Show simple item record

dc.contributor.authorTabasinezhad, M
dc.contributor.authorSamadi, N
dc.contributor.authorGhanbari, P
dc.contributor.authorMohseni, M
dc.contributor.authorSaei, AA
dc.contributor.authorSharifi, S
dc.contributor.authorSaeedi, N
dc.contributor.authorPourhassan, A
dc.date.accessioned2018-08-26T06:05:46Z
dc.date.available2018-08-26T06:05:46Z
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/41854
dc.description.abstractSphingosine-1 phosphate (S1P) is a bioactive lipid that mediates diverse cellular responses. Signaling of S1P is carried out by a family of G-protein coupled receptors (GPCRs), which show differential expression patterns depending on tissue and cell types. Activation of S1P receptors induces signaling pathway, which can subsequently lead to physiological process. Intercellular S1P concentration is regulated and determined by several enzymes including S1P lyase, S1P kinase and S1P phosphatase. Numerous studies showed the role of S1P in malignant behavior of cancer cells including breast, lung, colon, and leukemia cell lines. In the past decade, extensive research activities have focused on elucidating S1P signaling pathway, its receptors, enzymes involved in S1P metabolism, and its performance in cancer biology. In this review, we will explain the function of S1P in tumor progression that demonstrated in past research articles and we will express its importance as a target for designing futuristic anticancer drug.
dc.language.isoEnglish
dc.relation.ispartofJournal of cancer research and therapeutics
dc.subjectCell Movement
dc.subjectCell Proliferation
dc.subjectDisease Progression
dc.subjectDrug Resistance, Neoplasm
dc.subjectHumans
dc.subjectLysophospholipids
dc.subjectNeoplasm Invasiveness
dc.subjectNeoplasm Metastasis
dc.subjectNeoplasms
dc.subjectNeovascularization, Pathologic
dc.subjectReceptors, Lysosphingolipid
dc.subjectSecond Messenger Systems
dc.subjectSignal Transduction
dc.subjectSphingosine
dc.titleSphingosin 1-phosphate contributes in tumor progression.
dc.typearticle
dc.citation.volume9
dc.citation.issue4
dc.citation.spage556
dc.citation.epage63
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.4103/0973-1482.126446


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record