Annexin A1 and glucocorticoids as effectors of the resolution of inflammation

How do glucocorticoids influence stress responses? Integrating permissive, suppressive, stimulatory, and preparative actions

Sapolsky, R. M., Romero, L. M., & Munck, A. U. (2000) · Endocrine Reviews · doi:10.1210/edrv.21.1.0389 · Cited by 7,541

Antiinflammatory Action of Glucocorticoids — New Mechanisms for Old Drugs

Rhen, T., & Cidlowski, J. A. (2005) · New England Journal of Medicine · doi:10.1056/nejmra050541 · Cited by 3,149

Resolution of inflammation: the beginning programs the end

Serhan, C. N., & Savill, J. (2005) · Nature Immunology · doi:10.1038/ni1276 · Cited by 2,552

Annexins: linking Ca2+ signalling to membrane dynamics

Gerke, V., Creutz, C. E., & Moss, S. E. (2005) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1661 · Cited by 1,412

Resolution of in flammation: state of the art, definitions and terms

Serhan, C. N., Brain, S. D., Buckley, C. D., Gilroy, D. W., Haslett, C., O'Neill, L. A. J., Perretti, M., Rossi, A. G., & Wallace, J. L. (2007) · The FASEB Journal · doi:10.1096/fj.06-7227rev · Cited by 1,045 · cited 1×

Promotion of Tissue Inflammation by the Immune Receptor Tim-3 Expressed on Innate Immune Cells

Anderson, A. C., Anderson, D. E., Bregoli, L., Hastings, W. D., Kassam, N., Lei, C., Chandwaskar, R., Kármán, J., Su, E. W., Hirashima, M., et al. (2007) · Science · doi:10.1126/science.1148536 · Cited by 703

Histone deacetylase 2–mediated deacetylation of the glucocorticoid receptor enables NF-κB suppression

Ito, K., Yamamura, S., Essilfie-Quaye, S., Cosio, B., Ito, M., Barnes, P. J., & Adcock, I. M. (2006) · The Journal of Experimental Medicine · doi:10.1084/jem.20050466 · Cited by 638

Glucocorticoids and the Th1/Th2 Balance

Elenkov, I. J. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1321.010 · Cited by 618

Glucocorticoids promote a TH2 cytokine response by CD4+ T cells in vitro

Ramírez, F., Fowell, D. J., Puklavec, M. J., Simmonds, S. J., & Mason, D. (1996) · The Journal of Immunology · doi:10.4049/jimmunol.156.7.2406 · Cited by 483

The Lipoxin Receptor ALX: Potent Ligand-Specific and Stereoselective Actions in Vivo

Chiang, N., Serhan, C. N., Dahlén, S., Drazen, J. M., Hay, D. W. P., Rovati, G. E., Shimizu, T., Yokomizo, T., & Brink, C. (2006) · Pharmacological Reviews · doi:10.1124/pr.58.3.4 · Cited by 464

Annexins A2 and A5 are potential early biomarkers of hepatocarcinogenesis

Herrera-López, E. E., Guerrero‐Escalera, D., Aguirre-Maldonado, I., López-Hernández, A., Montero, H., Gutiérrez‐Nava, M. A., del Pozo‐Yauner, L., Arellanes‐Robledo, J., Camacho, J., & Pérez‐Carreón, J. I. (2023) · Scientific Reports · doi:10.1038/s41598-023-34117-8 · Cited by 19

Persulfidation of mitoKv7.4 channels contributes to the cardioprotective effects of the H2S-donor Erucin against ischemia/reperfusion injury

Testai, L., Montanaro, R., Flori, L., Pagnotta, E., Vellecco, V., Gorica, E., Ugolini, L., Righetti, L., Brancaleone, V., Bucci, M., et al. (2023) · Biochemical Pharmacology · doi:10.1016/j.bcp.2023.115728 · Cited by 19

Influence of Adipokines on Metabolic Dysfunction and Aging

Park, S., & Shimokawa, I. (2024) · Biomedicines · doi:10.3390/biomedicines12040873 · Cited by 20

Mass spectrometry based quantitative proteomics and integrative network analysis accentuates modulating roles of annexin‐1 in mammary tumorigenesis

Swa, H. L. F., Shaik, A. A., Lim, L. H. K., & Gunaratne, J. (2014) · PROTEOMICS · doi:10.1002/pmic.201400175 · Cited by 19

Annexin A1 in blood mononuclear cells from patients with coronary artery disease: Its association with inflammatory status and glucocorticoid sensitivity

Bergström, I., Lundberg, A. K., Jönsson, S., Särndahl, E., Ernerudh, J., & Jonasson, L. (2017) · PLoS ONE · doi:10.1371/journal.pone.0174177 · Cited by 19

