Breast cancer in postmenopausal women is associated with an altered gut metagenome

Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

Benjamini, Y., & Hochberg, Y. (1995) · Journal of the Royal Statistical Society Series B: Statistical Methodology · doi:10.1111/j.2517-6161.1995.tb02031.x · Cited by 109,482 · see citing works

A human gut microbial gene catalogue established by metagenomic sequencing

MetaHIT Consortium, Qin, J., Li, R., Raes, J., Arumugam, M., Burgdorf, K. S., Manichanh, C., Nielsen, T., Pons, N., Levenez, F., et al. (2010) · Nature · doi:10.1038/nature08821 · Cited by 11,624 · see citing works

Diversity of the Human Intestinal Microbial Flora

Eckburg, P. B., Bik, E. M., Bernstein, C. N., Purdom, E., Dethlefsen, L., Sargent, M., Gill, S. R., Nelson, K. E., & Relman, D. A. (2005) · Science · doi:10.1126/science.1110591 · Cited by 7,913 · see citing works

A core gut microbiome in obese and lean twins

Turnbaugh, P. J., Hamady, M., Yatsunenko, T., Cantarel, B. L., Duncan, A., Ley, R. E., Sogin, M. L., Jones, W. J., Roe, B. A., Affourtit, J. P., et al. (2009) · Nature · doi:10.1038/nature07540 · Cited by 7,823 · see citing works

Enterotypes of the human gut microbiome

MetaHIT Consortium (additional members), Arumugam, M., Raes, J., Pelletier, E., Le Paslier, D., Yamada, T., Mende, D. R., Fernandes, G. R., Tap, J., Bruls, T., et al. (2011) · Nature · doi:10.1038/nature09944 · Cited by 7,548 · see citing works

Changes of Intestinal Functions in Liver Cirrhosis

Fukui, H., & Wiest, R. (2016) · Inflammatory Intestinal Diseases · doi:10.1159/000444436 · Cited by 6,820 · see citing works

A metagenome-wide association study of gut microbiota in type 2 diabetes

Qin, J., Li, Y., Cai, Z., Li, S., Zhu, J., Zhang, F., Liang, S., Zhang, W., Guan, Y., Shen, D., et al. (2012) · Nature · doi:10.1038/nature11450 · Cited by 6,762 · see citing works

The ade4 Package: Implementing the Duality Diagram for Ecologists

Dray, S., & Dufour, A. (2007) · Journal of Statistical Software · doi:10.18637/jss.v022.i04 · Cited by 6,168 · see citing works

Gut flora metabolism of phosphatidylcholine promotes cardiovascular disease

Wang, Z., Klipfell, E., Bennett, B. J., Koeth, R., Levison, B. S., DuGar, B., Feldstein, A. E., Britt, E. B., Fu, X., Chung, Y.-M., et al. (2011) · Nature · doi:10.1038/nature09922 · Cited by 5,597 · see citing works

Role of the microbiota in immunity and inflammation.

Belkaid, Y., & Hand, T. W. (2014) · Cell · doi:10.1016/j.cell.2014.03.011 · Cited by 5,385 · see citing works

Metagenomic Analysis of the Human Distal Gut Microbiome

Gill, S. R., Pop, M., DeBoy, R. T., Eckburg, P. B., Turnbaugh, P. J., Samuel, B. S., Gordon, J. I., Relman, D. A., Fraser-Liggett, C. M., & Nelson, K. E. (2006) · Science · doi:10.1126/science.1124234 · Cited by 4,699 · see citing works

Molecular-phylogenetic characterization of microbial community imbalances in human inflammatory bowel diseases

Frank, D. N., St. Amand, A. L., Feldman, R. A., Boedeker, E. C., Harpaz, N., & Pace, N. R. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0706625104 · Cited by 4,611 · see citing works

The human microbiome: at the interface of health and disease

Cho, I., & Blaser, M. J. (2012) · Nature Reviews Genetics · doi:10.1038/nrg3182 · Cited by 3,449 · see citing works

Gut metagenome in European women with normal, impaired and diabetic glucose control

Karlsson, F. H., Tremaroli, V., Nookaew, I., Bergström, G., Behre, C. J., Fagerberg, B., Nielsen, J., & Bäckhed, F. (2013) · Nature · doi:10.1038/nature12198 · Cited by 3,115 · see citing works

The gut flora as a forgotten organ

O'Hara, A. M., & Shanahan, F. (2006) · The EMBO Reports · doi:10.1038/sj.embor.7400731 · Cited by 2,791 · see citing works

Obesity-induced gut microbial metabolite promotes liver cancer through senescence secretome

Yoshimoto, S., Loo, T. M., Atarashi, K., Kanda, H., Sato, S., Oyadomari, S., Iwakura, Y., Oshima, K., Morita, H., Hattori, M., et al. (2013) · Nature · doi:10.1038/nature12347 · Cited by 2,219 · see citing works

Alterations of the human gut microbiome in liver cirrhosis

Qin, N., Yang, F., Li, A., Prifti, E., Chen, Y., Shao, L., Guo, J., Le Chatelier, E., Yao, J., Wu, L., et al. (2014) · Nature · doi:10.1038/nature13568 · Cited by 2,177 · see citing works

An integrated catalog of reference genes in the human gut microbiome

MetaHIT Consortium, Li, J., Jia, H., Cai, X., Zhong, H., Feng, Q., Sunagawa, S., Arumugam, M., Kultima, J. R., Prifti, E., et al. (2014) · Nature Biotechnology · doi:10.1038/nbt.2942 · Cited by 2,164 · see citing works

Expansion of intestinal Prevotella copri correlates with enhanced susceptibility to arthritis

Scher, J. U., Sczesnak, A., Longman, R. S., Segata, N., Ubeda, C., Bielski, C., Rostron, T., Cerundolo, V., Pamer, E. G., Abramson, S. B., et al. (2013) · eLife · doi:10.7554/elife.01202 · Cited by 2,047 · see citing works

Endogenous Sex Hormones and Breast Cancer in Postmenopausal Women: Reanalysis of Nine Prospective Studies

The Endogenous Hormones and Breast Cancer Collaborative Group (2002) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/94.8.606 · Cited by 1,793 · see citing works

Gut microbiota dysbiosis contributes to the development of hypertension

Li, J., Zhao, F., Wang, Y., Chen, J., Tao, J., Tian, G., Wu, S., Liu, W., Cui, Q., Geng, B., et al. (2017) · Microbiome · doi:10.1186/s40168-016-0222-x · Cited by 1,685 · see citing works

VFDB 2016: hierarchical and refined dataset for big data analysis—10 years on

Chen, L., Zheng, D., Liu, B., Yang, J., & Jin, Q. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv1239 · Cited by 1,672 · see citing works

