Cited by 306Adipokines, Inflammation, and Metabolic DiseasesAdipose Tissue and MetabolismMuscle Physiology and Disorders

The DOI matches its Crossref record; 116 of the 118 references it cites were found in a registry or an index.

Myokines and adipokines: Involvement in the crosstalk between skeletal muscle and adipose tissue

Li, Fengna, Li, Yinghui, Duan, Yehui, Hu, Chien-An A., Tang, Yulong, Yin, Yulong·2017·Cytokine & Growth Factor Reviews

DOI 10.1016/j.cytogfr.2016.10.003

Open this paper in CoChat — free account

Abstract

Skeletal muscle and adipose tissue are the two largest organs in the body. Skeletal muscle is an effector organ, and adipose tissue is an organ that stores energy; in addition, they are endocrine organs that secrete cytokines, namely myokines and adipokines, respectively. Myokines consist of myostatin, interleukin (IL)-8, IL-15, irisin, fibroblast growth factor 21, and myonectin; adipokines include leptin, adiponectin, resistin, chemerin, and visfatin. Furthermore, certain cytokines, such as IL-6 and tumor necrosis factor-α, are released by both skeletal muscle and adipose tissue and exhibit a bioactive effect; thus, they are called adipo-myokines. Recently, novel myokines or adipokines were identified through the secretomic technique, which has expanded our knowledge on the previously unknown functions of skeletal muscle and adipose tissue and provide a new avenue of investigation for obesity treatment or animal production. This review focuses on the roles of and crosstalk between myokines and adipokines in skeletal muscle and adipose tissue that modulate the molecular events in the metabolic homeostasis of the whole body.

Integrity signals

Registry

Crossref · 10.1016/j.cytogfr.2016.10.003

Cites

116 of 116 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Positional cloning of the mouse obese gene and its human homologue
Zhang, Y., Proenca, R., Maffei, M., Barone, M., Leopold, L., & Friedman, J. M. (1994) · Nature · doi:10.1038/372425a0 · Cited by 13,419
Adipose Tissue as an Endocrine Organ
Kershaw, E. E., & Flier, J. S. (2004) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2004-0395 · Cited by 5,522
A PGC1-α-dependent myokine that drives brown-fat-like development of white fat and thermogenesis
Boström, P., Wu, J., Jedrychowski, M. P., Korde, A., Ye, L., Lo, J. C., Rasbach, K. A., Boström, E. A., Choi, J. H., Long, J. Z., et al. (2012) · Nature · doi:10.1038/nature10777 · Cited by 4,810
Regulation of skeletal muscle mass in mice by a new TGF-p superfamily member
McPherron, A. C., Lawler, A. M., & Lee, S.-J. (1997) · Nature · doi:10.1038/387083a0 · Cited by 4,013
Increased adipose tissue expression of tumor necrosis factor-alpha in human obesity and insulin resistance.
Hotamisligil, G. S., Arner, P., Caro, J. F., Atkinson, R. L., & Spiegelman, B. M. (1995) · Journal of Clinical Investigation · doi:10.1172/jci117936 · Cited by 3,543
Muscle as an Endocrine Organ: Focus on Muscle-Derived Interleukin-6
Pedersen, B. K., & Febbraio, M. A. (2008) · Physiological Reviews · doi:10.1152/physrev.90100.2007 · Cited by 2,388
Chemokines
Rollins, B. J. (1997) · Blood · doi:10.1182/blood.v90.3.909.909_909_928 · Cited by 2,126
The Effect of Insulin on the Disposal of Intravenous Glucose: Results from Indirect Calorimetry and Hepatic and Femoral Venous Catheterization
DeFronzo, R. A., Jacot, E., Jequier, E., Maeder, E., Wahren, J., & Felber, J. P. (1981) · Diabetes · doi:10.2337/diab.30.12.1000 · Cited by 1,770
FGF21 regulates PGC-1α and browning of white adipose tissues in adaptive thermogenesis
Fisher, F. M., Kleiner, S., Douris, N., Fox, E. C., Mepani, R. J., Verdeguer, F., Wu, J., Kharitonenkov, A., Flier, J. S., Maratos-Flier, E., et al. (2012) · Genes & Development · doi:10.1101/gad.177857.111 · Cited by 1,478
Myostatin Mutation Associated with Gross Muscle Hypertrophy in a Child
Schuelke, M., Wagner, K. R., Stolz, L. E., Hübner, C., Riebel, T., Kömen, W., Braun, T., Tobin, J. F., & Lee, S.-J. (2004) · New England Journal of Medicine · doi:10.1056/nejmoa040933 · Cited by 1,399