Fertility in classical galactosaemia, a study of N-glycan, hormonal and inflammatory gene interactions

Colhoun, H.-O., Rubio‐Gozalbo, M. E., Bosch, A. M., Knerr, I., Dawson, C., Brady, J. J., Galligan, M. C., Stępień, K. M., O’Flaherty, R., Moss, C. C., et al. (2018) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-018-0906-3 · Cited by 19

Associations of microRNA single nucleotide polymorphisms and disease risk and pathophysiology

Liu, X., Han, Z., & Yang, C. (2016) · Clinical Genetics · doi:10.1111/cge.12950 · Cited by 19

Proteome of the Triatomine Digestive Tract: From Catalytic to Immune Pathways; Focusing on Annexin Expression

Gumiel, M., de Mattos, D. P., Vieira, C. S., Moraes, C. D. S., Moreira, C. J. D. C., Gonzalez, M. S., Teixeira‐Ferreira, A., Waghabi, M. C., Azambuja, P., & Carels, N. (2020) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2020.589435 · Cited by 18

Immune modulation through secretory autophagy

Weigert, A., & Herhaus, L. (2023) · Journal of Cellular Biochemistry · doi:10.1002/jcb.30427 · Cited by 18

Immunomodulation of periodontitis with SPMs

Sahni, V., & Dyke, T. E. V. (2023) · Frontiers in Oral Health · doi:10.3389/froh.2023.1288722 · Cited by 20

The role of ANXA1 in the tumor microenvironment

Li, L., Wang, B., Zhao, S., Xiong, Q., & Cheng, A. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.111854 · Cited by 18

Development of Pro-resolving and Pro-efferocytic Nanoparticles for Atherosclerosis Therapy

Patel, Y., Manturthi, S., Tiwari, S., Gahunia, E., Courtemanche, A., Gandelman, M., Côté, M., & Gadde, S. (2024) · ACS Pharmacology & Translational Science · doi:10.1021/acsptsci.4c00292 · Cited by 18

Control of host inflammatory responsiveness by indigenous microbiota reveals an adaptive component of the innate immune system

Fagundes, C. T., Souza, D. G., Nicoli, J. R., & Teixeira, M. M. (2011) · Microbes and Infection · doi:10.1016/j.micinf.2011.07.012 · Cited by 18

Association Between Single-Nucleotide Polymorphism (SNP) in miR-146a, miR-196a2, and miR-499 and Risk of Ischemic Stroke: A Meta-Analysis

Zhu, J., Yue, H., Qiao, C., & Li, Y. (2015) · Medical Science Monitor · doi:10.12659/msm.895233 · Cited by 18

Annexin A1 sustains tumor metabolism and cellular proliferation upon stable loss of HIF1A

Rohwer, N., Bindel, F., Grimm, C., Lin, S. J., Wappler, J., Klinger, B., Blüthgen, N., Bois, I. D., Schmeck, B., Lehrach, H., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.6793 · Cited by 18

Proteomic signatures of neuroinflammation in Alzheimer’s disease, multiple sclerosis and ischemic stroke

Thygesen, C., Larsen, M. R., & Finsen, B. R. (2019) · Expert Review of Proteomics · doi:10.1080/14789450.2019.1633919 · Cited by 18

Pharmacogenomic Response of Inhaled Corticosteroids for the Treatment of Asthma: Considerations for Therapy

Cazzola, M., Rogliani, P., Calzetta, L., & Matera, M. G. (2020) · Pharmacogenomics and Personalized Medicine · doi:10.2147/pgpm.s231471 · Cited by 18

Resolution of leucocyte‐mediated mucosal diseases. A novel in vivo paradigm for drug development

Persson, C. G. A., & Uller, L. (2011) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2011.01772.x · Cited by 18

The anti-inflammatory potency of dexamethasone is determined by the route of application in vivo

Weichhart, T., Brandt, O., Lassnig, C., Müller, M. M., Hörl, W. H., Stingl, G., & Säemann, M. D. (2010) · Immunology Letters · doi:10.1016/j.imlet.2009.12.025 · Cited by 18

The essential role of annexin A1 mimetic peptide in the skin allograft survival

Teixeira, R. A. P., Mimura, K. K. O., Araújo, L. P., Greco, K. V., & Oliani, S. M. (2013) · Journal of Tissue Engineering and Regenerative Medicine · doi:10.1002/term.1773 · Cited by 18

Expression of annexin A1 in Leishmania-infected skin and its correlation with histopathological features

da Silva, H. A. L., Lima, G. S., Boité, M. C., Porrozzi, R., Hueb, M., & Damazo, A. S. (2015) · Revista da Sociedade Brasileira de Medicina Tropical · doi:10.1590/0037-8682-0183-2015 · Cited by 18

Decreased plasma concentrations of brain-derived neurotrophic factor in preeclampsia

Perucci, L. O., Vieira, É. L. M., Teixeira, A. L., Gomes, K. B., Dusse, L. M. S., & Sousa, L. P. (2016) · Clinica Chimica Acta · doi:10.1016/j.cca.2016.11.034 · Cited by 18

Purinergic Signaling and Cochlear Injury-Targeting the Immune System?