Reciprocal interactions of the intestinal microbiota and immune system

Maynard, C. L., Elson, C. O., Hatton, R. D., & Weaver, C. T. (2012) · Nature · doi:10.1038/nature11551 · Cited by 1,598 · see citing works

Gut microbiome development along the colorectal adenoma-carcinoma sequence

Feng, Q., Liang, S., Jia, H., Stadlmayr, A., Tang, L., Lan, Z., Zhang, D., Xia, H., Xu, X., Jie, Z., et al. (2015) · Nature Communications · doi:10.1038/ncomms7528 · Cited by 1,506 · see citing works

Potential of fecal microbiota for early-stage detection of colorectal cancer

Zeller, G., Tap, J., Voigt, A. Y., Sunagawa, S., Kultima, J. R., Costea, P. I., Amiot, A., Böhm, J., Brunetti, F., Habermann, N., et al. (2014) · Molecular Systems Biology · doi:10.15252/msb.20145645 · Cited by 1,375 · see citing works

Promotion of Hepatocellular Carcinoma by the Intestinal Microbiota and TLR4

Dapito, D. H., Mencin, A., Gwak, G.-Y., Pradere, J.-P., Jang, M.-K., Mederacke, I., Caviglia, J. M., Khiabanian, H., Adeyemi, A., Bataller, R., et al. (2012) · Cancer Cell · doi:10.1016/j.ccr.2012.02.007 · Cited by 1,346 · see citing works

Reduction in diversity of the colonic mucosa associated bacterial microflora in patients with active inflammatory bowel disease

Ott, S. J., Musfeldt, M., Wenderoth, D. F., Hampe, J., Brant, O., Fölsch, U. R., Timmis, K. N., & Schreiber, S. (2004) · Gut · doi:10.1136/gut.2003.025403 · Cited by 1,311 · see citing works

Characterization of fecal microbial communities in patients with liver cirrhosis

Chen, Y., Yang, F., Lu, H., Wang, B., Chen, Y., Lei, D., Wang, Y., Zhu, B., & Li, L. (2011) · Hepatology · doi:10.1002/hep.24423 · Cited by 1,038 · see citing works

Gut microbiota composition and development of atopic manifestations in infancy: the KOALA Birth Cohort Study

Penders, J., Thijs, C., van den Brandt, P. A., Kummeling, I., Snijders, B., Stelma, F., Adams, H., van Ree, R., & Stobberingh, E. E. (2007) · Gut · doi:10.1136/gut.2006.100164 · Cited by 844 · see citing works

Microbial Dysbiosis in Colorectal Cancer (CRC) Patients

Sobhani, I., Tap, J., Roudot‐Thoraval, F., Roperch, J. P., Letulle, S., Langella, P., Corthier, G., Nhieu, J. T. V., & Furet, J. (2011) · PLoS ONE · doi:10.1371/journal.pone.0016393 · Cited by 832 · see citing works

Differences between the gut microflora of children with autistic spectrum disorders and that of healthy children

Parracho, H. M., Bingham, M. O., Gibson, G. R., & McCartney, A. L. (2005) · Journal of Medical Microbiology · doi:10.1099/jmm.0.46101-0 · Cited by 784 · see citing works

Gut Microbiome Metagenomics Analysis Suggests a Functional Model for the Development of Autoimmunity for Type 1 Diabetes

Brown, C. T., Davis-Richardson, A. G., Giongo, A., Gano, K. A., Crabb, D. B., Mukherjee, N., Casella, G., Drew, J. C., Ilonen, J., Knip, M., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025792 · Cited by 778 · see citing works

Lipopolysaccharide Activates Distinct Signaling Pathways in Intestinal Epithelial Cell Lines Expressing Toll-Like Receptors

Cario, E., Rosenberg, I. M., Brandwein, S. L., Beck, P. L., Reinecker, H., & Podolsky, D. K. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.164.2.966 · Cited by 751 · see citing works

Microbiome and malignancy

Plottel, C. S., & Blaser, M. J. (2011) · Cell Host & Microbe · doi:10.1016/j.chom.2011.10.003 · Cited by 743 · see citing works

Uncovering transcriptional regulation of metabolism by using metabolic network topology

Patil, K. R., & NIELSEN, J. K. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0406811102 · Cited by 649 · see citing works

Iron Fortification Adversely Affects the Gut Microbiome, Increases Pathogen Abundance and Induces Intestinal Inflammation in Kenyan Infants

Jaeggi, T., Kortman, G. A. M., Moretti, D., Chassard, C., Holding, P., Dostal, A., Boekhorst, J., Timmerman, H. M., Swinkels, D. W., Tjalsma, H., et al. (2015) · Gut · doi:10.1136/gutjnl-2014-307720 · Cited by 622 · see citing works

Fecal microbial determinants of fecal and systemic estrogens and estrogen metabolites: a cross-sectional study

Flores, R., Shi, J., Fuhrman, B., Xu, X., Veenstra, T. D., Gail, M. H., Gajer, P., Ravel, J., & Goedert, J. J. (2012) · Journal of Translational Medicine · doi:10.1186/1479-5876-10-253 · Cited by 615 · see citing works

Status of the Microbial Census

Schloss, P. D., & Handelsman, J. (2004) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.68.4.686-691.2004 · Cited by 574 · see citing works

Real-Time PCR Quantitation of Clostridia in Feces of Autistic Children

Song, Y., Liu, C., & Finegold, S. M. (2004) · Applied and Environmental Microbiology · doi:10.1128/aem.70.11.6459-6465.2004 · Cited by 556 · see citing works

The luminal short-chain fatty acid butyrate modulates NF-κB activity in a human colonic epithelial cell line

Inan, M. S., Rasoulpour, R. J., Yin, L., Hubbard, A. K., Rosenberg, D. W., & Giardina, C. A. (2000) · Gastroenterology · doi:10.1016/s0016-5085(00)70142-9 · Cited by 502 · see citing works

Butyrate and other short-chain fatty acids as modulators of immunity: What relevance for health?

Meijer, K., de Vos, P., & Priebe, M. G. (2010) · Current Opinion in Clinical Nutrition and Metabolic Care · doi:10.1097/mco.0b013e32833eebe5 · Cited by 443 · see citing works

Fecal microbiota in early rheumatoid arthritis.

