Detailed Information

Cited 3 time in webofscience Cited 3 time in scopus
Metadata Downloads

Review fam72, glioblastoma multiforme (GBM) and beyond

Full metadata record
DC Field Value Language
dc.contributor.authorHo, Nguyen Thi Thanh-
dc.contributor.authorRahane, Chinmay Satish-
dc.contributor.authorPramanik, Subrata-
dc.contributor.authorKim, Pok-Son-
dc.contributor.authorKutzner, Arne-
dc.contributor.authorHeese, Klaus-
dc.date.accessioned2022-07-07T00:34:12Z-
dc.date.available2022-07-07T00:34:12Z-
dc.date.created2021-05-11-
dc.date.issued2021-03-
dc.identifier.issn2072-6694-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/142257-
dc.description.abstractNeural stem cells (NSCs) offer great potential for regenerative medicine due to their excellent ability to differentiate into various specialized cell types of the brain. In the central nervous system (CNS), NSC renewal and differentiation are under strict control by the regulation of the pivotal SLIT?ROBO Rho GTPase activating protein 2 (SRGAP2)?Family with sequence similarity to the 72 (FAM72) master gene (i.e., |?SRGAP2?FAM72?|) via a divergent gene transcription activation mechanism. If the gene transcription control unit (i.e., the intergenic region of the two sub?gene units, SRGAP2 and FAM72) gets out of control, NSCs may transform into cancer stem cells and generate brain tumor cells responsible for brain cancer such as glioblastoma multiforme (GBM). Here, we discuss the surveillance of this |?SRGAP2?FAM72?| master gene and its role in GBM, and also in light of FAM72 for diagnosing various types of cancers outside of the CNS.-
dc.language영어-
dc.language.isoen-
dc.publisherMDPI AG-
dc.titleReview fam72, glioblastoma multiforme (GBM) and beyond-
dc.typeArticle-
dc.contributor.affiliatedAuthorHeese, Klaus-
dc.identifier.doi10.3390/cancers13051025-
dc.identifier.scopusid2-s2.0-85101724494-
dc.identifier.wosid000627996400001-
dc.identifier.bibliographicCitationCancers, v.13, no.5, pp.1 - 28-
dc.relation.isPartOfCancers-
dc.citation.titleCancers-
dc.citation.volume13-
dc.citation.number5-
dc.citation.startPage1-
dc.citation.endPage28-
dc.type.rimsART-
dc.type.docTypeReview-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.subject.keywordPlusCELL-CYCLE TRANSCRIPTION-
dc.subject.keywordPlusLONG NONCODING RNAS-
dc.subject.keywordPlusDNA-METHYLATION-
dc.subject.keywordPlusGROWTH-FACTOR-
dc.subject.keywordPlusANTISENSE OLIGONUCLEOTIDE-
dc.subject.keywordPlusMOLECULAR-MECHANISMS-
dc.subject.keywordPlusGENOMIC CHARACTERIZATION-
dc.subject.keywordPlusSIGNALING PATHWAYS-
dc.subject.keywordPlusNEURONAL MIGRATION-
dc.subject.keywordPlusCHEMICAL TOXICITY-
dc.subject.keywordAuthorBrain cancer-
dc.subject.keywordAuthorCell cycle-
dc.subject.keywordAuthorDifferentiation-
dc.subject.keywordAuthorGlioblastoma-
dc.subject.keywordAuthorProliferation-
dc.subject.keywordAuthorRAS-
dc.subject.keywordAuthorSRGAP2-
dc.subject.keywordAuthorStem cell-
dc.subject.keywordAuthorTP53-
dc.identifier.urlhttps://www.mdpi.com/2072-6694/13/5/1025-
Files in This Item
Appears in
Collections
서울 의생명공학전문대학원 > 서울 의생명공학전문대학원 > 1. Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Related Researcher

Researcher Heese, Klaus photo

Heese, Klaus
GRADUATE SCHOOL OF BIOMEDICAL SCIENCE AND ENGINEERING (DEPARTMENT OF BIOMEDICAL SCIENCE)
Read more

Altmetrics

Total Views & Downloads

BROWSE