Show all 118 references

Research works printed but not linked: 1

Rollins, 1997, Chemokines, Blood, 90, 909, 10.1182/blood.V90.3.909 · DOI

Sorted by citations

Items 201–300 of 306

Are Aminoglycoside Antibiotics TRPing Your Metabolic Switches?
Franco‐Obregón, A., & Tai, Y. K. (2024) · Cells · doi:10.3390/cells13151273 · Cited by 5
The Significance of Longitudinal Psoas Muscle Loss in Predicting the Maintenance Efficacy of Durvalumab Treatment Following Concurrent Chemoradiotherapy in Patients with Non-Small Cell Lung Cancer: A Retrospective Study
Kuno, H., Nishioka, N., Yamada, T., Kunimatsu, Y., Yoshimura, A., Hirai, S., Futamura, S., Masui, T., Egami, M., Chihara, Y., et al. (2024) · Cancers · doi:10.3390/cancers16173037 · Cited by 4
Adiponectin and Leptin—Considerations in Adult Patients with Spinal Muscular Atrophy Type 3
Miletić, M., Stević, Z., Perić, S., Tančić‐Gajić, M., Rakočević, J., Stojanovic, M. M., Marković, B., & Žarković, M. (2025) · Diagnostics · doi:10.3390/diagnostics15050529 · Cited by 4
Enzymes in Physiological Samples
Pimentel, L. L., Rodríguez-Alcalá, L. M., Gomes, A., & Freitas, A. C. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-409547-2.14270-2 · Cited by 4
Bidirectional relationship between nonalcoholic fatty liver disease and serum creatinine‐to‐body weight ratio as a proxy for skeletal muscle mass index
Tong, C., Halengbieke, A., Ni, X., Han, Y., Tao, L., Zheng, D., Li, Q., & Yang, X. (2023) · Journal of Gastroenterology and Hepatology · doi:10.1111/jgh.16333 · Cited by 4
The Hormone-like Myokines Irisin as Novel Biomarker for Cardiovascular Risk Stratification”,
Berezin, A. A., Myrnyi, D. P., Myrnyi, S. P., & Berezin, A. Е. (2021) · Pharmacophore · doi:10.51847/cx5vhf76yw · Cited by 4
Exercise-induced exerkines in multiple sclerosis: Emphasizing the pivotal role of myokines
Alifarsangi, A., Khaksari, M., Rajizadeh, M. A., Zadeh, N. A., & Rafie, F. (2025) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2025.111565 · Cited by 3
Osteosarcopenia in metabolic dysfunction–associated steatotic liver disease: from mechanisms to management
Fan, A., Zhang, J., & Ye, Q. (2025) · Frontiers in Endocrinology · doi:10.3389/fendo.2025.1706068 · Cited by 4
Docosahexaenoic and Eicosapentaenoic Acids Promote the Accumulation of Browning-Related Myokines via Calcium Signaling in Insulin-Resistant Mice
Wei, W., Yu, S., Zeng, H., Tan, W., Hu, M., Huang, J., Li, X., & Mao, L. (2024) · Journal of Nutrition · doi:10.1016/j.tjnut.2024.02.016 · Cited by 3
Myokines Produced by Cultured Bovine Satellite Cells Harvested from 3- and 11-Month-Old Angus Steers
Shira, K. A., Murdoch, B. M., Thornton, K. J., Reichhardt, C. C., Becker, G. M., Chibisa, G. E., & Murdoch, G. K. (2024) · Animals · doi:10.3390/ani14050709 · Cited by 3
Association of Initial and Changes in Serum A-FABP Level With the Development and Improvement of Presarcopenia
Hu, T., Xu, Y., Li, X., Xiao, Y., Wang, Y., Bao, Y., & Ma, X. (2024) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/clinem/dgae531 · Cited by 3
Maternal Nutrient Excess Induces Stress Signaling and Decreases Mitochondrial Number in Term Fetal Baboon Skeletal Muscle
Yan, X., Tocantins, C., Zhu, M. J., Pereira, S. P., & Du, ‬. (2025) · Biology · doi:10.3390/biology14070868 · Cited by 3
Adiponectin Concentration and Chronic Stroke Individuals, Associations with Body Composition, Physical Activity Levels and Lipid Profile: A Cross-Sectional Explorative Study
García-Salazar, L. F., Ribeiro, J. A. M., Saade-Pacheco, C. R., Mattiello, S. M., Catai, A. M., Garcia-Araújo, A. S., & Russo, T. L. (2021) · Journal of Stroke and Cerebrovascular Diseases · doi:10.1016/j.jstrokecerebrovasdis.2021.105993 · Cited by 3
The Outstanding Beneficial Roles of Irisin in Depressive Disorders
Algül, Ş., Ilcin, S., & Özçelik, O. (2021) · Endokrynologia Polska · doi:10.5603/ep.a2021.0088 · Cited by 3
Incretin-induced changes in the transcriptome of skeletal muscles of fa/fa Zucker rat (ZFR) with obesity, without diabetes
Colin, I. M., Knoops, B., & Gérard, A.-C. (2022) · International Journal of Obesity · doi:10.1038/s41366-022-01114-2 · Cited by 3
Exploring the Diversity of Visceral, Subcutaneous and Perivascular Adipose Tissue in a Vascular Surgery Population
Ferreira, J., Afonso, J., Carneiro, A. L., Vila, I., Cunha, C., Roque, S., Silva, C., Mesquita, A. V. S. C., Cotter, J., Correia‐Neves, M., et al. (2023) · Journal of Cardiovascular Development and Disease · doi:10.3390/jcdd10070271 · Cited by 4
