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Autotaxin-Lysophosphatidate Axis: Promoter of Cancer Development and Possible Therapeutic Implications.
- Source :
-
International journal of molecular sciences [Int J Mol Sci] 2024 Jul 15; Vol. 25 (14). Date of Electronic Publication: 2024 Jul 15. - Publication Year :
- 2024
-
Abstract
- Autotaxin (ATX) is a member of the ectonucleotide pyrophosphate/phosphodiesterase ( ENPP ) family; it is encoded by the ENPP2 gene. ATX is a secreted glycoprotein and catalyzes the hydrolysis of lysophosphatidylcholine to lysophosphatidic acid (LPA). LPA is responsible for the transduction of various signal pathways through the interaction with at least six G protein-coupled receptors, LPA Receptors 1 to 6 (LPAR1-6). The ATX-LPA axis is involved in various physiological and pathological processes, such as angiogenesis, embryonic development, inflammation, fibrosis, and obesity. However, significant research also reported its connection to carcinogenesis, immune escape, metastasis, tumor microenvironment, cancer stem cells, and therapeutic resistance. Moreover, several studies suggested ATX and LPA as relevant biomarkers and/or therapeutic targets. In this review of the literature, we aimed to deepen knowledge about the role of the ATX-LPA axis as a promoter of cancer development, progression and invasion, and therapeutic resistance. Finally, we explored its potential application as a prognostic/predictive biomarker and therapeutic target for tumor treatment.
- Subjects :
- Humans
Animals
Cell Transformation, Neoplastic
Tumor Escape
Drug Resistance, Neoplasm
Disease Progression
Phosphoric Diester Hydrolases genetics
Phosphoric Diester Hydrolases metabolism
Lysophospholipids metabolism
Neoplasms genetics
Neoplasms immunology
Neoplasms metabolism
Neoplasms pathology
Phosphodiesterase Inhibitors therapeutic use
Subjects
Details
- Language :
- English
- ISSN :
- 1422-0067
- Volume :
- 25
- Issue :
- 14
- Database :
- MEDLINE
- Journal :
- International journal of molecular sciences
- Publication Type :
- Academic Journal
- Accession number :
- 39062979
- Full Text :
- https://doi.org/10.3390/ijms25147737