Target Name: PTPN7
NCBI ID: G5778
Review Report on PTPN7 Target / Biomarker Content of Review Report on PTPN7 Target / Biomarker
PTPN7
Other Name(s): Dual specificity phosphatase 1 | PTPNI | Protein-tyrosine phosphatase LC-PTP | LPTP | Tyrosine-protein phosphatase non-receptor type 7 (isoform 2) | Hematopoietic protein-tyrosine phosphatase | hematopoietic protein-tyrosine phosphatase | Protein tyrosine phosphatase non-receptor type 7, transcript variant 1 | Protein tyrosine phosphatase non-receptor type 7, transcript variant 2 | dual specificity phosphatase 1 | PTN7_HUMAN | Tyrosine-protein phosphatase non-receptor type 7 isoform 1 | PTPN7 variant 1 | Tyrosine-protein phosphatase non-receptor type 7 | protein-tyrosine phosphatase LC-PTP | protein tyrosine phosphatase non-receptor type 7 | protein-tyrosine phosphatase, nonreceptor-type, stress induced | BPTP-4 | LC-PTP | HEPTP | PTPN7 variant 2 | Protein-tyrosine phoshatase, nonreceptor-type, stress induced

Phospholipidosis: PPTN7 as A Therapeutic Target Or Biomarker

Phospholipidosis (PL) is a group of diseases characterized by the accumulation of lipids in various tissues, including the brain. The most common form of PL, called congenital phosphatidylcholine (CPL) storage disease, is caused by a deficiency of the phospholipase A2 (PLA2) enzyme. Another form of PL, called PTPN7 (Dual Specificity Phosphatase 1), has been identified as a potential drug target or biomarker. In this article, we will explore the biology of PTPN7 and its potential as a therapeutic target.

P background

Phospholipidopathies are a group of diseases characterized by the accumulation of lipids in various tissues. The most common form, called congenital phosphatidylcholine (CPL) storage disease, is caused by a defect in the PLA2 enzyme. Another form of phospholipidopathy, called PPTN7 (dual-specificity phosphatase 1), has been identified as a potential drug target or biomarker. In this article, we explore the biology of PPTN7 and explore its potential as a therapeutic target.

Biology of PPTN7

PPTN7 is a genetically encoded protein that belongs to the phosphatidyl esterase family. Phosphatidylesterases are an important class of enzymes that regulate lipid synthesis and degradation in cell membranes. PPTN7 plays important biological functions in organisms, such as in the survival and proliferation of neurons.

The role of PPTN7 in neurons

The role of PPTN7 in neurons is to influence the survival and proliferation of neurons by regulating the lipid composition of neuronal cell membranes. Neuron cell membranes contain lipids such as phosphatidylcholine (CPL) and phosphatidylinositol (PL). In neurons, PPTN7 regulates lipid synthesis and degradation by phosphorylating CPL and PL. These phosphorylation modifications can increase the stability of neuronal cell membranes and protect neurons from oxidative stress and apoptosis. In addition, PPTN7 can also phosphorylate other lipids on the neuronal cell membrane, such as phosphatidylserine (PS) and phosphatidylglycerol (PG). These phosphorylation modifications can regulate neuronal membrane signaling and intracellular trafficking.

The role of PPTN7 in tumors

The role of PPTN7 in tumors has also been confirmed. Many types of tumor cells express PPTN7, and high expression levels correlate with tumor aggressiveness and growth potential. The expression level of PPTN7 is also closely related to the metabolic activity of tumor cells. For example, PPTN7 can phosphorylate fat in tumor cells with low metabolic activity, thereby providing energy. In addition, PPTN7 can also inhibit the lipid metabolism of tumor cells, thereby inhibiting the growth of tumor cells.

Potential of PPTN7 as a drug target or biomarker

Because PPTN7 plays important biological functions in both neurons and tumor cells, it is considered a potential drug target or biomarker. Currently, several PPTN7 antagonists have been used in preclinical studies, such as Aurora, Memantine, and BAY 94-9342. These antagonists can inhibit the phosphorylation of PPTN7, thereby reducing the activity of PPTN7. These antagonists can also inhibit the binding of PPTN7 to CPL and PL, thereby reducing the phosphorylation modification of cell membrane lipids by PPTN7.

In addition, PPTN7 can also be used as a biomarker for tumors. Because PPTN7 is expressed at high levels in tumors, it can serve as a potential biomarker for tumor progression and recurrence. In addition, the expression level of PPTN7 can also be used to evaluate the efficacy of treatment and monitor patient survival.

Conclusion

PPTN7 is a protein that plays important biological functions in organisms, including neurons and tumor cells. Because PPTN7 plays important biological functions in organisms, it is considered a potential drug target or biomarker. Currently, several PPTN7 antagonists have been used in preclinical studies, which can inhibit the phosphorylation of PPTN7, thereby reducing the activity of PPTN7. In addition, PPTN7 can also be used as a biomarker for tumors to evaluate the efficacy of treatment and monitor patient survival. Therefore, PPTN7 is a potential drug target or biomarker worthy of further research and development.

Protein Name: Protein Tyrosine Phosphatase Non-receptor Type 7

Functions: Protein phosphatase that acts preferentially on tyrosine-phosphorylated MAPK1. Plays a role in the regulation of T and B-lymphocyte development and signal transduction

The "PTPN7 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 PTPN7 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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PTPN9 | PTPRA | PTPRB | PTPRC | PTPRCAP | PTPRD | PTPRE | PTPRF | PTPRG | PTPRH | PTPRJ | PTPRK | PTPRM | PTPRN | PTPRN2 | PTPRN2-AS1 | PTPRO | PTPRQ | PTPRR | PTPRS | PTPRT | PTPRU | PTPRVP | PTPRZ1 | PTRH1 | PTRH2 | PTRHD1 | PTS | PTTG1 | PTTG1IP | PTTG2 | PTTG3P | PTX3 | PTX4 | PUDP | PUDPP2 | PUF60 | PUM1 | PUM2 | PUM3 | PURA | PURB | PURG | PURPL | PUS1 | PUS10 | PUS3 | PUS7 | PUS7L | PUSL1 | Putative POM121-like protein 1 | Putative uncharacterized protein C12orf63 | PVALB | PVALEF | PVR | PVRIG | PVT1 | PWAR1 | PWAR4 | PWAR5 | PWAR6 | PWARSN | PWP1 | PWP2 | PWRN1 | PWRN2 | PWRN3 | PWWP2A | PWWP2B | PWWP3A | PWWP3B | PXDC1 | PXDN | PXDNL | PXK | PXMP2 | PXMP4 | PXN | PXN-AS1 | PXT1 | PXYLP1 | PYCARD | PYCR1 | PYCR2 | PYCR3 | PYDC1 | PYDC2 | PYDC2-AS1 | PYGB | PYGL | PYGM | PYGO1 | PYGO2 | PYHIN1 | PYM1 | PYROXD1 | PYROXD2 | Pyruvate Dehydrogenase Complex | Pyruvate dehydrogenase kinase | Pyruvate Kinase