Alterations in serum concentrations of visfatin and betatrophin in dogs with hypothyroidism
Mazaki‐Tovi, M., Shachar, O., & Zur, T. E. (2023) · Journal of Veterinary Internal Medicine · doi:10.1111/jvim.16904 · Cited by 2
Factors Associated With Longitudinal QOL Change in Patients With Chronic Liver Diseases
Nishikawa, H., Yoh, K., Enomoto, H., Nishimura, T., Nishiguchi, S., & Iijima, H. (2021) · In Vivo · doi:10.21873/invivo.12524 · Cited by 3
Chronic Central Leptin Infusion Promotes an Anti-Inflammatory Cytokine Profile Related to the Activation of Insulin Signaling in the Gastrocnemius of Male Rats
Barrios, V., Guerra-Cantera, S., Martín‐Rivada, Á., Canelles, S., Campillo-Calatayud, A., Arilla, E., Frago, L. M., Chowen, J. A., & Argente, J. (2022) · Biomedicines · doi:10.3390/biomedicines10071465 · Cited by 3
Resistance Exercise in Treating Heart Failure with Preserved Ejection Fraction (HFpEF) and Obesity: Targeting Skeletal Muscle Abnormalities and Ectopic Adipose Depots
McDonough, D. J. (2025) · Physiologia · doi:10.3390/physiologia5010010 · Cited by 2
The role of adipose tissue in critical illness-induced skeletal muscle wasting—new considerations for treatment approaches
Sexton, C. L., Meza‐Perez, S., Παπανικολάου, Κ., Kaminski, T. M., Nowacka-Chmielewska, M. M., Rodak, P., Lin, Y., Buford, T. W., Morris, P. E., Englund, D. A., et al. (2025) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00203.2025 · Cited by 2
Handgrip Strength Asymmetry Predicts Mortality Risk: A Prospective Cohort Study From the UK Biobank
Li, Y., Li, D., Ren, Z., Chen, C., Guo, S., Talifu, Z., & Zheng, X. (2025) · Journal of the American Medical Directors Association · doi:10.1016/j.jamda.2025.105995 · Cited by 2
Muscle and fat matter: Automated CT-based body composition analysis predicts survival in Hepatocellular carcinoma patients undergoing radioembolization
Steinberg, H., Ketelsen, A., Schuch, T., Theysohn, J. M., Schaarschmidt, B. M., Haubold, J., Noghani, F. V., Jeschke, M., Jochheim, L. S., & Ludwig, J. M. (2026) · European Journal of Radiology Open · doi:10.1016/j.ejro.2025.100721 · Cited by 2
Relationship between meteorin-like peptide (Metrnl) serum levels and inflammatory cytokines, oxidative stress biomarkers and body composition parameters in type 2 diabetes patients
Khajebishak, Y., Madani, S., Faghfouri, A. H., Soleimani, A., Ilaei, S., Peyrovi, S., & Payahoo, L. (2022) · Nutrition & Food Science · doi:10.1108/nfs-06-2022-0186 · Cited by 2
The longitudinal association of adipose-to-lean ratio with incident cardiometabolic morbidity: The CARDIA study
Booker, R., Wong, M., Bancks, M. P., Carnethon, M. R., Chow, L. S., Lewis, C. E., Schreiner, P. J., & Alexandria, S. J. (2024) · Journal of Diabetes and its Complications · doi:10.1016/j.jdiacomp.2024.108725 · Cited by 2
Yam glycoprotein promotes white adipose tissue browning, enhances metabolism, and boosts exercise tolerance in mice: A novel Strategy for metabolic disease prevention
Li, W., Rang, Y., Shi, J. G., Mei, M., Qiu, H., Liu, Y., Liang, B., & Liu, C. (2025) · Food Bioscience · doi:10.1016/j.fbio.2024.105818 · Cited by 2
The Relevance of Metabotrophic Factors in Pathobiology and Therapy of Obesity and Related Diseases
Chaldakov, G. N., Aloe, L., Rančić, G., Pancheva, R., Hiriart, M., Fiore, M., & Yanev, S. G. (2021) · Advances in biochemistry in health and disease · doi:10.1007/978-3-030-84763-0_16 · Cited by 2
The Mediterranean diet, dietary inflammatory index, and adiposity
Galarregui, C., Zulet, M. Á., Martínez, J. A., & Abete, I. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-818649-7.00030-8 · Cited by 2
Introduction to Cultivated meat and tissue engineering
Mall, E., Andriessen, V., Doğan, A., Paes, D., Altuntaş, E., Post, M. J., & Jackisch, L. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-18767-4.00015-9 · Cited by 2
Variation in myokine and adipokine levels according to menstrual cycle following regular resistance exercise
Kang, S., Kim, E., Ju, S.-B., & Lim, S. (2021) · The Journal of Sports Medicine and Physical Fitness · doi:10.23736/s0022-4707.21.12785-9 · Cited by 1
Secretory Malfunction
Eckel, J. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-809518-8.00005-2 · Cited by 1
