维生素C抗肿瘤机制

赵文芝,石汉平

肿瘤代谢与营养电子杂志 ›› 2019, Vol. 6 ›› Issue (4) : 409-414.

PDF(1447 KB)
PDF(1447 KB)
肿瘤代谢与营养电子杂志 ›› 2019, Vol. 6 ›› Issue (4) : 409-414. DOI: 10.16689/j.cnki.cn11-9349/r.2019.04.004
专家论坛

维生素C抗肿瘤机制

  • 赵文芝,石汉平
作者信息 +

The anti-tumor mechanism of vitamin C

  • ZHAO Wen-zhi, SHI Han-ping
Author information +
文章历史 +

摘要

维生素C是具有重要生理作用的必需营养素,具有抗氧化、抗衰老、预防和治疗缺铁性贫血的作用,参与胶原、肉碱、儿茶酚胺类激素、酰胺化肽激素的合成,能够羟化转录因子。维生素C抗肿瘤研究已接近半个世纪,其抗肿瘤效果由肯定到否定、再到肯定,经历了质疑与验证的沉浮。维生素C的抗肿瘤机制目前主要有3种假说,即维生素C通过诱导的过氧化应激杀伤肿瘤细胞、通过调节表观遗传学改变及调节低氧诱导因子-1的活性改变肿瘤细胞的恶性程度,即兼具杀伤肿瘤细胞和增强肿瘤细胞对治疗敏感性的功能。维生素C诱导的过氧化应激反应过程中,由于产生过氧化氢或者由于脱氢抗坏血酸的氧化还原,导致细胞内部能量耗竭;维生素C调节表观遗传学改变过程中,通过增强具有脱甲基作用的酶的活性,降低DNA或组蛋白甲基化水平,从而降低肿瘤细胞的恶性程度;维生素C调节低氧诱导因子-1活性的过程中,通过增强细胞内低氧诱导因子羟化酶活性抑制低氧诱导因子-1转录反应,从而降低肿瘤细胞的恶性程度。关于其抗肿瘤的效果和应用前景目前仍存在争议,促使人们去探索关于其敏感性、用药剂量等问题。维生素C的抗肿瘤研究有望为肿瘤治疗提供新的思路。

Abstract

Vitamin C is an essential nutrient with important physiological function of anti-oxidant activity, anti-aging activity, preventing and treating iron deficiency anemia, being involved in synthesis of collagen, carnitine, catecholamines, and aminopeptide hormones, and biochemical reaction of hydroxylation of transcription factors. It has been nearly half a century since the beginning of researches of anti-tumor effect of vitamin C and the effect was challenged and verified repeatedly. At present, there are three main hypotheses about the anti-tumor mechanism of vitamin C, that is targeting redox imbalance to kill tumor cells, or targeting epigenetic regulators or targeting hypoxia-inducible factor 1(HIF-1) signaling to reduce the malignancy and enhance the sensitivity to treatment of cancer cells. In the mechanism of targeting redox imbalance, intracellular energy is exhausted due to the generation of H2O2 or the oxidation and reduction of the dehydroascorbic acid. In the mechanism of targeting epigenetic regulators, malignancy of the tumor cells is reducing through demethylation of DNA or histone catalyzed by enhancing activity of the related enzyme. In the mechanism of targeting HIF-1, malignancy of the tumor cells is reducing through inhibiting transcription of HIF-1 by enhancing activity of HIF hydroxylase. Its controversial about the efficiency and the prospect of vitamin C in treatment of cancer, which has led to the exploration of the question of drug sensitivity and dosage. Research on the anti-tumor effect of vitamin C is expected to provide a new way for the treatment of cancer.

