Associations between Dietary Fiber, the Fecal Microbiota and Estrogen Metabolism in Postmenopausal Women with Breast Cancer

References

• Siegel RL, Miller KD, Jemal A. Cancer statistics, 2018. CA Cancer J Clin. 2018;68(1):7–30. doi:10.3322/caac.21442
   PubMed Web of Science ®Google Scholar
• American Cancer Society. Breast Cancer Facts & Figures 2018. Atlanta: American Cancer Society, 2018.
   Google Scholar
• Munsell MF, Sprague BL, Berry DA, Chisholm G, Trentham-Dietz A. Body mass index and breast cancer risk according to postmenopausal estrogen-progestin use and hormone receptor status. Epidemiol Rev. 2014;36(1):114–36. doi:10.1093/epirev/mxt010
   PubMed Web of Science ®Google Scholar
• Renehan AG, Tyson M, Egger M, Heller RF, Zwahlen M. Body-mass index and incidence of cancer: a systematic review and meta-analysis of prospective observational studies. Lancet. 2008;371(9612):569–78. doi:10.1016/S0140-6736(08)60269-X
   PubMed Web of Science ®Google Scholar
• Rossi RE, Pericleous M, Mandair D, Whyand T, Caplin ME. The role of dietary factors in prevention and progression of breast cancer. Anticancer Res. 2014;34(12):6861–75.
   PubMed Web of Science ®Google Scholar
• Kapil U, Bhadoria AS, Sareen N, Singh P, Dwivedi SN. Total cholesterol and triglyceride levels in patients with breast cancer. J Breast Cancer. 2013;16(1):129–30. doi:10.4048/jbc.2013.16.1.129
   PubMed Web of Science ®Google Scholar
• Farvid MS, Cho E, Chen WY, Eliassen AH, Willett WC. Dietary protein sources in early adulthood and breast cancer incidence: prospective cohort study. BMJ. 2014;348:g3437doi:10.1136/bmj.g3437
   PubMed Web of Science ®Google Scholar
• Catsburg C, Kim RS, Kirsh VA, Soskolne CL, Kreiger N, Rohan TE. Dietary patterns and breast cancer risk: a study in 2 cohorts. Am J Clin Nutr. 2015;101(4):817–23. doi:10.3945/ajcn.114.097659
   PubMed Web of Science ®Google Scholar
• Link LB, Canchola AJ, Bernstein L, Clarke CA, Stram DO, Ursin G, Horn-Ross PL. Dietary patterns and breast cancer risk in the California Teachers Study cohort. Am J Clin Nutr. 2013;98(6):1524–32. doi:10.3945/ajcn.113.061184
   PubMed Web of Science ®Google Scholar
• Aune D, Chan DSM, Greenwood DC, Vieira AR, Rosenblatt DAN, Vieira R, Norat T. Dietary fiber and breast cancer risk: a systematic review and meta-analysis of prospective studies. Ann Oncol. 2012;23(6):1394–402. doi:10.1093/annonc/mdr589
   PubMed Web of Science ®Google Scholar
• Anderson JW, Baird P, Davis RH, Ferreri S, Knudtson M, Koraym A, Waters V, Williams CL. Health benefits of dietary fiber. Nutr Rev. 2009;67(4):188–205. doi:10.1111/j.1753-4887.2009.00189.x
   PubMed Web of Science ®Google Scholar
• Fujii H, Iwase M, Ohkuma T, Ogata-Kaizu S, Ide H, Kikuchi Y, Idewaki Y, Joudai T, Hirakawa Y, Uchida K, et al. Impact of dietary fiber intake on glycemic control, cardiovascular risk factors and chronic kidney disease in Japanese patients with type 2 diabetes mellitus: the Fukuoka Diabetes Registry. Nutr J. 2013;12:159. doi:10.1186/1475-2891-12-159
   PubMed Web of Science ®Google Scholar
• Gaskins AJ, Mumford SL, Zhang C, Wactawski-Wende J, Hovey KM, Whitcomb BW, Howards PP, Perkins NJ, Yeung E, Schisterman EF, BioCycle Study Group, et al. Effect of daily fiber intake on reproductive function: the BioCycle study. Am J Clin Nutr. 2009;90(4):1061–9.: doi:10.3945/ajcn.2009.27990
   PubMed Web of Science ®Google Scholar
• Suzuki R, Rylander-Rudqvist T, Ye W, Saji S, Adlercreutz H, Wolk A. Dietary fiber intake and risk of postmenopausal breast cancer defined by estrogen and progesterone receptor status-a prospective cohort study among Swedish women. Int J Cancer. 2008;122(2):403–12. doi:10.1002/ijc.23060
   PubMed Web of Science ®Google Scholar
• Kwa M, Plottel CS, Blaser MJ, Adams S. The intestinal microbiome and estrogen receptor–positive female breast cancer. J National Cancer Inst. 2016;108:djw029. doi:10.1093/jnci/djw029
   PubMedGoogle Scholar
• Raftogianis R, Creveling C, Weinshilboum R, Weisz J. Estrogen metabolism by conjugation. JNCI Monogr. 2000;2000(27):113–24. doi:10.1093/oxfordjournals.jncimonographs.a024234
   Google Scholar
