Please use this identifier to cite or link to this item:
http://hdl.handle.net/11452/29587
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.date.accessioned | 2022-11-28T08:10:48Z | - |
dc.date.available | 2022-11-28T08:10:48Z | - |
dc.date.issued | 2016-09-30 | - |
dc.identifier.citation | Sevinç, E. D. vd. (2016). "Expression and clinical significance of miRNAs that may be associated with the FHIT gene in breast cancer". Gene, 590(2), 278-284. | en_US |
dc.identifier.issn | 0378-1119 | - |
dc.identifier.issn | 1879-0038 | - |
dc.identifier.uri | https://doi.org/10.1016/j.gene.2016.05.033 | - |
dc.identifier.uri | https://www.sciencedirect.com/science/article/pii/S0378111916304103 | - |
dc.identifier.uri | http://hdl.handle.net/11452/29587 | - |
dc.description.abstract | The dysregulation of miRNA expression has frequently been observed in breast cancer. Therefore, we investigated the expression profile of miRNAs that may be associated with expression of the FHIT gene in breast cancer and assessed their clinicopathological significance. The expression levels of miR-143, miR-663a, miR-668, miR-922 and FHIT were analyzed in normal and malignant breast tissues from 65 patients with breast cancer. We studied the correlation between the expression of miR-143, miR-663a, miR-668, miR-922 and FHIT and the clinicopathological features presented by the patients. The expression levels of the miRNAs and FHIT were downregulated in breast cancer tissue. The expression levels of miR-143, miR-663a and miR-668 were significantly reduced in FHIT downregulated tumors. miR-668 expression was also significantly altered relative to FHIT down- and up- regulated tumor tissues. Reduced miR-663a expression was statistically associated with high-grade ER/PR (+) status, benign reactive hyperplasia, lymph-node metastasis, in-situ component >25% and Ki 67 > 15% compared with non-tumor tissues. Additionally, reduced miR-668 expression was significantly different between tumors with and without lymph-node metastasis. miR-668 may play an important role in breast cancer development and progression by regulating the expression of FHIT. Furthermore, miR-668 and miR-663a may be potential prognostic biomarkers for breast cancer. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Genetics & heredity | en_US |
dc.subject | Breast cancer | en_US |
dc.subject | FHIT | en_US |
dc.subject | miR-143 | en_US |
dc.subject | miR-663a | en_US |
dc.subject | miR-668 | en_US |
dc.subject | miR-922 | en_US |
dc.subject | Cell-proliferation | en_US |
dc.subject | Micrornas | en_US |
dc.subject | Classification | en_US |
dc.subject | Biomarkers | en_US |
dc.subject | Phenotype | en_US |
dc.subject | Rnas | en_US |
dc.subject.mesh | Acid anhydride hydrolases | en_US |
dc.subject.mesh | Adolescent | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Aged | en_US |
dc.subject.mesh | Aged, 80 and over | en_US |
dc.subject.mesh | Breast neoplasms | en_US |
dc.subject.mesh | Computational biology | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Gene expression profiling | en_US |
dc.subject.mesh | Gene expression regulation, neoplastic | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | MicroRNAs | en_US |
dc.subject.mesh | Middle aged | en_US |
dc.subject.mesh | Neoplasm proteins | en_US |
dc.subject.mesh | Young adult | en_US |
dc.title | Expression and clinical significance of miRNAs that may be associated with the FHIT gene in breast cancer | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000381842700011 | tr_TR |
dc.identifier.scopus | 2-s2.0-84976465950 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Biyoloji Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Genel Cerrahi Anabilim Dalı. | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Patoloji Anabilim Dalı. | tr_TR |
