Inflammation and Colon Cancer

A genetic model for colorectal tumorigenesis

Fearon, E. R., & Vogelstein, B. (1990) · Cell · doi:10.1016/0092-8674(90)90186-i · Cited by 12,132

Cancer-related inflammation

Mantovani, A., Allavena, P., Sica, A., & Balkwill, F. (2008) · Nature · doi:10.1038/nature07205 · Cited by 11,399

Immunity, Inflammation, and Cancer

Grivennikov, S. I., Greten, F. R., & Karin, M. (2010) · Cell · doi:10.1016/j.cell.2010.01.025 · Cited by 10,755

The basics of epithelial-mesenchymal transition

Kalluri, R., & Weinberg, R. A. (2009) · Journal of Clinical Investigation · doi:10.1172/jci39104 · Cited by 10,196

Cancer Statistics, 2008

Jemal, A., Siegel, R. L., Ward, E., Hao, Y., Xu, J., Murray, T., & Thun, M. J. (2008) · CA A Cancer Journal for Clinicians · doi:10.3322/ca.2007.0010 · Cited by 10,184

Reciprocal developmental pathways for the generation of pathogenic effector TH17 and regulatory T cells

Bettelli, E., Carrier, Y., Gao, W., Korn, T., Strom, T. B., Oukka, M., Weiner, H. L., & Kuchroo, V. K. (2006) · Nature · doi:10.1038/nature04753 · Cited by 6,992

Myeloid-derived-suppressor cells as regulators of the immune system

Gabrilovich, D. I., & Nagaraj, S. (2009) · Nature Reviews Immunology · doi:10.1038/nri2506 · Cited by 6,753

Type, Density, and Location of Immune Cells Within Human Colorectal Tumors Predict Clinical Outcome

Galon, J., Costes, A., Sanchez-Cabo, F., Kirilovsky, A., Mlecnik, B., Lagorce-Pagès, C., Tosolini, M., Camus, M., Berger, A., Wind, P., et al. (2006) · Science · doi:10.1126/science.1129139 · Cited by 6,516

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

STATs in cancer inflammation and immunity: a leading role for STAT3

Yu, H., Pardoll, D., & Jove, R. (2009) · Nature reviews. Cancer · doi:10.1038/nrc2734 · Cited by 4,383

Antitumor Activity of Nitazoxanide against Colon Cancers: Molecular Docking and Experimental Studies Based on Wnt/β-Catenin Signaling Inhibition

El‐Fadeal, N. M. A., Nafie, M. S., El-Kherbetawy, M. K., Elmistekawy, A., Mohammad, H. M. F., Elbahaie, A. M., Hashish, A. A., Alomar, S. Y., Aloyouni, S. Y., El-dosoky, M., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22105213 · Cited by 24

A Signaling View into the Inflammatory Tumor Microenvironment

Pereira, J., Jordan, P., & Matos, P. (2021) · Immuno · doi:10.3390/immuno1020007 · Cited by 24

Association between post-treatment circulating biomarkers of inflammation and survival among stage II–III colorectal cancer patients

Hua, X., Kratz, M., Malen, R. C., Dai, J. Y., Lindström, S., Zheng, Y., & Newcomb, P. A. (2021) · British Journal of Cancer · doi:10.1038/s41416-021-01458-y · Cited by 24

Microbiome in drug resistance to colon cancer

Pandey, K. R., & Umar, S. (2021) · Current Opinion in Physiology · doi:10.1016/j.cophys.2021.100472 · Cited by 24

Chitosan-Decorated PLGA-NPs Loaded with Tannic Acid/Vitamin E Mitigate Colon Cancer via the NF-κB/β-Cat/EMT Pathway

Nag, S., & Saha, K. D. (2021) · ACS Omega · doi:10.1021/acsomega.1c03477 · Cited by 24

Inhibitory Effect of Dietary Defatted Rice Bran in an AOM/DSS-Induced Colitis-Associated Colorectal Cancer Experimental Animal Model

