Structural segregation of gut microbiota between colorectal cancer patients and healthy volunteers

Global cancer statistics

Jemal, A., Bray, F., Ferlay, J., Ward, E., & Forman, D. (2011) · CA A Cancer Journal for Clinicians · doi:10.3322/caac.20107 · Cited by 55,044

Profiling of complex microbial populations by denaturing gradient gel electrophoresis analysis of polymerase chain reaction-amplified genes coding for 16S rRNA

Muyzer, G., de Waal, E. C., & Uitterlinden, A. G. (1993) · Applied and Environmental Microbiology · doi:10.1128/aem.59.3.695-700.1993 · Cited by 11,490

Cd-hit: a fast program for clustering and comparing large sets of protein or nucleotide sequences

Li, W.-Z., & Godzik, A. (2006) · Bioinform. · doi:10.1093/bioinformatics/btl158 · Cited by 10,996

ARB: a software environment for sequence data

Ludwig, W. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh293 · Cited by 6,714

Impact of diet in shaping gut microbiota revealed by a comparative study in children from Europe and rural Africa

De Filippo, C., Cavalieri, D., Di Paola, M., Ramazzotti, M., Poullet, J. B., Massart, S., Collini, S., Pieraccini, G., & Lionetti, P. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1005963107 · Cited by 5,579

The Ribosomal Database Project: improved alignments and new tools for rRNA analysis

Cole, J. R., Wang, Q., Cardenas, E., Fish, J., Chai, B., Farris, R. J., Kulam-Syed-Mohideen, A. S., McGarrell, D. M., Marsh, T. L., Garrity, G. M., et al. (2008) · Nucleic Acids Research · doi:10.1093/nar/gkn879 · Cited by 4,873

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

THE POPULATION FREQUENCIES OF SPECIES AND THE ESTIMATION OF POPULATION PARAMETERS

Good, I. J. (1953) · Biometrika · doi:10.1093/biomet/40.3-4.237 · Cited by 3,427

de la Chapelle, A.

Beighton, P., & Beighton, G. (1997) · Springer eBooks · doi:10.1007/978-1-4471-0925-9_118 · Cited by 3,165

Introducing DOTUR, a Computer Program for Defining Operational Taxonomic Units and Estimating Species Richness

Schloss, P. D., & Handelsman, J. (2005) · Applied and Environmental Microbiology · doi:10.1128/aem.71.3.1501-1506.2005 · Cited by 2,529

IP6 reduces colorectal cancer metastasis by mediating the interaction of gut microbiota with host genes

Lan, T., Song, Y., Liu, X., Liu, C., Zhao, H.-C., Han, Y.-S., Wang, C.-H., Yang, N., Xu, Z., Meng, T., et al. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.979135 · Cited by 20

Novel Phocaeicola Strain Ameliorates Dextran Sulfate Sodium-induced Colitis in Mice

Sun, Z., Jiang, X., Wang, B., Tian, F., Zhang, H., & Yu, L. (2022) · Current Microbiology · doi:10.1007/s00284-022-03054-6 · Cited by 20

Bacterial communities of Beijing surface waters as revealed by 454 pyrosequencing of the 16S rRNA gene

Wei, Y., Wang, J., Liu, T., Kong, W., Chen, N., He, X., & Jin, Y. (2015) · Environmental Science and Pollution Research · doi:10.1007/s11356-015-4534-3 · Cited by 20

Development and application of a real‐time polymerase chain reaction assay for detection of a novel gut bacteriophage (crAssphage)

Liang, Y., Jin, X., Huang, Y., & Chen, S. (2017) · Journal of Medical Virology · doi:10.1002/jmv.24974 · Cited by 20

Leveraging Fecal Bacterial Survey Data to Predict Colorectal Tumors

Zhang, B., Xu, S., Xu, W., Chen, Q., Chen, Z., Yan, C., Fan, Y., Zhang, H., Liu, Q., Yang, J., et al. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2019.00447 · Cited by 20

Parvimonas micra forms a distinct bacterial network with oral pathobionts in colorectal cancer patients

Löwenmark, T., Köhn, L., Kellgren, T. G., Rosenbaum, W., Bronnec, V., Löfgren‐Burström, A., Zingmark, C., Larsson, P. G., Dahlberg, M. L., Schroeder, B. O., et al. (2024) · Journal of Translational Medicine · doi:10.1186/s12967-024-05720-8 · Cited by 19

Bioconversion variation of ginsenoside CK mediated by human gut microbiota from healthy volunteers and colorectal cancer patients

Guo, Y., Shao, L., Wang, L., Chen, M., Zhang, W., & Huang, W. (2021) · Chinese Medicine · doi:10.1186/s13020-021-00436-z · Cited by 19