关键词

维生素C / 过氧化应激 / 脱甲基 / 缺氧诱导因子

Key words

Vitamin C / Pro-oxidative stress / Demethylation / Hypoxia-inducible factor

引用本文

导出引用
赵文芝,石汉平. 维生素C抗肿瘤机制[J]. 肿瘤代谢与营养电子杂志. 2019, 6(4): 409-414 https://doi.org/10.16689/j.cnki.cn11-9349/r.2019.04.004
ZHAO Wen-zhi, SHI Han-ping. The anti-tumor mechanism of vitamin C[J]. Electronic Journal of Metabolism and Nutrition of Cancer. 2019, 6(4): 409-414 https://doi.org/10.16689/j.cnki.cn11-9349/r.2019.04.004

参考文献

1.孙长颢. 营养与食品卫生学.第8版. 北京: 人民卫生出版社,2018.
2.Corti A, Casini AF, Pompella A. Cellular pathways for transport and efflux of ascorbate and dehydroascorbate. Arch Biochem Biophys. 2010;500(2):107-115.
3.Wilson JX. The physiological role of dehydroascorbic acid. FEBS Lett. 2002;527(1-3):5-9.
4.Mandl J, Szarka A, Banhegyi G. Vitamin C: update on physiology and pharmacology. Br J Pharmacol. 2009;157(7):1097-1110.
5.Englard S, Seifter S. The biochemical functions of ascorbic acid. Annu Rev Nutr.1986;6:365-406.
6.Cameron E, Campbell A. The orthomolecular treatment of cancer. II. Clinical trial of high-dose ascorbic acid supplements in advanced human cancer. Chem Biol Interact.1974;9(4):285-315.
7.Cameron E, Pauling L. Supplemental ascorbate in the supportive treatment of cancer: prolongation of survival times in terminal human cancer. Proc Natl Acad Sci U S A.1976;73(10):3685-3689.
8.Cameron E, Pauling L. Supplemental ascorbate in the supportive treatment of cancer: reevaluation of prolongation of survival times in terminal human cancer. Proc Natl Acad Sci U S A. 1978;75(9):4538-4542.
9.Creagan ET, Moertel CG, OFallon JR, et al. Failure of high-dose vitamin C (ascorbic acid) therapy to benefit patients with advanced cancer. A controlled trial. N Engl J Med.1979;301(13):687-690.
10.Moertel CG, Fleming TR, Creagan ET, et al. High-dose vitamin C versus placebo in the treatment of patients with advanced cancer who have had no prior chemotherapy. A randomized double-blind comparison. N Engl J Med.1985;312(3):137-141.
11.Chen Q, Espey MG, Sun AY, et al. Ascorbate in pharmacologic concentrations selectively generates ascorbate radical and hydrogen peroxide in extracellular fluid in vivo. Proc Natl Acad Sci U S A. 2007;104(21):8749-8754.
12.Carr AC, Cook J. Intravenous vitamin C for cancer therapy - identifying the current gaps in our knowledge. Front Physiol. 2018;9:1182.
13.Nielsen TK, Hojgaard M, Andersen JT, et al. Elimination of ascorbic acid after high-dose infusion in prostate cancer patients: a pharmacokinetic evaluation. Basic Clin Pharmacol Toxicol. 2015;116(4):343-348.
14.张婷,饶本强,江波.维生素C在肿瘤治疗中的作用. 肿瘤代谢与营养电子杂志. 2016;3(3):135-138.
15.Duarte TL, Almeida GM, Jones GD. Investigation of the role of extracellular H2O2 and transition metal ions in the genotoxic action of ascorbic acid in cell culture models. Toxicol Lett. 2007;170(1):57-65.
16.Lee YJ, Shacter E. Oxidative stress inhibits apoptosis in human lymphoma cells. J Biol Chem.1999;274(28):19792-19798.
17.Schraufstatter IU, Hinshaw DB, Hyslop PA, et al. Oxidant injury of cells. DNA strand-breaks activate polyadenosine diphosphate-ribose polymerase and lead to depletion of nicotinamide adenine dinucleotide. J Clin Invest.1986;77(4):1312-1320.
18.Kroemer G. Mitochondria in cancer. Oncogene. 2006;25(34):4630-4632.