Tajasuwan, L., Kettawan, A., Rungruang, T., Wunjuntuk, K., Prombutara, P., Muangnoi, C., & Kettawan, A. K. (2022) · Foods · doi:10.3390/foods11213488 · Cited by 24

Exercise‐induced changes to the human gut microbiota and implications for colorectal cancer: a narrative review

Boytar, A. N., Nitert, M. D., Morrison, M., Skinner, T. L., & Jenkins, D. G. (2022) · The Journal of Physiology · doi:10.1113/jp283702 · Cited by 28

Application of chitosan as nano carrier in the treatment of inflammatory bowel disease

Liu, X., Dong, Y., Wang, C., & Guo, Z. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.134899 · Cited by 24

Inactivation of the Transcription Factor GLI1 Accelerates Pancreatic Cancer Progression

Mills, L. D., Zhang, L., Marler, R. J., Svingen, P. A., Fernández‐Barrena, M. G., Dave, M., Bamlet, W. R., McWilliams, R. R., Petersen, G. M., Faubion, W. A., et al. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.539031 · Cited by 24

From Molecular Biology to Clinical Trials: Toward Personalized Colorectal Cancer Therapy

Palma, S., Zwenger, A. O., Croce, M. V., Abba, M. C., & Lacunza, E. (2015) · Clinical Colorectal Cancer · doi:10.1016/j.clcc.2015.11.001 · Cited by 25

Association Between Dietary Inflammation Index and The Risk of Colorectal Cancer: A Meta-Analysis

Zhang, C., Wang, W., & Zhang, D. (2017) · Nutrition and Cancer · doi:10.1080/01635581.2017.1374418 · Cited by 24

Anti-inflammatory nitro-fatty acids suppress tumor growth by triggering mitochondrial dysfunction and activation of the intrinsic apoptotic pathway in colorectal cancer cells

Kuhn, B. R., Brat, C., Fettel, J., Hellmuth, N., Maucher, I. V., Bulut, U., Hock, K. J., Grimmer, J., Manolikakes, G., Rühl, M., et al. (2018) · Biochemical Pharmacology · doi:10.1016/j.bcp.2018.06.014 · Cited by 25

Development of a series of 4-hydroxycoumarin platinum(IV) hybrids as antitumor agents: Synthesis, biological evaluation and action mechanism investigation

Li, G., Zhang, J., Liu, Z., Wang, Q., Chen, Y., Liu, M., Li, D., Han, J., & Wang, B. (2019) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2019.02.011 · Cited by 24

Potential applications of multifunctional mesoporous carbon nanoplatform for tumor microenvironment improving by combined chemo-/phototherapy

Zhang, Y., Zhu, J., Huang, G., Zhu, J., & He, D. (2020) · Carbon · doi:10.1016/j.carbon.2020.02.029 · Cited by 24

SIRT5 Contributes to Colorectal Cancer Growth by Regulating T Cell Activity

Wang, K., Hu, Z., Zhang, C., Yang, L., Li, F., Yang, P., & Yu, H. (2020) · Journal of Immunology Research · doi:10.1155/2020/3792409 · Cited by 24

Intratumorally CpG immunotherapy with carbon nanotubes inhibits local tumor growth and liver metastasis by suppressing the epithelial–mesenchymal transition of colon cancer cells

Jin, H., Gao, S., Song, D., Liu, Y., & Chen, X. (2020) · Anti-Cancer Drugs · doi:10.1097/cad.0000000000001000 · Cited by 24

Endometrial polyps in infertile patients: do high concentrations of interferon-gamma play a role?

Mollo, A., Stile, A., Alviggi, C., Granata, M., Placido, G. D., Perrella, A., D'Antonio, A., & Cicinelli, E. (2011) · Fertility and Sterility · doi:10.1016/j.fertnstert.2011.08.001 · Cited by 24

Neohesperidin protects against colitis-associated colorectal cancer in mice via suppression of the NF-κB/p65 and MAPK pathways

Cao, X., Li, L., Hu, J., Zhu, S., Song, S., Kong, S., Zhou, L., & Huang, Y. (2024) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2024.109804 · Cited by 23

