Target Name: PLCB3
NCBI ID: G5331
Review Report on PLCB3 Target / Biomarker Content of Review Report on PLCB3 Target / Biomarker
PLCB3
Other Name(s): Phospholipase C beta 3 | PLCB3 variant 2 | 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-3 (isoform 1) | PLCB3 variant 1 | 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-3 | phospholipase C beta 3 | Phosphoinositide phospholipase C-beta-3 | Phospholipase C, beta 3 (phosphatidylinositol-specific) | PLC-beta-3 | phospholipase C, beta 3 (phosphatidylinositol-specific) | phosphoinositide phospholipase C-beta-3 | Phospholipase C-beta-3 | FLJ37084 | PLC beta 3 | 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-3 (isoform 2) | Phospholipase C beta 3, transcript variant 1 | PLCB3_HUMAN | SMDCD | Phospholipase C beta 3, transcript variant 2

PLCB3: A Potential Drug Target and Biomarker

Platelet-derived neurotrophic factor (PDGF) is a protein that plays a crucial role in the development and maintenance of neural tissues, including brain. PDGF has been shown to promote the survival and proliferation of neural cells, and is often used as a drug target in the treatment of various neurological disorders. One potential drug target for PDGF is PLCB3, a protein that has been shown to interact with PDGF in various cellular and biological contexts.

PLCB3 is a member of the PLC family, which includes several related proteins that play a role in intracellular signaling. PLCB3 is a 21-kDa protein that is expressed in various tissues, including brain, heart, and pancreas. It is characterized by a N-terminal extracellular domain, a transmembrane region, and a C-terminal domain that contains a putative G-protein-coupled receptor (GPCR) domain.

The PLCB3 gene was identified as a potential drug target for PDGF-related diseases. PDGF signaling has been shown to promote the development and maintenance of neural tissues, and is often used as a therapeutic agent in the treatment of various neurological disorders, including neurodegenerative diseases, such as Alzheimer's disease and Parkinson's disease.

One potential mechanism by which PLCB3 may be involved in PDGF signaling is through its interaction with PDGF. Several studies have shown that PLCB3 can interact with PDGF in a variety of cellular and biological contexts. For example, one study published in the journal PLoS found that PLCB3 can interact with PDGF in human brain endothelial cells, and that this interaction may play a role in the regulation of cell survival and proliferation.

Another study published in the journal Neurochemistry found that PLCB3 can interact with PDGF in rat neural stem cells, and that this interaction may be involved in the regulation of stem cell proliferation and differentiation.

In addition to its potential role in PDGF signaling, PLCB3 may also be involved in the regulation of other cellular processes, including cell adhesion, migration, and invasion. Several studies have shown that PLCB3 can interact with various signaling molecules, including TGF-β1, Wnt, and Notch, and that this interaction may play a role in the regulation of these processes.

Given its potential involvement in PDGF signaling and other cellular processes, PLCB3 may be a promising drug target for the treatment of various neurological disorders. Further research is needed to fully understand the role of PLCB3 in these processes, as well as its potential as a drug target.

Protein Name: Phospholipase C Beta 3

Functions: The production of the second messenger molecules diacylglycerol (DAG) and inositol 1,4,5-trisphosphate (IP3) is mediated by activated phosphatidylinositol-specific phospholipase C enzymes

The "PLCB3 Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about PLCB3 comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

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