Vaahtovuo, J., Munukka, E., Korkeamäki, M., Luukkainen, R., & Toivanen, P. (2008) · PubMed · Cited by 426 · see citing works

Investigation of the Association Between the Fecal Microbiota and Breast Cancer in Postmenopausal Women: a Population-Based Case-Control Pilot Study

Goedert, J. J., Jones, G., Hua, X., Xu, X., Yu, G., Flores, R., Falk, R. T., Gail, M. H., Shi, J., Ravel, J., et al. (2015) · JNCI: Journal of the National Cancer Institute · doi:10.1093/jnci/djv147 · Cited by 393 · see citing works

Circulating sex hormones and breast cancer risk factors in postmenopausal women: reanalysis of 13 studies

Endogenous Hormones and Breast Cancer Collaborative Group (2011) · British Journal of Cancer · doi:10.1038/bjc.2011.254 · Cited by 391 · see citing works

Roseburia intestinalis sp. nov., a novel saccharolytic, butyrate-producing bacterium from human faeces.

Duncan, S. H., Hold, G. L., Barcenilla, A., Stewart, C. S., & Flint, H. J. (2002) · INTERNATIONAL JOURNAL OF SYSTEMATIC AND EVOLUTIONARY MICROBIOLOGY · doi:10.1099/00207713-52-5-1615 · Cited by 368 · see citing works

Molecular mechanisms of innate memory and tolerance to LPS

Seeley, J. J., & Ghosh, S. (2016) · Journal of Leukocyte Biology · doi:10.1189/jlb.3mr0316-118rr · Cited by 366 · see citing works

Shotgun Metagenomics of 250 Adult Twins Reveals Genetic and Environmental Impacts on the Gut Microbiome

Xie, H., Guo, R., Zhong, H., Feng, Q., Lan, Z., Qin, B., Ward, K. J., Jackson, M. A., Xia, Y., Chen, X., et al. (2016) · Cell Systems · doi:10.1016/j.cels.2016.10.004 · Cited by 341 · see citing works

Culture‐independent analysis of the gut microbiota in colorectal cancer and polyposis

Scanlan, P. D., Shanahan, F., Clune, Y., Collins, J. K., O'Sullivan, G. C., O'Riordan, M., Holmes, E., Wang, Y., & Marchesi, J. R. (2008) · Environmental Microbiology · doi:10.1111/j.1462-2920.2007.01503.x · Cited by 245 · see citing works

PHI-base: a new interface and further additions for the multi-species pathogen–host interactions database

Urban, M., Cuzick, A., Rutherford, K., Irvine, A. G., Pedro, H., Pant, R., Sadanadan, V., Khamari, L., Billal, S., Mohanty, S., et al. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw1089 · Cited by 224 · see citing works

Estrogen Metabolism and Risk of Breast Cancer in Postmenopausal Women

Fuhrman, B. J., Schairer, C., Gail, M. H., Boyd-Morin, J., Xu, X., Sue, L. Y., Buys, S. S., Isaacs, C. J., Keefer, L. K., Veenstra, T. D., et al. (2012) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/djr531 · Cited by 206 · see citing works

Substrate-driven gene expression in Roseburia inulinivorans : Importance of inducible enzymes in the utilization of inulin and starch

Scott, K. P., Martin, J. C., Chassard, C., Clerget, M., Potrykus, J., Campbell, G., Mayer, C., Young, P., Rucklidge, G. J., Ramsay, A. G., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1000091107 · Cited by 144 · see citing works

Urinary Estrogens and Estrogen Metabolites and Subsequent Risk of Breast Cancer among Premenopausal Women

Eliassen, A. H., Spiegelman, D. L., Xu, X., Keefer, L. K., Veenstra, T. D., Barbieri, R. L., Willett, W. C., Hankinson, S. E., & Ziegler, R. G. (2011) · Cancer Research · doi:10.1158/0008-5472.can-11-2507 · Cited by 94 · see citing works

Diversity and Composition of the Adult Fecal Microbiome Associated with History of Cesarean Birth or Appendectomy: Analysis of the American Gut Project

Goedert, J. J., Hua, X., Yu, G., & Shi, J. (2014) · EBioMedicine · doi:10.1016/j.ebiom.2014.11.004 · Cited by 84 · see citing works

Diet, Hormones, and Cancer

Rose, D. P. (1993) · Annual Review of Public Health · doi:10.1146/annurev.pu.14.050193.000245 · Cited by 75 · see citing works

Estrogen metabolism and breast cancer risk among postmenopausal women: a case–cohort study within B~FIT

Dallal, C. M., Tice, J. A., Buist, D. S. M., Bauer, D. C., Lacey, J. V., Cauley, J. A., Hue, T. F., LaCroix, A. Z., Falk, R. T., Pfeiffer, R. M., et al. (2013) · Carcinogenesis · doi:10.1093/carcin/bgt367 · Cited by 73 · see citing works

Expression and Functional Research of TLR4 in Human Colon Carcinoma

Tang, X., Wang, H., Zhu, Y., & Wei, B. (2010) · The American Journal of the Medical Sciences · doi:10.1097/maj.0b013e3181cef1b7 · Cited by 53 · see citing works

Biomarkers of folate and vitamin B12 and breast cancer risk: report from the EPIC cohort

Matejcic, M., de Batlle, J., Ricci, C., Biessy, C., Perrier, F., Huybrechts, I., Weiderpass, E., Boutron‐Ruault, M., Cadeau, C., His, M., et al. (2016) · International Journal of Cancer · doi:10.1002/ijc.30536 · Cited by 51 · see citing works

Species richness in soil bacterial communities: A proposed approach to overcome sample size bias

Youssef, N. H., & Elshahed, M. S. (2008) · Journal of Microbiological Methods · doi:10.1016/j.mimet.2008.05.009 · Cited by 41 · see citing works

Intestinal Microflora as an Alternative Metabolic Source of Estrogens in Women with Uterine Leiomyoma and Breast Cancer

Minelli, E. B., Beghini, A. M., Vesentini, S., Marchiori, L., Nardo, G., Cerutti, R., & Mortani, E. (1990) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1990.tb34337.x · Cited by 39 · see citing works

Culture‐independent analysis of the gut microbiota in colorectal cancer and polyposis

Scanlan, P. D., Shanahan, F., Clune, Y., Collins, J. K., O’Sullivan, G. C., O'Riordan, M., Holmes, E. C., Wang, Y., & Marchesi, J. R. (2008) · Environmental Microbiology · doi:10.1111/j.1462-2920.2008.01622.x · Cited by 29 · see citing works

Rhizosphere Engineering With Plant Growth-Promoting Microorganisms for Agriculture and Ecological Sustainability

Hakim, S., Naqqash, T., Nawaz, M. S., Laraib, I., Siddique, M. J., Zia, R., Mirza, M. S., & Imran, A. (2021) · Frontiers in Sustainable Food Systems · doi:10.3389/fsufs.2021.617157 · Cited by 507 · see citing works

A systematic review of antibiotics and antibiotic resistance genes in estuarine and coastal environments