Colorectal cancer mouse models: Integrating inflammation and the stroma

Ernst, M., & Ramsay, R. G. (2011) · Journal of Gastroenterology and Hepatology · doi:10.1111/j.1440-1746.2011.06883.x · Cited by 23

Blood cell markers that can predict the long-term outcomes of patients with colorectal cancer

Mizuno, H., Yuasa, N., Takeuchi, E., Miyake, H., Nagai, H., Yoshioka, Y., & Miyata, K. (2019) · PLoS ONE · doi:10.1371/journal.pone.0220579 · Cited by 23

Do Aspirin and Flavonoids Prevent Cancer through a Common Mechanism Involving Hydroxybenzoic Acids?—The Metabolite Hypothesis

Sankaranarayanan, R., Kumar, D. R., Patel, J., & Bhat, G. J. (2020) · Molecules · doi:10.3390/molecules25092243 · Cited by 23

Non‐genetic biomarkers and colorectal cancer risk: Umbrella review and evidence triangulation

Zhang, X., Gill, D., He, Y., Yang, T., Li, X., Monori, G., Campbell, H. J., Dunlop, M. G., Tsilidis, K. K., Timofeeva, M. N., et al. (2020) · Cancer Medicine · doi:10.1002/cam4.3051 · Cited by 22

TIAM2S Mediates Serotonin Homeostasis and Provokes a Pro-Inflammatory Immune Microenvironment Permissive for Colorectal Tumorigenesis

Chan, Y., Lai, W., Chen, J., Tseng, J. T.-C., Chuang, P.-C., Jou, J., Lee, C., & Sun, H. S. (2020) · Cancers · doi:10.3390/cancers12071844 · Cited by 23

Impact of Appendectomy on Gut Microbiota

Бабаханов, А. Т., ДЖУМАБЕКОВ, А. Т., Zhao, A., Kuandykov, Y., Tanabayeva, S. B., Fakhradiyev, I. R., Nazarenko, Y., & Saliev, T. M. (2021) · Surgical Infections · doi:10.1089/sur.2020.422 · Cited by 26

Suppression of ELF4 in ulcerative colitis predisposes host to colorectal cancer

Du, H., Xia, H., Liu, T., Li, Y., Liu, J., Xie, B., Chen, J., Liu, T., Cao, L., Liu, S., et al. (2021) · iScience · doi:10.1016/j.isci.2021.102169 · Cited by 22

B cell-mediated regulatory mechanisms control tumor-promoting intestinal inflammation

Melcher, C., Yu, J., Duong, V. H. H., Westphal, K., Farimany, N. H. S., Shaverskyi, A., Zhao, B., Strowig, T., Glage, S., Brand, K., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111051 · Cited by 25

Enterobacter Strains Might Promote Colon Cancer

Yurdakul, D., Karataş, A. Y., & Şahi̇n, F. (2015) · Current Microbiology · doi:10.1007/s00284-015-0867-x · Cited by 22

TNF-α potentiates lysophosphatidic acid-induced COX-2 expression via PKD in human colonic myofibroblasts

Rodríguez-Pérez, C. E., Nie, W., Sinnett‐Smith, J. W., Rozengurt, E., & Yoo, J. (2011) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00381.2010 · Cited by 23

Evaluation of Antiproliferative Activity, Safety and Biodistribution of Oxaliplatin and 5-Fluorouracil Loaded Lactoferrin Nanoparticles for the Management of Colon Adenocarcinoma: an In Vitro and an In Vivo Study

Ahmed, F., Kumari, S., & Kondapi, A. K. (2018) · Pharmaceutical Research · doi:10.1007/s11095-018-2457-7 · Cited by 24

miR-21: a promising biomarker for the early detection of colon cancer

Dehghan, F., Boozarpour, S., Torabizadeh, Z., & Alijanpour, S. (2019) · OncoTargets and Therapy · doi:10.2147/ott.s199508 · Cited by 23

Development of Aldose Reductase Inhibitors for the Treatment of Inflammatory Disorders and Cancer: Current Drug Design Strategies and Future Directions

Sonowal, H., & Ramana, K. V. (2020) · Current Medicinal Chemistry · doi:10.2174/0929867327666201027152737 · Cited by 23

