc.subjectAscorbic acid
dc.subjectBraf mutation
dc.subjectColorectal cancer
dc.subjectEgfr resistance
dc.subjectKras mutation
dc.subjectVitamin c
dc.titleOvercoming EGFR Resistance in Metastatic Colorectal Cancer Using Vitamin C: A Review
dc.typeReview

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