CX3CL1 induces cell migration and invasion through ICAM‐1 expression in oral squamous cell carcinoma cells
Human oral squamous cell carcinoma (OSCC) has been associated with a relatively low survival rate over the years and is characterized by a poor prognosis. C‐X3‐C motif chemokine ligand 1 (CX3CL1) has been involved in advanced migratory cells. Overexpressed CX3CL1 promotes several cellular responses...
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Published in | Journal of Cellular and Molecular Medicine Vol. 27; no. 11; pp. 1509 - 1522 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Wiley
01.06.2023
John Wiley & Sons, Inc John Wiley and Sons Inc |
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Abstract | Human oral squamous cell carcinoma (OSCC) has been associated with a relatively low survival rate over the years and is characterized by a poor prognosis. C‐X3‐C motif chemokine ligand 1 (CX3CL1) has been involved in advanced migratory cells. Overexpressed CX3CL1 promotes several cellular responses related to cancer metastasis, including cell movement, migration and invasion in tumour cells. However, CX3CL1 controls the migration ability, and its molecular mechanism in OSCC remains unknown. The present study confirmed that CX3CL1 increased cell movement, migration and invasion. The CX3CL1‐induced cell motility is upregulated through intercellular adhesion molecule‐1 (ICAM‐1) expression in OSCC cells. These effects were significantly suppressed when OSCC cells were pre‐treated with CX3CR1 monoclonal antibody (mAb) and small‐interfering RNA (siRNA). The CX3CL1‐CX3CR1 axis activates promoted PLCβ/PKCα/c‐Src phosphorylation. Furthermore, CX3CL1 enhanced activator protein‐1 (AP‐1) activity. The CX3CR1 mAb and PLCβ, PKCα, c‐Src inhibitors reduced CX3CL1‐induced c‐Jun phosphorylation, c‐Jun translocation into the nucleus and c‐Jun binding to the ICAM‐1 promoter. The present results reveal that CX3CL1 induces the migration of OSCC cells by promoting ICAM‐1 expression through the CX3CR1 and the PLCβ/PKCα/c‐Src signal pathway, suggesting that CX3CL1‐CX3CR1‐mediated signalling is correlated with tumour motility and appealed to be a precursor for prognosis in human OSCC. |
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AbstractList | Human oral squamous cell carcinoma (OSCC) has been associated with a relatively low survival rate over the years and is characterized by a poor prognosis. C‐X3‐C motif chemokine ligand 1 (CX3CL1) has been involved in advanced migratory cells. Overexpressed CX3CL1 promotes several cellular responses related to cancer metastasis, including cell movement, migration and invasion in tumour cells. However, CX3CL1 controls the migration ability, and its molecular mechanism in OSCC remains unknown. The present study confirmed that CX3CL1 increased cell movement, migration and invasion. The CX3CL1‐induced cell motility is upregulated through intercellular adhesion molecule‐1 (ICAM‐1) expression in OSCC cells. These effects were significantly suppressed when OSCC cells were pre‐treated with CX3CR1 monoclonal antibody (mAb) and small‐interfering RNA (siRNA). The CX3CL1‐CX3CR1 axis activates promoted PLCβ/PKCα/c‐Src phosphorylation. Furthermore, CX3CL1 enhanced activator protein‐1 (AP‐1) activity. The CX3CR1 mAb and PLCβ, PKCα, c‐Src inhibitors reduced CX3CL1‐induced c‐Jun phosphorylation, c‐Jun translocation into the nucleus and c‐Jun binding to the ICAM‐1 promoter. The present results reveal that CX3CL1 induces the migration of OSCC cells by promoting ICAM‐1 expression through the CX3CR1 and the PLCβ/PKCα/c‐Src signal pathway, suggesting that CX3CL1‐CX3CR1‐mediated signalling is correlated with tumour motility and appealed to be a precursor for prognosis in human OSCC. Human oral squamous cell carcinoma (OSCC) has been associated with a relatively low survival rate over