Down regulation of the inverse relationship between parathyroid hormone and irisin in male vitamin D-sufficient HIV patients
Karras, S. Ν., Koufakis, T., Dimakopoulos, G., Zisimopoulou, E., Mourampetzis, P., Manthou, E., Karalazou, P., Thisiadou, K., Tsachouridou, Ο., Zebekakis, P. E., et al. (2023) · Journal of Endocrinological Investigation · doi:10.1007/s40618-023-02112-5 · Cited by 1
Effects of weight loss rate on myostatin and follistatin dynamics in patients with obesity
Kurose, S., Onishi, K., Miyauchi, T., Takahashi, K., & Kimura, Y. (2024) · Frontiers in Endocrinology · doi:10.3389/fendo.2024.1418177 · Cited by 2
Longitudinal Study Involving Obesity in Women and Bariatric Surgery: An Electromyographic Approach to the Masseter and Temporal Muscles
Malek-Zadeh, C. H., Palinkas, M., Watanabe, L. M., Salgado, W., de Vasconcelos, P. B., Regalo, I. H., Siéssere, S., Regalo, S. C. H., & Nonino, C. B. (2024) · Prague Medical Report · doi:10.14712/23362936.2024.30 · Cited by 1
Neurovascular Impairment in Type 2 Diabetes Mellitus: The Role of Adipocyte-Derived Exosomes
Sawant, H., & Bihl, J. C. (2026) · Biomolecules · doi:10.3390/biom16020233 · Cited by 1
Targeting the activin/myostatin - actrii pathway to preserve skeletal muscle mass in obesity: mechanistic insights and therapeutic perspectives
Lisco, G., Tullio, A. D., Disoteo, O., Dicorato, P., Tortora, A., Geronimo, V. D., & Triggiani, V. (2026) · Reviews in Endocrine and Metabolic Disorders · doi:10.1007/s11154-026-10033-w · Cited by 1
Toward bioengineered muscle–fat microphysiological systems for sports medicine and obesity therapeutics
Kim, M. Y., Harriot, A. D., & Kim, D. (2026) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2026.115896 · Cited by 1
Cellular and molecular pathways linking obesity to skeletal muscle dysfunction
PINHEIRO, D., & Cornachione, A. S. (2026) · Molecular Biology Reports · doi:10.1007/s11033-026-12146-6 · Cited by 2
Reduced grip strength is associated with progression of depressive status in chronic liver diseases
Nishikawa, H., Yoh, K., Enomoto, H., Ikeda, N., Takashima, T., Aizawa, N., Nishimura, T., Nishiguchi, S., & Iijima, H. (2021) · Annals of Palliative Medicine · doi:10.21037/apm-20-2059 · Cited by 1
The molecular mechanism by which miR-206-regulated JunD expression influences myoblast proliferation and differentiation in yaks
Li, H., Peng, W., Huang, R. S., Chang, J., Su, H., He, Y., Lei, C., Zhang, J., Zhao, Z., & Huang, Y. (2025) · Comparative Biochemistry and Physiology Part D Genomics and Proteomics · doi:10.1016/j.cbd.2025.101600 · Cited by 1
Biomarkers of Insulin Resistance
Cox‐York, K. A., & Pereira, R. I. (2019) · Contemporary Endocrinology · doi:10.1007/978-3-030-25057-7_11 · Cited by 1
Relationship between adult handgrip strength and metabolic syndrome.
Baek, S., & Shin, J. (2020) · Ethiopian Journal of Health Development · Cited by 1
Resistin As a Biomarker and Applications to PreDiabetes
Üstünsoy, S. (2022) · Biomarkers in disease · doi:10.1007/978-3-030-81303-1_4-1 · Cited by 1
Resistin as a Biomarker and Applications to Prediabetes
Üstünsoy, S. (2022) · Biomarkers in disease · doi:10.1007/978-3-031-08014-2_4 · Cited by 1
Efeito de diferentes periodizações no treinamento concorrente sobre parâmetros imunológicos, metabólicos, ponderais e de qualidade de vida relacionada à saúde em mulheres com sobrepeso e/ou obesidade
Bertazone, T. M. A. (2019) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.22.2019.tde-29072019-172909 · Cited by 1
Role of Adipose-to-Muscle Communication in PCB126-induced Metabolic Defects
Caron, A. (2018) · uO Research (University of Ottawa) · doi:10.20381/ruor-22048
Obesity and Immunity
Sabour, H. (2019) · Springer eBooks · doi:10.1007/978-3-030-16073-9_18
PCB126-mediated effects on adipocyte energy metabolism and adipokine secretion may result in abnormal glucose uptake in muscle cellsPreprint
Caron, A., Ahmed, F., Peshdary, V., Garneau, L., Atlas, E., & Aguer, C. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.07.07.192245
Decrease in grip strength is associated with the progression of sleep disturbances in chronic liver diseases
Nishikawa, H., Yoh, K., Enomoto, H., Nishimura, T., Nishiguchi, S., & Iijima, H. (2021) · World Academy of Sciences Journal · doi:10.3892/wasj.2021.87
Association between Bone Biomarkers Osteoactivin and OPG with Plasma Levels of Irisin and Meteorin-like Protein in People with T2D and ObesityPreprint
