Negative Association of Serum β-Cryptoxanthin With Benzene and Its Derivatives

References

• International Agency for Research on Cancer. Benzene. Vol. 120. World Health Organization; 2018.
   Google Scholar
• IARC. IARC monographs on the evaluation of carcinogenic risks to humans; 2000. p. 257. https://publications.iarc.fr/_publications/media/download/2931/d7a4e802483b1374482768a36a7c78e1b33aa1c8.pdf
   Google Scholar
• Cancer IAfRo. Chemical agents and related occupations. World Health Organization; 2012. p. 250. https://monographs.iarc.who.int/wp-content/uploads/2018/06/mono100F.pdf
   Google Scholar
• World Health Organization. Exposure to benzene—a major public health concern; 2019. p. 2. https://www.who.int/publications/i/item/WHO-CED-PHE-EPE-19.4.2
   Google Scholar
• Jiao Y, Reuss L, Wang Y. β-Cryptoxanthin: chemistry, occurrence, and potential health benefits. Curr Pharmacol Rep. 2019;5(1):20–34. doi:10.1007/s40495-019-00168-7.
   Google Scholar
• Burri BJ, La Frano MR, Zhu C. Absorption, metabolism, and functions of β-cryptoxanthin. Nutr Rev. 2016;74(2):69–82. doi:10.1093/nutrit/nuv064.
   PubMed Web of Science ®Google Scholar
• Saini RK, Keum YS, Daglia M, Rengasamy KR. Dietary carotenoids in cancer chemoprevention and chemotherapy: a review of emerging evidence. Pharmacol Res. 2020;157:104830. doi:10.1016/j.phrs.2020.104830.
   PubMed Web of Science ®Google Scholar
• Männistö S, Smith-Warner SA, Spiegelman D, Albanes D, Anderson K, van den Brandt PA, Cerhan JR, Colditz G, Feskanich D, Freudenheim JL, et al. Dietary carotenoids and risk of lung cancer in a pooled analysis of seven cohort studies. Cancer Epidemiol Biomarkers Prev. 2004;13(1):40–8. doi:10.1158/1055-9965.epi-038-3.
   PubMed Web of Science ®Google Scholar
• De Stefani E, Brennan P, Boffetta P, Ronco AL, Mendilaharsu M, Deneo-Pellegrini H. Vegetables, fruits, related dietary antioxidants, and risk of squamous cell carcinoma of the esophagus: a case-control study in Uruguay. Nutr Cancer. 2000;38(1):23–9. doi:10.1207/S15327914NC381_4.
   PubMed Web of Science ®Google Scholar
• (2003-2004) NCfHS. National Health and Nutrition Examination Survey; [cited 2023 Mar 4]. Available from: https://wwwn.cdc.gov/Nchs/Nhanes/continuousnhanes/default.aspx?BeginYear=2003.
   Google Scholar
• Survey NHaNE. 2003-2004 Data Documentation, Codebook, and Frequencies; 2006; [cited 2023 Mar 20]. Available from: https://wwwn.cdc.gov/Nchs/Nhanes/2003-2004/SMQ_C.htm#SMQ020
   Google Scholar
• Collins JJ, Anteau SE, Swaen GM, Bodner KM, Bodnar CM. Lymphatic and hematopoietic cancers among benzene-exposed workers. J Occup Environ Med. 2015;57(2):159–63. doi:10.1097/JOM.0000000000000324.
   PubMed Web of Science ®Google Scholar
• Wong O, Harris F, Armstrong TW, Hua F. A hospital-based case-control study of acute myeloid leukemia in Shanghai: analysis of environmental and occupational risk factors by subtypes of the WHO classification. Chem Biol Interact. 2010;184(1-2):112–28. doi:10.1016/j.cbi.2009.10.017.
   PubMed Web of Science ®Google Scholar
• Saberi Hosnijeh F, Christopher Y, Peeters P, Romieu I, Xun W, Riboli E, Raaschou-Nielsen O, Tjønneland A, Becker N, Nieters A, et al. Occupation and risk of lymphoid and myeloid leukaemia in the European Prospective Investigation into Cancer and Nutrition (EPIC). Occup Environ Med. 2013;70(7):464–70. doi:10.1136/oemed-2012-101135.
