Retinoic acid-inducible orphan G protein-coupled receptor

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Retinoic acid-inducible orphan G protein-coupled receptor (RAI3) is a protein that in humans is encoded by the GPRC5A gene. This receptor is part of the G protein-coupled receptor (GPCR) family, which is one of the largest and most diverse protein families in the mammalian genome. GPCRs play a crucial role in cell signaling and are involved in various physiological processes including sensory perception, immune response, and hormone signaling.

Function[edit | edit source]

The Retinoic acid-inducible orphan G protein-coupled receptor is implicated in mediating the effects of retinoic acid, which is a metabolite of vitamin A involved in cellular growth, differentiation, and apoptosis. Although the precise function of RAI3 remains to be fully elucidated, it is believed to play a role in the regulation of gene expression in response to retinoic acid. This receptor may also be involved in the development and progression of certain cancers, making it a potential target for cancer therapy.

Gene[edit | edit source]

The GPRC5A gene is located on chromosome 12 in humans and consists of multiple exons that encode the RAI3 protein. The gene is expressed in various tissues, with higher expression levels observed in lung and pancreas tissues. The expression of GPRC5A can be induced by retinoic acid, which suggests its role in retinoic acid signaling pathways.

Clinical Significance[edit | edit source]

Alterations in the expression of the GPRC5A gene have been associated with several types of cancers, including lung, breast, and pancreatic cancers. Overexpression or underexpression of RAI3 may influence the progression and metastasis of these cancers. Research is ongoing to understand the potential role of RAI3 as a biomarker for cancer diagnosis and prognosis, as well as its utility as a target for therapeutic interventions.

Research Directions[edit | edit source]

Future research on Retinoic acid-inducible orphan G protein-coupled receptor may focus on elucidating its signaling mechanisms and interactions with other molecules in the retinoic acid pathway. Understanding the structural characteristics of RAI3 and its ligands could also pave the way for the development of novel drugs targeting this receptor. Additionally, studies investigating the role of RAI3 in non-cancerous conditions could further expand our knowledge of its physiological functions.


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Contributors: Prab R. Tumpati, MD