dc.relation.bap | UAP(T)-2011/7 | tr_TR |
dc.contributor.orcid | 0000-0002-3820-424X | tr_TR |
dc.contributor.orcid | 0000-0001-7904-883X | tr_TR |
dc.contributor.orcid | 0000-0002-1619-6680 | tr_TR |
dc.identifier.startpage | 278 | tr_TR |
dc.identifier.endpage | 284 | tr_TR |
dc.identifier.volume | 590 | tr_TR |
dc.identifier.issue | 2 | tr_TR |
dc.relation.journal | Gene | en_US |
dc.contributor.buuauthor | Sevinç, Elif Demirdöğen | - |
dc.contributor.buuauthor | Çeçener, Gülşah | - |
dc.contributor.buuauthor | Ak, Seçil | - |
dc.contributor.buuauthor | Tunca, Berrin | - |
dc.contributor.buuauthor | Egeli, Ünal | - |
dc.contributor.buuauthor | Gökgöz, Şehsuvar | - |
dc.contributor.buuauthor | Tolunay, Şahsine | - |
dc.contributor.buuauthor | Taşdelen, İsmet | - |
dc.contributor.researcherid | AAP-9988-2020 | tr_TR |
dc.contributor.researcherid | AAH-1420-2021 | tr_TR |
dc.contributor.researcherid | AAI-1612-2021 | tr_TR |
dc.contributor.researcherid | ABI-6078-2020 | tr_TR |
dc.identifier.pubmed | 27236032 | tr_TR |
dc.subject.wos | Genetics & heredity | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | PubMed | en_US |
dc.wos.quartile | Q3 | en_US |
dc.contributor.scopusid | 56508326500 | tr_TR |
dc.contributor.scopusid | 6508156530 | tr_TR |
dc.contributor.scopusid | 55253485700 | tr_TR |
dc.contributor.scopusid | 6602965754 | tr_TR |
dc.contributor.scopusid | 55665145000 | tr_TR |
dc.contributor.scopusid | 6603238737 | tr_TR |
dc.contributor.scopusid | 6602604390 | tr_TR |
dc.contributor.scopusid | 9637821500 | tr_TR |
dc.subject.scopus | Nucleotide Binding Protein; Histidine; Triad | en_US |
dc.subject.emtree | Estrogen receptor | en_US |
dc.subject.emtree | Fragile histidine triad protein | en_US |
dc.subject.emtree | Ki 67 antigen | en_US |
dc.subject.emtree | MicroRNA | en_US |
dc.subject.emtree | MicroRNA 143 | en_US |
dc.subject.emtree | MicroRNA 663a | en_US |
dc.subject.emtree | MicroRNA 668 | en_US |
dc.subject.emtree | MicroRNA 922 | en_US |
dc.subject.emtree | Progesterone receptor | en_US |
dc.subject.emtree | Unclassified drug | en_US |
dc.subject.emtree | Acid anhydride hydrolase | en_US |
dc.subject.emtree | Fragile histidine triad protein | en_US |
dc.subject.emtree | MicroRNA | en_US |
dc.subject.emtree | Tumor protein | en_US |
dc.subject.emtree | 3' untranslated region | en_US |
dc.subject.emtree | Adult | en_US |
dc.subject.emtree | Aged | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Breast cancer | en_US |
dc.subject.emtree | Cancer prognosis | en_US |
dc.subject.emtree | Cancer tissue | en_US |
dc.subject.emtree | Controlled study | en_US |
dc.subject.emtree | Down regulation | en_US |
dc.subject.emtree | Gene expression profiling | en_US |
dc.subject.emtree | Gene expression regulation | en_US |
dc.subject.emtree | Genetic association | en_US |
dc.subject.emtree | Histopathology | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Human tissue | en_US |
dc.subject.emtree | Hyperplasia | en_US |
dc.subject.emtree | Lymph node metastasis | en_US |
dc.subject.emtree | Major clinical study | en_US |
dc.subject.emtree | Middle aged | en_US |
dc.subject.emtree | Priority journal | en_US |
dc.subject.emtree | Tumor gene | en_US |
dc.subject.emtree | Upregulation | en_US |
dc.subject.emtree | Adolescent | en_US |
dc.subject.emtree | Biology | en_US |
dc.subject.emtree | Breast tumor | en_US |
dc.subject.emtree | Female | en_US |
dc.subject.emtree | Genetics | en_US |
dc.subject.emtree | Metabolism | en_US |
dc.subject.emtree | Pathology | en_US |
dc.subject.emtree | Very elderly | en_US |
dc.subject.emtree | Young adult | en_US |
Appears in Collections: | Scopus Web of Science |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.