   PubMed Web of Science ®Google Scholar
• Talibov M, Lehtinen-Jacks S, Martinsen JI, Kjærheim K, Lynge E, Sparén P, Tryggvadottir L, Weiderpass E, Kauppinen T, Kyyrönen P, et al. Occupational exposure to solvents and acute myeloid leukemia: a population-based, case-control study in four Nordic countries. Scand J Work Environ Health. 2014;40(5):511–7. doi:10.5271/sjweh.3436.
   PubMed Web of Science ®Google Scholar
• Rhomberg L, Goodman J, Tao G, Zu K, Chandalia J, Williams PRD, Allen B. Evaluation of acute nonlymphocytic leukemia and its subtypes with updated benzene exposure and mortality estimates: a lifetable analysis of the pliofilm cohort. J Occup Environ Med. 2016;58(4):414–20. doi:10.1097/JOM.0000000000000689.
   PubMed Web of Science ®Google Scholar
• Kirkeleit J, Riise T, Bråtveit M, Moen BE. Increased risk of acute myelogenous leukemia and multiple myeloma in a historical cohort of upstream petroleum workers exposed to crude oil. Cancer Causes Control. 2008;19(1):13–23. doi:10.1007/s10552-007-9065-x.
   PubMed Web of Science ®Google Scholar
• Schnatter AR, Glass DC, Tang G, Irons RD, Rushton L. Myelodysplastic syndrome and benzene exposure among petroleum workers: an international pooled analysis. J Natl Cancer Inst. 2012;104(22):1724–37. doi:10.1093/jnci/djs411.
   PubMedGoogle Scholar
• Stenehjem JS, Kjærheim K, Bråtveit M, Samuelsen SO, Barone-Adesi F, Rothman N, Lan Q, Grimsrud TK. Benzene exposure and risk of lymphohaematopoietic cancers in 25 000 offshore oil industry workers. Br J Cancer. 2015;112(9):1603–12. doi:10.1038/bjc.2015.108.
   PubMed Web of Science ®Google Scholar
• Ireland B, Collins JJ, Buckley CF, Riordan SG. Cancer mortality among workers with benzene exposure. Epidemiology. 1997;8(3):318–20. doi:10.1097/00001648-199705000-00016.
   PubMed Web of Science ®Google Scholar
• Iskandar AR, Miao B, Li X, Hu KQ, Liu C, Wang XD. β-Cryptoxanthin reduced lung tumor multiplicity and inhibited lung cancer cell motility by downregulating nicotinic acetylcholine receptor α7 signaling. Cancer Prev Res (Phila). 2016;9(11):875–86. doi:10.1158/1940-6207.CAPR-16-0161.
   PubMed Web of Science ®Google Scholar
• San Millán C, Soldevilla B, Martín P, Gil-Calderón B, Compte M, Pérez-Sacristán B, Donoso E, Peña C, Romero J, Granado-Lorencio F, et al. β-Cryptoxanthin synergistically enhances the antitumoral activity of oxaliplatin through ΔNP73 negative regulation in colon cancer. Clin Cancer Res. 2015;21(19):4398–409. doi:10.1158/1078-0432.CCR-14-2027.
   PubMed Web of Science ®Google Scholar
• Gao M, Dang F, Deng C. β-Cryptoxanthin induced anti-proliferation and apoptosis by G0/G1 arrest and AMPK signal inactivation in gastric cancer. Eur J Pharmacol. 2019;859:172528. doi:10.1016/j.ejphar.2019.172528.
   PubMed Web of Science ®Google Scholar
• Miyazawa K, Miyamoto S, Suzuki R, Yasui Y, Ikeda R, Kohno H, et al. Dietary β-cryptoxanthin inhibits N-butyl-N-(4-hydroxybutyl)nitrosamine-induced urinary bladder carcinogenesis in male ICR mice. Oncol Rep. 2007;17(2):297–304.