Cherian, P., Al‐Khairi, I., Jamal, M. H., Al‐Sabah, S., Ali, H., Dsouza, C. L., ALSHAWAF, E. M. M., Al-Ali, W., Al‐Khaledi, G., Al‐Mulla, F., et al. (2021) · Preprints.org · doi:10.20944/preprints202104.0655.v1
General Introduction
Eckel, J. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-809518-8.00001-5
Obesity, inflammation and muscle weakness
Hasselgren, P.-O. J. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-90960-0.00014-x · Cited by 1
Adipomyobiology Of Obesity And Related Diseases: Therapy Insights
Chaldakov, G. N., Aloe, L., Vinciguerra, M., Tonchev, A. B., Fiore, M., & Öztürk, L. (2021) · Adipobiology · doi:10.14748/adipo.v11.8561
The Pathological Changes Seen in Cardiac Diseases Indicated for Transplantation
Al‐Obaidi, A. D., Mutar, M. T., Majid, M., Ahmad, S. S., Bakose, R. Y., Al‐Obaidi, M. N., Al-Abbasi, H., Shaalan, S. S., & Ismail, M. (2022) · Springer eBooks · doi:10.1007/978-3-031-17311-0_4
Role of Taurine Supplementation in Obesity: Stimulating Fats to Burn in Cellular Power Plants
Heidari, R., & Ommati, M. M. (2023) · BENTHAM SCIENCE PUBLISHERS eBooks · doi:10.2174/9789815124484123010013
Study protocol: Identification and validation of integrative biomarkers of physical activity level and health in children and adolescents (INTEGRActiv)
Picó, C., Lurbe, E., Keijer, J., Kopecký, J., Landrier, J., Álvarez‐Pitti, J., Martin, J., Oliver, P., Palou, A., Palou, M., et al. (2023) · Frontiers in Pediatrics · doi:10.3389/fped.2023.1250731
Total and regional fat-to-muscle mass ratio and risk of incident breast and ovarian cancers
Li, H., Huang, N., Wang, W., Huang, T., & Wang, L. (2023) · Journal of Public Health · doi:10.1007/s10389-023-02116-8
Association between muscle-fat ratio and sarcopenia in older adults with hypothyroidismPreprint
yang, R., pan, Y., Lei, H., guo, W., wen, Z., Yang, F., & zhang, Q. (2023) · Research Square · doi:10.21203/rs.3.rs-3648960/v1
Prognostic significance of CT-determined sarcopenia in older patients with advanced squamous cell lung cancer treated with programmed death-1 inhibitorsPreprint
Qin, Z., Lin, Y., Liqian, X., & Ji, Y. (2024) · Research Square · doi:10.21203/rs.3.rs-3848515/v1
Additional file 6 of MYOD1 inhibits avian adipocyte differentiation via miRNA-206/KLF4 axis
Wang, Z., Zhao, Q., Li, X., Yin, Z., Chen, S., Wu, S., Yang, N., & Hou, Z. (2021) · Figshare · doi:10.6084/m9.figshare.14544732
Additional file 7 of MYOD1 inhibits avian adipocyte differentiation via miRNA-206/KLF4 axis
Wang, Z., Zhao, Q., Li, X., Yin, Z., Chen, S., Wu, S., Yang, N., & Hou, Z. (2021) · Figshare · doi:10.6084/m9.figshare.14544735
Additional file 8 of MYOD1 inhibits avian adipocyte differentiation via miRNA-206/KLF4 axis
Wang, Z., Zhao, Q., Li, X., Yin, Z., Chen, S., Wu, S., Yang, N., & Hou, Z. (2021) · Figshare · doi:10.6084/m9.figshare.14544738
Additional file 4 of The whole-transcriptome landscape of muscle and adipose tissues reveals the ceRNA regulation network related to intramuscular fat deposition in yak
Wang, H., Zhong, J., Zhang, C., Chai, Z., Cao, H., Wang, J., Zhu, J., Wang, J., & Ji, Q. (2020) · Figshare · doi:10.6084/m9.figshare.12269654
Additional file 3 of The whole-transcriptome landscape of muscle and adipose tissues reveals the ceRNA regulation network related to intramuscular fat deposition in yak
Wang, H., Zhong, J., Zhang, C., Chai, Z., Cao, H., Wang, J., Zhu, J., Wang, J., & Ji, Q. (2020) · Figshare · doi:10.6084/m9.figshare.12269648
Additional file 1 of MYOD1 inhibits avian adipocyte differentiation via miRNA-206/KLF4 axis
Wang, Z., Zhao, Q., Li, X., Yin, Z., Chen, S., Wu, S., Yang, N., & Hou, Z. (2021) · Figshare · doi:10.6084/m9.figshare.14544717
Additional file 1 of The whole-transcriptome landscape of muscle and adipose tissues reveals the ceRNA regulation network related to intramuscular fat deposition in yak
Wang, H., Zhong, J., Zhang, C., Chai, Z., Cao, H., Wang, J., Zhu, J., Wang, J., & Ji, Q. (2020) · Figshare · doi:10.6084/m9.figshare.12269636
Additional file 8 of The whole-transcriptome landscape of muscle and adipose tissues reveals the ceRNA regulation network related to intramuscular fat deposition in yak
Wang, H., Zhong, J., Zhang, C., Chai, Z., Cao, H., Wang, J., Zhu, J., Wang, J., & Ji, Q. (2020) · Figshare · doi:10.6084/m9.figshare.12269681