19.Ahmad IM, Aykin-Burns N, Sim JE, et al. Mitochondrial O2*-and H2O2 mediate glucose deprivation-induced stress in human cancer cells. J Biol Chem. 2005;280(6):4254-4263.
20.Comelli M, Di Pancrazio F, Mavelli I. Apoptosis is induced by decline of mitochondrial ATP synthesis in erythroleukemia cells. Free Radic Biol Med. 2003;34(9):1190-1199.
21.DeBerardinis RJ, Chandel NS. Fundamentals of cancer metabolism. Sci Adv. 2016;2(5):e1600200.
22.Liberti MV, Locasale JW. The Warburg effect: how does it benefit cancer cells? Trends Biochem Sci. 2016;41(3):211-218.
23.Parker WH, Qu ZC, May JM. Ascorbic acid transport in brain microvascular pericytes. Biochem Biophys Res Commun. 2015;458(2):262-267.
24.Corpe CP, Eck P, Wang J, et al. Intestinal dehydroascorbic acid (DHA) transport mediated by the facilitative sugar transporters, GLUT2 and GLUT8. J Biol Chem. 2013;288(13):9092-9101.
25.Lu YX, Wu QN, Chen DL, et al. Pharmacological ascorbate suppresses growth of gastric cancer cells with glut1 overexpression and enhances the efficacy of oxaliplatin through redox modulation. Theranostics. 2018;8(5):1312-1326.
26.Yun J, Mullarky E, Lu C, et al. Vitamin C selectively kills KRAS and BRAF mutant colorectal cancer cells by targeting GAPDH. Science. 2015;350(6266):1391-1396.
27.Linster CL, Van Schaftingen E. Vitamin C. Biosynthesis, recycling and degradation in mammals. FEBS J. 2007;274(1):1-22.
28.杨柳青, 石汉平. 维生素C对KRAS突变型结直肠癌的治疗作用. 肿瘤代谢与营养电子杂志. 2015;2(4):76-79.
29.Cimmino L, Neel BG, Aifantis I. Vitamin C in stem cell reprogramming and cancer. Trends Cell Biol. 2018;28(9):698-708.
30.Gillberg L, Orskov AD, Liu M, et al. Vitamin C - A new player in regulation of the cancer epigenome. Semin Cancer Biol. 2018;51:59-67.
31.Agathocleous M, Meacham CE, Burgess RJ, et al. Ascorbate regulates haematopoietic stem cell function and leukaemogenesis. Nature. 2017;549(7673):476-481.
32.Cimmino L, Dolgalev I, Wang Y, et al. Restoration of TET2 function blocks aberrant self-renewal and leukemia progression. Cell. 2017;170(6):1079-1095.
33.Shenoy N, Bhagat T, Nieves E, et al. Upregulation of TET activity with ascorbic acid induces epigenetic modulation of lymphoma cells. Blood Cancer J. 2017;7(7):e587.
34.Baylin SB, Jones PA. A decade of exploring the cancer epigenome - biological and translational implications. Nat Rev Cancer. 2011;11(10):726-734.
35.Bejar R, Lord A, Stevenson K, et al. TET2 mutations predict response to hypomethylating agents in myelodysplastic syndrome patients. Blood. 2014;124(17):2705-2712.
36.Hu CY, Mohtat D, Yu Y, et al. Kidney cancer is characterized by aberrant methylation of tissue-specific enhancers that are prognostic for overall survival. Clin Cancer Res. 2014;20(16):4349-4360.
37.Jiang Y, Dunbar A, Gondek LP, et al. Aberrant DNA methylation is a dominant mechanism in MDS progression to AML. Blood. 2009;113(6):1315-1325.
38.Letouze E, Martinelli C, Loriot C, et al. SDH mutations establish a hypermethylator phenotype in paraganglioma. Cancer Cell. 2013;23(6):739-752.
39.Patnaik MM, Tefferi A. Chronic myelomonocytic leukemia: 2016 update on diagnosis, risk stratification, and management. Am J Hematol. 2016;91(6):631-642.
40.Rasmussen KD, Helin K. Role of TET enzymes in DNA methylation, development, and cancer. Genes Dev. 2016;30(7):733-750.
41.Wu SC, Zhang Y. Active DNA demethylation: many roads lead to Rome. Nat Rev Mol Cell Biol. 2010;11(9):607-620.