Zheng, D., Yin, G., Liu, M., Chen, C., Jiang, Y., Hou, L., & Zheng, Y. (2021) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2021.146009 · Cited by 353 · see citing works

A faecal microbiota signature with high specificity for pancreatic cancer

Kartal, E., Schmidt, T. S. B., Molina-Montes, E., Rodríguez-Perales, S., Wirbel, J., Maistrenko, O. M., Akanni, W. A., Alashkar Alhamwe, B., Alves, R. J., Carrato, A., et al. (2022) · Gut · doi:10.1136/gutjnl-2021-324755 · Cited by 290 · see citing works

Gut microbial beta-glucuronidase: a vital regulator in female estrogen metabolism

Hu, S., Ding, Q., Zhang, W. K., Kang, M., Ma, J., & Zhao, L. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2236749 · Cited by 304 · see citing works

A Procarcinogenic Colon Microbe Promotes Breast Tumorigenesis and Metastatic Progression and Concomitantly Activates Notch and β-Catenin Axes

Parida, S., Wu, S., Siddharth, S., Wang, G., Muniraj, N., Nagalingam, A., Hum, C., Mistriotis, P., Hao, H., Talbot, C. C., et al. (2021) · Cancer Discovery · doi:10.1158/2159-8290.cd-20-0537 · Cited by 257 · see citing works

Demystifying the manipulation of host immunity, metabolism, and extraintestinal tumors by the gut microbiome

Zhang, Z., Tang, H., Chen, P., Xie, H., & Tao, Y. (2019) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-019-0074-5 · Cited by 251 · see citing works

The Microbiome–Estrogen Connection and Breast Cancer Risk

Parida, S., & Sharma, D. (2019) · Cells · doi:10.3390/cells8121642 · Cited by 248 · see citing works

Microbe to Microbiome: A Paradigm Shift in the Application of Microorganisms for Sustainable Agriculture

Ray, P., Lakshmanan, V., Labbé, J., & Craven, K. D. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.622926 · Cited by 232 · see citing works

Microbiome—Microbial Metabolome—Cancer Cell Interactions in Breast Cancer—Familiar, but Unexplored

Mikó, E., Kovàcs, T., Sebő, É., Tóth, J., Csonka, T., Ujlaki, G., Sipos, A., Szabó, J., Méhes, G., & Bai, P. (2019) · Cells · doi:10.3390/cells8040293 · Cited by 220 · see citing works

Breast and Gut Microbiota Action Mechanisms in Breast Cancer Pathogenesis and Treatment

Laborda-Illanes, A., Sánchez‐Alcoholado, L., Domínguez-Recio, M. E., Jiménez-Rodríguez, B., Lavado-Valenzuela, R., Comino‐Méndez, I., Alba, E., & Queipo‐Ortuño, M. I. (2020) · Cancers · doi:10.3390/cancers12092465 · Cited by 208 · see citing works

Plant microbiome structure and benefits for sustainable agriculture

dos Santos, L. F., & Olivares, F. L. (2021) · Current Plant Biology · doi:10.1016/j.cpb.2021.100198 · Cited by 195 · see citing works

Intestinal microbiota influences clinical outcome and side effects of early breast cancer treatment

Terrisse, S., Derosa, L., Iebba, V., Ghiringhelli, F., Vaz-Luis, I., Kroemer, G., Fidelle, M., Christodoulidis, S., Segata, N., Thomas, A. M., et al. (2021) · Cell Death & Differentiation · doi:10.1038/s41418-021-00784-1 · Cited by 172 · see citing works

The Role of Gut Microbial β-Glucuronidase in Estrogen Reactivation and Breast Cancer

Sui, Y., Wu, J., & Chen, J. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.631552 · Cited by 170 · see citing works

Indolepropionic Acid, a Metabolite of the Microbiome, Has Cytostatic Properties in Breast Cancer by Activating AHR and PXR Receptors and Inducing Oxidative Stress

Sári, Z., Mikó, E., Kovàcs, T., Jankó, L., Csonka, T., Lente, G., Sebő, É., Tóth, J., Tóth, D., Árkosy, P., et al. (2020) · Cancers · doi:10.3390/cancers12092411 · Cited by 153 · see citing works

Dysbiosis of the gut microbiome is associated with thyroid cancer and thyroid nodules and correlated with clinical index of thyroid function

Zhang, J., Zhang, F., Zhao, C., Xu, Q., Liang, C., Yang, Y., Wang, H., Shang, Y., Wang, Y., Mu, X., et al. (2018) · Endocrine · doi:10.1007/s12020-018-1831-x · Cited by 142 · see citing works

Compositional and functional features of the female premenopausal and postmenopausal gut microbiota

Zhao, H., Chen, J., Li, X., Sun, Q., Qin, P., & Wang, Q. (2019) · FEBS Letters · doi:10.1002/1873-3468.13527 · Cited by 138 · see citing works

The microbiome and cancer for clinicians

Picardo, S. L., Coburn, B. A., & Hansen, A. R. (2019) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2019.06.004 · Cited by 135 · see citing works

Metagenomic analysis of the human microbiome reveals the association between the abundance of gut bile salt hydrolases and host health

Jia, B., Park, D., Hahn, Y., & Jeon, C. O. (2020) · Gut Microbes · doi:10.1080/19490976.2020.1748261 · Cited by 135 · see citing works

Gut Microbiota as an Objective Measurement for Auxiliary Diagnosis of Insomnia Disorder

Liu, B., Lin, W., Chen, S., Xiang, T., Yang, Y., Yin, Y., Xu, G., Liu, Z., Liu, L., Pan, J., et al. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.01770 · Cited by 132 · see citing works

Breast and gut microbiome in health and cancer

Zhang, J., Xia, Y., & Sun, J. (2020) · Genes & Diseases · doi:10.1016/j.gendis.2020.08.002 · Cited by 130 · see citing works

A genomic compendium of cultivated human gut fungi characterizes the gut mycobiome and its relevance to common diseases

Yan, Q., Li, S., Yan, Q., Huo, X., Wang, C., Wang, X., Sun, Y., Zhao, W., Yu, Z., Zhang, Y., et al. (2024) · Cell · doi:10.1016/j.cell.2024.04.043 · Cited by 121 · see citing works

Human Microbiota and Breast Cancer—Is There Any Relevant Link?—A Literature Review and New Horizons Toward Personalised Medicine

Costa, D. A., Nobre, J. G., Batista, M. V., Ribeiro, C., Callé, C., Cortés, A., Marhold, M., Negreiros, I., Borralho, P., Brito, M., et al. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.584332 · Cited by 123 · see citing works

Role of microbial diversity to influence the growth and environmental remediation capacity of bamboo: A review

