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Expression of Cyr61, CTGF, and WISP-1 Correlates with Clinical Features of Lung Cancer
BACKGROUND: CCN family, comprising six members (Cyr61, CTGF, Nov, WISP-1, WISP-2, WISP-3), is involved in the stimulation of cell proliferation, migration, adhesion, angiogenesis, and tumorigenesis. Several studies have shown that expression of Cyr61, CTGF, and WISP-1 affects the tumorigenic potenti...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1888724/ https://www.ncbi.nlm.nih.gov/pubmed/17579708 http://dx.doi.org/10.1371/journal.pone.0000534 |
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author | Chen, Ping-Ping Li, Wen-Jie Wang, Yan Zhao, Song Li, De-Yun Feng, Li-Yun Shi, Xiang-Lin Koeffler, H. Phillip Tong, Xiang-Jun Xie, Dong |
author_facet | Chen, Ping-Ping Li, Wen-Jie Wang, Yan Zhao, Song Li, De-Yun Feng, Li-Yun Shi, Xiang-Lin Koeffler, H. Phillip Tong, Xiang-Jun Xie, Dong |
author_sort | Chen, Ping-Ping |
collection | PubMed |
description | BACKGROUND: CCN family, comprising six members (Cyr61, CTGF, Nov, WISP-1, WISP-2, WISP-3), is involved in the stimulation of cell proliferation, migration, adhesion, angiogenesis, and tumorigenesis. Several studies have shown that expression of Cyr61, CTGF, and WISP-1 affects the tumorigenic potential of lung cancer cells in vitro. However, the correlation of expression of CCN family proteins and clinical features of lung cancer remains unknown. METHODOLOGY AND PRINCIPAL FINDINGS: In the present work, we quantified the mRNA levels of Cyr61, CTGF, and WISP-1 in samples from 60 primary lung cancers and their matched normal lung tissues by quantitative real-time PCR assay. Downregulation of the Cyr61 and CTGF genes and upregulation of the WISP-1 gene were found in primary lung cancers compared to the paired normal lung tissues. Immunohistochemistry analysis also disclosed a similar expression pattern of Cyr61, CTGF, and WISP-1 protein in paired lung cancer tissues. Statistical analysis revealed significant associations between expression of either Cyr61 or CTGF with tumor stage, tumor histology, metastasis, smoking, and family history at diagnosis. A significant correlation also existed between WISP-1 expression with tumor histology, and patient age. Moreover, expression levels of Cyr61 and CTGF correlated with survival of the lung-cancer patients. CONCLUSIONS: Our results suggest that Cyr61, CTGF, and WISP-1 might be implicated in the development and progression of primary lung cancers, and their levels might serve as valuable prognostic markers, as well as potential targets for therapeutic intervention. |
format | Text |
id | pubmed-1888724 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-18887242007-06-20 Expression of Cyr61, CTGF, and WISP-1 Correlates with Clinical Features of Lung Cancer Chen, Ping-Ping Li, Wen-Jie Wang, Yan Zhao, Song Li, De-Yun Feng, Li-Yun Shi, Xiang-Lin Koeffler, H. Phillip Tong, Xiang-Jun Xie, Dong PLoS One Research Article BACKGROUND: CCN family, comprising six members (Cyr61, CTGF, Nov, WISP-1, WISP-2, WISP-3), is involved in the stimulation of cell proliferation, migration, adhesion, angiogenesis, and tumorigenesis. Several studies have shown that expression of Cyr61, CTGF, and WISP-1 affects the tumorigenic potential of lung cancer cells in vitro. However, the correlation of expression of CCN family proteins and clinical features of lung cancer remains unknown. METHODOLOGY AND PRINCIPAL FINDINGS: In the present work, we quantified the mRNA levels of Cyr61, CTGF, and WISP-1 in samples from 60 primary lung cancers and their matched normal lung tissues by quantitative real-time PCR assay. Downregulation of the Cyr61 and CTGF genes and upregulation of the WISP-1 gene were found in primary lung cancers compared to the paired normal lung tissues. Immunohistochemistry analysis also disclosed a similar expression pattern of Cyr61, CTGF, and WISP-1 protein in paired lung cancer tissues. Statistical analysis revealed significant associations between expression of either Cyr61 or CTGF with tumor stage, tumor histology, metastasis, smoking, and family history at diagnosis. A significant correlation also existed between WISP-1 expression with tumor histology, and patient age. Moreover, expression levels of Cyr61 and CTGF correlated with survival of the lung-cancer patients. CONCLUSIONS: Our results suggest that Cyr61, CTGF, and WISP-1 might be implicated in the development and progression of primary lung cancers, and their levels might serve as valuable prognostic markers, as well as potential targets for therapeutic intervention. Public Library of Science 2007-06-20 /pmc/articles/PMC1888724/ /pubmed/17579708 http://dx.doi.org/10.1371/journal.pone.0000534 Text en Chen et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Chen, Ping-Ping Li, Wen-Jie Wang, Yan Zhao, Song Li, De-Yun Feng, Li-Yun Shi, Xiang-Lin Koeffler, H. Phillip Tong, Xiang-Jun Xie, Dong Expression of Cyr61, CTGF, and WISP-1 Correlates with Clinical Features of Lung Cancer |
title | Expression of Cyr61, CTGF, and WISP-1 Correlates with Clinical Features of Lung Cancer |
title_full | Expression of Cyr61, CTGF, and WISP-1 Correlates with Clinical Features of Lung Cancer |
title_fullStr | Expression of Cyr61, CTGF, and WISP-1 Correlates with Clinical Features of Lung Cancer |
title_full_unstemmed | Expression of Cyr61, CTGF, and WISP-1 Correlates with Clinical Features of Lung Cancer |
title_short | Expression of Cyr61, CTGF, and WISP-1 Correlates with Clinical Features of Lung Cancer |
title_sort | expression of cyr61, ctgf, and wisp-1 correlates with clinical features of lung cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1888724/ https://www.ncbi.nlm.nih.gov/pubmed/17579708 http://dx.doi.org/10.1371/journal.pone.0000534 |
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