Köles, L., Szepesy, J., Berekméri, E., & Zelles, T. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20122979 · Cited by 18

Therapeutic Potential of Annexin A1 Modulation in Kidney and Cardiovascular Disorders

Mozaffari, M. S. (2021) · Cells · doi:10.3390/cells10123420 · Cited by 17

Annexin A1 affects tumor metastasis through epithelial-mesenchymal transition: a narrative review

Zheng, L., Li, L., Wang, B., Zhang, S., Fu, Z., Cheng, A., & Liang, X. (2022) · Translational Cancer Research · doi:10.21037/tcr-22-1544 · Cited by 17

Downstream Gene Activation of the Receptor ALX by the Agonist Annexin A1

Renshaw, D. W., Montero‐Melendez, T., Dalli, J., Kamal, A. M., Brancaleone, V., D’Acquisto, F., Cirino, G., & Perretti, M. (2010) · PLoS ONE · doi:10.1371/journal.pone.0012771 · Cited by 17

Glucocorticoids: Molecular Mechanisms of Action

Cruz‐Topete, D., & Cidlowski, J. A. (2018) · Springer eBooks · doi:10.1007/978-3-319-77658-3_11 · Cited by 17

Immuno-moodulin: A new anxiogenic factor produced by Annexin-A1 transgenic autoimmune-prone T cells

Piras, G., Rattazzi, L., Paschalidis, N., Oggero, S., Berti, G., Ono, M., Bellia, F., D’Addario, C., Dell’Osso, B. M., Pariante, C. M., et al. (2020) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2020.02.015 · Cited by 17

Annexin-A1-Derived Peptide Ac2-26 Suppresses Allergic Airway Inflammation and Remodelling in Mice

Ferreira, T. P. T., Guimarães, F. V., de Sá, Y. A. P. J., Ribeiro, N. B. D. S., de Arantes, A. C. S., Carvalho, V. F., Sousa, L. P., Perretti, M., Martins, M. A., & Silva, P. (2022) · Cells · doi:10.3390/cells11050759 · Cited by 17

Interaction of the Anti-Inflammatory Annexin A1 Protein and Tacrolimus Immunosuppressant in the Renal Function of Rats

Araújo, L. P., Truzzi, R. R., Mendes, G. E. F., Luz, M. A. M., Burdmann, E. A., & Oliani, S. M. (2010) · American Journal of Nephrology · doi:10.1159/000309756 · Cited by 17

Regulation of Interleukin-6 in Head and Neck Squamous Cell Carcinoma Is Related to Papillomavirus Infection

Guerrera, I. C., Quétier, I., Fetouchi, R., Moreau, F., Vauloup‐Fellous, C., Lekbaby, B., Rousselot, C., Chhuon, C., Edelman, A., Lefèvre, M., et al. (2014) · Journal of Proteome Research · doi:10.1021/pr401009f · Cited by 17

Biology and pathobiology of lipid droplets and their potential role in the protection of the organ of Corti

Urrutia, R. A., & Kalinec, F. (2015) · Hearing Research · doi:10.1016/j.heares.2015.04.015 · Cited by 17

Single-cell transcriptional dissection illuminates an evolution of immunosuppressive microenvironment during pancreatic ductal adenocarcinoma metastasis

Liu, X., Song, J., Yuan, M., Zuo, F., Li, H., Tang, L., Wang, X., Wang, X., Xiao, Q., Li, L., et al. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02265-0 · Cited by 16

Transduced Tat-Annexin protein suppresses inflammation-associated gene expression in lipopolysaccharide (LPS)-stimulated Raw 264.7 cells

Lee, S. H., Kim, D. W., Back, S. S., Hwang, H. S., Park, E. Y., Kang, T., Kwon, O., Park, J. H., Cho, S., Han, K. H., et al. (2011) · BMB Reports · doi:10.5483/bmbrep.2011.44.7.484 · Cited by 16

Augmenting Endogenous Levels of Retinal Annexin A1 Suppresses Uveitis in Mice

Gardner, P. J., Yazid, S., Ribeiro, J., Ali, R. R., & Dick, A. D. (2017) · Translational Vision Science & Technology · doi:10.1167/tvst.6.5.10 · Cited by 16