Fuke, P., Mohan Manu, T., Kumar, M., Sawarkar, A. D., Pandey, A., & Singh, L. (2021) · Industrial Crops and Products · doi:10.1016/j.indcrop.2021.113567 · Cited by 117 · see citing works

Emerging role of ferroptosis in breast cancer: New dawn for overcoming tumor progression

Sui, S., Xu, S., & Pang, D. (2021) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2021.107992 · Cited by 114 · see citing works

The gut microbiome and cancer: from tumorigenesis to therapy

Nobels, A., van Marcke, C., Jordan, B. F., Hul, M. V., & Cani, P. D. (2025) · Nature Metabolism · doi:10.1038/s42255-025-01287-w · Cited by 119 · see citing works

Adjunctive Probiotic Lactobacillus rhamnosus Probio-M9 Administration Enhances the Effect of Anti-PD-1 Antitumor Therapy via Restoring Antibiotic-Disrupted Gut Microbiota

Gao, G., Ma, T., Zhang, T., Jin, H., Li, Y., Kwok, L.-Y., Zhang, H., & Sun, Z. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.772532 · Cited by 111 · see citing works

Rare gut microbiota associated with breeding success, hormone metabolites and ovarian cycle phase in the critically endangered eastern black rhino

Antwis, R. E., Edwards, K. L., Unwin, B., Walker, S. L., & Shultz, S. (2019) · Microbiome · doi:10.1186/s40168-019-0639-0 · Cited by 107 · see citing works

Underground gas storage as a promising natural methane bioreactor and reservoir?

Molíková, A., Vítězová, M., Vítěz, T., Buriánková, I., Huber, H., Dengler, L., Hanišáková, N., Onderka, V., & Urbanová, I. (2021) · Journal of Energy Storage · doi:10.1016/j.est.2021.103631 · Cited by 101 · see citing works

Impact of the Gut Microbiota Balance on the Health–Disease Relationship: The Importance of Consuming Probiotics and Prebiotics

Olvera-Rosales, L. B., Cruz-Guerrero, A. E., Ramírez‐Moreno, E., Lira, A. Q., Contreras‐López, E., Ordaz, J. J., Ovando, A. C., Añorve‐Morga, J., Calderón‐Ramos, Z. G., Arias‐Rico, J., et al. (2021) · Foods · doi:10.3390/foods10061261 · Cited by 101 · see citing works

The Gut Microbiome and Female Health

Siddiqui, R., Makhlouf, Z., Alharbi, A. M., Alfahemi, H. H., & Khan, N. A. (2022) · Biology · doi:10.3390/biology11111683 · Cited by 101 · see citing works

The gut microbiota in breast cancer development and treatment: The good, the bad, and the useful!

Nandi, D., Parida, S., & Sharma, D. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2221452 · Cited by 98 · see citing works

Synergistic effects of antimony and arsenic contaminations on bacterial, archaeal and fungal communities in the rhizosphere of Miscanthus sinensis: Insights for nitrification and carbon mineralization

Huang, Y., Zheng, X., Weng, W., Yan, X., Chen, P., Liu, X., Peng, T., Zhong, Q., Xu, K., Wang, C., et al. (2021) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2021.125094 · Cited by 96 · see citing works

Abundant fungal and rare bacterial taxa jointly reveal soil nutrient cycling and multifunctionality in uneven-aged mixed plantations

Haidong, X., Yu, M., & Cheng, X. (2021) · Ecological Indicators · doi:10.1016/j.ecolind.2021.107932 · Cited by 93 · see citing works

Comprehensive review on the electrochemical biosensors of different breast cancer biomarkers

Mostafa, I. M., Tian, Y., Anjum, S., Hanif, S., Hosseini, M., Lou, B., & Xu, G. (2022) · Sensors and Actuators B Chemical · doi:10.1016/j.snb.2022.131944 · Cited by 91 · see citing works

Rare prokaryotic sub-communities dominate the complexity of ecological networks and soil multinutrient cycling during long-term secondary succession in China's Loess Plateau

Shu, D., Guo, Y., Zhang, B., Zhang, C., Nostrand, J. D. V., Lin, Y., Zhou, J. Z., & Wei, G. (2021) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2021.145737 · Cited by 84 · see citing works

Role of Gut Microbiota Dysbiosis in Breast Cancer and Novel Approaches in Prevention, Diagnosis, and Treatment

Ruo, S. W., Alkayyali, T., Win, M. T. T., Tara, A., Joseph, C. G., Kannan, A., Srivastava, K., Ochuba, O., Sandhu, J. K., Went, T. R., et al. (2021) · Cureus · doi:10.7759/cureus.17472 · Cited by 87 · see citing works

Productivity and quality of banana in response to chemical fertilizer reduction with bio-organic fertilizer: Insight into soil properties and microbial ecology

Li, Z., Jiao, Y., Yin, J., Li, D. W., Wang, B., Zhang, K., Zheng, X., Hong, Y., Zhang, H., Xie, C., et al. (2021) · Agriculture Ecosystems & Environment · doi:10.1016/j.agee.2021.107659 · Cited by 86 · see citing works

Gut Microbiota and Breast Cancer: The Dual Role of Microbes

Álvarez‐Mercado, A. I., Cano, A. D. V., Fernández, M. F., & Fontana, L. (2023) · Cancers · doi:10.3390/cancers15020443 · Cited by 88 · see citing works

Soil type shapes the antibiotic resistome profiles of long-term manured soil

Zhang, Y., Cheng, D., Zhang, Y., Xie, J., Xiong, H., Wan, Y., Zhang, Y., Chen, X., & Shi, X. (2021) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2021.147361 · Cited by 84 · see citing works

Gut microbiota and risk of five common cancers: A univariable and multivariable Mendelian randomization study

Wei, Z., Yang, B., Tang, T., Xiao, Z., Ye, F., Li, X., Wu, S., Huang, J., & Jiang, S. (2023) · Cancer Medicine · doi:10.1002/cam4.5772 · Cited by 79 · see citing works

The Clinical Link between Human Intestinal Microbiota and Systemic Cancer Therapy

Aarnoutse, R., Ziemons, J., Penders, J., Rensen, S. S., de Vos‐Geelen, J., & Smidt, M. L. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20174145 · Cited by 84 · see citing works

Associations of fecal microbial profiles with breast cancer and nonmalignant breast disease in the Ghana Breast Health Study

Byrd, D. A., Vogtmann, E., Wu, Z., Han, Y., Wan, Y., Clegg‐Lamptey, J., Yarney, J., Wiafe‐Addai, B., Wiafe, S., Awuah, B., et al. (2021) · International Journal of Cancer · doi:10.1002/ijc.33473 · Cited by 83 · see citing works

