Orphan G protein–coupled receptor GPR56 plays a role in cell transformation and tumorigenesis involving the cell adhesion pathway
| Autor: | Guohong Liu, Dehua Yu, Ning Ke, Flossie Wong-Staal, Mirta Grifman, Roshni Sundaram, John Chionis, Wufang Fan, Qi-Xiang Li, Tarif Awad, Cheryl Rogers |
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| Rok vydání: | 2007 |
| Předmět: |
Cancer Research
Biology medicine.disease_cause Cell Line Receptors G-Protein-Coupled Extracellular matrix Cell Adhesion medicine Animals Humans Gene silencing Anoikis Gene Silencing Cell adhesion DNA Primers Base Sequence Reverse Transcriptase Polymerase Chain Reaction Gene Expression Profiling Cancer medicine.disease Cell biology Cell Transformation Neoplastic GPR56 Oncology Cancer cell Carcinogenesis |
| Zdroj: | Molecular Cancer Therapeutics. 6:1840-1850 |
| ISSN: | 1538-8514 1535-7163 |
| DOI: | 10.1158/1535-7163.mct-07-0066 |
| Popis: | GPR56 is an orphan G protein–coupled receptor, mutations of which have recently been associated with bilateral frontoparietal polymicrogyria, a rare neurologic disease that has implications in brain development. However, no phenotype beyond central nervous system has yet been described for the GPR56-null mutations despite abundant GPR56 expression in many non–central nervous system adult tissues. In the present study, we show that higher GPR56 expression is correlated with the cellular transformation phenotypes of several cancer tissues compared with their normal counterparts, implying a potential oncogenic function. RNA interference–mediated GPR56 silencing results in apoptosis induction and reduced anchorage-independent growth of cancer cells via increased anoikis, whereas cDNA overexpression resulted in increased foci formation in mouse fibroblast NIH3T3 cell line. When GPR56 silencing was induced in vivo in several xenograft tumor models, significant tumor responses (including regression) were observed, suggesting the potential of targeting GPR56 in the development of tumor therapies. The expression profiling of GPR56-silenced A2058 melanoma cell line revealed several genes whose expression was affected by GPR56 silencing, particularly those in the integrin-mediated signaling and cell adhesion pathways. The potential role of GPR56 in cancer cell adhesion was further confirmed by the observation that GPR56 silencing also reduced cell adhesion to the extracellular matrix, which is consistent with the observed increase in anoikis and reduction in anchorage-independent growth phenotypes. The oncogenic potential and apparent absence of physiologic defects in adult human tissues lacking GPR56, as well as the targetable nature of G protein–coupled receptor by small molecule or antibody, make GPR56 an attractive drug target for the development of cancer therapies. [Mol Cancer Ther 2007;6(6):1840–50] |
| Databáze: | OpenAIRE |
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