Gut microbiota in gastrointestinal diseases

Bhattacharjee, G., Khambhati, K., Gohil, N., Singh, P., Gohil, J., Gautam, H., Maurya, R., Chu, D., Ramakrishna, S., & Singh, V. (2022) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2022.06.028 · Cited by 19

Multi-Fold Computational Analysis to Discover Novel Putative Inhibitors of Isethionate Sulfite-Lyase (Isla) from Bilophila wadsworthia: Combating Colorectal Cancer and Inflammatory Bowel Diseases

Waqas, M. S., Halim, S. A., Ullah, A., Ali, A. A. M., Khalid, A., Abdalla, A. N., Khan, A., & Al‐Harrasi, A. (2023) · Cancers · doi:10.3390/cancers15030901 · Cited by 20

Modulating gut microbiota using nanotechnology to increase anticancer efficacy of the treatments

Jalil, A. T., Thabit, S. N., Hanan, Z. K., Alasheqi, M. Q., Al-Azzawi, A. K. J., Zabibah, R. S., & Fadhil, A. A. (2023) · Macromolecular Research · doi:10.1007/s13233-023-00168-z · Cited by 19

Microbiome and intestinal pathophysiology in post-acute sequelae of COVID-19

Zhang, J., Zhang, Y., Xia, Y., & Sun, J. (2023) · Genes & Diseases · doi:10.1016/j.gendis.2023.03.034 · Cited by 19

Gut microbiome and serum short-chain fatty acids are associated with responses to chemo- or targeted therapies in Chinese patients with lung cancer

Chen, H., Wu, Q., Zhang, T., & Zhao, Y. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1165360 · Cited by 19

Lack of significant association between serum inflammatory cytokine profiles and the presence of colorectal adenoma

Henry, C. J., Sedjo, R. L., Rozhok, A. I., Salstrom, J. L., Ahnen, D. J., Levin, T. R., D’Agostino, R., Haffner, S. M., DeGregori, J. V., & Byers, T. (2015) · BMC Cancer · doi:10.1186/s12885-015-1115-2 · Cited by 19

Clinical detection of human probiotics and human pathogenic bacteria by using a novel high-throughput platform based on next generation sequencing

Chiu, C.-M., Lin, F.-M., Chang, T., Huang, W.-C., Liang, C., Yang, T., Wu, W.-Y., Yang, T.-L., Weng, S.-L., & Huang, H. (2014) · Journal of Clinical Bioinformatics · doi:10.1186/2043-9113-4-1 · Cited by 19

Impact of dietary compounds on cancer-related gut microbiota and microRNA

Rajoka, M. S. R., Jin, M., Zhao, H., Li, Q., Shao, D., Huang, Q., & Shi, J. (2018) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-018-8935-3 · Cited by 19

The Viral Janus: Viruses as Aetiological Agents and Treatment Options in Colorectal Cancer

Turkington, C. J. R., Varadan, A. C., Grenier, S. F., & Grasis, J. A. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.601573 · Cited by 19

Correction: The chemopreventive effects of Huangqin-tea against AOM-induced preneoplastic colonic aberrant crypt foci in rats and omics analysis

Shen, J., Li, P., Liu, S., Liu, Q., Li, Y., Zhang, Z., Yang, C., Hu, M., Sun, Y., He, C., et al. (2021) · Food & Function · doi:10.1039/d1fo90005f · Cited by 19

Role of signaling pathways in the interaction between microbial, inflammation and cancer

Kamdje, A. H. N., Simo, R. T., Dongmo, H. P. F., Bidias, A. R., & Netongo, P. M. (2023) · Holistic Integrative Oncology · doi:10.1007/s44178-023-00064-7 · Cited by 19

Overcoming Microbiome-Acquired Gemcitabine Resistance in Pancreatic Ductal Adenocarcinoma

Mendes, I., & Vale, N. (2024) · Biomedicines · doi:10.3390/biomedicines12010227 · Cited by 20

Emerging risk factors and the role of gut microbiota in immunomodulation and therapeutic implications in colorectal cancer

Modeel, S., Siwach, S., Dolkar, P., Chaurasia, M., Yadav, P., Atri, A., Yadav, A., Negi, T., & Negi, R. K. (2025) · Cancer Pathogenesis and Therapy · doi:10.1016/j.cpt.2025.06.007 · Cited by 20

Differences in Anxiety Levels of Various Murine Models in Relation to the Gut Microbiota Composition

Huang, E., Kang, S., Park, H., Park, S., Ji, Y., & Holzapfel, W. H. (2018) · Biomedicines · doi:10.3390/biomedicines6040113 · Cited by 18