Additional file 5 of The whole-transcriptome landscape of muscle and adipose tissues reveals the ceRNA regulation network related to intramuscular fat deposition in yak
Wang, H., Zhong, J., Zhang, C., Chai, Z., Cao, H., Wang, J., Zhu, J., Wang, J., & Ji, Q. (2020) · Figshare · doi:10.6084/m9.figshare.12269663
Additional file 9 of MYOD1 inhibits avian adipocyte differentiation via miRNA-206/KLF4 axis
Wang, Z., Zhao, Q., Li, X., Yin, Z., Chen, S., Wu, S., Yang, N., & Hou, Z. (2021) · Figshare · doi:10.6084/m9.figshare.14544741
Additional file 7 of The whole-transcriptome landscape of muscle and adipose tissues reveals the ceRNA regulation network related to intramuscular fat deposition in yak
Wang, H., Zhong, J., Zhang, C., Chai, Z., Cao, H., Wang, J., Zhu, J., Wang, J., & Ji, Q. (2020) · Figshare · doi:10.6084/m9.figshare.12269675
Additional file 6 of The whole-transcriptome landscape of muscle and adipose tissues reveals the ceRNA regulation network related to intramuscular fat deposition in yak
Wang, H., Zhong, J., Zhang, C., Chai, Z., Cao, H., Wang, J., Zhu, J., Wang, J., & Ji, Q. (2020) · Figshare · doi:10.6084/m9.figshare.12269672
Additional file 5 of MYOD1 inhibits avian adipocyte differentiation via miRNA-206/KLF4 axis
Wang, Z., Zhao, Q., Li, X., Yin, Z., Chen, S., Wu, S., Yang, N., & Hou, Z. (2021) · Figshare · doi:10.6084/m9.figshare.14544729
Additional file 4 of MYOD1 inhibits avian adipocyte differentiation via miRNA-206/KLF4 axis
Wang, Z., Zhao, Q., Li, X., Yin, Z., Chen, S., Wu, S., Yang, N., & Hou, Z. (2021) · Figshare · doi:10.6084/m9.figshare.14544726
Additional file 3 of MYOD1 inhibits avian adipocyte differentiation via miRNA-206/KLF4 axis
Wang, Z., Zhao, Q., Li, X., Yin, Z., Chen, S., Wu, S., Yang, N., & Hou, Z. (2021) · Figshare · doi:10.6084/m9.figshare.14544723
Additional file 2 of The whole-transcriptome landscape of muscle and adipose tissues reveals the ceRNA regulation network related to intramuscular fat deposition in yak
Wang, H., Zhong, J., Zhang, C., Chai, Z., Cao, H., Wang, J., Zhu, J., Wang, J., & Ji, Q. (2020) · Figshare · doi:10.6084/m9.figshare.12269642
Additional file 10 of MYOD1 inhibits avian adipocyte differentiation via miRNA-206/KLF4 axis
Wang, Z., Zhao, Q., Li, X., Yin, Z., Chen, S., Wu, S., Yang, N., & Hou, Z. (2021) · Figshare · doi:10.6084/m9.figshare.14544714
Sarcopenia and inflammatory bowel disease: current information
Tikhonravova, D. V., & Равильевна, Б. Г. (2023) · Scientific Bulletin of the Omsk State Medical University · doi:10.61634/2782-3024-2023-12-36-44
RELATIONSHIP OF THE LEVELS OF TRYPTOFAN METABOLITES WITH ADIPOKINES AND MYOKINES IN PATIENTS WITH VARIOUS OBESITY PHENOTYPES
Shatova, O. P., Appolonova, S. A., Roumiantsev, S. A., & Shestopalov, A. (2023) · Problems of Biological Medical and Pharmaceutical Chemistry · doi:10.29296/25877313-2023-03-05
An auxiliary diagnostic approach based on traditional Chinese medicine constitutions for older patients with frailty
Gu, X., Wang, X., Yang, Y., Guan, K., Chang, H.-C., Liu, D., Wang, W., Wu, T., He, P., Wang, J., et al. (2024) · Clinical and Translational Discovery · doi:10.1002/ctd2.70019
Significance of Adipose Tissue as an Endocrine Organ
Avtanski, D. B., & Stojchevski, R. (2024) · Contemporary Endocrinology · doi:10.1007/978-3-031-72570-8_1
Intramuscular adipose tissue physically restricts functional muscle recoveryPreprint
Norris, A. M., Palzkill, V. R., Appu, A. B., RYAN, T. E., & Kopinke, D. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.17.628009
Multiple omics analysis reveals the regulation of SIRT4 on lipid deposition and metabolism during the differentiation of bovine preadipocytes
Ma, H., Lu, Y. C., Chen, W. J., Gao, Z., Wu, D., Chong, Y., Wu, J., Xi, D., Deng, W., & Hong, J. (2025) · Genomics · doi:10.1016/j.ygeno.2025.111006
Comparative Analysis of Physical Function and Adipomyokines According to Exercise Type in Obese Elderly Women
Kim, C.-Y., & Byun, Y.-H. (2025) · Exercise Science · doi:10.15857/ksep.2025.00108
Resistance training volume dictates distinct redox molecular signature in white adipose tissue: a high-sensitivity proteomics study
Neto, I. V. D. S., Luz, I. S., da Silva, A. S. R., Silveira, W. A. A., Tahir, M., Veiga-Souza, F. H., de Souza, P. E. N., Tibana, R. A., Petriz, B. A., Rosa, T. D. S., et al. (2025) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00231.2025
Co-cultured adipocytes alter the expression of genes involved in extracellular matrix remodeling and metabolic adaptation in muscle cells
