نمایش پرونده ساده آیتم

dc.contributor.authorShotorbani, SS
dc.contributor.authorBaradarn, B
dc.contributor.authorGhadim, HH
dc.contributor.authorBabaloo, Z
dc.contributor.authorSadat-Hatamnezhad, L
dc.contributor.authorGhareaghaji-Zare, A
dc.contributor.authorShotorbani, BS
dc.contributor.authorAzimi, H
dc.date.accessioned2018-08-26T07:13:38Z
dc.date.available2018-08-26T07:13:38Z
dc.date.issued2017
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/44998
dc.description.abstractContext: MicroRNAs (miRNAs) have recently been found to be important targets for cancer therapy in innate immunity. Such molecules are highly expressed in a wide variety of tumor cells and play an important role in immune responses, such as apoptosis. Evidence Acquisition: We searched PubMed, Medline, Scopus and google scholar databases for the studies published from January, 1998 to October, 2017 with the following keywords: "TLRS", "MicroRNA", "cancer", "HMGB1", and "Melanoma" Results: MiRNAs are mainly classified into 2 different groups, tumor suppressors and oncogenes. MiRNAs are closely related to damage-associated molecular patterns and pathogen-associated molecular patterns through the innate immunity signaling pathways, such as Toll-like receptors (TLRs). This review was carried out to find the relation between melanoma miRNAs with innate immune signaling pathways, such as toll-like receptors and high-mobility group box 1. High-mobility groups (HMG) are danger signal molecules, which can involve damage-associated molecular patterns and manage microRNAs. Conclusions: The important point in this field is that miRNA targeted in the immune defense can regulate inflammatory cytokines and alter cancerous phenotypes.
dc.language.isoEnglish
dc.relation.ispartofINTERNATIONAL JOURNAL OF CANCER MANAGEMENT
dc.subjectToll-Like Receptors
dc.subjectHigh-Mobility Groups
dc.subjectMicroRNAs
dc.subjectMelanoma
dc.titleAssociation of Toll-like Receptors and High-mobility Group Proteins with MicroRNAs in Melanoma
dc.typeReview
dc.citation.volume10
dc.citation.issue12
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.5812/ijcm.11935


فایلهای درون آیتم

فایلهاسایزفرمتنمایش

هیچ فایل مرتبطی وجود ندارد

این آیتم در مجموعه های زیر مشاهده می شود

نمایش پرونده ساده آیتم