the years and is characterized by a poor prognosis. C-X3-C motif chemokine ligand 1 (CX3CL1) has been involved in advanced migratory cells. Overexpressed CX3CL1 promotes several cellular responses related to cancer metastasis, including cell movement, migration and invasion in tumour cells. However, CX3CL1 controls the migration ability, and its molecular mechanism in OSCC remains unknown. The present study confirmed that CX3CL1 increased cell movement, migration and invasion. The CX3CL1-induced cell motility is upregulated through intercellular adhesion molecule-1 (ICAM-1) expression in OSCC cells. These effects were significantly suppressed when OSCC cells were pre-treated with CX3CR1 monoclonal antibody (mAb) and small-interfering RNA (siRNA). The CX3CL1-CX3CR1 axis activates promoted PLCβ/PKCα/c-Src phosphorylation. Furthermore, CX3CL1 enhanced activator protein-1 (AP-1) activity. The CX3CR1 mAb and PLCβ, PKCα, c-Src inhibitors reduced CX3CL1-induced c-Jun phosphorylation, c-Jun translocation into the nucleus and c-Jun binding to the ICAM-1 promoter. The present results reveal that CX3CL1 induces the migration of OSCC cells by promoting ICAM-1 expression through the CX3CR1 and the PLCβ/PKCα/c-Src signal pathway, suggesting that CX3CL1-CX3CR1-mediated signalling is correlated with tumour motility and appealed to be a precursor for prognosis in human OSCC.Human oral squamous cell carcinoma (OSCC) has been associated with a relatively low survival rate over the years and is characterized by a poor prognosis. C-X3-C motif chemokine ligand 1 (CX3CL1) has been involved in advanced migratory cells. Overexpressed CX3CL1 promotes several cellular responses related to cancer metastasis, including cell movement, migration and invasion in tumour cells. However, CX3CL1 controls the migration ability, and its molecular mechanism in OSCC remains unknown. The present study confirmed that CX3CL1 increased cell movement, migration and invasion. The CX3CL1-induced cell motility is upregulated through intercellular adhesion molecule-1 (ICAM-1) expression in OSCC cells. These effects were significantly suppressed when OSCC cells were pre-treated with CX3CR1 monoclonal antibody (mAb) and small-interfering RNA (siRNA). The CX3CL1-CX3CR1 axis activates promoted PLCβ/PKCα/c-Src phosphorylation. Furthermore, CX3CL1 enhanced activator protein-1 (AP-1) activity. The CX3CR1 mAb and PLCβ, PKCα, c-Src inhibitors reduced CX3CL1-induced c-Jun phosphorylation, c-Jun translocation into the nucleus and c-Jun binding to the ICAM-1 promoter. The present results reveal that CX3CL1 induces the migration of OSCC cells by promoting ICAM-1 expression through the CX3CR1 and the PLCβ/PKCα/c-Src signal pathway, suggesting that CX3CL1-CX3CR1-mediated signalling is correlated with tumour motility and appealed to be a precursor for prognosis in human OSCC. |
Author | Tsung‐Ming Chang Ju‐Fang Liu Pei‐Wen Peng Chia‐Yu Wu Augusta I‐Chin Wei Chia‐Jung Lee Ting‐Yi Renn |
AuthorAffiliation | 1 School of Dental Technology, College of Oral Medicine Taipei Medical University Taipei City Taiwan 6 Institute of Physiology, School of Medicine National Yang Ming Chiao Tung University Taipei City Taiwan 2 Division of Oral and Maxillofacial Surgery, Department of Dentistry Taipei Medical University Hospital Taipei City Taiwan 9 Department of Medical Research China Medical University Hospital, China Medical University Taichung City Taiwan 4 Department of Otolaryngology Head and Neck Surgery Shin‐Kong Wu‐Ho‐Su Memorial Hospital Taipei City Taiwan 5 School of Medicine Fu‐Jen Catholic University Taipei City Taiwan 7 Translational Medicine Center Shin‐Kong Wu Ho‐Su Memorial Hospital Taipei City Taiwan 8 School of Oral Hygiene, College of Oral Medicine Taipei Medical University Taipei City Taiwan 3 Department of Oral and Maxillofacial Pathobiology, Graduate School of Biomedical and Health Sciences Hiroshima University Hiroshima Japan |