Protective effect of hesperidin against N,N′‐dimethylhydrazine induced oxidative stress, inflammation, and apoptotic response in the colon of Wistar rats

Afzal, S. M., Vafa, A., Rashid, S., Barnwal, P., Shahid, A., Shree, A., Islam, J., Ali, N., & Sultana, S. (2020) · Environmental Toxicology · doi:10.1002/tox.23068 · Cited by 23

CXCR4 engagement triggers CD47 internalization and antitumor immunization in a mouse model of mesothelioma

Mezzapelle, R., Marchis, F. D., Passera, C., Leo, M., Brambilla, F., Colombo, F., Casalgrandi, M., Preti, A., Zambrano, S., Castellani, P., et al. (2021) · EMBO Molecular Medicine · doi:10.15252/emmm.202012344 · Cited by 21

Gut microbiota: an Indicator to Gastrointestinal Tract Diseases

Patel, T., Bhattacharya, P., & Das, S. (2016) · Journal of Gastrointestinal Cancer · doi:10.1007/s12029-016-9820-x · Cited by 26

Gut microbiota protect against colorectal tumorigenesis through lncRNA Snhg9

Wang, M., Liu, K., Bao, W., Hang, B., Chen, X., Zhu, X., Li, G., Liu, L., Xiang, H., Hu, H., et al. (2025) · Developmental Cell · doi:10.1016/j.devcel.2024.12.013 · Cited by 24

Concerted actions of ameliorated colitis, aberrant crypt foci inhibition and 15‐hydroxyprostaglandin dehydrogenase induction by sonic hedgehog inhibitor led to prevention of colitis‐associated cancer

Kangwan, N., Kim, Y. T., Han, Y., Jeong, M., Park, J., & Hahm, K. (2015) · International Journal of Cancer · doi:10.1002/ijc.29892 · Cited by 22

The Role and Underlying Mechanism of miR-1299 in Cancer

Deng, K., Huang, L., Sun, X., & Zang, Y. (2021) · Future Science OA · doi:10.2144/fsoa-2021-0014 · Cited by 22

“Nanomaterials of curcumin-hyaluronic acid”: their various methods of formulations, clinical and therapeutic applications, present gap, and future directions

Charan, T. R., Bhutto, M. A., Bhutto, M. A., Tunio, A. A., Khuhro, G. M., Khaskheli, S. A., & Mughal, A. A. (2021) · Future Journal of Pharmaceutical Sciences · doi:10.1186/s43094-021-00281-9 · Cited by 22

Antitumor and hepatoprotective effect of Cuscuta reflexa Roxb. in a murine model of colon cancer

Mishra, S., Alhodieb, F. S., Barkat, M. A., Hassan, M. Z., Barkat, H. A., Ali, R., Alam, P., & Alam, O. (2021) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2021.114597 · Cited by 24

The Transcription Factor IRF9 Promotes Colorectal Cancer via Modulating the IL-6/STAT3 Signaling Axis

Sharma, B. R., Karki, R., Sundaram, B., Wang, Y., Vogel, P., & Kanneganti, T. (2022) · Cancers · doi:10.3390/cancers14040919 · Cited by 20

A microRNA panel that regulates proinflammatory cytokines as diagnostic and prognosis biomarkers in colon cancer

Martínez-Gutiérrez, A. D., Carbajal-López, B., Bui, T. M., Mendoza-Rodríguez, M., Campos-Parra, A. D., Calderillo-Ruiz, G., León, D. F. C.-D., Madrigal‐Santillán, E., Sumagin, R., Pérez‐Plasencia, C., et al. (2022) · Biochemistry and Biophysics Reports · doi:10.1016/j.bbrep.2022.101252 · Cited by 22

Surgical site infection after laparoscopic resection of colorectal cancer is associated with compromised long-term oncological outcome

Sugamata, N., Okuyama, T., Takeshita, E., Oi, H., Hakozaki, Y., Miyazaki, S., Takada, M., Mitsui, T., Noro, T., Yoshitomi, H., et al. (2022) · World Journal of Surgical Oncology · doi:10.1186/s12957-022-02578-2 · Cited by 22

