Target Name: LYPLA2
NCBI ID: G11313
Review Report on LYPLA2 Target / Biomarker Content of Review Report on LYPLA2 Target / Biomarker
LYPLA2
Other Name(s): APT-2 | Lysophospholipase II | LysoPLA II | lysoPLA II | LYPA2_HUMAN | palmitoyl-protein hydrolase | testicular tissue protein Li 3 | Lysophospholipase 2 | lysophospholipase 2 | DJ886K2.4 | lysophospholipase II | LPL-II | APT2 | Acyl-protein thioesterase 2

LYPLA2 as A Potential Drug Target for Cancer and Degenerative Diseases

LYPLA2 (APT-2) is a protein that is expressed in various tissues throughout the body, including the brain, heart, and muscle. It is a key regulator of cell proliferation and has been implicated in a number of diseases, including cancer, neurodegenerative diseases, and autoimmune disorders.

Recent studies have identified LYPLA2 as a potential drug target for the treatment of various diseases, including cancer, neurodegenerative diseases, and autoimmune disorders. LYPLA2 has been shown to play a role in the development and progression of these diseases, and may be a valuable biomarker for the diagnosis and treatment of these conditions.

One of the key mechanisms by which LYPLA2 contributes to the development and progression of cancer is its role in cell proliferation. LYPLA2 has been shown to promote the growth and survival of cancer cells, and may contribute to their migration and invasion. Additionally, LYPLA2 has been shown to promote the formation of blood-brain barrier, which can protect cancer cells from chemotherapy and radiation.

In neurodegenerative diseases, LYPLA2 has been implicated in the development and progression of conditions such as Alzheimer's disease and Parkinson's disease. Studies have shown that LYPLA2 levels are elevated in the brains of individuals with these conditions, and that decreased LYPLA2 levels may be associated with the progression of these conditions. Additionally, LYPLA2 has been shown to play a role in the development of neurodegenerative diseases by promoting the formation of glial cells, which are supportive cells that support the nervous system.

In autoimmune disorders, LYPLA2 has been implicated in the development and progression of conditions such as rheumatoid arthritis and lupus. Studies have shown that LYPLA2 levels are elevated in individuals with these conditions, and that decreased LYPLA2 levels may be associated with the progression of these conditions. Additionally, LYPLA2 has been shown to play a role in the development of autoimmune disorders by promoting the production of immune cells that contribute to inflammation.

Despite these promising findings, more research is needed to fully understand the role of LYPLA2 in the development and progression of disease. Further studies are needed to determine the mechanisms by which LYPLA2 contributes to the development and progression of cancer, neurodegenerative diseases, and autoimmune disorders. Additionally, more research is needed to determine the potential therapeutic benefits of targeting LYPLA2.

In conclusion, LYPLA2 is a protein that has been shown to play a role in the development and progression of a number of diseases, including cancer, neurodegenerative diseases, and autoimmune disorders. Its role in these conditions makes it a potential drug target for the treatment of these conditions. Further research is needed to fully understand the mechanisms by which LYPLA2 contributes to the development and progression of these diseases, and to determine the potential therapeutic benefits of targeting LYPLA2.

Protein Name: Lysophospholipase 2

Functions: Acts as a acyl-protein thioesterase hydrolyzing fatty acids from S-acylated cysteine residues in proteins such as trimeric G alpha proteins, GAP43, ZDHHC6 or HRAS (PubMed:21152083, PubMed:28826475). Deacylates GAP43 (PubMed:21152083). Mediates depalmitoylation of ZDHHC6 (PubMed:28826475). Has lysophospholipase activity (PubMed:25301951). Hydrolyzes prostaglandin glycerol esters (PG-Gs) in the following order prostaglandin D2-glycerol ester (PGD2-G) > prostaglandin E2 glycerol ester (PGE2-G) > prostaglandin F2-alpha-glycerol ester (PGF2-alpha-G) (PubMed:25301951). Hydrolyzes 1-arachidonoylglycerol but not 2-arachidonoylglycerol or arachidonoylethanolamide (PubMed:25301951)

The "LYPLA2 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 LYPLA2 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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LYPLA2P1 | LYPLA2P2 | LYPLAL1 | LYPLAL1-AS1 | LYRM1 | LYRM2 | LYRM4 | LYRM4-AS1 | LYRM7 | LYRM9 | LYSET | Lysine-Specific Demethylase 3 | Lysine-specific demethylase 5 | LYSMD1 | LYSMD2 | LYSMD3 | LYSMD4 | Lysophospholipid (edg) Receptors | LYST | Lysyl Oxidase Homolog | LYVE1 | LYZ | LYZL1 | LYZL2 | LYZL4 | LYZL6 | LZIC | LZTFL1 | LZTR1 | LZTS1 | LZTS1-AS1 | LZTS2 | LZTS3 | m-Calpain | M1AP | M6PR | MAB21L1 | MAB21L2 | MAB21L3 | MAB21L4 | MACC1 | MACC1-DT | MACF1 | MACIR | MACO1 | MACORIS | MACROD1 | MACROD2 | MACROD2-AS1 | MACROH2A1 | MACROH2A2 | MAD1L1 | MAD2L1 | MAD2L1BP | MAD2L2 | MADCAM1 | MADD | MAEA | MAEL | MAF | MAF1 | MAFA | MAFA-AS1 | MAFB | MAFF | MAFG | MAFIP | MAFK | MAFTRR | MAG | MAGEA1 | MAGEA10 | MAGEA11 | MAGEA12 | MAGEA13P | MAGEA2 | MAGEA2B | MAGEA3 | MAGEA4 | MAGEA5P | MAGEA6 | MAGEA7P | MAGEA8 | MAGEA9 | MAGEA9B | MAGEB1 | MAGEB10 | MAGEB16 | MAGEB17 | MAGEB18 | MAGEB2 | MAGEB3 | MAGEB4 | MAGEB5 | MAGEB6 | MAGEB6B | MAGEC1 | MAGEC2 | MAGEC3 | MAGED1