CX3CL1(+) Microparticles-Induced MFG-E8 Enhances Apoptotic Cell Clearance by Alveolar Macrophages

Tsai, W.-H., Chang, S.-C., Lin, Y.-C., & Hsu, H.-C. (2021) · Cells · doi:10.3390/cells10102583 · Cited by 16

Suppression of FPR2 expression inhibits inflammation in preeclampsia by improving the biological functions of trophoblast via NF-κB pathway

Li, S., Li, A., Zhai, L., Sun, Y., Yu, L., Fang, Z., Zhang, L., Peng, Y., Zhang, M., & Wang, X. (2022) · Journal of Assisted Reproduction and Genetics · doi:10.1007/s10815-022-02395-2 · Cited by 16

Proteomic Portrait of Human Lymphoma Reveals Protein Molecular Fingerprint of Disease Specific Subtypes and Progression

Ku, X., Wang, J., Li, H., Meng, C., Yu, F., Yu, W., Li, Z., Zhou, Z., Zhang, C., Ying, H., et al. (2022) · Phenomics · doi:10.1007/s43657-022-00075-w · Cited by 16

Quantitative Proteome Profiling of CNS-Infiltrating Autoreactive CD4+ Cells Reveals Selective Changes during Experimental Autoimmune Encephalomyelitis

Turvey, M. E., Koudelka, T., Comerford, I., Greer, J. M., Carroll, W. M., Bernard, C. C. A., Hoffmann, P., & McColl, S. R. (2014) · Journal of Proteome Research · doi:10.1021/pr500158r · Cited by 16

Annexin A1 promotes the nuclear localization of the epidermal growth factor receptor in castration-resistant prostate cancer

Mota, S. T. S., Vecchi, L., Alves, D. A., Cordeiro, A. O., Guimarães, G. S., Campos‐Fernández, E., Maia, Y. C. D. P., Dornelas, B. D. C., Bezerra, S. M., de Andrade, V. P., et al. (2020) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2020.105838 · Cited by 17

Red light-emitting diode treatment improves tissue recovery in DSS-induced colitis in mice

de Paula-Silva, M., Broering, M. F., Scharf, P. R. D. S., da Rocha, G. H. O., Farsky, S. H. P., & Lino‐dos‐Santos‐Franco, A. (2020) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2020.112018 · Cited by 16

Chronic Glucocorticoids Consumption Triggers and Worsens Experimental Alzheimer’s Disease-Like Pathology by Detrimental Immune Modulations

Canet, G., Zussy, C., Hernandez, C., Chevallier, N., Marchi, N., Desrumaux, C. M., & Givalois, L. (2021) · Neuroendocrinology · doi:10.1159/000521559 · Cited by 16

Pro-resolving therapies as potential adjunct treatment for infectious diseases: Evidence from studies with annexin A1 and angiotensin-(1-7)

Tavares, L. P., Melo, E. M., Sousa, L. P., & Teixeira, M. M. (2022) · Seminars in Immunology · doi:10.1016/j.smim.2022.101601 · Cited by 16

ANXA1 Silencing Increases the Sensitivity of Cancer Cells to Low-concentration Arsenic Trioxide Treatment by Inhibiting ERK MAPK Activation

Zhang, X., Li, X., Li, X., Zheng, L., & Lei, L. (2015) · Tumori Journal · doi:10.5301/tj.5000315 · Cited by 16

Annexin A1 as a target for managing murine pristane-induced systemic lupus erythematosus

Mihaylova, N., Bradyanova, S. L., Chipinski, P., Herbáth, M., Chausheva, S., Kyurkchiev, D. S., Prechl, J., & Tchorbanov, A. I. (2017) · Autoimmunity · doi:10.1080/08916934.2017.1300884 · Cited by 16

Effects on pig immunophysiology, PBMC proteome and brain neurotransmitters caused by group mixing stress and human-animal relationship

Valent, D., Arroyo, L., Peña, R., Yu, K., Carreras, R., Mainau, E., Velarde, A., & Bassols, A. (2017) · PLoS ONE · doi:10.1371/journal.pone.0176928 · Cited by 16

Single-cell screens identify ADAM12 as a fibroblast checkpoint impeding anti-tumor immunity

Li, J., Liu, H., Guo, Q., Zhang, Y., Li, J., Diao, T., Zheng, L., Deng, Z., Yang, Y., Chen, X., et al. (2026) · Cancer Cell · doi:10.1016/j.ccell.2025.12.018 · Cited by 16

Molecular analysis of Annexin expression in cancer

Hein, T., Krammer, P. H., & Weyd, H. (2022) · BMC Cancer · doi:10.1186/s12885-022-10075-8 · Cited by 15