Antibiotic-induced disturbances of the gut microbiota result in accelerated breast tumor growth

McKee, A. M., Kirkup, B. M., Madgwick, M., Fowler, W. J., Price, C. A., Dreger, S. A., Ansorge, R., Makin, K. A., Caim, S., Gall, G. L., et al. (2021) · iScience · doi:10.1016/j.isci.2021.103012 · Cited by 83 · see citing works

Dysbiosis of human tumor microbiome and aberrant residence of Actinomyces in tumor-associated fibroblasts in young-onset colorectal cancer

Xu, Z., Lv, Z., Chen, F., Zhang, Y., Xu, Z., Huo, J., Liu, W., Yu, S., Tuersun, A., Zhao, J., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1008975 · Cited by 83 · see citing works

The Human Microbiome in Relation to Cancer Risk: A Systematic Review of Epidemiologic Studies

Huybrechts, I., Zouiouich, S., Loobuyck, A., Vandenbulcke, Z., Vogtmann, E., Pisanu, S., Iguacel, I., Scalbert, A., Indave, I., Smelov, V., et al. (2020) · Cancer Epidemiology, Biomarkers & Prevention · doi:10.1158/1055-9965.epi-20-0288 · Cited by 80 · see citing works

Microbial investigations of new hydrogel-biochar composites as soil amendments for simultaneous nitrogen-use improvement and heavy metal immobilization

Zhang, L., & Guan, Y. (2021) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2021.127154 · Cited by 78 · see citing works

Omics-Based Investigations of Breast Cancer

Neagu, A.-N., Whitham, D., Bruno, P. S., Morrissiey, H., Darie, C. A., & Darie, C. C. (2023) · Molecules · doi:10.3390/molecules28124768 · Cited by 79 · see citing works

The Cancer Microbiota: EMT and Inflammation as Shared Molecular Mechanisms Associated with Plasticity and Progression

Vergara, D., Simeone, P., Damato, M., Maffia, M., Lanuti, P., & Trerotola, M. (2019) · Journal of Oncology · doi:10.1155/2019/1253727 · Cited by 77 · see citing works

Probiotic Consortia and Their Metabolites Ameliorate the Symptoms of Inflammatory Bowel Diseases in a Colitis Mouse Model

Xu, L., Liu, B., Huang, L., Li, Z., Cheng, Y., Tian, Y., Pan, G., Li, H., Xu, Y., Wu, W., et al. (2022) · Microbiology Spectrum · doi:10.1128/spectrum.00657-22 · Cited by 78 · see citing works

Gut Microbiota as Potential Biomarker and/or Therapeutic Target to Improve the Management of Cancer: Focus on Colibactin-Producing Escherichia coli in Colorectal Cancer

Véziant, J., Villéger, R., Barnich, N., & Bonnet, M. (2021) · Cancers · doi:10.3390/cancers13092215 · Cited by 72 · see citing works

The Gut Microbiota: A Potential Gateway to Improved Health Outcomes in Breast Cancer Treatment and Survivorship

Sampsell, K., Hao, D., & Reimer, R. A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21239239 · Cited by 70 · see citing works

Longitudinal study on the effects of growth-promoting and therapeutic antibiotics on the dynamics of chicken cloacal and litter microbiomes and resistomes

Gupta, C. L., Blum, S. E., Kattusamy, K., Daniel, T., Druyan, S., Shapira, R., Krifucks, O., Zhu, Y., Zhou, X., Su, J., et al. (2021) · Microbiome · doi:10.1186/s40168-021-01136-4 · Cited by 72 · see citing works

The estrobolome: Estrogen‐metabolizing pathways of the gut microbiome and their relation to breast cancer

Larnder, A., Manges, A. R., & Murphy, R. A. (2025) · International Journal of Cancer · doi:10.1002/ijc.35427 · Cited by 70 · see citing works

Endobolome, a New Concept for Determining the Influence of Microbiota Disrupting Chemicals (MDC) in Relation to Specific Endocrine Pathogenesis

Aguilera, J., Gálvez-Ontiveros, Y., & Rivas, A. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.578007 · Cited by 70 · see citing works

Statistical normalization methods in microbiome data with application to microbiome cancer research

Xia, Y. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2244139 · Cited by 71 · see citing works

The role of the gut microbiota in tumor, immunity, and immunotherapy

Xie, Y., & Liu, F. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1410928 · Cited by 70 · see citing works

The Microbiome and Atopic Dermatitis: A Review

Pothmann, A., Illing, T., Wiegand, C., HARTMANN, A. A., & Elsner, P. U. (2019) · American Journal of Clinical Dermatology · doi:10.1007/s40257-019-00467-1 · Cited by 65 · see citing works

Obesity and breast cancer

Bakar, D., & Mehrzad, R. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-90965-5.00006-4 · Cited by 65 · see citing works

Changes of intestinal microflora of breast cancer in premenopausal women

He, C. H., Liu, Y., Ye, S., Yin, S., & Gu, J. (2020) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-020-04036-x · Cited by 64 · see citing works

Comprehensive profiles and diagnostic value of menopausal-specific gut microbiota in premenopausal breast cancer

Hou, M., Ou‐Yang, F., Li, C.-L., Chen, F., Chuang, C., Kan, J., Wu, C.-C., Shih, S., Shiau, J., Kao, L.-C., et al. (2021) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00686-9 · Cited by 65 · see citing works

Microbial interkingdom associations across soil depths reveal network connectivity and keystone taxa linked to soil fine-fraction carbon content

Banerjee, S., Zhao, C., Kirkby, C. A., Coggins, S., Zhao, S., Bissett, A. B., van der Heijden, M. G. A., Kirkegaard, J. A., & Richardson, A. E. (2021) · Agriculture Ecosystems & Environment · doi:10.1016/j.agee.2021.107559 · Cited by 63 · see citing works

Assembly processes and co-occurrence relationships in the bacterioplankton communities of a large river system

Sun, H., Pan, B., He, H., Zhao, G., Hou, Y., & Zhu, P. (2021) · Ecological Indicators · doi:10.1016/j.ecolind.2021.107643 · Cited by 62 · see citing works

The complex interplay of gut microbiota with the five most common cancer types: From carcinogenesis to therapeutics to prognoses

Jaye, K. M., Li, C. G., & Bhuyan, D. J. (2021) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2021.103429 · Cited by 62 · see citing works

Intestinal Microbiota Influence Doxorubicin Responsiveness in Triple-Negative Breast Cancer

Bawaneh, A., Wilson, A. S., Levi, N., Howard-McNatt, M. M., Chiba, A., Soto‐Pantoja, D. R., & Cook, K. L. (2022) · Cancers · doi:10.3390/cancers14194849 · Cited by 62 · see citing works

