The Role of Connexins in Breast Cancer: From Misregulated Cell Communication To Aberrant Intracellular Signaling

dc.contributor.author Ünal, Yağmur Ceren
dc.contributor.author Yavuz, Büşra
dc.contributor.author Özçivici, Engin
dc.contributor.author Meşe Özçivici, Gülistan
dc.date.accessioned 2021-11-06T09:46:57Z
dc.date.available 2021-11-06T09:46:57Z
dc.date.issued 2022
dc.description.abstract In spite of clinical advancements and improved diagnostic techniques, breast cancers are the leading cause of cancer-associated deaths in women worldwide. Although 70% of early breast cancers can be cured, there are no efficient therapies against metastatic breast cancers. Several factors including connexins and gap junctions play roles in breast tumorigenesis. Connexins are critical for cellular processes as a linkage between connexin mutations and hereditary disorders demonstrated their importance for tissue homeostasis. Further, alterations in their expression, localization and channel activities were observed in many cancers including breast cancer. Both channel-dependent and independent functions of connexins were reported in initiation and progression of cancers. Unlike initial reports suggesting tumor suppressor functions, connexins and gap junctions have stage, context and isoform dependent effects in breast cancers similar to other cancers. In this review, we tried to describe the current understanding of connexins in tumorigenesis specifically in breast cancers. en_US
dc.description.sponsorship Scientific and Technological Research Council of TurkeyTurkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) [114Z874, 119Z294]; Turkish Academy of SciencesTurkish Academy of Sciences en_US
dc.description.sponsorship Financial supports by The Scientific and Technological Research Council of Turkey (114Z874 and 119Z294 to GM) and The Young Investigator Award by the Turkish Academy of Sciences (GM) are highly appreciated. We would like to apologize to the researchers whose studies could not be included due to space constraints. en_US
dc.identifier.doi 10.1080/21688370.2021.1962698
dc.identifier.issn 2168-8370
dc.identifier.scopus 2-s2.0-85112658477
dc.identifier.uri https://doi.org/10.1080/21688370.2021.1962698
dc.identifier.uri https://hdl.handle.net/11147/11346
dc.language.iso en en_US
dc.publisher Taylor & Francis en_US
dc.relation.ispartof Tissue Barriers en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Connexin en_US
dc.subject Gap junctions (Cell biology) en_US
dc.subject GJIC en_US
dc.subject Breast cancer en_US
dc.subject Cancer cells en_US
dc.title The Role of Connexins in Breast Cancer: From Misregulated Cell Communication To Aberrant Intracellular Signaling en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id 0000-0003-4464-0475
gdc.bip.impulseclass C5
gdc.bip.influenceclass C5
gdc.bip.popularityclass C4
gdc.coar.access metadata only access
gdc.coar.type text::journal::journal article
gdc.collaboration.industrial false
gdc.description.department İzmir Institute of Technology. Bioengineering en_US
gdc.description.department İzmir Institute of Technology. Molecular Biology and Genetics en_US
gdc.description.publicationcategory Diğer en_US
gdc.description.scopusquality Q1
gdc.description.volume 10
gdc.description.wosquality Q2
gdc.identifier.openalex W3190424751
gdc.identifier.pmid 34355641
gdc.identifier.wos WOS:000682487700001
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed
gdc.oaire.diamondjournal false
gdc.oaire.impulse 4.0
gdc.oaire.influence 2.779701E-9
gdc.oaire.isgreen true
gdc.oaire.keywords Gap Junctions
gdc.oaire.keywords Humans
gdc.oaire.keywords Breast Neoplasms
gdc.oaire.keywords Female
gdc.oaire.keywords Cell Communication
gdc.oaire.keywords Connexins
gdc.oaire.keywords Signal Transduction
gdc.oaire.popularity 5.724611E-9
gdc.oaire.publicfunded false
gdc.oaire.sciencefields 0301 basic medicine
gdc.oaire.sciencefields 03 medical and health sciences
gdc.openalex.collaboration National
gdc.openalex.fwci 0.58519456
gdc.openalex.normalizedpercentile 0.62
gdc.opencitations.count 6
gdc.plumx.crossrefcites 3
gdc.plumx.mendeley 30
gdc.plumx.pubmedcites 4
gdc.plumx.scopuscites 8
gdc.scopus.citedcount 8
gdc.wos.citedcount 8
relation.isAuthorOfPublication.latestForDiscovery 0fe91b63-51f9-4201-90a3-132b1f2c627c
relation.isOrgUnitOfPublication.latestForDiscovery 9af2b05f-28ac-4015-8abe-a4dfe192da5e

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