The role of lipoxin in regulating tumor immune microenvironments

Zhang, T., Hao, H., & Zhou, X. (2019) · Prostaglandins & Other Lipid Mediators · doi:10.1016/j.prostaglandins.2019.106341 · Cited by 15

Innovative Anti-Inflammatory and Pro-resolving Strategies for Pulmonary Hypertension: High Blood Pressure Research Council of Australia Award 2019

Scott, T., Qin, C. X., Drummond, G. R., Hobbs, A. J., & Kemp‐Harper, B. K. (2021) · Hypertension · doi:10.1161/hypertensionaha.120.14525 · Cited by 15

Role of annexin A family in tumorigenesis and chemoresistance of gastric cancer

Zhao, R.-R., Mao, X.-R., Wang, X.-F., Zheng, Y., Wang, Y.-P., & Zhou, Y.-N. (2022) · Neoplasma · doi:10.4149/neo_2021_210629n872 · Cited by 15

Annexin A1 is a polarity cue that directs mitotic spindle orientation during mammalian epithelial morphogenesis

Fankhaenel, M., Hashemi, F. S. G., Mourão, L., Lucas, E., Hosawi, M. M., Skipp, P. J. S., Morin, X., Scheele, C. L. G. J., & Élias, S. (2023) · Nature Communications · doi:10.1038/s41467-023-35881-x · Cited by 15

Microbiota-Induced Antibodies Are Essential for Host Inflammatory Responsiveness to Sterile and Infectious Stimuli

Cisalpino, D., Fagundes, C. T., de Brito, C. B., Ascenção, F. R., Queiroz‐Junior, C. M., Vieira, A. T., Sousa, L. P., Amaral, F. A., Vieira, L. Q., Nicoli, J. R., et al. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1600852 · Cited by 15

Ocimum Phytochemicals and Their Potential Impact on Human Health

Bhattacharjya, D., Adhikari, S., Biswas, A., Bhuimali, A., Ghosh, P., & Saha, S. (2019) · IntechOpen eBooks · doi:10.5772/intechopen.88555 · Cited by 15

Identification, phylogenetic relationships, characterization and gene expression patterns of six different annexins of channel catfish (Ictalurus punctatus Rafinesque, 1818)

Yeh, H., & Klesius, P. H. (2010) · Veterinary Immunology and Immunopathology · doi:10.1016/j.vetimm.2010.02.013 · Cited by 15

An overview of the regulatory role of annexin A1 in the tumor microenvironment and its prospective clinical application (Review)

Gao, K., Li, X., Luo, S., & Zhao, L. (2024) · International Journal of Oncology · doi:10.3892/ijo.2024.5639 · Cited by 14

Proteomic Analysis of Heat Shock-Induced Protection in Acute Pancreatitis

Fétaud-Lapierre, V., Pastor, C. M., Farina, A., Hochstrasser, D. F., Frossard, J., & Lescuyer, P. (2010) · Journal of Proteome Research · doi:10.1021/pr100695d · Cited by 14

Emerging functions as host cell factors – an encyclopedia of annexin-pathogen interactions

Kühnl, A., Musiol, A., Raabe, C. A., & Rescher, U. (2016) · Biological Chemistry · doi:10.1515/hsz-2016-0183 · Cited by 14

The N-Formyl Peptide Receptors and Rheumatoid Arthritis: A Dangerous Liaison or Confusing Relationship?

Mormile, I., Rossi, F. W., Prevete, N., Granata, F., Pucino, V., & de Paulis, A. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.685214 · Cited by 14

Molecular Characterization and Clinical Relevance of ANXA1 in Gliomas via 1,018 Chinese Cohort Patients

Qian, Z., Fan, W., Meng, F., Sun, Z., Li, G., Zhai, Y., Chang, Y., Yang, C., Zeng, F., Chai, R., et al. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.777182 · Cited by 14

Lipidomics Revealed Aberrant Lipid Metabolism Caused by Inflammation in Cardiac Tissue in the Early Stage of Systemic Lupus Erythematosus in a Murine Model

Zhang, J., Lu, L., Tian, X., Wang, K., Xie, G., Li, H., Wen, C., & Hu, C. (2022) · Metabolites · doi:10.3390/metabo12050415 · Cited by 14

Overexpression of Annexin A1 Suppresses Pro-Inflammatory Factors in PC12 Cells Induced by 1-Methyl-4-Phenylpyridinium.