AuthorAffiliation_xml | – name: 1 School of Dental Technology, College of Oral Medicine Taipei Medical University Taipei City Taiwan – name: 9 Department of Medical Research China Medical University Hospital, China Medical University Taichung City Taiwan – name: 5 School of Medicine Fu‐Jen Catholic University Taipei City Taiwan – name: 2 Division of Oral and Maxillofacial Surgery, Department of Dentistry Taipei Medical University Hospital Taipei City Taiwan – name: 8 School of Oral Hygiene, College of Oral Medicine Taipei Medical University Taipei City Taiwan – name: 6 Institute of Physiology, School of Medicine National Yang Ming Chiao Tung University Taipei City Taiwan – name: 4 Department of Otolaryngology Head and Neck Surgery Shin‐Kong Wu‐Ho‐Su Memorial Hospital Taipei City Taiwan – name: 7 Translational Medicine Center Shin‐Kong Wu Ho‐Su Memorial Hospital Taipei City Taiwan – name: 3 Department of Oral and Maxillofacial Pathobiology, Graduate School of Biomedical and Health Sciences Hiroshima University Hiroshima Japan |
Author_xml | – sequence: 1 givenname: Chia‐Yu surname: Wu fullname: Wu, Chia‐Yu organization: Taipei Medical University Hospital – sequence: 2 givenname: Pei‐Wen surname: Peng fullname: Peng, Pei‐Wen organization: Taipei Medical University – sequence: 3 givenname: Ting‐Yi surname: Renn fullname: Renn, Ting‐Yi organization: Hiroshima University – sequence: 4 givenname: Chia‐Jung surname: Lee fullname: Lee, Chia‐Jung organization: Fu‐Jen Catholic University – sequence: 5 givenname: Tsung‐Ming surname: Chang fullname: Chang, Tsung‐Ming organization: National Yang Ming Chiao Tung University – sequence: 6 givenname: Augusta I‐Chin surname: Wei fullname: Wei, Augusta I‐Chin organization: Shin‐Kong Wu Ho‐Su Memorial Hospital – sequence: 7 givenname: Ju‐Fang orcidid: 0000-0002-0887-6096 surname: Liu fullname: Liu, Ju‐Fang email: jufangliu@tmu.edu.tw organization: China Medical University Hospital, China Medical University |
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CitedBy_id | crossref_primary_10_1038_s41598_023_44598_2 crossref_primary_10_1016_j_ecoenv_2024_116172 crossref_primary_10_1186_s12967_023_04449_0 crossref_primary_10_3390_ijms25094679 |
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Keywords | ICAM-1 human oral squamous cell carcinoma (OSCC) CX3CL1 PLCβ/PKCα/c-Src pathway tumour motility |
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SubjectTerms | Activator protein 1 Antibodies c-Jun protein Carcinoma, Squamous Cell Carcinoma, Squamous Cell - pathology Cell adhesion Cell adhesion & migration Cell culture Cell Line, Tumor Cell migration Cell Movement Chemokine CX3CL1 Chemokine CX3CL1 - genetics Chemokine CX3CL1 - metabolism Chemokines CX3CL1 CX3CR1 protein Experiments Gene expression Head and Neck Neoplasms human oral squamous cell carcinoma (OSCC) Humans ICAM‐1 Intercellular Adhesion Molecule-1 Intercellular Adhesion Molecule-1 - genetics Intercellular Adhesion Molecule-1 - metabolism Kinases Lung cancer Medical prognosis Metastases Metastasis Molecular modelling Monoclonal antibodies Mouth Neoplasms Mouth Neoplasms - pathology Oral cancer Oral carcinoma Oral squamous cell carcinoma Original Original Articles Phosphorylation PLCβ/PKCα/c‐Src pathway tumour motility Prognosis Protein kinase C Protein Kinase C-alpha Proteins RNA, Small Interfering RNA, Small Interfering - genetics RNA, Small Interfering - pharmacology Signal transduction siRNA Software Squamous cell carcinoma Squamous Cell Carcinoma of Head and Neck Src protein Transcription factors Tumorigenesis Tumors |
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Title | CX3CL1 induces cell migration and invasion through ICAM‐1 expression in oral squamous cell carcinoma cells |
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