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Cited 3 time in webofscience Cited 3 time in scopus
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Review fam72, glioblastoma multiforme (GBM) and beyondopen access

Authors
Ho, Nguyen Thi ThanhRahane, Chinmay SatishPramanik, SubrataKim, Pok-SonKutzner, ArneHeese, Klaus
Issue Date
Mar-2021
Publisher
MDPI AG
Keywords
Brain cancer; Cell cycle; Differentiation; Glioblastoma; Proliferation; RAS; SRGAP2; Stem cell; TP53
Citation
Cancers, v.13, no.5, pp.1 - 28
Indexed
SCIE
SCOPUS
Journal Title
Cancers
Volume
13
Number
5
Start Page
1
End Page
28
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/142257
DOI
10.3390/cancers13051025
ISSN
2072-6694
Abstract
Neural 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.
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Heese, Klaus
GRADUATE SCHOOL OF BIOMEDICAL SCIENCE AND ENGINEERING (DEPARTMENT OF BIOMEDICAL SCIENCE)
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