Altered expression of phosphatase of regenerating liver gene family in non-small cell lung cancer
Protein tyrosine phophatases (PTPs) are implicated in the tumorigenesis and metastasis of human cancer. The phosphatase of regenerating liver (PRL) gene family, a subgroup of PTPs is also linked to these processes. In many solid cancers, high levels of PRL-3 expression are related with metastasis an...
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Published in | Oncology reports Vol. 27; no. 2; pp. 535 - 540 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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Spandidos
01.02.2012
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Abstract | Protein tyrosine phophatases (PTPs) are implicated in the tumorigenesis and metastasis of human cancer. The phosphatase of regenerating liver (PRL) gene family, a subgroup of PTPs is also linked to these processes. In many solid cancers, high levels of PRL-3 expression are related with metastasis and poor prognosis. However, the expression patterns of PRL-1 and -2 have not been explored in lung cancer yet. Thus, we investigated the expression levels of PRL-1, -2 and -3 in the tissues of primary lung cancer patients. The protein expression levels of PRL-2, but not PRL-1 and -3 were increased in cancer tissues. However, there was no correlation between mRNA and protein expression levels of the PRLs. Reporter assays showed that PRLs suppressed the activity of the p21 promoter but promoted AP-1 activity. Furthermore, transfection of PRLs showed significantly increased cell proliferation. Therefore, these results suggest that PRL-2 plays an important role in lung cancer and can be a biomarker of lung cancer, substituting for the function of other PRLs. |
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AbstractList | Protein tyrosine phophatases (PTPs) are implicated in the tumorigenesis and metastasis of human cancer. The phosphatase of regenerating liver (PRL) gene family, a subgroup of PTPs is also linked to these processes. In many solid cancers, high levels of PRL-3 expression are related with metastasis and poor prognosis. However, the expression patterns of PRL-1 and -2 have not been explored in lung cancer yet. Thus, we investigated the expression levels of PRL-1, -2 and -3 in the tissues of primary lung cancer patients. The protein expression levels of PRL-2, but not PRL-1 and -3 were increased in cancer tissues. However, there was no correlation between mRNA and protein expression levels of the PRLs. Reporter assays showed that PRLs suppressed the activity of the p21 promoter but promoted AP-1 activity. Furthermore, transfection of PRLs showed significantly increased cell proliferation. Therefore, these results suggest that PRL-2 plays an important role in lung cancer and can be a biomarker of lung cancer, substituting for the function of other PRLs. |
Author | LEE, Seung-Hyo MIN, Sang-Hyun YOO, Ook-Joon KIM, Kil-Dong HWANG, Jung-Joo HEO, Young-Shin SIN, Ki-Hyuk |
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Keywords | Cell proliferation non-small cell lung cancer Lung disease PRL-2 Digestive system Enzyme Respiratory disease Lung cancer Liver CDKN1A Gene Phosphoric monoester hydrolases Esterases Malignant tumor non-small cell lung carcinoma AP-1 p21 Cancerology Hydrolases Bronchus disease Multigene family Cancer Tumor suppressor gene Transcription factor AP1 |
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SubjectTerms | Aged Animals Biological and medical sciences Carcinoma, Non-Small-Cell Lung - enzymology Carcinoma, Non-Small-Cell Lung - genetics Cell Line, Tumor Cell Proliferation Cyclin-Dependent Kinase Inhibitor p21 - genetics Female Gene Expression Gene Expression Regulation, Neoplastic Humans Lung Neoplasms - enzymology Lung Neoplasms - genetics Male Medical sciences Mice Middle Aged NIH 3T3 Cells Pneumology Protein Tyrosine Phosphatases - genetics Protein Tyrosine Phosphatases - metabolism Transcription Factor AP-1 - genetics Transcription, Genetic Tumors Tumors of the respiratory system and mediastinum |
Title | Altered expression of phosphatase of regenerating liver gene family in non-small cell lung cancer |
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