42.He YF, Li BZ, Li Z, et al. Tet-mediated formation of 5-carboxylcytosine and its excision by TDG in mammalian DNA. Science. 2011;333(6047):1303-1307.
43.Kohli RM, Zhang Y. TET enzymes, TDG and the dynamics of DNA demethylation. Nature. 2013;502(7472):472-479.
44.Lian CG, Xu Y, Ceol C, et al. Loss of 5-hydroxymethylcytosine is an epigenetic hallmark of melanoma. Cell. 2012;150(6):1135-1146.
45.Tsukada Y, Fang J, Erdjument-Bromage H, et al. Histone demethylation by a family of JmjC domain-containing proteins. Nature. 2006;439(7078):811-816.
46.Suzuki T, Minehata K, Akagi K, et al. Tumor suppressor gene identification using retroviral insertional mutagenesis in Blm-deficient mice. EMBO J. 2006;25(14):3422-3431.
47.Mustafi S, Camarena V, Volmar CH, et al. Vitamin C sensitizes melanoma to BET inhibitors. Cancer Res. 2018;78(2):572-583.
48.Peng D, Ge G, Gong Y, et al. Vitamin C increases 5-hydroxymethylcytosine level and inhibits the growth of bladder cancer. Clin Epigenetics. 2018;10(1):94.
49.Masoud GN, Li W. HIF-1alpha pathway: role, regulation and intervention for cancer therapy. Acta Pharm Sin B. 2015;5(5):378-389.
50.Kuiper C, Dachs GU, Currie MJ, et al. Intracellular ascorbate enhances hypoxia-inducible factor (HIF)-hydroxylase activity and preferentially suppresses the HIF-1 transcriptional response. Free Radic Biol Med. 2014;69:308-317.
51.Vadde R, Vemula S, Jinka R, et al. Role of hypoxia-inducible factors (HIF) in the maintenance of stemness and malignancy of colorectal cancer. Crit Rev Oncol Hematol. 2017;113:22-27.
52.Koivunen P, Hirsila M, Gunzler V, et al. Catalytic properties of the asparaginyl hydroxylase (FIH) in the oxygen sensing pathway are distinct from those of its prolyl 4-hydroxylases. J Biol Chem. 2004;279(11):9899-9904.
53.Lando D, Peet DJ, Gorman JJ, et al. FIH-1 is an asparaginyl hydroxylase enzyme that regulates the transcriptional activity of hypoxia-inducible factor. Genes Dev. 2002;16(12):1466-1471.
54.Ngo B, Van Riper JM, Cantley LC, et al. Targeting cancer vulnerabilities with high-dose vitamin C. Nat Rev Cancer. 2019;19(5):271-282.
55.Kuiper C, Dachs GU, Currie MJ, et al. Intracellular ascorbate enhances hypoxia-inducible factor (HIF)-hydroxylase activity and preferentially suppresses the HIF-1 transcriptional response. Free Radic Biol Med. 2014;69:308-317.
56.Jozwiak P, Ciesielski P, Zaczek A, et al. Expression of hypoxia inducible factor 1alpha and 2alpha and its association with vitamin C level in thyroid lesions. J Biomed Sci. 2017;24(1):83.
57.Wohlrab C, Vissers M, Phillips E, et al. The association between ascorbate and the hypoxia-inducible factors in human renal cell carcinoma requires a functional von hippel-lindau protein. Front Oncol. 2018;8:574.
58.Kuiper C, Molenaar IG, Dachs GU, et al. Low ascorbate levels are associated with increased hypoxia-inducible factor-1 activity and an aggressive tumor phenotype in endometrial cancer. Cancer Res. 2010;70(14):5749-5758.
59.Campbell EJ, Vissers MC, Dachs GU. Ascorbate availability affects tumor implantation-take rate and increases tumor rejection in Gulo(-/-) mice. Hypoxia (Auckl). 2016;4:41-52.
60.徐一杰, 王志超, 侯高峰, 等. 大剂量维生素C在肿瘤患者应用的安全性观察. 肿瘤代谢与营养电子杂志. 2018;5(4):399-402.

基金

国家重点研发计划项目(2017YFC1309200)
北京市临床重点专科(肿瘤科)建设项目(2018ZLLCZDZK4) 

PDF(1447 KB)

Accesses

Citation

Detail

段落导航
相关文章

/