Kiani‐Esfahani, A., Kazemi, S., Peymani, M., Hashemi, M., Ghaedi, K., & Nasr‐Esfahani, M. H. (2016) · Europe PMC (PubMed Central) · doi:10.22074/cellj.2016.4314 · Cited by 14

New insight into the role of ANXA1 in melanoma progression: involvement of stromal expression in dissemination.

Delorme, S., Privat, M., Sonnier, N., Rouanet, J., Witkowski, T., Kossaï, M., Mishellany, F., Radosevic‐Robin, N., Juban, G., Molnar, I., et al. (2021) · PubMed Central · Cited by 14

Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders

Correia, C., Conceição, I. C., Oliveira, B., Coelho, J., Sousa, I., Sequeira, A. F., Almeida, J., Café, C., Duque, F., Mouga, S., et al. (2014) · Molecular Autism · doi:10.1186/2040-2392-5-28 · Cited by 15

Single-cell transcriptomic analysis reveals heterogeneous features of myeloid-derived suppressor cells in newborns

Meng, Y., Cao, Y., He, J., Dong, R., Liu, G., Chen, Y., Wang, J., & Zhou, J. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1367230 · Cited by 13

Protective effect of soybean oil- or fish oil-rich diets on allergic airway inflammation

Silveira, V. L. F., Navarro-Xavier, R., de Barros, K. V., de Andrade, I. S., Palomino, Z., & Casarini, D. E. (2016) · Journal of Inflammation Research · doi:10.2147/jir.s102221 · Cited by 13

High co-expression of the SDF1/CXCR4 axis in hepatocarcinoma cells is regulated by AnnexinA7 in vitro and in vivo

Wang, J., Huang, Y., Zhang, J., Xing, B., Wei, X., Wang, H., Huang, H., Yang, J., & Tang, J. (2018) · Cell Communication and Signaling · doi:10.1186/s12964-018-0234-1 · Cited by 13

TAM receptors and their ligand-mediated activation: Role in atherosclerosis

Cai, B., & Kasikara, C. (2020) · International review of cytology · doi:10.1016/bs.ircmb.2020.09.001 · Cited by 13

Exploiting oxidized lipids and the lipid‐binding GPCRs against cardiometabolic diseases

Guimarães, R. C., Gonçalves, T. T., & Leiria, L. O. (2020) · British Journal of Pharmacology · doi:10.1111/bph.15321 · Cited by 15

Prednisolone in Dogs—Plasma Exposure and White Blood Cell Response

Ekstrand, C., Pettersson, H., Gehring, R., Hedeland, M., Adolfsson, S., & Lilliehöök, I. E. (2021) · Frontiers in Veterinary Science · doi:10.3389/fvets.2021.666219 · Cited by 13

The poorly conducted orchestra of steroid hormones, oxidative stress and inflammation in frailty needs a maestro: Regular physical exercise

Barros, M. P., Bachi, A. L. L., Santos, J. M. B., Lambertucci, R. H., Figueirôa, R. I., Polotow, T. G., Caldo‐Silva, A., Valente, P. A., Hogervorst, E., & Furtado, G. E. (2021) · Experimental Gerontology · doi:10.1016/j.exger.2021.111562 · Cited by 13

Subtyping of Human Papillomavirus-Positive Cervical Cancers Based on the Expression Profiles of 50 Genes

Zhu, X., Li, S., Luo, J., Ying, X., Li, Z., Wang, Y., Zhang, M., Zhang, T., Jiang, P., & Wang, X. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.801639 · Cited by 13

Insights into the role of the resolvin D2-GPR18 signaling axis in cardiovascular physiology and disease

Spite, M. R., & Fredman, G. (2023) · Advances in pharmacology · doi:10.1016/bs.apha.2022.12.005 · Cited by 13

Comparative Analysis of Transcriptional Profiles of Adult Schistosoma japonicum from Different Laboratory Animals and the Natural Host, Water Buffalo

Liu, S., Zhou, X., Piao, X., Wu, C., Hou, N., & Chen, Q. (2015) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0003993 · Cited by 13

Alterations in the profile of blood neutrophil membrane receptors caused by in vivo adrenocorticotrophic hormone actions

Machado, I. D., Santin, J. R., Drewes, C. C., Gil, C. D., Oliani, S. M., Perretti, M., & Farsky, S. H. P. (2014) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00227.2014 · Cited by 13

Connections of annexin A1 and translocator protein-18 kDa on toll like receptor stimulated BV-2 cells

Pantaleão, L. D. N., da Rocha, G. H. O., Reutelingsperger, C. P. M., Tiago, M., Maria–Engler, S. S., Solito, E., & Farsky, S. P. (2018) · Experimental Cell Research · doi:10.1016/j.yexcr.2018.04.008 · Cited by 13