The Effects of the Food Additive Titanium Dioxide (E171) on Tumor Formation and Gene Expression in the Colon of a Transgenic Mouse Model for Colorectal Cancer

Bischoff, N. S., Proquin, H., Jetten, M. J., Schrooders, Y., Jonkhout, M. C. M., Briedé, J. J., van Breda, S. G., Jennen, D. G. J., Medina‐Reyes, E. I., Delgado‐Buenrostro, N. L., et al. (2022) · Nanomaterials · doi:10.3390/nano12081256 · Cited by 22

STING promotes proliferation and induces drug resistance in colorectal cancer by regulating the AMPK-mTOR pathway

Yao, H., Wang, S., Zhou, X., Sun, J., Zhou, G., Zhou, D., Chen, G., Shi, X., Chen, J., Shi, B., et al. (2022) · Journal of Gastrointestinal Oncology · doi:10.21037/jgo-22-957 · Cited by 22

Contribution of natural killer cells in innate immunity against colorectal cancer

Ghazvinian, Z., Abdolahi, S., Tokhanbigli, S., Tarzemani, S., Piccin, A., Zali, M. R., Verdi, J., & Baghaei, K. (2023) · Frontiers in Oncology · doi:10.3389/fonc.2022.1077053 · Cited by 23

Cathelicidin, an antimicrobial peptide produced by macrophages, promotes colon cancer by activating the Wnt/β-catenin pathway

Li, D., Liu, W., Wang, X., Wu, J., Quan, W., Yao, Y., Bals, R., Ji, S., Wu, K., Guo, J., et al. (2014) · Oncotarget · doi:10.18632/oncotarget.2845 · Cited by 22

Human Pol ɛ-dependent replication errors and the influence of mismatch repair on their correction

Agbor, A. A., Goksenin, A. Y., LeCompte, K. G., Hans, S. H., & Pursell, Z. F. (2013) · DNA repair · doi:10.1016/j.dnarep.2013.08.012 · Cited by 22

Inflammatory cues acting on the adult intestinal stem cells and the early onset of cancer (Review)

Barbaro, A. D. L., Perletti, G., Bonapace, I. M., & Monti, E. (2014) · International Journal of Oncology · doi:10.3892/ijo.2014.2490 · Cited by 22

Drug delivery by polymeric micelles: an in vitro and in vivo study to deliver lipophilic substances to colonocytes and selectively target inflamed colon

Valerii, M. C., Benaglia, M., Caggiano, C., Papi, A., Strillacci, A., Lazzarini, G., Campieri, M., Gionchetti, P., Rizzello, F., & Spisni, E. (2012) · Nanomedicine Nanotechnology Biology and Medicine · doi:10.1016/j.nano.2012.11.007 · Cited by 22

Urokinase-Type Plasminogen Activator Deficiency Promotes Neoplasmatogenesis in the Colon of Mice

Karamanavi, E., Angelopoulou, K., Lavrentiadou, S. N., Tsingotjidou, A., Abas, Z., Taitzoglou, I., Vlemmas, I., Erdman, S. E., & Poutahidis, T. (2014) · Translational Oncology · doi:10.1016/j.tranon.2014.02.002 · Cited by 22

Dysregulation of laminins in intestinal inflammation

Spenlé, C., Hussenet, T., Lacroute, J., Lefèbvre, O., Kédinger, M., Orend, G., & Simon-Assmann, P. M. (2011) · Pathologie Biologie · doi:10.1016/j.patbio.2011.10.005 · Cited by 22

Prostatitis, other genitourinary infections and prostate cancer: results from a population-based case–control study

Böehm, K., Valdivieso, R. F., Meskawi, M., Larcher, A., Schiffmann, J., Sun, M., Graefen, M., Fred Saad, C., Parent, M., & Karakiewicz, P. I. (2015) · World Journal of Urology · doi:10.1007/s00345-015-1625-1 · Cited by 22

In silico and Ex vivo approaches identify a role for toll-like receptor 4 in colorectal cancer