Associations Among Estrogens, the Gut Microbiome and Osteoporosis

Kverka, M., & Stepan, J. J. (2024) · Current Osteoporosis Reports · doi:10.1007/s11914-024-00896-w · Cited by 63 · see citing works

Prevotella copri exhausts intrinsic indole-3-pyruvic acid in the host to promote breast cancer progression: inactivation of AMPK via UHRF1-mediated negative regulation

Su, J., Lin, X., Li, D., Yang, C.-M., Lv, S., Chen, X., Yang, X., Pan, B., Xu, R. P., Ren, L., et al. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2347757 · Cited by 58 · see citing works

Indoxylsulfate, a Metabolite of the Microbiome, Has Cytostatic Effects in Breast Cancer via Activation of AHR and PXR Receptors and Induction of Oxidative Stress

Sári, Z., Mikó, E., Kovàcs, T., Boratkó, A., Ujlaki, G., Jankó, L., Kiss, B., Uray, K., & Bai, P. (2020) · Cancers · doi:10.3390/cancers12102915 · Cited by 57 · see citing works

Small-Scale Heterogeneity in Drinking Water Biofilms

Neu, L., Proctor, C. R., Walser, J., & Hammes, F. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.02446 · Cited by 55 · see citing works

How the Gut Microbiome Links to Menopause and Obesity, with Possible Implications for Endometrial Cancer Development

Schreurs, M. P. H., van Steenwijk, P. J. D. V., Romano, A., Dieleman, S., & Werner, H. M. J. (2021) · Journal of Clinical Medicine · doi:10.3390/jcm10132916 · Cited by 55 · see citing works

Response of Sugarcane Rhizosphere Bacterial Community to Drought Stress

Liu, Q., Zhao, X., Liu, Y., Xie, S., Xing, Y., Dao, J., Wei, B., Peng, Y., Duan, W., & Wang, Z. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.716196 · Cited by 55 · see citing works

Analysis of Gut Microbiota in Patients with Breast Cancer and Benign Breast Lesions

Ma, Z., Qu, M., & Wang, X. (2022) · Polish Journal of Microbiology · doi:10.33073/pjm-2022-019 · Cited by 54 · see citing works

Legacy effects of 8-year nitrogen inputs on bacterial assemblage in wheat rhizosphere

Liu, W., Ling, N., Guo, J., Ruan, Y., Zhu, C., Shen, Q., & Guo, S. (2020) · Biology and Fertility of Soils · doi:10.1007/s00374-020-01435-2 · Cited by 54 · see citing works

Understanding variations in soil properties and microbial communities in bamboo plantation soils along a chromium pollution gradient

Zhang, X., Gai, X., Zhong, Z., Bian, F., Yang, C., Li, Y., & Wen, X. (2021) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2021.112507 · Cited by 54 · see citing works

Gut and Breast Microbiota as Endocrine Regulators of Hormone Receptor-positive Breast Cancer Risk and Therapy Response

Arnone, A. A., & Cook, K. L. (2022) · Endocrinology · doi:10.1210/endocr/bqac177 · Cited by 53 · see citing works

Soil and plant health in relation to dynamic sustainment of Eh and pH homeostasis: A review

Husson, O., Sarthou, J., Bousset, L., Ratnadass, A., Schmidt, H., Kempf, J., Husson, B., Tingry, S., Aubertot, J., Deguine, J., et al. (2021) · Plant and Soil · doi:10.1007/s11104-021-05047-z · Cited by 53 · see citing works

Impact of diet on human gut microbiome and disease risk

Mansour, S. R., Moustafa, M., Saad, B. M., hamed, R. A., & Moustafa, A. (2021) · New Microbes and New Infections · doi:10.1016/j.nmni.2021.100845 · Cited by 55 · see citing works

Modulating Microbiota as a New Strategy for Breast Cancer Prevention and Treatment

Wu, H., Ganguly, S., & Tollefsbol, T. O. (2022) · Microorganisms · doi:10.3390/microorganisms10091727 · Cited by 53 · see citing works

Human gut, breast, and oral microbiome in breast cancer: A systematic review and meta-analysis

Thu, M. S., Chotirosniramit, K., Nopsopon, T., Hirankarn, N., & Pongpirul, K. (2023) · Frontiers in Oncology · doi:10.3389/fonc.2023.1144021 · Cited by 52 · see citing works

Effect of Two Different Sugarcane Cultivars on Rhizosphere Bacterial Communities of Sugarcane and Soybean Upon Intercropping

Liu, Y., Yang, H., Liu, Q., Zhao, X., Xie, S., Wang, Z., Wen, R., Zhang, M., & Chen, B. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.596472 · Cited by 51 · see citing works

Mycorrhizosphere bacteria and plant-plant interactions facilitate maize P acquisition in an intercropping system

Song, C. Y., Sarpong, C. K., Zhang, X., Wang, W., Wang, L., Gan, Y., Yong, T., Chang, X., Wang, Y., & Yang, W. (2021) · Journal of Cleaner Production · doi:10.1016/j.jclepro.2021.127993 · Cited by 51 · see citing works

An emerging strategy: probiotics enhance the effectiveness of tumor immunotherapy via mediating the gut microbiome

Jiang, S., Ma, W., Ma, C., Zhang, Z., Zhang, W., & Zhang, J. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2341717 · Cited by 52 · see citing works

Gut Microbiota Profiling in Patients With HER2-Negative Metastatic Breast Cancer Receiving Metronomic Chemotherapy of Capecitabine Compared to Those Under Conventional Dosage

Guan, X., Ma, F., Sun, X., Li, C., Li, L., Liang, F., Li, S., Yi, Z., Liu, B., & Xu, B. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.00902 · Cited by 52 · see citing works

The involvement of oncobiosis and bacterial metabolite signaling in metastasis formation in breast cancer

Kovàcs, T., Mikó, E., Ujlaki, G., Yousef, H., Csontos, V., Uray, K., & Bai, P. (2021) · Cancer and Metastasis Reviews · doi:10.1007/s10555-021-10013-3 · Cited by 52 · see citing works

Red Raspberry and Fructo-Oligosaccharide Supplementation, Metabolic Biomarkers, and the Gut Microbiota in Adults with Prediabetes: A Randomized Crossover Clinical Trial

Zhang, X., Zhao, A., Sandhu, A. K., Edirisinghe, I., & Burton‐Freeman, B. M. (2022) · Journal of Nutrition · doi:10.1093/jn/nxac037 · Cited by 51 · see citing works

Microbial Therapy and Breast Cancer Management: Exploring Mechanisms, Clinical Efficacy, and Integration within the One Health Approach

Filippou, C., Themistocleous, S., Marangos, G., Panayiotou, Y., Fyrilla, M., Kousparou, C. A., Pana, Z. D., Tsioutis, C., Johnson, E. O., & Yiallouris, A. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25021110 · Cited by 49 · see citing works

Proteomics and its applications in breast cancer.