Reduction of faecal immunochemical test false‐positive results using a signature based on faecal bacterial markers

Malagón, M., Ramió‐Pujol, S., Serrano, M., Serra‐Pagès, M., Amoedo, J., Oliver, L., Bahí, A., Mas-De-Xaxars, T., Torrealba, L., Gilabert, P., et al. (2019) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.15251 · Cited by 20

Biological Activity of an Epilobium angustifolium L. (Fireweed) Infusion after In Vitro Digestion

Kowalik, K., Polak‐Berecka, M., Prendecka, M., Pigoń-Zając, D., Niedźwiedź, I., Szwajgier, D., Baranowska‐Wójcik, E., & Waśko, A. D. (2022) · Molecules · doi:10.3390/molecules27031006 · Cited by 18

Enterobacteria impair host p53 tumor suppressor activity through mRNA destabilization

Aschtgen, M., Fragkoulis, K., Sanz, G., Normark, S. J., Selivanova, G., Henriques‐Normark, B., & Peuget, S. (2022) · Oncogene · doi:10.1038/s41388-022-02238-5 · Cited by 18

Fecal and Tissue Microbiota Are Associated with Tumor T-Cell Infiltration and Mesenteric Lymph Node Involvement in Colorectal Cancer

Luu, K., Ye, J. Y., Lagishetty, V., Liang, F., Hauer, M. C., Sedighian, F., Kwaan, M. R., Kazanjian, K. K., Hecht, J. R., Lin, A., et al. (2023) · Nutrients · doi:10.3390/nu15020316 · Cited by 18

Altered intestinal microbiota composition with epilepsy and concomitant diarrhea and potential indicator biomarkers in infants

Liu, T., Jia, F., Guo, Y., Wang, Q., Zhang, X., Chang, F., & Xie, Y. X. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.1081591 · Cited by 19

The Fungal and Bacterial Interface in the Respiratory Mycobiome with a Focus on Aspergillus spp.

Rozaliyani, A., Antariksa, B., Nurwidya, F., Zaini, J., Setianingrum, F., Hasan, F. N., Nugrahapraja, H., Yusva, H., Wibowo, H., Bowolaksono, A., et al. (2023) · Life · doi:10.3390/life13041017 · Cited by 19

Immuno-oncology-microbiome axis of gastrointestinal malignancy

Lin, Q., Guan, S.-W., & Yu, H. (2023) · World Journal of Gastrointestinal Oncology · doi:10.4251/wjgo.v15.i5.757 · Cited by 20

Gut microbiota: a perspective for colorectal cancer

Milani, P. G., Soleimani, R. A., Khani, N., & Rad, A. H. (2023) · Gastrointestinal Nursing · doi:10.12968/gasn.2023.21.7.26 · Cited by 19

Berberine attenuates 5-fluorouracil-induced intestinal mucosal injury by modulating the gut microbiota without compromising its anti-tumor efficacy

Wu, C., Yang, J., Ye, C., Wu, H., Shu, W., Li, R., Wang, S., Lü, Y., Chen, H., Zhang, Z., et al. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e34528 · Cited by 18

SMAD4 haploinsufficiency associates with augmented colonic inflammation in select humans and mice.

Szigeti, R. G., Pangas, S. A., Nagy‐Szakal, D., Dowd, S. E., Shulman, R. J., Olivé, A., Popek, E. J., Finegold, M. J., & Kellermayer, R. (2012) · PubMed · Cited by 18

Sodium butyrate inhibits colitis-associated colorectal cancer through preventing the gut microbiota dysbiosis and reducing the expression of NLRP3 and IL-1β

Liu, H., Bian, Z., Zhang, Q., Xiao, Z., Cao, Y., Sun, X., Qin, Y., Mao, L., Chu, X., Liao, W., et al. (2021) · Journal of Functional Foods · doi:10.1016/j.jff.2021.104862 · Cited by 18

Diet, Microbes, and Cancer Across the Tree of Life: a Systematic Review

Kapsetaki, S. E., Alcaraz, G. M., Maley, C. C., Whisner, C. M., & Aktipis, A. (2022) · Current Nutrition Reports · doi:10.1007/s13668-022-00420-5 · Cited by 19

Dietary components regulate chronic diseases through gut microbiota: a review

Zhang, Y., Zhou, M., Zhou, Y., & Xiao, G. (2023) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.12732 · Cited by 19

Histone hypoacetylation contributes to CXCL12 downregulation in colon cancer: impact on tumor growth and cell migration

