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ING4 regulates JWA in angiogenesis and their prognostic value in melanoma patients

BACKGROUND: We previously showed that inhibitor of growth family member 4 (ING4) inhibits melanoma angiogenesis, and JWA suppresses the metastasis of melanoma cells. As angiogenesis is essential for tumour metastasis, further investigation of the function of ING4 and JWA in melanoma angiogenesis is...

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Autores principales: Lu, J, Tang, Y, Cheng, Y, Zhang, G, Yip, A, Martinka, M, Dong, Z, Zhou, J, Li, G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3844917/
https://www.ncbi.nlm.nih.gov/pubmed/24157826
http://dx.doi.org/10.1038/bjc.2013.670
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author Lu, J
Tang, Y
Cheng, Y
Zhang, G
Yip, A
Martinka, M
Dong, Z
Zhou, J
Li, G
author_facet Lu, J
Tang, Y
Cheng, Y
Zhang, G
Yip, A
Martinka, M
Dong, Z
Zhou, J
Li, G
author_sort Lu, J
collection PubMed
description BACKGROUND: We previously showed that inhibitor of growth family member 4 (ING4) inhibits melanoma angiogenesis, and JWA suppresses the metastasis of melanoma cells. As angiogenesis is essential for tumour metastasis, further investigation of the function of ING4 and JWA in melanoma angiogenesis is needed, and their prognostic value are of great interest. METHODS: Western blot, tube-formation assays and luciferase assays were used to investigate the correlation between ING4 and JWA in melanoma angiogenesis. JWA and integrin-linked kinase (ILK) expression was determined on a tissue microarray constructed from 175 biopsies. RESULTS: ING4 promoted JWA expression by activating JWA promoter. Furthermore, the regulation of growth and tube formation of endothelial cells by ING4 was partially JWA dependent. Also, ING4 inhibited the ILK-induced angiogenesis signalling pathway via JWA. Moreover, reduced JWA, or increased ILK, expression was closely associated with 5-year disease-specific survival of melanoma patients (P=0.001 and 0.007, respectively). There was also a positive correlation between ING4 and JWA yet a negative correlation between ING4 and ILK. Importantly, their concomitant expressions were significantly related to 5-year survival of melanoma patients (P=0.002 and 0.003, respectively). CONCLUSION: JWA has an important role in ING4-regulated melanoma angiogenesis, and ING4/JWA/ILK are promising prognostic markers and may be used as anti-angiogenic therapeutic targets for melanoma.
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spelling pubmed-38449172014-11-26 ING4 regulates JWA in angiogenesis and their prognostic value in melanoma patients Lu, J Tang, Y Cheng, Y Zhang, G Yip, A Martinka, M Dong, Z Zhou, J Li, G Br J Cancer Molecular Diagnostics BACKGROUND: We previously showed that inhibitor of growth family member 4 (ING4) inhibits melanoma angiogenesis, and JWA suppresses the metastasis of melanoma cells. As angiogenesis is essential for tumour metastasis, further investigation of the function of ING4 and JWA in melanoma angiogenesis is needed, and their prognostic value are of great interest. METHODS: Western blot, tube-formation assays and luciferase assays were used to investigate the correlation between ING4 and JWA in melanoma angiogenesis. JWA and integrin-linked kinase (ILK) expression was determined on a tissue microarray constructed from 175 biopsies. RESULTS: ING4 promoted JWA expression by activating JWA promoter. Furthermore, the regulation of growth and tube formation of endothelial cells by ING4 was partially JWA dependent. Also, ING4 inhibited the ILK-induced angiogenesis signalling pathway via JWA. Moreover, reduced JWA, or increased ILK, expression was closely associated with 5-year disease-specific survival of melanoma patients (P=0.001 and 0.007, respectively). There was also a positive correlation between ING4 and JWA yet a negative correlation between ING4 and ILK. Importantly, their concomitant expressions were significantly related to 5-year survival of melanoma patients (P=0.002 and 0.003, respectively). CONCLUSION: JWA has an important role in ING4-regulated melanoma angiogenesis, and ING4/JWA/ILK are promising prognostic markers and may be used as anti-angiogenic therapeutic targets for melanoma. Nature Publishing Group 2013-11-26 2013-10-24 /pmc/articles/PMC3844917/ /pubmed/24157826 http://dx.doi.org/10.1038/bjc.2013.670 Text en Copyright © 2013 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Molecular Diagnostics
Lu, J
Tang, Y
Cheng, Y
Zhang, G
Yip, A
Martinka, M
Dong, Z
Zhou, J
Li, G
ING4 regulates JWA in angiogenesis and their prognostic value in melanoma patients
title ING4 regulates JWA in angiogenesis and their prognostic value in melanoma patients
title_full ING4 regulates JWA in angiogenesis and their prognostic value in melanoma patients
title_fullStr ING4 regulates JWA in angiogenesis and their prognostic value in melanoma patients
title_full_unstemmed ING4 regulates JWA in angiogenesis and their prognostic value in melanoma patients
title_short ING4 regulates JWA in angiogenesis and their prognostic value in melanoma patients
title_sort ing4 regulates jwa in angiogenesis and their prognostic value in melanoma patients
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3844917/
https://www.ncbi.nlm.nih.gov/pubmed/24157826
http://dx.doi.org/10.1038/bjc.2013.670
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