Major Apoptotic Mechanisms and Genes Involved in Apoptosis

dc.contributor.author Kiraz, Yağmur
dc.contributor.author Adan, Aysun
dc.contributor.author Kartal Yandım, Melis
dc.contributor.author Baran, Yusuf
dc.coverage.doi 10.1007/s13277-016-5035-9
dc.date.accessioned 2017-08-23T11:42:09Z
dc.date.available 2017-08-23T11:42:09Z
dc.date.issued 2016
dc.description.abstract As much as the cellular viability is important for the living organisms, the elimination of unnecessary or damaged cells has the opposite necessity for the maintenance of homeostasis in tissues, organs and the whole organism. Apoptosis, a type of cell death mechanism, is controlled by the interactions between several molecules and responsible for the elimination of unwanted cells from the body. Apoptosis can be triggered by intrinsically or extrinsically through death signals from the outside of the cell. Any abnormality in apoptosis process can cause various types of diseases from cancer to auto-immune diseases. Different gene families such as caspases, inhibitor of apoptosis proteins, B cell lymphoma (Bcl)-2 family of genes, tumor necrosis factor (TNF) receptor gene superfamily, or p53 gene are involved and/or collaborate in the process of apoptosis. In this review, we discuss the basic features of apoptosis and have focused on the gene families playing critical roles, activation/inactivation mechanisms, upstream/downstream effectors, and signaling pathways in apoptosis on the basis of cancer studies. In addition, novel apoptotic players such as miRNAs and sphingolipid family members in various kind of cancer are discussed. en_US
dc.identifier.citation Kiraz, Y., Adan, A., Kartal Yandım, M., and Baran, Y. (2016). Major apoptotic mechanisms and genes involved in apoptosis. Tumor Biology, 37(7), 8471-8486. doi:10.1007/s13277-016-5035-9 en_US
dc.identifier.doi 10.1007/s13277-016-5035-9 en_US
dc.identifier.doi 10.1007/s13277-016-5035-9
dc.identifier.issn 1423-0380
dc.identifier.issn 1010-4283
dc.identifier.scopus 2-s2.0-84964033724
dc.identifier.uri http://doi.org/10.1007/s13277-016-5035-9
dc.identifier.uri https://hdl.handle.net/11147/6170
dc.language.iso en en_US
dc.publisher SAGE Publications en_US
dc.relation.ispartof Tumor Biology en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Caspase en_US
dc.subject Protein bcl 2 en_US
dc.subject Protein p53 en_US
dc.subject Tumor necrosis factor en_US
dc.title Major Apoptotic Mechanisms and Genes Involved in Apoptosis en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.id 0000-0003-3508-5617
gdc.author.id 0000-0003-3508-5617 en_US
gdc.author.institutional Yağmur, Kiraz
gdc.author.institutional Adan, Aysun
gdc.author.institutional Baran, Yusuf
gdc.bip.impulseclass C2
gdc.bip.influenceclass C3
gdc.bip.popularityclass C2
gdc.coar.access open access
gdc.coar.type text::journal::journal article
gdc.collaboration.industrial false
gdc.description.department İzmir Institute of Technology. Molecular Biology and Genetics en_US
gdc.description.endpage 8486 en_US
gdc.description.issue 7 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q3
gdc.description.startpage 8471 en_US
gdc.description.volume 37 en_US
gdc.identifier.openalex W2325008670
gdc.identifier.pmid 27059734
gdc.identifier.wos WOS:000382174500001
gdc.index.type WoS
gdc.index.type Scopus
gdc.index.type PubMed
gdc.oaire.accesstype GOLD
gdc.oaire.diamondjournal false
gdc.oaire.impulse 158.0
gdc.oaire.influence 1.7759405E-8
gdc.oaire.isgreen false
gdc.oaire.keywords Neoplasms
gdc.oaire.keywords Animals
gdc.oaire.keywords Humans
gdc.oaire.keywords Apoptosis
gdc.oaire.keywords Apoptosis Regulatory Proteins
gdc.oaire.keywords Signal Transduction
gdc.oaire.popularity 2.308032E-7
gdc.oaire.publicfunded false
gdc.oaire.sciencefields 0301 basic medicine
gdc.oaire.sciencefields 0303 health sciences
gdc.oaire.sciencefields 03 medical and health sciences
gdc.openalex.collaboration National
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gdc.opencitations.count 456
gdc.plumx.crossrefcites 387
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gdc.scopus.citedcount 539
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relation.isOrgUnitOfPublication.latestForDiscovery 9af2b05f-28ac-4013-8abe-a4dfe192da5e

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