Romain, B., Benbrika, R., Marisa, L., Legrain, M., Lobstein, V., Oravecz, A., Poidevin, L., Bour, C., Freund, J., Duluc, I., et al. (2017) · Oncotarget · doi:10.18632/oncotarget.16323 · Cited by 18

Novel Biomarkers in the Diagnosis of Benign and Malignant Gastrointestinal Diseases

Jonaitis, P., Kiudelis, V., Streleckienė, G., Gedgaudas, R., Skiecevičienė, J., & Kupčinskas, J. (2021) · Digestive Diseases · doi:10.1159/000515522 · Cited by 17

Metagenomic analysis of the interaction between the gut microbiota and colorectal cancer: a paired-sample study based on the GMrepo database

Chen, H., Jiao, J., Wei, M., Jiang, X., Yang, R., Yu, X., Zhang, G., & Zhou, X. (2022) · Gut Pathogens · doi:10.1186/s13099-022-00527-8 · Cited by 18

Ginsenoside Rb1 Suppresses AOM/DSS-induced Colon Carcinogenesis

Wang, L., Zhang, Q., Xu, Y., Zhang, R., Zhao, Q., Zhang, Y., Huang, X.-H., Jiang, B., & Ni, M. (2023) · Anti-Cancer Agents in Medicinal Chemistry · doi:10.2174/1871520623666230119092735 · Cited by 17

Prospective Analysis Reveals Associations between Carbohydrate Intakes, Genetic Predictors of Short-Chain Fatty Acid Synthesis, and Colorectal Cancer Risk

Watling, C. Z., Kelly, R. K., Murphy, N., Gunter, M. J., Piernas, C., Bradbury, K. E., Schmidt, J. A., Key, T. J., & Perez‐Cornago, A. (2023) · Cancer Research · doi:10.1158/0008-5472.can-22-3755 · Cited by 17

Expanding the repertoire of counterselection markers for markerless gene deletion in the human gut bacterium Phocaeicola vulgatus

Neff, A., Lück, R., Hövels, M., & Deppenmeier, U. (2023) · Anaerobe · doi:10.1016/j.anaerobe.2023.102742 · Cited by 17

Gut bacteria and sex differences in colorectal cancer

Yang, X., Li, P., Qu, Z., Jing, Z., Wu, Y., Wu, W., & Wei, Q. (2023) · Journal of Medical Microbiology · doi:10.1099/jmm.0.001706 · Cited by 17

Nutrition Support and the Gastrointestinal Microbiota: A Systematic Review

Andersen, S., Banks, M., & Bauer, J. D. (2020) · Journal of the Academy of Nutrition and Dietetics · doi:10.1016/j.jand.2020.04.024 · Cited by 17

Microbiomes and Resistomes in Biopsy Tissue and Intestinal Lavage Fluid of Colorectal Cancer

Yuan, Y., Chen, Y., Yao, F., Zeng, M., Xie, Q., Shafiq, M., Noman, S. M., & Jiao, X. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.736994 · Cited by 17

Bornlisy Attenuates Colitis-Associated Colorectal Cancer via Inhibiting GPR43-Mediated Glycolysis

Lu, X., Qiao, S., Chen, P., Yan, W., Xu, Z., Qu, J., Hou, Y., Zhao, S., Chen, P., & Wang, T. (2021) · Frontiers in Nutrition · doi:10.3389/fnut.2021.706382 · Cited by 17

Does the Microbiota Composition Influence the Efficacy of Colorectal Cancer Immunotherapy?

Lin, Y., Kong, D.-X., & Zhang, Y.-N. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.852194 · Cited by 17

Deciphering the interdependent labyrinth between gut microbiota and the immune system

Saini, A., Dalal, P., & Sharma, D. (2022) · Letters in Applied Microbiology · doi:10.1111/lam.13775 · Cited by 18

Fecal Bacterial Composition of Sichuan Snub-Nosed Monkeys (Rhinopithecus roxellana)

Su, C., Zuo, R., Liu, W., Sun, Y., Li, Z., Jin, X., Jia, K.-S., Yang, Y. M., & Zhang, H. (2016) · International Journal of Primatology · doi:10.1007/s10764-016-9918-9 · Cited by 18

The interplay between tissue‐resident microbiome and host proteins by integrated multi‐omics during progression of colorectal adenoma to carcinoma

Wu, D., Wang, A., Bu, D., Sun, Y., Li, C., Hong, Y.-M., Zhang, S., Chen, S., Zhou, J., Zhang, T., et al. (2025) · iMeta · doi:10.1002/imt2.70090 · Cited by 16

