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- W145418268 abstract "Metastasis is a complex process composed of sequential events involving host celltumor cell interactions, which enable tumor cells to disseminate from the primary site to distant locations (1). To successfully establish a secondary metastatic colony, tumor cells must be able to overcome all of the steps in the metastatic cascade, including detachment, intravasation, arrest, extravasation and proliferation. Ample cell-host interactions, such as tumor cell-platelet, tumor cell-endothelial cell and tumor cell-matrix protein interaction, are influenced by positive and negative regulatory factors. Eicosanoids and other bioactive lipids have been shown to be involved in various aspects of neoplasia including cell transformation, proliferation, apoptosis, invasion and metastasis. Platelets and endothelial cells with which tumor cells interaction during hematogenous metastasis are capable of producing a vast array of lipid mediators by either direct or transcellular metabolism of precursors. Platelets and some tumor cells are capable of converting arachidonic acid (AA) through the 12-lipoxygenase (12-LOX) pathway into 12(S)-hydroxyeicosatetraenoic acid (12(S)-HETE). A large collection of experimental data suggest that 12(S)-HETE plays a pivotal role in multiple steps of the metastatic cascade encompassing tumor cell-vasculature interaction, tumor cell motility, proteolysis, invasion, and angiogenesis. In this review we summarize the effects of 12(S)-HETE in modulating tumor metastasis." @default.
- W145418268 created "2016-06-24" @default.
- W145418268 creator A5044817021 @default.
- W145418268 creator A5046194281 @default.
- W145418268 date "1999-01-01" @default.
- W145418268 modified "2023-09-27" @default.
- W145418268 title "12(S)-HETE in Cancer Metastasis" @default.
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- W145418268 doi "https://doi.org/10.1007/978-1-4615-4861-4_17" @default.
- W145418268 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/10086194" @default.
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