Annexin A1 mediates the anti‐adhesive effects of dexamethasone during the cell–cell interaction between the all‐trans retinoic acid‐treated acute promyelocytic leukemic cells and endothelial cells

Tsai, W., Lai, S., Li, I., Chien, H., Shih, C., Kou, Y. R., & Hsu, H. (2012) · Journal of Cellular Biochemistry · doi:10.1002/jcb.24394 · Cited by 13

wRAPping Up Early Monocyte and Neutrophil Recruitment in Atherogenesis via AnnexinA1/FPR2 Signaling

Butcher, M. J., & Galkina, E. (2015) · Circulation Research · doi:10.1161/circresaha.115.305920 · Cited by 13

An in vitro menstrual cycle using organoids captures epithelial cell transitions during menstruation and regeneration of the human endometrium

Νικολακοπούλου, Κ., Ybañez, W. S., Klaeylé, L., Frugoli, L., Cindrová‐Davies, T., Hotz, H.-R., Soneson, C., & Turco, M. Y. (2026) · Cell stem cell · doi:10.1016/j.stem.2026.04.005 · Cited by 12

Illumination of Molecular Pathways in Multiple Sclerosis Lesions and the Immune Mechanism of Matrine Treatment in EAE, a Mouse Model of MS

Dou, M., Zhou, X., Li, L., Zhang, M., Wang, W., Wang, M., Jing, Y., Ma, R., Zhao, J., & Zhu, L. D. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.640778 · Cited by 13

Ac2‑26 alleviates hepatic ischemia‑reperfusion injury based on inhibiting the positive feedback loop of HMGB1/TLR4/NF‑κB/neutrophils

Bai, C., Jiang, Z., Jiang, H., Yu, S., Li, M., Chu, F., Sheng, Y., Li, J., Jiang, J., & Li, W. (2022) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2022.11609 · Cited by 12

Molecular signature of neutrophil extracellular trap mediating disease module in idiopathic inflammatory myopathy

Moon, S., Jung, S. M., Baek, I., Park, K., & Kim, K. (2023) · Journal of Autoimmunity · doi:10.1016/j.jaut.2023.103063 · Cited by 12

Exploring the role of LIAS-related cuproptosis in systemic lupus erythematosus

Li, Y., Xu, B., Zhang, J., Liu, X., Ganesan, K., & Shi, G. (2023) · Lupus · doi:10.1177/09612033231211429 · Cited by 12

Pathways involved in the resolution of inflammatory joint disease

Haworth, O., & Buckley, C. D. (2015) · Seminars in Immunology · doi:10.1016/j.smim.2015.04.002 · Cited by 13

Cytokine/Chemokine Secretion and Proteomic Identification of Upregulated Annexin A1 from Peripheral Blood Mononuclear Cells Cocultured with the Liver Fluke Opisthorchis viverrini

Hongsrichan, N., Intuyod, K., Pinlaor, P., Khoontawad, J., Yongvanit, P., Wongkham, C., Roytrakul, S., & Pinlaor, S. (2014) · Infection and Immunity · doi:10.1128/iai.00901-13 · Cited by 12

Pro-resolution therapeutics for cardiovascular diseases

Heinz, J., Marinello, M., & Fredman, G. (2017) · Prostaglandins & Other Lipid Mediators · doi:10.1016/j.prostaglandins.2017.03.004 · Cited by 12

Age-related response to an acute innate immune challenge in mice: proteomics reveals a telomere maintenance-related cost

Criscuolo, F., Sorci, G., Benhaim-Delarbre, M., Zahn, S., Faivre, B., & Bertile, F. (2018) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2018.1877 · Cited by 12

Dexamethasone and Tofacitinib suppress NADPH oxidase expression and alleviate very-early-onset ileocolitis in mice deficient in GSH peroxidase 1 and 2

Chu, F., Esworthy, R. S., Shen, B., Gao, Q., & Doroshow, J. H. (2019) · Life Sciences · doi:10.1016/j.lfs.2019.116884 · Cited by 12

Values of natural products to future antiinflammatory pharmaceutical discovery

Amalraj, A., & Gopi, S. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819218-4.00009-2 · Cited by 12

Annexin A1 Is Required for Efficient Tumor Initiation and Cancer Stem Cell Maintenance in a Model of Human Breast Cancer

Johnstone, C. N., Tu, Y., Langenbach, S. Y., Baloyan, D., Pattison, A., Lock, P., Britt, K. L., Lehmann, B. D., Beilharz, T. H., Ernst, M., et al. (2021) · Cancers · doi:10.3390/cancers13051154 · Cited by 12

Leukocytes in Inflammation, Resolution of Inflammation, Autoimmune Diseases and Cancer