Altered Mucosal Immune-Microbiota Interactions in Familial Adenomatous Polyposis

Noble, A., Durant, L. R., Dilke, S. M., Man, R., Martín, I. R., Patel, R., Hoyles, L., Pring, E. T., Latchford, A. R., Clark, S. K., et al. (2022) · Clinical and Translational Gastroenterology · doi:10.14309/ctg.0000000000000428 · Cited by 16

The animal's microbiome and cancer: A translational perspective

Aluai‐Cunha, C., Pinto, C. A., Correia, A., Serra, C. R., & Santos, A. A. F. (2023) · Veterinary and Comparative Oncology · doi:10.1111/vco.12892 · Cited by 17

Microbiome Dysbiosis, Dietary Intake and Lifestyle-Associated Factors Involve in Epigenetic Modulations in Colorectal Cancer: A Narrative Review

Kwao‐Zigah, G., Bediako‐Bowan, A., Boateng, P. A., Aryee, G. K., Abbang, S. M., Atampugbire, G. A., Quaye, O., & Tagoe, E. A. (2024) · Cancer Control · doi:10.1177/10732748241263650 · Cited by 19

Dysbiosis Triggers ACF Development in Genetically Predisposed Subjects

Santis, S. D., Liso, M., Vacca, M., Verna, G., Cavalcanti, E., Coletta, S., Calabrese, F. M., Eri, R. D., Lippolis, A., Armentano, R., et al. (2021) · Cancers · doi:10.3390/cancers13020283 · Cited by 16

Machine learning on microbiome research in gastrointestinal cancer

Cheung, H., & Yu, J. Q. (2021) · Journal of Gastroenterology and Hepatology · doi:10.1111/jgh.15502 · Cited by 16

Extracellular vesicles in Inter-Kingdom communication in gastrointestinal cancer.

Chen, Y., Xu, Y., Zhong, H., Yuan, H., Liang, F., Liu, J., & Tang, W. (2021) · PubMed Central · Cited by 16

Colonic Microbial Abundances Predict Adenoma Formers

Watson, K. M., Gardner, I. H., Anand, S., Siemens, K. N., Sharpton, T. J., Kasschau, K. D., Dewey, E. N., Martindale, R. G., Gaulke, C. A., & Tsikitis, V. L. (2021) · Annals of Surgery · doi:10.1097/sla.0000000000005261 · Cited by 16

A two-front nutritional environment fuels colorectal cancer: perspectives for dietary intervention

Alderweireldt, E., Grootaert, C., Wever, O. D., & Camp, J. V. (2021) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2021.11.002 · Cited by 16

Microbiome analysis reveals universal diagnostic biomarkers for colorectal cancer across populations and technologies

Zhang, H., Wu, J., Ji, D., Liu, Y., Lu, S., Lin, Z., Chen, T., & Ao, L. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.1005201 · Cited by 17

Lipopolysaccharide exacerbates to the migration, invasion, and epithelial‐mesenchymal transition of esophageal cancer cells by TLR4 / NF‐κB axis

Peng, Z., Wan, P., Deng, Y., Shen, W., & Liu, R. (2023) · Environmental Toxicology · doi:10.1002/tox.23750 · Cited by 18

Luminally expressed gastrointestinal biomarkers

Cummins, G., Yung, D. E., Cox, B. F., Koulaouzidis, A., Desmulliez, M. P. Y., & Cochran, S. (2017) · Expert Review of Gastroenterology & Hepatology · doi:10.1080/17474124.2017.1373017 · Cited by 17

The rise and evolving role of Fusobacterium nucleatum subspecies

Wolf, M., Steinberg, T., Scholz, K. J., Kruse, A., Rezasoltani, S., Conrads, G., Al‐Ahmad, A., & Cieplik, F. (2025) · Current Research in Microbial Sciences · doi:10.1016/j.crmicr.2025.100414 · Cited by 15

Colorectal cancer biofilm composition reveals distinct bacterial species signature

Kushwaha, M., Dalal, N., Chaudhary, S., Ahmed, A., Makharia, G. K., Singh, A. K., & Kumar, A. (2025) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-025-13537-8 · Cited by 16

Electromagnetic field exposure-induced depression features could be alleviated by heat acclimation based on remodeling the gut microbiota

Luo, X. G., Huang, X., Luo, Z., Wang, Z., He, G., Tan, Y., Zhang, B., Zhou, H., Li, P., Shen, T., et al. (2021) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2021.112980 · Cited by 15

Promotion of Deoxycholic Acid Effect on Colonic Cancer Cell Lines In Vitro by Altering the Mucosal Microbiota

Ma, Y., Zhang, Y., Qu, R., Zhou, X., Sun, L., Wang, K., Jiang, C., Zhang, Z., & Fu, W. (2022) · Microorganisms · doi:10.3390/microorganisms10122486 · Cited by 16

