# Vitamin C in the Treatment of Colorectal Cancer: Between Hope and Despair

**Authors:** Mathias Wasmer, Markus Weber, Seraina Faes

PMC · DOI: 10.3390/cancers18040654 · 2026-02-17

## TL;DR

This review explores the potential of high-dose vitamin C as a treatment for colorectal cancer, highlighting its mechanisms and the gap between experimental and clinical results.

## Contribution

The paper provides a comprehensive analysis of vitamin C's anti-cancer mechanisms and treatment protocols in colorectal cancer.

## Key findings

- High-dose vitamin C shows anti-cancer effects in colorectal cancer models, especially in tumors with KRAS or BRAF mutations.
- Intravenous vitamin C enhances the efficacy of chemotherapies, targeted therapies, and immunotherapies in experimental settings.
- Clinical trials have not yet confirmed the anti-cancer benefits observed in preclinical studies, indicating a need for improved patient selection and treatment protocols.

## Abstract

Vitamin C displays anti-cancer properties in part via its pro-oxidative activity. Whereas most evidence has been obtained in preclinical studies, recent clinical trials suggest that vitamin C might provide anti-cancer benefits in cancer patients. In this review, we summarize the available evidence for a role of vitamin C in the treatment of colorectal cancer. Importantly, understanding the anti-cancer mechanisms of vitamin C could help design pertinent treatment protocols for colorectal cancer patients.

Despite recent progress in different treatment modalities, colorectal cancer remains a leading cause of cancer-related death, highlighting the need to further develop novel treatment strategies. In this context, over recent decades, several experimental studies have demonstrated that high doses of vitamin C provide anti-cancer benefits in various colorectal cancer models. Intravenous administrations of vitamin C are necessary to reach these high concentrations in tumors. Tumors harboring KRAS or BRAF mutations or driven by the HIF1α signaling pathway are particularly sensitive to high-dose vitamin C. In addition, high doses of vitamin C increase the efficacy of other treatments when used in combination, including chemotherapies, targeted therapies, and immunotherapies. Whilst results of experimental studies were promising, their translation into clinical protocols has been disappointing. So far, very few clinical data support the anti-cancer benefits of vitamin C in colorectal cancer patients. This lack of success highlights the need to ameliorate the selection of patients based on biomarkers and to refine treatment protocols to achieve high-dose vitamin C in tumors. In this review, we analyze in vitro and in vivo studies that investigated the effect of vitamin C in colorectal cancer cells and point out the anti-cancer mechanisms of vitamin C. We further examine clinical trials that tested vitamin C in colorectal cancer patients and address several points that still need to be investigated in order to fully define the role of vitamin C in the treatment of colorectal cancer.

## Linked entities

- **Genes:** KRAS (KRAS proto-oncogene, GTPase) [NCBI Gene 3845], BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673]
- **Proteins:** HIF1A (hypoxia inducible factor 1 subunit alpha)
- **Chemicals:** vitamin C (PubChem CID 54670067)
- **Diseases:** colorectal cancer (MONDO:0005575)

