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E-cadherin can limit the transforming properties of activating beta-catenin mutations
Canc Res UK Beatson Inst, Glasgow, Lanark, Scotland..
Canc Res UK Beatson Inst, Glasgow, Lanark, Scotland..
Canc Res UK Beatson Inst, Glasgow, Lanark, Scotland..
ASTAR, Inst Med Biol, Singapore, Singapore..
Vise andre og tillknytning
2015 (engelsk)Inngår i: EMBO Journal, ISSN 0261-4189, E-ISSN 1460-2075, Vol. 34, nr 18, s. 2321-2333Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Wnt pathway deregulation is a common characteristic of many cancers. Only colorectal cancer predominantly harbours mutations in APC, whereas other cancer types (hepatocellular carcinoma, solid pseudopapillary tumours of the pancreas) have activating mutations in beta-catenin (CTNNB1). We have compared the dynamics and the potency of beta-catenin mutations in vivo. Within the murine small intestine (SI), an activating mutation of beta-catenin took much longer to achieve Wnt deregulation and acquire a crypt-progenitor cell (CPC) phenotype than Apc or Gsk3 loss. Within the colon, a single activating mutation of beta-catenin was unable to drive Wnt deregulation or induce the CPC phenotype. This ability of beta-catenin mutation to differentially transform the SI versus the colon correlated with higher expression of E-cadherin and a higher number of E-cadherin: beta-catenin complexes at the membrane. Reduction in E-cadherin synergised with an activating mutation of beta-catenin resulting in a rapid CPC phenotype within the SI and colon. Thus, there is a threshold of beta-catenin that is required to drive transformation, and E-cadherin can act as a buffer to sequester mutated beta-catenin.

sted, utgiver, år, opplag, sider
2015. Vol. 34, nr 18, s. 2321-2333
Emneord [en]
APC, beta-catenin, colorectal cancer, E-cadherin
HSV kategori
Identifikatorer
URN: urn:nbn:se:uu:diva-265922DOI: 10.15252/embj.201591739ISI: 000362457500004PubMedID: 26240067OAI: oai:DiVA.org:uu-265922DiVA, id: diva2:867009
Forskningsfinansiär
EU, FP7, Seventh Framework Programme, 278568Tilgjengelig fra: 2015-11-04 Laget: 2015-11-04 Sist oppdatert: 2018-01-10bibliografisk kontrollert

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