   PubMed Web of Science ®Google Scholar
• Lim JY, Liu C, Hu K-Q, Smith DE, Wu D, Lamon-Fava S, Ausman LM, Wang X-D. Dietary β-cryptoxanthin inhibits high-refined carbohydrate diet–induced fatty liver via differential protective mechanisms depending on carotenoid cleavage enzymes in male mice. J Nutr. 2019;149(9):1553–64. doi:10.1093/jn/nxz106.
   PubMed Web of Science ®Google Scholar
• Powley MW, Carlson GP. Cytochromes P450 involved with benzene metabolism in hepatic and pulmonary microsomes. J Biochem Mol Toxicol. 2000;14(6):303–9. doi:10.1002/1099-0461(2000)14:6<303::AID-JBT2>3.0.CO;2-8.
   PubMed Web of Science ®Google Scholar
• Chaney AM, Carlson GP. Comparison of rat hepatic and pulmonary microsomal metabolism of benzene and the lack of benzene-induced pneumotoxicity and hepatotoxicity. Toxicology. 1995;104(1-3):53–62. doi:10.1016/0300-483x(95)03129-4.
   PubMed Web of Science ®Google Scholar
• Rappaport SM, Kim S, Lan Q, Vermeulen R, Waidyanatha S, Zhang L, Li G, Yin S, Hayes RB, Rothman N, et al. Evidence that humans metabolize benzene via two pathways. Environ Health Perspect. 2009;117(6):946–52. doi:10.1289/ehp.0800510.
   PubMed Web of Science ®Google Scholar
• Glatt H, Padykula R, Berchtold GA, Ludewig G, Platt KL, Klein J, Oesch F. Multiple activation pathways of benzene leading to products with varying genotoxic characteristics. Environ Health Perspect. 1989;82:81–9. doi:10.1289/ehp.898281.
   PubMed Web of Science ®Google Scholar
• Schattenberg DG, Stillman WS, Gruntmeir JJ, Helm KM, Irons RD, Ross D. Peroxidase activity in murine and human hematopoietic progenitor cells: potential relevance to benzene-induced toxicity. Mol Pharmacol. 1994;46(2):346–51.
   PubMed Web of Science ®Google Scholar
• Gut I, Nedelcheva V, Soucek P, Stopka P, Tichavská B. Cytochromes P450 in benzene metabolism and involvement of their metabolites and reactive oxygen species in toxicity. Environ Health Perspect. 1996;104(suppl 6):1211–8. doi:10.1289/ehp.961041211.
   PubMedGoogle Scholar
• Snyder R, Hedli CC. An overview of benzene metabolism. Environ Health Perspect. 1996;104(suppl 6):1165–71. doi:10.1289/ehp.961041165.
   PubMed Web of Science ®Google Scholar
• Ross D. The role of metabolism and specific metabolites in benzene-induced toxicity: evidence and issues. J Toxicol Environ Health A. 2000;61(5-6):357–72. doi:10.1080/00984100050166361.
   PubMed Web of Science ®Google Scholar
• Darwish WS, Ikenaka Y, Nakayama S, Mizukawa H, Thompson LA, Ishizuka M. β-Carotene and retinol reduce benzo [a] pyrene-induced mutagenicity and oxidative stress via transcriptional modulation of xenobiotic metabolizing enzymes in human HepG2 cell line. Environ Sci Pollut Res Int. 2018;25(7):6320–8. doi:10.1007/s11356-017-0977-z.
   PubMed Web of Science ®Google Scholar
• Turner T, Burri BJ, Jamil KM, Jamil M. The effects of daily consumption of β-cryptoxanthin-rich tangerines and β-carotene-rich sweet potatoes on vitamin A and carotenoid concentrations in plasma and breast milk of Bangladeshi women with low vitamin A status in a randomized controlled trial. Am J Clin Nutr. 2013;98(5):1200–8. doi:10.3945/ajcn.113.058180.
   PubMed Web of Science ®Google Scholar