Anti-tumour effect of Huangqin Decoction on colorectal cancer mice through microbial butyrate mediated PI3K/Akt pathway suppression

Zhu, J., Liu, H., Yang, L., Fang, Z., Fu, R., Chen, J., Liu, S., & Fei, B. (2023) · Journal of Medical Microbiology · doi:10.1099/jmm.0.001692 · Cited by 15

Expanding germ-organ theory: Understanding non-communicable diseases through enterobacterial translocation

Boopathi, S., Priya, P. S., Haridevamuthu, B., Nayak, S. P. R. R., Chandrasekar, M., Arockiaraj, J., & Jia, A. (2023) · Pharmacological Research · doi:10.1016/j.phrs.2023.106856 · Cited by 17

Influence of gut microbiome on health and development of penaeid shrimps

Hembrom, P. S., Barik, S., Deepthi, M., Kannoth, S., & Grace, T. (2023) · Aquatic Sciences · doi:10.1007/s00027-023-01018-x · Cited by 15

Integrating functional metagenomics to decipher microbiome–immune interactions

Sardar, P., Almeida, A., & Pedicord, V. A. (2024) · Immunology and Cell Biology · doi:10.1111/imcb.12798 · Cited by 15

Involvement of autophagy and gut dysbiosis in ambient particulate matter-induced colonic inflammation

Cheng, H., Hsu, W., Lin, P., Chen, Y., Lin, T.-H., Fang, S.-S., Tsai, M., Lin, Y., Wang, S.-P., Chen, H., et al. (2024) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2024.117171 · Cited by 15

Meta-analysis of gut microbiota alterations in patients with irritable bowel syndrome

Li, X., Li, X., Xiao, H., Xu, J., He, J., Xiao, C., Zhang, B., Cao, M., & Hong, W. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1492349 · Cited by 15

Gut microbiome in colorectal cancer: metagenomics from bench to bedside

Esfahani, A. T., Zafarjafarzadeh, N., Vakili, F., Bizhanpour, A., Mashaollahi, A., Kordestani, B. K., Baratinamin, M., & Mohammadpour, S. (2025) · JNCI Cancer Spectrum · doi:10.1093/jncics/pkaf026 · Cited by 15

Coupling culturomics and metagenomics sequencing to characterize the gut microbiome of patients with cancer treated with immune checkpoint inhibitors

Diop, K., Mbaye, B., Nili, S., Filin, A., Benlaïfaoui, M., Malo, J., Renaud, A. S., Belkaïd, W., Hunter, S., Messaoudene, M., et al. (2025) · Gut Pathogens · doi:10.1186/s13099-025-00694-4 · Cited by 15

Evidence for Contributions of Gut Microbiota to Colorectal Carcinogenesis

Culpepper, B. S. T., & Mai, V. (2012) · Current Nutrition Reports · doi:10.1007/s13668-012-0032-0 · Cited by 16

Microbiota in digestive cancers: our new partner?

Lopez, A., Hansmannel, F., Kökten, T., Bronowicki, J., Melhem, H., Sokol, H., & Peyrin‐Biroulet, L. (2017) · Carcinogenesis · doi:10.1093/carcin/bgx087 · Cited by 16

Influence of diet and dietary nanoparticles on gut dysbiosis

Jiang, Z., Jacob, J. A., Jian-yue, L., Wu, X., Wei, G., Arunprasanna, V., Mani, R., Nainangu, P., Rajadurai, U. M., & Chen, B. (2018) · Microbial Pathogenesis · doi:10.1016/j.micpath.2018.03.017 · Cited by 15

The gut microbiota of hand, foot and mouth disease patients demonstrates down‐regulated butyrate‐producing bacteria and up‐regulated inflammation‐inducing bacteria

Li, W., Zhu, Y., Li, Y., Shu, M., Yang, W. K., Gao, X., & Wan, C. (2018) · Acta Paediatrica · doi:10.1111/apa.14644 · Cited by 15

Gut Flora-Mediated Metabolic Health, the Risk Produced by Dietary Exposure to Acetamiprid and Tebuconazole

Liu, J., Zhao, F., Xu, Y., Li, N., Qiu, J., & Qian, Y. (2021) · Foods · doi:10.3390/foods10040835 · Cited by 15

The hidden threat: Microplastics and cancer biology

Cirillo, F., Gianì, F., Sergi, V., Scordamaglia, D., Giallongo, S., Tibullo, D., Volti, G. L., Maggiolini, M., Malaguarnera, R., Lappano, R., et al. (2026) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2026.141332 · Cited by 15

Modulation of intestinal metabolites by calorie restriction and its association with gut microbiota in a xenograft model of colorectal cancer