Neagu, A.-N., Whitham, D., Buonanno, E., Jenkins, A., Alexa‐Stratulat, T., Tamba, B.-I., & Darie, C. C. (2021) · PubMed Central · Cited by 48 · see citing works

The Relationship of Tumor Microbiome and Oral Bacteria and Intestinal Dysbiosis in Canine Mammary Tumor

Zheng, H.-H., Du, C.-T., Yu, C., Tang, X.-Y., Huang, R., Zhang, Y., Gao, W., & Xie, G.-H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231810928 · Cited by 49 · see citing works

Metagenomic Analyses Reveal Distinct Gut Microbiota Signature for Predicting the Neoadjuvant Chemotherapy Responsiveness in Breast Cancer Patients

Li, Y., Dong, B., Wu, W., Wang, J., Jin, H., Chen, K., Huang, K., Huang, S., & Yao, Y. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.865121 · Cited by 48 · see citing works

Harness the functions of gut microbiome in tumorigenesis for cancer treatment

Lee, M. (2021) · Cancer Communications · doi:10.1002/cac2.12200 · Cited by 50 · see citing works

Probiotics and Prebiotics: Any Role in Menopause-Related Diseases?

Barrea, L., Verde, L., Auriemma, R. S., Vetrani, C., Cataldi, M., Frías-Toral, E., Pugliese, G., Camajani, E., Savastano, S., Colao, A., et al. (2023) · Current Nutrition Reports · doi:10.1007/s13668-023-00462-3 · Cited by 52 · see citing works

Breast cancer patients from the Midwest region of the United States have reduced levels of short-chain fatty acid-producing gut bacteria

Shrode, R. L., Knobbe, J. E., Cady, N. M., Yadav, M., Hoang, J., Cherwin, C. H., Curry, M. A., Garje, R., Vikas, P., Sugg, S. L., et al. (2023) · Scientific Reports · doi:10.1038/s41598-023-27436-3 · Cited by 43 · see citing works

The Rhizosphere Microbiome of Mikania micrantha Provides Insight Into Adaptation and Invasion

Yin, L., Liu, B., Wang, H., Zhang, Y., Wang, S., Jiang, F., Ren, Y., Liu, H., Liu, C., Wan, F., et al. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.01462 · Cited by 47 · see citing works

Comparison of the Gut Microbiota in Patients with Benign and Malignant Breast Tumors: A Pilot Study

Yang, P., Wang, Z., Peng, Q., Lian, W., & Chen, D. (2021) · Evolutionary Bioinformatics · doi:10.1177/11769343211057573 · Cited by 45 · see citing works

The Relationship Between Microbial Community and Breast Cancer

Song, X., Wei, C., & Li, X. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.849022 · Cited by 45 · see citing works

Systematic Review and Meta-analysis: Changes of Gut Microbiota before and after Menopause

Yang, M., Wen, S., Zhang, J., Peng, J., Shen, X., & Xu, L. (2022) · Disease Markers · doi:10.1155/2022/3767373 · Cited by 45 · see citing works

The conundrum of breast cancer and microbiome - A comprehensive review of the current evidence

Papakonstantinou, A., Nuciforo, P. G., Borrell, M., Zamora, E., Pimentel, I., Saura, C., & Oliveira, M. (2022) · Cancer Treatment Reviews · doi:10.1016/j.ctrv.2022.102470 · Cited by 45 · see citing works

Afforestation suppresses soil nitrogen availability and soil multifunctionality on a subtropical grassland

Ding, L., & Wang, P. (2020) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2020.143663 · Cited by 45 · see citing works

Composition of intestinal flora affects the risk relationship between Alzheimer's disease/Parkinson's disease and cancer.

Hang, Z.-C., Lei, T., Zeng, Z.-H., Cai, S.-L., Bi, W.-Y., & Du, H. (2021) · Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · doi:10.1016/j.biopha.2021.112343 · Cited by 39 · see citing works

Microbiome Markers of Pancreatic Cancer Based on Bacteria-Derived Extracellular Vesicles Acquired from Blood Samples: A Retrospective Propensity Score Matching Analysis

Kim, J. R., Han, K., Han, Y., Kang, N., Shin, T.-S., Park, H. J., Kim, H., Kwon, W., Lee, S., Kim, Y.-K., et al. (2021) · Biology · doi:10.3390/biology10030219 · Cited by 44 · see citing works

Variations in the Gut Microbiota in Breast Cancer Occurrence and Bone Metastasis

Yu, W., Xie, Z., Kai, C., Zhaopeng, C., Li, J., Mengjun, M., Su, Z., Yunshu, C., Wang, P., Wu, Y., et al. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.894283 · Cited by 43 · see citing works

Breast cancer but not the menopausal status is associated with small changes of the gut microbiota

Żeber‐Lubecka, N., Kulecka, M., Jagiełło-Gruszfeld, A., Dąbrowska, M., Kluska, A., Piątkowska, M., Bagińska, K., Głowienka, M., Surynt, P., Tenderenda, M., et al. (2024) · Frontiers in Oncology · doi:10.3389/fonc.2024.1279132 · Cited by 14 · see citing works

Additional file 2: of Breast cancer in postmenopausal women is associated with an altered gut metagenome

Zhu, J., Liao, M., Yao, Z., Liang, W., Li, Q., Liu, J., Yang, H., Ji, Y., Wei, W., Tan, A., et al. (2018) · Figshare · doi:10.6084/m9.figshare.6938867

Abstract PS2-28: The gut microbial signatures of premenopausal breast cancer in Taiwan

Hou, M., Chiang, C.-P., & Yeh, Y. (2021) · Cancer Research · doi:10.1158/1538-7445.sabcs20-ps2-28

Comprehensive profiles and diagnostic value of menopausal-specific gut microbiota in premenopausal breast cancer

Hou, M., Ou‐Yang, F., Li, C.-L., Chen, F., Chuang, C., Kan, J., Wu, C.-C., Shih, S., Shiau, J., Kao, L.-C., et al. (2021) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00686-9 · Cited by 65 · see citing works

Differences in composition and diversity of the gut microbiota of post-menopausal breast cancer patients

Kabbej, N., Sommerville, J. D., Gharaibeh, R. Z., Dang, K., Atencio, E., Rosenkrantz, E., Day, D., Ashby, F. J., Naas, T., Gauthier, J., et al. (2026) · Scientific Reports · doi:10.1038/s41598-026-47558-8