Filep, J. G. (2021) · Cells · doi:10.3390/cells10071735 · Cited by 13

Annexins: Involvement in cholesterol homeostasis, inflammatory response and atherosclerosis

Méndez‐Barbero, N., Gutiérrez‐Muñoz, C., Blázquez‐Serra, R., Martı́n-Ventura, J. L., & Blanco‐Colio, L. M. (2021) · Clínica e Investigación en Arteriosclerosis (English Edition) · doi:10.1016/j.artere.2021.07.001 · Cited by 12

Electrical Stimulation of the Auricular Branch Vagus Nerve Using Random and Alternating Frequencies Triggers a Rapid Onset and Pronounced Antihyperalgesia via Peripheral Annexin A1-Formyl Peptide Receptor 2/ALX Pathway in a Mouse Model of Persistent Inflammatory Pain

Salm, D. C., Horewicz, V. V., Tanaka, F., Ferreira, J. K., de Oliveira, B. H., Maio, J. M. B., Donatello, N. N., Lüdtke, D. D., Mazzardo‐Martins, L., Dutra, A. R., et al. (2023) · Molecular Neurobiology · doi:10.1007/s12035-023-03237-7 · Cited by 12

Annexin A1 negatively regulates viral RNA replication of hepatitis C virus.

Hiramoto, H., Dansako, H., Takeda, M., Satoh, S., Wakita, T., Ikeda, M., & Kato, N. (2015) · PubMed · doi:10.18926/amo/53335 · Cited by 12

IMMUNOSTIMULATORY AND BIOCHEMICAL EFFECTS OF ETHANOLIC EXTRACT OF MANGIFERA INDICA STEM BARK ON DEXAMETHASONE-INDUCED IMMUNOSUPPRESSED MALE RATS

Grace, U., Ogbonnia, S. O., Ehianeta, T., & Shakirat, B. (2013) · Cited by 12

Unifying considerations and evidence of macrophage activation mosaicism through human CSF1R and M1/M2 genes

Orsenigo, F., Stewart, A., Hammer, C., Clarke, E., Simpkin, D., Attia, H., Rockall, T., Gordon, S., & Martínez, F. O. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114352 · Cited by 11

Resistance to anti-LAG-3 plus anti-PD-1 therapy in head and neck cancer is mediated by Sox9+ tumor cells interaction with Fpr1+ neutrophils

Wang, X., Cheng, M., Chen, S., Zhang, C., Ling, R., Qiu, S., Chen, K., Zhou, B., Li, Q., Lei, W., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-59050-4 · Cited by 11

Panoramic lead-immune system interactome reveals diversified mechanisms of immunotoxicity upon chronic lead exposure

Hong, Y., Ye, T., Jiang, H., Wang, A., Wang, B., Li, Y., Xie, H., Meng, H., Shen, C., & Ding, X. (2025) · Cell Biology and Toxicology · doi:10.1007/s10565-025-10034-6 · Cited by 11

Molecular Circuits of Resolution in Airway Inflammation

Carlo, T., & Levy, B. D. (2010) · The Scientific World JOURNAL · doi:10.1100/tsw.2010.143 · Cited by 11

Macrophage migration inhibitory factor counter‐regulates dexamethasone‐induced annexin 1 expression and influences the release of eicosanoids in murine macrophages

Sun, Y., Wang, Y., Li, J., Zhu, S., Tang, H., & Xia, Z. (2013) · Immunology · doi:10.1111/imm.12135 · Cited by 11

Annexin‐A1: a pivotal regulator of the innate and adaptive immune systems

D’Acquisto, F., Perretti, M., & Flower, R. J. (2008) · British Journal of Pharmacology · doi:10.1038/bjp.2008.252 · Cited by 194

[Annexin-1: 2nd messanger of the anti-inflammatory actions of glucocorticoids].

Castro‐Caldas, M. (2006) · PubMed · Cited by 4

Overview of the Role of Annexin 1 in the Innate and Adaptive Immune Response

D’Acquisto, F., & Perretti, M. (2008) · Immunology Endocrine & Metabolic Agents - Medicinal Chemistry · doi:10.2174/187152208785748313

Annexin-1 regulates inflammatory response via glucocorticoid-induced genes

Yang, Y. H., Rao, Z., Aeberli, D., Liu, J., Leech, M. T., Dacumos, A., Xue, J., & Morand, E. F. (2009)

The annexin-1 knockout mouse: what it tells us about the inflammatory response.

Roviezzo, F., Getting, S. J., Paul‐Clark, M. J., Yona, S., Gavins, F. N. E., Perretti, M., Hannon, R., Croxtall, J. D., Buckingham, J. C., & Flower, R. J. (2002) · PubMed · Cited by 82