Zhang, Y., Dong, L., Dai, X., Huang, Y., Gao, Y., & Wang, F. (2024) · Discover Oncology · doi:10.1007/s12672-024-00897-2 · Cited by 14

Association between gut microbiota and onset of type 2 diabetes mellitus: a two-sample Mendelian randomization study

Zhang, H., Ma, L., Peng, W., Wang, B., & Sun, Y. (2024) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2024.1327032 · Cited by 16

The immune interactions of gut glycans and microbiota in health and disease

(2024) · doi:10.1111/mmi.15267 · Cited by 14

Shaping the future of gastrointestinal cancers through metabolic interactions with host gut microbiota

Xie, W., Sharma, A., Kaushik, H. K., Sharma, L., Nistha, Anwer, M. K., Sachdeva, M., Elossaily, G. M., Zhang, Y., Pillappan, R., et al. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e35336 · Cited by 14

Osteopontin associated Bifidobacterium bifidum microencapsulation modulates infant fecal fermentation and gut microbiota development

Huang, Y., Lu, Z., Liu, F., Lane, J. A., Chen, J., Huang, Q., Hu, R., & Zhang, B. (2024) · Food Research International · doi:10.1016/j.foodres.2024.115211 · Cited by 14

Butyrate suppresses abnormal proliferation in colonic epithelial cells under diabetic state by targeting HMGB1

Wang, S.-Y., Li, J., Xu, J., Xia, Z., Cheng, D., Zhong, W., Lai, Y., Yu, T., & Chen, Q. (2018) · Journal of Pharmacological Sciences · doi:10.1016/j.jphs.2018.07.012 · Cited by 15

Effects of dachaihu decoction and its “prescription elements” on intestinal flora of nonalcoholic fatty liver disease model rats

Li, Y., Sun, Y., Wang, M., Zhang, S., Gao, Y.-S., Chen, L., Wu, M., Zhang, X., Zhou, L., Yuan, H.-M., et al. (2020) · World Journal of Traditional Chinese Medicine · doi:10.4103/wjtcm.wjtcm_38_19 · Cited by 14

Cancer Risk in Pediatric-Onset Inflammatory Bowel Disease

El‐Matary, W., & Bernstein, C. N. (2020) · Frontiers in Pediatrics · doi:10.3389/fped.2020.00400 · Cited by 14

A low molecular weight brown algae Laminaria japonica glycan modulation of gut microbiota and body weight in mice

Jin, Z., Fang, Z., Pei, Z., Wang, H., Zhu, J., Lee, Y. K., Zhang, H., Zhao, J., Lu, W., & Chen, W. (2021) · Food & Function · doi:10.1039/d1fo03024h · Cited by 14

Role of Toll-like receptors in microbiota-associated gastrointestinal cancer metastasis

Ding, H., Lu, Q., & Li, W. (2013) · Journal of Cancer Research and Therapeutics · doi:10.4103/0973-1482.122509 · Cited by 14

ISN Forefronts Symposium 2015: IgA Nephropathy, the Gut Microbiota, and Gut−Kidney Crosstalk

Han, L., Fang, X., He, Y., & Ruan, X. Z. (2016) · Kidney International Reports · doi:10.1016/j.ekir.2016.08.002 · Cited by 15

Bifidogenic and butyrogenic effects of young barely leaf extract in an in vitro human colonic microbiota model

Sasaki, D., Sasaki, K., Kadowaki, Y., Aotsuka, Y., & Kondo, A. (2019) · AMB Express · doi:10.1186/s13568-019-0911-5 · Cited by 14

Metagenomics analysis reveals universal signatures of the intestinal microbiota in colorectal cancer, regardless of regional differences

Berbert, L., Santos, A., Magro, D. O., Guadagnini, D., Assalin, H. B., Lourenço, L. H., Martinez, C. A. R., Saad, M. J. A., & Coy, C. S. R. (2022) · Brazilian Journal of Medical and Biological Research · doi:10.1590/1414-431x2022e11832 · Cited by 14

The Interplay Between the Gut Microbiota and Colorectal Cancer: A Review of the Literature

Cintoni, M., Palombaro, M., Zoli, E., D’Agostino, G., Pulcini, G., Leonardi, E., Raoul, P. C., Rinninella, E., Maio, F. D., Capristo, E., et al. (2025) · Microorganisms · doi:10.3390/microorganisms13061410 · Cited by 14

The Correlation Between Probiotics and Anxiety and Depression Levels in Cancer Patients: A Retrospective Cohort Study

Ye, Z., Zhang, Y., Du, M., Lu, S., Zhao, Q., & Yang, S. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.830081 · Cited by 15