Sussman, D. A., Santaolalla, R., Bejarano, P. A., Garcia-Buitrago, M. T., Perez, M. T., Abreu, M. T., & Clarke, J. (2014) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/1756-9966-33-45 · Cited by 22

Promotion of malignant phenotype after disruption of the three-dimensional structure of cultured spheroids from colorectal cancer

Piulats, J. M., Kondo, J., Endo, H., Ono, H., Hagihara, T., Okuyama, H., Nishizawa, Y., Tomita, Y., Ohue, M., Okita, K., et al. (2018) · Oncotarget · doi:10.18632/oncotarget.24641 · Cited by 22

FORMATION OF THE INTESTINAL MICROBIOTA OF CHILDREN AND THE FACTORS THAT INFLUENCE THIS PROCESS

Nikolaeva, I. V., Царегородцев, А. Д., & Shaikhieva, G. S. (2018) · Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) · doi:10.21508/1027-4065-2018-63-3-13-18 · Cited by 27

Styrylcoumarin 7-SC2 induces apoptosis in SW480 human colon adenocarcinoma cells and inhibits azoxymethane-induced aberrant crypt foci formation in BALB/c mice

Herrera-R, A., Naranjo, T. W., Celis, M. E. M., Moreno, G., Yepes, A. F., & Cardona‐Galeano, W. (2019) · Medicinal Chemistry Research · doi:10.1007/s00044-019-02487-2 · Cited by 22

TLR9 induces colitis‑associated colorectal carcinogenesis by regulating NF‑κB expression levels

Luo, Q., Zeng, L., Tang, C., Zhang, Z., Chen, Y., & Zeng, C. (2020) · Oncology Letters · doi:10.3892/ol.2020.11971 · Cited by 24

Bioengineered Colorectal Cancer Drugs: Orally Delivered Anti-Inflammatory Agents

Urbanska, A. M., Zhang, X., & Prakash, S. (2015) · Cell Biochemistry and Biophysics · doi:10.1007/s12013-015-0528-5 · Cited by 22

Early life environment and developmental immunotoxicity in inflammatory dysfunction and disease

Leifer, C. A., & Dietert, R. R. (2011) · Toxicological & Environmental Chemistry Reviews · doi:10.1080/02772248.2011.586114 · Cited by 22

The alleviating effect of Akkermansia muciniphila PROBIO on AOM/DSS-induced colorectal cancer in mice and its regulatory effect on gut microbiota

Ma, X., LvjunYan, Yu, X., Guo, H., He, Y., Wen, S., Yu, T., & Wang, W. (2024) · Journal of Functional Foods · doi:10.1016/j.jff.2024.106091 · Cited by 21

Preoperative monocyte-lymphocyte and neutrophil-lymphocyte but not platelet-lymphocyte ratios are predictive of clinical outcomes in resected patients with non-metastatic Siewert type II/III adenocarcinoma of esophagogastric junction: a prospective cohort study (the AMONP corhort)

Zhang, J., Huang, L., & Xu, A. (2017) · Oncotarget · doi:10.18632/oncotarget.15497 · Cited by 21

Antidepressant Use and Risk of Colorectal Cancer in the Women's Health Initiative

Kiridly, J. F., Sturgeon, S. R., Kroenke, C. H., & Reeves, K. W. (2018) · Cancer Epidemiology Biomarkers & Prevention · doi:10.1158/1055-9965.epi-17-1035 · Cited by 21

Genome‐wide DNA methylation analysis of colorectal adenomas with and without recurrence reveals an association between cytosine‐phosphate‐guanine methylation and histological subtypes

Fiedler, D., Hirsch, D. D., Hajj, N. E., Yang, H. H., Hu, Y., Sticht, C., Nanda, I., Belle, S., Rueschoff, J., Lee, M. P., et al. (2019) · Genes Chromosomes and Cancer · doi:10.1002/gcc.22787 · Cited by 21

Impact of Benign Prostatic Hyperplasia and/or Prostatitis on the Risk of Prostate Cancer in Korean Patients

