Title |
Targeting 20-HETE producing enzymes in cancer – rationale, pharmacology, and clinical potential
|
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Published in |
OncoTargets and therapy, March 2013
|
DOI | 10.2147/ott.s31586 |
Pubmed ID | |
Authors |
Anna Alexanian, Andrey Sorokin |
Abstract |
Studies demonstrate that lipid mediator 20-Hydroxyeicosatetraenoic acid (20-HETE) synthesis and signaling are associated with the growth of cancer cells in vitro and in vivo. Stable 20-HETE agonists promote the proliferation of cancer cells, whereas selective inhibitors of the 20-HETE-producing enzymes of the Cytochrome (CYP450)4A and CYP4F families can block the proliferation of glioblastoma, prostate, renal cell carcinoma, and breast cancer cell lines. A recent observation that the expression of CYP4A/4F genes was markedly elevated in thyroid, breast, colon, and ovarian cancer further highlights the significance of 20-HETE-producing enzymes in the progression of different types of human cancer. These findings provide the rationale for targeting 20-HETE-producing enzymes in human cancers and set the basis for the development of novel therapeutic strategies for anticancer treatment. |
X Demographics
Geographical breakdown
Country | Count | As % |
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Unknown | 1 | 100% |
Demographic breakdown
Type | Count | As % |
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Practitioners (doctors, other healthcare professionals) | 1 | 100% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
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South Africa | 1 | 3% |
Unknown | 36 | 97% |
Demographic breakdown
Readers by professional status | Count | As % |
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Researcher | 8 | 22% |
Student > Doctoral Student | 6 | 16% |
Student > Master | 6 | 16% |
Student > Ph. D. Student | 4 | 11% |
Student > Bachelor | 2 | 5% |
Other | 3 | 8% |
Unknown | 8 | 22% |
Readers by discipline | Count | As % |
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Agricultural and Biological Sciences | 8 | 22% |
Biochemistry, Genetics and Molecular Biology | 7 | 19% |
Medicine and Dentistry | 5 | 14% |
Pharmacology, Toxicology and Pharmaceutical Science | 2 | 5% |
Chemistry | 2 | 5% |
Other | 5 | 14% |
Unknown | 8 | 22% |