Intestinal changes associated with nitrite exposure in Bufo gargarizans larvae: Histological damage, immune response, and microbiota dysbiosis

Liu, Y., Wang, H., Wu, L., Han, J. Z., Sui, B., Meng, L., Xu, Y., Lu, S., Wang, H., & Peng, J. (2022) · Aquatic Toxicology · doi:10.1016/j.aquatox.2022.106228 · Cited by 13

Microbiome-Metabolome Responses in Ruminal Content and Feces of Lactating Dairy Cows With N-Carbamylglutamate Supplementation Under Heat Stress

Li, Y., Ma, N., Ren, L., Wang, M., Hu, L., Shen, Y., Cao, Y., Li, Q., Li, J., & Gao, Y. (2022) · Frontiers in Veterinary Science · doi:10.3389/fvets.2022.902001 · Cited by 13

The impact of bariatric surgery on colorectal cancer risk

D’Amato, S., Sofia, M., Agosta, M., Litrico, G., Sarvà, I., Greca, G. L., & Latteri, S. (2022) · Surgery for Obesity and Related Diseases · doi:10.1016/j.soard.2022.10.016 · Cited by 15

The difference of human gut microbiome in colorectal cancer with and without metastases

Sun, L., Zhu, Z., Jia, X., Ying, X., Wang, B., Wang, P., Zhang, S., & Yu, J. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.982744 · Cited by 13

Inflammatory profiles, gut microbiome, and kidney function are impacted after high-fidelity firefighter training

Houser, M. C., Smith, D. J., Rhodes, D., Glick-Smith, J. L., Chovan, P., Ferranti, E. P., Dunbar, S. B., Tansey, M. G., Hertzberg, V., & Mac, V. (2022) · International Journal of Hygiene and Environmental Health · doi:10.1016/j.ijheh.2022.114107 · Cited by 13

The Gut Microbiome Correlated to Chemotherapy Efficacy in Diffuse Large B-Cell Lymphoma Patients

Xu, Z., Li, Y., Zhang, Y., Zhang, W., Wei, C., Wang, W., Zhao, D., Zhou, D., & Li, J. (2024) · Hematology Reports · doi:10.3390/hematolrep16010007 · Cited by 13

Seaweeds as emerging functional foods and therapeutics for colorectal cancer management

Gengatharan, A., Mohamad, N.-V., Zahari, C. N. M. C., & Vijayakumar, R. (2025) · Discover Food · doi:10.1007/s44187-025-00383-w · Cited by 14

Effect of Overgrowth or Decrease in Gut Microbiota on Health and Disease

Nojoomi, F., & Ghasemian, A. (2016) · Archives of Pediatric Infectious Diseases · doi:10.5812/pedinfect.34558 · Cited by 15

Dysbiosis Signature of Fecal Microbiota in Colorectal Cancer Patients

Wu, N., Yang, X., Zhang, R., Li, J., Xiao, X., Hu, Y., Chen, Y., Yang, F., Lu, N., Wang, Z., et al. (2013) · Microbial Ecology · doi:10.1007/s00248-013-0245-9 · Cited by 454

Changes in Intestinal Microbiota and Their Relationship With Patient Characteristics in Colorectal Cancer

Zhao, L., Fang, Y., Zhang, J., Chen, W., Ji, H., Zhao, J., Wang, D., & Tang, D. (2024) · Clinical Medicine Insights Oncology · doi:10.1177/11795549241307632 · Cited by 4

Study of the 16s rRNA gene sequences of Gut Microbiome in some Egyptian Patients with Colorectal Cancer

Fawzy, M. A., Afifi, M. S., Ahmed, S. M., & Shamseya, A. M. (2025) · SVU-International Journal of Medical Sciences · doi:10.21608/svuijm.2023.220485.1609 · Cited by 1

Altered profile of gut microbiota and the level short chain fatty acids in colorectal cancer patients

Yusuf, F., Adewiah, S., Syam, A. F., & Fatchiyah, F. (2019) · Journal of Physics Conference Series · doi:10.1088/1742-6596/1146/1/012037 · Cited by 43

Metagenomic analysis of gut microbiota of patients with colorectal cancer at the Federal Medical Centre (FMC), Abeokuta, Ogun State, Nigeria.

Sulaimon, L. A., Joel, I. Y., Sanusi, O. S., Olanipekun, Q. A.-K., Haliru, A. M., Ajanaku, Z. A., Hassan, A. E., Zakariyah, I. F., Ajibade, F. B., Olajide, M., et al. (2023) · Journal of Clinical Oncology · doi:10.1200/jco.2023.41.4_suppl.195 · Cited by 2