Kim, S. H., Kwon, W., & Joung, J. Y. (2020) · The World Journal of Men s Health · doi:10.5534/wjmh.190135 · Cited by 21

Posttranslational modifications as therapeutic targets for intestinal disorders

Choo, J., Heo, G., Pothoulakis, C., & Im, E. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2020.105412 · Cited by 21

Impact of skeletal muscle mass in patients with unresectable gastric cancer who received palliative first-line chemotherapy based on 5-fluorouracil

Matsunaga, T., Saito, H., Miyauchi, W., Shishido, Y., Miyatani, K., Morimoto, M., Murakami, Y., Hanaki, T., Kihara, K., Yamamoto, M., et al. (2021) · BMC Cancer · doi:10.1186/s12885-021-08953-8 · Cited by 22

Characteristics of mesenteric adipose tissue attached to different intestinal segments and their roles in immune regulation

Zhang, H., Ding, Y., Zeng, Q., Wang, D., Liu, G., Hussain, Z. S., Xiao, B., Liu, W., & Deng, T. (2022) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00256.2021 · Cited by 21

MUC1-mediated Macrophage Activation Promotes Colitis-associated Colorectal Cancer via Activating the Interleukin-6/ Signal Transducer and Activator of Transcription 3 Axis

Sheng, Y., Davies, J. M., Wang, R., Wong, K. Y., Giri, R., Yang, Y., Begun, J., Florin, T. H., Hasnain, S. Z., & McGuckin, M. A. (2022) · Cellular and Molecular Gastroenterology and Hepatology · doi:10.1016/j.jcmgh.2022.06.010 · Cited by 21

Correlation between Lymphocyte-to-Monocyte Ratio (LMR), Neutrophil-to-Lymphocyte Ratio (NLR), Platelet-to-Lymphocyte Ratio (PLR) and Extramural Vascular Invasion (EMVI) in Locally Advanced Rectal Cancer

Gawiński, C., Hołdakowska, A., & Wyrwicz, L. S. (2022) · Current Oncology · doi:10.3390/curroncol30010043 · Cited by 21

Sleeping Beauty transposon mutagenesis identified genes and pathways involved in inflammation-associated colon tumor development

Shimomura, K., Hattori, N., Iida, N., Muranaka, Y., Sato, K., Shiraishi, Y., Arai, Y., Hama, N., Shibata, T., Narushima, D., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-42228-z · Cited by 21

MUSCLE: multi-view and multi-scale attentional feature fusion for microRNA–disease associations prediction

Ji, B., Zou, H., Xu, L., Xie, X., & Peng, S. (2024) · Briefings in Bioinformatics · doi:10.1093/bib/bbae167 · Cited by 21

Genetic variation in prostaglandin synthesis and related pathways, NSAID use and colorectal cancer risk in the Colon Cancer Family Registry

Resler, A. J., Makar, K. W., Heath, L., Whitton, J. A., Potter, J. D., Poole, E. M., Habermann, N., Scherer, D., Duggan, D. J., Wang, H., et al. (2014) · Carcinogenesis · doi:10.1093/carcin/bgu119 · Cited by 21

Wheat germ agglutinin-functionalised crosslinked polyelectrolyte microparticles for local colon delivery of 5-FU:in vitroefficacy andin vivogastrointestinal distribution

Dodov, M. G., Steffansen, B., Crcarevska, M. S., Geškovski, N., Dimchevska, S., Kuzmanovska, S., & Goračinova, K. (2013) · Journal of Microencapsulation · doi:10.3109/02652048.2013.770099 · Cited by 21

Role of Matrix Metalloproteinases in Inflammation/Colitis-Associated Colon Cancer

Walter, L. (2013) · ImmunoGastroenterology · doi:10.7178/ig.29 · Cited by 21

Evaluation of anti-inflammatory activity of Boswellia serrata on carrageenan induced paw edema in albino Wistar rats

Ismail, S., Rao, K., & Bhaskar, M. (2016) · International Journal of Research in Medical Sciences · doi:10.18203/2320-6012.ijrms20161989 · Cited by 21

Anticancer Efficacy of Some Plant Phenolics - A Recent Scenario

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