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Integrin beta 8

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Integrin beta-8 is a protein that in humans is encoded by the ITGB8 gene.[5]

AliasesITGB8, integrin subunit beta 8
End20,415,754 bp[1]
Quick facts ITGB8, Identifiers ...
ITGB8
Identifiers
AliasesITGB8, integrin subunit beta 8
External IDsOMIM: 604160; MGI: 1338035; GeneCards: ITGB8
Orthologs
DatabasesNCBI: entry; OMA: entry
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_002214

NM_177290

RefSeq (protein)

NP_002205

NP_796264

Location (UCSC)Chr 7: 20.33 – 20.42 MbChr 12: 119.12 – 119.2 Mb
PubMed search[3][4]
Wikidata
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Function

This gene is a member of the integrin beta chain family and encodes a single-pass type I membrane protein with a VWFA domain and four cysteine-rich repeats. This protein noncovalently binds to an alpha subunit to form a heterodimeric integrin complex. In general, integrin complexes mediate cell-cell and cell-extracellular matrix interactions and this complex plays a role in human airway epithelial proliferation. Alternatively spliced variants which encode different protein isoforms have been described; however, not all the variants have been fully characterized.[5] Additionally, it has been shown to interact with RhoGDI1 to alter the activation of Rho GTPases to promote Glioblastoma cell invasiveness. Uncoupling the αvβ8-RhoGDI1 interaction has been seen to block GBM cell invasion by hyperactivating Rho GTPases.[6]

Clinical significance

High expression levels of ITGB8 are associated with high angiogenic and poorly invasive glioblastoma tumors. Conversely low expression of ITGB8 correlates with highly invasive but low angiogenic tumors.[7]

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