GPCRs: Exploring New Paradigms
| by S.Jones | October 08, 2007
As one of the largest and most diverse protein families in nature, the G-protein coupled receptor (GPCR) superfamily play important roles in a variety of biological and pathological processes such as development and proliferation, neuromodulation, angiogenesis, metabolic disorders, inflammation, and viral infection. Not surprisingly, it is one of the most targeted protein families in pharmaceutical research today (Schlyer 2006).
All members of this superfamily share a similar seven transmembrane domain, but are grouped on the basis of shared sequence motifs into the following broad classes:
Class A Rhodopsin-like
Class B Secretin-like
Class C Metabotropic glutamate/pheromone
Class D Fungal pheromone
Class E cAMP receptors
Frizzled/Smoothened
Vomeronasal receptors
Putative/unclassified
The pharmaceutical industry has focused on development of modulators to this protein family, but GPCRs also represent an attractive target as biomarkers. Recent studies have implicated endothelin receptors, chemokine receptors and lysophosphatidic acid receptors in tumorgenesis and metastasis, and a recent in silico analysis found a number of GPCRs that were up-regulated in various cancers which suggests not only targets of therapeutic value, but of diagnostic and prognostic value as well. A summary of these up-regulated receptors is below.
Lung cancer
Edg2, P2Y purinoceptor 6, PAR-2, PAR-3, GPR68
Breast cancer
CCR1, CXCR-4, PAR-2
Prostate cancer
Beta 2 adrenergic receptor, CXCR-3, CXCR-4, GPR68
Melanoma
Edg6, PAR-2, mGluR1
Gastric cancer
CXCR-4, P2Y purinoceptor 5
Lymphoma
Beta 2 adrenergic receptor, Edg1, CCR7
While research continues, it is evident that GPCRs are critical in countless biological functions--and disfunctions. While the emphasis is on their role in drug development, it is becoming increasingly clear that G-protein coupled receptors will play a critical role as indicators of disease with diagnostic and prognostic potential. IMGENEX carries over 900 IHC, WB, and flow validated GPCR antibodies. View our complete GPCRs antibody list grouped by class and family. Also see our complete list of Tissue Microarray slides--perfect for GPCR localization.
Find out more information about GPCRs.
All members of this superfamily share a similar seven transmembrane domain, but are grouped on the basis of shared sequence motifs into the following broad classes:
Class A Rhodopsin-like
Class B Secretin-like
Class C Metabotropic glutamate/pheromone
Class D Fungal pheromone
Class E cAMP receptors
Frizzled/Smoothened
Vomeronasal receptors
Putative/unclassified
The pharmaceutical industry has focused on development of modulators to this protein family, but GPCRs also represent an attractive target as biomarkers. Recent studies have implicated endothelin receptors, chemokine receptors and lysophosphatidic acid receptors in tumorgenesis and metastasis, and a recent in silico analysis found a number of GPCRs that were up-regulated in various cancers which suggests not only targets of therapeutic value, but of diagnostic and prognostic value as well. A summary of these up-regulated receptors is below.
Lung cancer
Edg2, P2Y purinoceptor 6, PAR-2, PAR-3, GPR68
Breast cancer
CCR1, CXCR-4, PAR-2
Prostate cancer
Beta 2 adrenergic receptor, CXCR-3, CXCR-4, GPR68
Melanoma
Edg6, PAR-2, mGluR1
Gastric cancer
CXCR-4, P2Y purinoceptor 5
Lymphoma
Beta 2 adrenergic receptor, Edg1, CCR7
While research continues, it is evident that GPCRs are critical in countless biological functions--and disfunctions. While the emphasis is on their role in drug development, it is becoming increasingly clear that G-protein coupled receptors will play a critical role as indicators of disease with diagnostic and prognostic potential. IMGENEX carries over 900 IHC, WB, and flow validated GPCR antibodies. View our complete GPCRs antibody list grouped by class and family. Also see our complete list of Tissue Microarray slides--perfect for GPCR localization.
Find out more information about GPCRs.
Article Source: http://www.articleset.com

You are welcome to publish or reprint this article free of charge, provided:
- you include the entire article, unchanged, including the "About The Author" box
- all hyperlinks remain active, including the bottom ArticleSet.com link (does not apply to print publications)
- you agree not to hold the authors nor ArticleSet.com liable for any loss profits, expenses, or any other damages resulting from the use or misuse of articles published on this website