Ojima, K., Muroya, S., Oe, M., & Nishimura, T. (2025) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1007/s11626-025-01092-5 · Cited by 1
Prognostic predictive value of sarcopenia and systemic immune-inflammatory index in patients after radical surgery for distal cholangiocarcinoma
Ma, Z., Lin, Y., Zhang, B., Yue, P., Li, B., & Meng, W. (2025) · Scientific Reports · doi:10.1038/s41598-025-30485-5
Additional file 2 of MYOD1 inhibits avian adipocyte differentiation via miRNA-206/KLF4 axis
Wang, Z., Zhao, Q., Li, X., Yin, Z., Chen, S., Wu, S., Yang, N., & Hou, Z. (2021) · Figshare · doi:10.6084/m9.figshare.14544720
Additional file 1 of Is inflammation a missing link between relative handgrip strength with hyperlipidemia? Evidence from a large population-based study
La, R., Yin, Y., Ding, W., He, Z., Lu, L., Xu, B., Jiang, D., Huang, L., Jiang, J., Zhou, L., et al. (2024) · Figshare · doi:10.6084/m9.figshare.25909969
Additional file 1 of A potential correlation between adipokines, skeletal muscle function and bone mineral density in middle-aged and elderly individuals
Wang, W., Gu, X., Cao, Z., Wang, X., Lei, Y., Xu, X., Wang, S., Wu, T., & Bao, Z. (2023) · Figshare · doi:10.6084/m9.figshare.23812367
Additional file 2 of Nomogram for predicting the overall survival of underweight patients with colorectal cancer: a clinical study
Bong, J. W., Na, Y., Ju, Y., Cheong, C., Kang, S., Lee, S. I., & Min, B. W. (2023) · Figshare · doi:10.6084/m9.figshare.22612406
Additional file 2 of Impact of baseline body composition on prognostic outcomes in urological malignancies treated with immunotherapy: a pooled analysis of 10 retrospective studies
Ma, W., Shi, Q., Zhang, L., Qiu, Z., Kuang, T., Zhao, K., & Wang, W. (2024) · Figshare · doi:10.6084/m9.figshare.26748305
Additional file 6 of Impact of baseline body composition on prognostic outcomes in urological malignancies treated with immunotherapy: a pooled analysis of 10 retrospective studies
Ma, W., Shi, Q., Zhang, L., Qiu, Z., Kuang, T., Zhao, K., & Wang, W. (2024) · Figshare · doi:10.6084/m9.figshare.26748317
Additional file 5 of Impact of baseline body composition on prognostic outcomes in urological malignancies treated with immunotherapy: a pooled analysis of 10 retrospective studies
Ma, W., Shi, Q., Zhang, L., Qiu, Z., Kuang, T., Zhao, K., & Wang, W. (2024) · Figshare · doi:10.6084/m9.figshare.26748314
Additional file 1 of Nomogram for predicting the overall survival of underweight patients with colorectal cancer: a clinical study
Bong, J. W., Na, Y., Ju, Y., Cheong, C., Kang, S., Lee, S. I., & Min, B. W. (2023) · Figshare · doi:10.6084/m9.figshare.22612403
Additional file 4 of Impact of baseline body composition on prognostic outcomes in urological malignancies treated with immunotherapy: a pooled analysis of 10 retrospective studies
Ma, W., Shi, Q., Zhang, L., Qiu, Z., Kuang, T., Zhao, K., & Wang, W. (2024) · Figshare · doi:10.6084/m9.figshare.26748311
Additional file 3 of Impact of baseline body composition on prognostic outcomes in urological malignancies treated with immunotherapy: a pooled analysis of 10 retrospective studies
Ma, W., Shi, Q., Zhang, L., Qiu, Z., Kuang, T., Zhao, K., & Wang, W. (2024) · Figshare · doi:10.6084/m9.figshare.26748308
Additional file 7 of Impact of baseline body composition on prognostic outcomes in urological malignancies treated with immunotherapy: a pooled analysis of 10 retrospective studies
Ma, W., Shi, Q., Zhang, L., Qiu, Z., Kuang, T., Zhao, K., & Wang, W. (2024) · Figshare · doi:10.6084/m9.figshare.26748320
Additional file 1 of Impact of baseline body composition on prognostic outcomes in urological malignancies treated with immunotherapy: a pooled analysis of 10 retrospective studies
Ma, W., Shi, Q., Zhang, L., Qiu, Z., Kuang, T., Zhao, K., & Wang, W. (2024) · Figshare · doi:10.6084/m9.figshare.26748302
Adipocyte‐specific ablation of plakoglobin in mice does not affect adiposity but results in sexual‐dimorphic effects on weight gain
Azar, F. A., Vivoli, A., Machuca‐Parra, A. I., Paré, F., Civelek, M., Shou, W., & Lim, G. E. (2025) · Physiological Reports · doi:10.14814/phy2.70681
Biocommunication entre le tissu adipeux viscéral et la cellule bêta-pancréatique : isoprostanes et microARNs
Laget, J. (2019) · theses.fr (ABES) · doi:10.70675/ed653ea5z6ff4z4915za368z0d23f0cd9829

