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Mechanisms of Lysophosphatidic Acid-Mediated Lymphangiogenesis in Prostate Cancer
- Source :
- Cancers, Vol 10, Iss 11, p 413 (2018), Cancers
- Publication Year :
- 2018
- Publisher :
- MDPI AG, 2018.
-
Abstract
- Prostate cancer (PCa) is the most common noncutaneous cancer in men worldwide. One of its major treatments is androgen deprivation therapy, but PCa frequently relapses as aggressive castration resistant local tumors and distal metastases. Hence, the development of novel agents or treatment modalities for advanced PCa is crucial. Many tumors, including PCa, first metastasize to regional lymph nodes via lymphatic vessels. Recent findings demonstrate that the bioactive lipid lysophosphatidic acid (LPA) promotes PCa progression by regulating vascular endothelial growth factor-C (VEGF-C), a critical mediator of tumor lymphangiogenesis and lymphatic metastasis. Many of the underlying molecular mechanisms of the LPA–VEGF-C axis have been described, revealing potential biomarkers and therapeutic targets that may aid in the diagnosis and treatment of advanced PCa. Herein, we review the literature that illustrates a functional role for LPA signaling in PCa progression. These discoveries may be especially applicable to anti-lymphangiogenic strategies for the prevention and therapy of metastatic PCa.
- Subjects :
- 0301 basic medicine
Cancer Research
LPA receptor
VEGF-C
Review
urologic and male genital diseases
lcsh:RC254-282
Androgen deprivation therapy
03 medical and health sciences
Prostate cancer
chemistry.chemical_compound
Mediator
Lysophosphatidic acid
medicine
business.industry
Cancer
prostate cancer
lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
medicine.disease
Lymphangiogenesis
LPA
lymphangiogenesis
030104 developmental biology
Lymphatic system
Oncology
chemistry
Potential biomarkers
Cancer research
business
Subjects
Details
- ISSN :
- 20726694
- Volume :
- 10
- Database :
- OpenAIRE
- Journal :
- Cancers
- Accession number :
- edsair.doi.dedup.....6e307eeaa4121150541ae735b97d04e7
- Full Text :
- https://doi.org/10.3390/cancers10110413