## Full-text entities

- **Genes:** VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673] {aka B-RAF1, B-raf, BRAF-1, BRAF1, NS7, RAFB1}, Pdcd1 (programmed cell death 1) [NCBI Gene 18566] {aka Ly101, PD-1, Pdc1}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, CA9 (carbonic anhydrase 9) [NCBI Gene 768] {aka CAIX, MN}, MALAT1 (metastasis associated lung adenocarcinoma transcript 1) [NCBI Gene 378938] {aka HCN, LINC00047, NCRNA00047, NEAT2, PRO2853, miPEP-52}, MAP2K7 (mitogen-activated protein kinase kinase 7) [NCBI Gene 5609] {aka JNKK2, MAPKK7, MEK, MEK 7, MKK7, PRKMK7}, POU5F1 (POU class 5 homeobox 1) [NCBI Gene 5460] {aka OCT3, OCT4, OCT4Borf1, OTF-3, OTF3, OTF4}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, PKM (pyruvate kinase M1/2) [NCBI Gene 5315] {aka CTHBP, HEL-S-30, OIP3, PK3, PKM2, TCB}, PECAM1 (platelet and endothelial cell adhesion molecule 1) [NCBI Gene 5175] {aka CD31, CD31/EndoCAM, GPIIA', PECA1, PECAM-1, endoCAM}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, APC (APC regulator of Wnt signaling pathway) [NCBI Gene 324] {aka BTPS2, DESMD, DP2, DP2.5, DP3, GS}, COL18A1 (collagen type XVIII alpha 1 chain) [NCBI Gene 80781] {aka GLCC, KNO, KNO1, KS}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, PDK1 (pyruvate dehydrogenase kinase 1) [NCBI Gene 5163], TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, BMI1 (BMI1 proto-oncogene, polycomb ring finger) [NCBI Gene 648] {aka FLVI2/BMI1, PCGF4, RNF51, flvi-2/bmi-1}, PARP1 (poly(ADP-ribose) polymerase 1) [NCBI Gene 142] {aka ADPRT, ADPRT 1, ADPRT1, ARTD1, PARP, PARP-1}, SOX2 (SRY-box transcription factor 2) [NCBI Gene 6657] {aka ANOP3, MCOPS3}, CEACAM3 (CEA cell adhesion molecule 3) [NCBI Gene 1084] {aka CD66D, CEA, CGM1, CGM1a, W264, W282}, H3P16 (H3 histone pseudogene 16) [NCBI Gene 644914] {aka H3.6, H3F3AP6, p21}, VEGFD (vascular endothelial growth factor D) [NCBI Gene 2277] {aka FIGF, VEGF-D}, HIF1A (hypoxia inducible factor 1 subunit alpha) [NCBI Gene 3091] {aka HIF-1-alpha, HIF-1A, HIF-1alpha, HIF1, HIF1-ALPHA, MOP1}, ARNT (aryl hydrocarbon receptor nuclear translocator) [NCBI Gene 405] {aka ARNT1, HIF-1-beta, HIF-1beta, HIF1-beta, HIF1B, HIF1BETA}, GULOP (gulonolactone (L-) oxidase, pseudogene) [NCBI Gene 2989] {aka GULO, SCURVY}, CXCR4 (C-X-C motif chemokine receptor 4) [NCBI Gene 7852] {aka CD184, D2S201E, FB22, HM89, HSY3RR, LCR1}, SLC2A1 (solute carrier family 2 member 1) [NCBI Gene 6513] {aka CSE, DYT17, DYT18, DYT9, EIG12, GLUT}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, HMOX1 (heme oxygenase 1) [NCBI Gene 3162] {aka HMOX1D, HO-1, HSP32, bK286B10}, IDH1 (isocitrate dehydrogenase (NADP(+)) 1) [NCBI Gene 3417] {aka HEL-216, HEL-S-26, IDCD, IDH, IDP, IDPC}, GAPDH (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 2597] {aka G3PD, GAPD, HEL-S-162eP}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, Ctla4 (cytotoxic T-lymphocyte-associated protein 4) [NCBI Gene 12477] {aka Cd152, Ctla-4, Ly-56}, KRAS (KRAS proto-oncogene, GTPase) [NCBI Gene 3845] {aka 'C-K-RAS, C-K-RAS, CFC2, K-RAS2A, K-RAS2B, K-RAS4A}, CAT (catalase) [NCBI Gene 847], CASP1 (caspase 1) [NCBI Gene 834] {aka ICE, IL1BC, P45}, AFP (alpha fetoprotein) [NCBI Gene 174] {aka AFPD, FETA, HPAFP}, SLC2A3 (solute carrier family 2 member 3) [NCBI Gene 6515] {aka GLUT3}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}, TXN (thioredoxin) [NCBI Gene 7295] {aka TRDX, TRX, TRX1, TXN1, Trx80}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, SLC23A2 (solute carrier family 23 member 2) [NCBI Gene 9962] {aka NBTL1, SLC23A1, SVCT2, YSPL2}
- **Diseases:** Lynch syndrome (MESH:D003123), hypoxia (MESH:D000860), vomiting (MESH:D014839), hemolysis (MESH:D006461), iron deficient (MESH:D000090463), fatigue (MESH:D005221), diarrhea (MESH:D003967), obesity (MESH:D009765), hypoxic (MESH:D002534), nausea (MESH:D009325), gastric cancer (MESH:D013274), intestinal tumors (MESH:D007414), microsatellite instability (MESH:D053842), rectal cancer (MESH:D012004), edema (MESH:D004487), neurotoxicity (MESH:D020258), Tumors (MESH:D009369), pain (MESH:D010146), headache (MESH:D006261), injury to (MESH:D014947), colon (MESH:D003108), necrosis (MESH:D009336), hypokalemia (MESH:D007008), appetite loss (MESH:D001068), dry mouth (MESH:D014987), inflammatory bowel diseases (MESH:D015212), polyps (MESH:D011127), Toxicities (MESH:D064420), kidney stone (MESH:D007669), familial adenomatous polyposis (MESH:D011125), stomatitis (MESH:D013280), deficient (MESH:D007153), neutropenia (MESH:D009503), death (MESH:D003643), CRC (MESH:D015179), glucose-6-phosphate dehydrogenase deficiency (MESH:D005955), metastasis (MESH:D009362)
- **Chemicals:** bevacizumab (MESH:D000068258), sulindac (MESH:D013467), oxaliplatin (MESH:D000077150), decitabine (MESH:D000077209), lapatinib (MESH:D000077341), hemin (MESH:D006427), hydroxyl radical (MESH:D017665), ipilimumab (MESH:D000074324), norepinephrine (MESH:D009638), Ascorbate (MESH:D001205), Iron (MESH:D007501), adagrasib (MESH:C000718190), leucovorin (MESH:D002955), pertuzumab (MESH:C485206), encorafenib (MESH:C000601108), panitumumab (MESH:D000077544), 5-FU (MESH:D005472), tyrosine (MESH:D014443), cytosine (MESH:D003596), iron sucrose (MESH:D000077605), metformin (MESH:D008687), ferric ammonium citrate (MESH:C013531), FeCl3 (MESH:C024555), trastuzumab (MESH:D000068878), pentose phosphate (MESH:D010428), desferrioxamine (MESH:D003676), glyceraldehyde 3-phosphate (MESH:D005986), arsenic trioxide (MESH:D000077237), TCA (MESH:D014233), lactate (MESH:D019344), irinotecan (MESH:D000077146), DHA (MESH:D003683), azoxymethane (MESH:D001397), O2 (MESH:D010100), ramucirumab (MESH:C543333), 2-hydroxyglutarate (MESH:C019417), glucose (MESH:D005947), CoCl2 (MESH:C018021), ROS (MESH:D017382), calcium (MESH:D002118), morphine (MESH:D009020), NAD (MESH:D009243), nivolumab (MESH:D000077594), DFO (MESH:C000709069), N-acetylcysteine (MESH:D000111), alcohol (MESH:D000438), balstilimab (MESH:C000720935), ATP (MESH:D000255), GSH (MESH:D005978), cetuximab (MESH:D000068818), GSSG (MESH:D019803), fruquintinib (MESH:C000591844), pembrolizumab (MESH:C582435), 1,2-dimethylhydrazine (MESH:D019813), carnitine (MESH:D002331), threonic acids (MESH:C011369), cisplatin (MESH:D002945), sotorasib (MESH:C000706028), H2O2 (MESH:D006861), 2,3-L-diketogluconate (-)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]
- **Mutations:** A600E, C in 14, E545K, H1047R, G12C, Y103fs, R273H, A146T, C at 1, T119S, G12V, R132C, G13D
- **Cell lines:** WiDr — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_2760), HCT8 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_2478), SW48 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_1724), HCT116 — Homo sapiens (Human), Colon carcinoma, Cancer cell line (CVCL_0291), CCK81 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_2873), FHC — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_3688), CT26 — Mus musculus (Mouse), Mouse colon adenocarcinoma, Cancer cell line (CVCL_7254), LoVo — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0399), DLD-1 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0248), HT-29 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0320), Colon 26 — Mus musculus (Mouse), Mouse colon adenocarcinoma, Cancer cell line (CVCL_0240), LS174T — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_1384), MC38 — Mus musculus (Mouse), Mouse colon adenocarcinoma, Cancer cell line (CVCL_B288), HCT15 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0292), C2BBe1 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_1096), SW620 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0547), SW480 — Homo sapiens (Human), Colon adenocarcinoma, Cancer cell line (CVCL_0546), LS1034 — Homo sapiens (Human), Cecum adenocarcinoma, Cancer cell line (CVCL_1382), CMT-93 — Mus musculus (Mouse), Mouse rectum carcinoma, Cancer cell line (CVCL_1986)

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12939454/full.md

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Source: https://tomesphere.com/paper/PMC12939454