Authors: Li, F., Li, Y., Duan, Y., Hu, C.-A. A., Tang, Y., & Yin, Y.
Affiliations: Chinese Academy of Sciences (CN)
University of New Mexico (US)
Hunan Normal University (CN)
Corresponding author: Tang, Yulong
Yin, Yulong
ORCID: Li, Fengna
Li, Yinghui
Duan, Yehui
Hu, Chien-An A.
Tang, Yulong
Yin, Yulong
Venue: Cytokine & Growth Factor Reviews
Publisher: Elsevier BV
Published: 2017-02
Volume: 33
Pages: 73-82
ISSN: 1359-6101 (ISSN-L)
DOI: 10.1016/j.cytogfr.2016.10.003
OpenAlex: W2531173597
Cited by: 288
References: 118
Citations by year: 2026: 11 · 2025: 32 · 2024: 35 · 2023: 34 · 2022: 32 · 2021: 47 · 2020: 31 · 2019: 26 · 2018: 25 · 2017: 15
FWCI: 2.98
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Cytokine & Growth Factor Reviews (publishedVersion)
PubMed (publishedVersion)
Funders: National Basic Research Program of China (2013CB127305, 2012CB124704)
Youth Innovation Promotion Association CAS (2016326)
Nature Science Foundation of Hunan Province (2015JJ2146)
Topics: Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adipokines, Inflammation, and Metabolic Diseases
Health Sciences › Medicine › Physiology (medical) › Adipose Tissue and Metabolism
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
Keywords: myokines, adipokines, skeletal muscle, adipose tissue, myostatin, irisin, FGF21, leptin, adiponectin, resistin, chemerin, visfatin, interleukin-6, TNF-α, secretome, obesity, metabolic homeostasis, animal husbandry
MeSH terms: Adipose Tissue, Animals, Cell Communication, Humans, Muscle Proteins, Obesity, Signal Transduction, Interleukin-6, Interleukin-8, Adipocytes, Muscle, Skeletal, Interleukin-15, Proteome, Muscle Cells, Mice, Adipokines

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Myokines and adipokines: Involvement in the crosstalk between skeletal muscle and adipose tissue

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks