Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/34640
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    CNU IR > Offices > 123 >  Item 310902800/34640
    Please use this identifier to cite or link to this item: https://ir.cnu.edu.tw/handle/310902800/34640


    Title: Growth regulated oncogene-? contribute to EMT/MMPs pathway by binding its receptors in head and neck squamous cell carcinoma
    Authors: Chan, Leong-Perng
    Tseng, Ya-Ping
    Wang, Hui-Ching
    Chien, Chen-Yu
    Wu, Che-Wei
    Wang, Ling-Feng
    Liang, Chia-Hua
    Contributors: Kaohsiung Medical University
    Kaohsiung Medical University Hospital
    Kaohsiung Medical University
    Kaohsiung Municipal Ta-Tung Hospital
    National Cheng Kung University
    Kaohsiung Medical University
    Kaohsiung Medical University Hospital
    Kaohsiung Medical University
    Kaohsiung Municipal Siao-Gang Hospital
    Chia Nan University of Pharmacy & Science
    Chia Nan University of Pharmacy & Science
    Keywords: metastasis
    axis
    Date: 2022
    Issue Date: 2023-12-11 14:02:04 (UTC+8)
    Publisher: PERGAMON-ELSEVIER SCIENCE LTD
    Abstract: Squamous cell carcinoma (SCC) is the most common malignant tumor of the head and neck and generally detected in the late stages when the cancer has advanced, and therefore has a poor prognosis and survival rate. A high expression of growth-related oncogene alpha (Gro alpha) is associated with tumor metastasis and invasion and the poor survival rate of patients. Microarray reveals that Gro alpha exhibits a cancer-specific response in HNSCC. Quantitative real-time PCR (qRT-PCR) results concerning the mRNA expression of Gro alpha in HNSCC tissues; indicate that Gro alpha was more highly expressed in HNSCC than in non-cancerous matched tissue (NCMT). The serum of HNSCC patients and healthy subjects demonstrates that the expression of Gro alpha in the HNSCC patients significantly exceeded than in healthy subjects. Furthermore, exposure Gro alpha to stimulated the proliferation, clonogenicity and migration with HNSCC cells (SCC4, SCC9, SCC25 and OECM-1), yielding a stronger response than in non-malignant HaCaT and DOK cells. A high expression of Gro alpha and its receptors CXCR1/2 (chemokine (C-X-C motif) receptor) in HNSCC tissues are highly correlated with tumor progression stage and metastasis. Following the treatment of SCC25 and OECM-1 cells with Gro alpha, beta-catenin, matrix metalloproteinases (MMP)-2, MMP-7 and MMP-9 expressions significantly increased but E-cadherin expression was slightly decreased, sug-gesting that the EMT and metastasis processes were activated by Gro alpha. These findings constitute the first evi-dence that Gro alpha promotes epithelial mesenchymal transition (EMT) and MMPs expressions in HNSCC via activating CXCR1/2, suggesting a role for Gro alpha in mediating metastasis and its potential as a therapeutic target.
    Relation: LIFE SCIENCES, v.306, n.CB2, pp.CC2, pp.-,
    Appears in Collections:[Offices] 123

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