• Tsuruta Y, Rogers LQ, Krontiras H, Grizzle WE, Frugé AD, Oster RA, Umphrey HR, Jones LW, Azrad M, Demark-Wahnefried W, et al. Exploring effects of presurgical weight loss among women with stage 0-II breast cancer: protocol for a randomised controlled feasibility trial. BMJ Open. 2016;6(9):e012320. doi:10.1136/bmjopen-2016-012320
   PubMed Web of Science ®Google Scholar
• Tai SS, Welch MJ. Development and evaluation of a reference measurement procedure for the determination of estradiol-17beta in human serum using isotope-dilution liquid chromatography-tandem mass spectrometry. Anal Chem. 2005;77(19):6359–63. doi:10.1021/ac050837i
   PubMed Web of Science ®Google Scholar
• Kumar R, Eipers P, Little RB, Crowley M, Crossman DK, Lefkowitz EJ, Morrow CD. Getting started with microbiome analysis: sample acquisition to bioinformatics. Curr Protoc Hum Genet. 2014;82:18.8.1–29. doi:10.1002/0471142905.hg1808s82
   PubMedGoogle Scholar
• Frugé AD, Ptacek T, Tsuruta Y, Morrow CD, Azrad M, Desmond RA, Hunter GR, Rais-Bahrami S, Demark-Wahnefried W. Dietary changes impact the gut microbe composition in overweight and obese men with prostate cancer undergoing radical prostatectomy. J Acad Nutr Diet. 2018;118(4):714–23.e1. doi:10.1016/j.jand.2016.10.017
   PubMed Web of Science ®Google Scholar
• Fruge AD, Van der Pol W, Rogers LQ, Morrow CD, Tsuruta Y, et al. Fecal akkermansia muciniphila is associated with body composition and microbiota diversity in overweight and obese women with breast cancer participating in a presurgical weight loss trial. J Acad Nutr Diet. 2020;120(4):650–9. doi:10.1016/j.jand.2018.08.164
   PubMed Web of Science ®Google Scholar
• Steer T, Collins MD, Gibson GR, Hippe H, Lawson PA. Clostridium hathewayi sp. nov., from human faeces. Syst Appl Microbiol. 2001;24(3):353–7. doi:10.1078/0723-2020-00044
   PubMed Web of Science ®Google Scholar
• Linscott AJ, Flamholtz RB, Shukla D, Song Y, Liu C, Finegold SM. Fatal septicemia due to Clostridium hathewayi and Campylobacter hominis. Anaerobe. 2005;11(1–2):97–8. doi:10.1016/j.anaerobe.2004.10.002
   PubMed Web of Science ®Google Scholar
• Woo PCY, Lau SKP, Woo GKS, Fung AMY, Yiu VPY, Yuen K-Y. Bacteremia due to Clostridium hathewayi in a patient with acute appendicitis. J Clin Microbiol. 2004;42(12):5947–9. doi:10.1128/jcm.42.12.5947-5949.2004
   PubMed Web of Science ®Google Scholar
• Tena D, Losa C, Medina-Pascual MJ, Sáez-Nieto JA. Fournier's gangrene caused by Actinomyces funkei, Fusobacterium gonidiaformans and Clostridium hathewayi. Anaerobe. 2014;27:14–6. doi:10.1016/j.anaerobe.2014.02.004
   PubMed Web of Science ®Google Scholar
• Dababneh AS, Nagpal A, Palraj BR, Sohail MR. Clostridium hathewayi bacteraemia and surgical site infection after uterine myomectomy. BMJ Case Rep. 2014;2014. doi:10.1136/bcr-2013-009322
   PubMedGoogle Scholar
• Sameer E, Kunyan Z. Human infection caused by Clostridium hathewayi. Emerg Infect Dis J. 2004;10:1950. doi:10.3201/eid1011.040006
   PubMed Web of Science ®Google Scholar
• Chinda D, Nakaji S, Fukuda S, Sakamoto J, Shimoyama T, Nakamura T, Fujisawa T, Terada A, Sugawara K. The fermentation of different dietary fibers is associated with fecal clostridia levels in men. J Nutr. 2004;134(8):1881–6. doi:10.1093/jn/134.8.1881
   PubMed Web of Science ®Google Scholar
• Bang S-J, Kim G, Lim MY, Song E-J, Jung D-H, Kum J-S, Nam Y-D, Park C-S, Seo D-H. The influence of in vitro pectin fermentation on the human fecal microbiome. AMB Express. 2018;8(1):98. doi:10.1186/s13568-018-0629-9
   PubMed Web of Science ®Google Scholar
• Benítez-Páez A, Gómez del Pulgar EM, Sanz Y. The glycolytic versatility of bacteroides uniformis CECT 7771 and its genome response to oligo and polysaccharides. Front Cell Infect Microbiol. 2017;7:383. doi:10.3389/fcimb.2017.00383
   PubMed Web of Science ®Google Scholar
• Rivenzon-Segal D, Margalit R, Degani H. Glycolysis as a metabolic marker in orthotopic breast cancer, monitored by in vivo (13)C MRS. Am J Physiol Endocrinol Metab. 2002;283(4):E623–E630. doi:10.1152/ajpendo.00050.2002
   PubMed Web of Science ®Google Scholar
• van der Hiel B, Pauwels EK, Stokkel MP. Positron emission tomography with 2-[18F]-fluoro-2-deoxy-D-glucose in oncology. Part IIIa: therapy response monitoring in breast cancer, lymphoma and gliomas. J Cancer Res Clin Oncol. 2001;127(5):269–77. doi:10.1007/s004320000191
   PubMed Web of Science ®Google Scholar