Details

Autor(en) / Beteiligte

• Wappenschmidt, B.
• Wardelmann, E.
• Gehrig, A.
• Schöndorf, T.
• Maass, N.
• Bonatz, G.
• Gassel, A.-M.
• Pietsch, T.
• Mallmann, P.
• Weber, B.H.F.
• Schmutzler, R.K.

Titel

PTEN mutations do not cause nuclear β-catenin accumulation in endometrial carcinomas

Ist Teil von

• Human pathology, 2004-10, Vol.35 (10), p.1260-1265

Ort / Verlag

New York, NY: Elsevier Inc

Erscheinungsjahr

2004

Quelle

MEDLINE

Beschreibungen/Notizen

• PTEN and β-catenin mutations constitute the predominant genetic alterations in endometrioid carcinomas of the endometrium. PTEN encodes a dual-specificity phosphatase with lipid phosphatase and protein tyrosine phosphatase activities that regulate both apoptosis and interactions with the extracellular matrix. Recent studies have associated PTEN mutations with tumorigenesis of prostate carcinoma via the Wnt signaling pathway, leading to nuclear β-catenin accumulation. To elucidate the potential interaction of PTEN and β-catenin in endometrial cancer, we performed mutation analyses of the entire PTEN gene and of exon 3 of the β-catenin gene that is most frequently targeted by mutations. A total of 82 endometrial carcinomas comprising 62 type I endometrioid carcinomas and 20 type II high-grade carcinomas were investigated. In addition in a subset of 22 carcinomas, the intracellular β-catenin distribution was analyzed by immunohistochemistry. Overall, 20 (24.4%) of 82 tumors revealed mutations in the PTEN gene, and 16 (19.5%) of 82, in the β-catenin gene. Six tumors (7.3%) showed mutations in both the PTEN and β-catenin gene. Mutations were mainly detected in endometrioid carcinomas of the endometrium. As expected, a striking nuclear accumulation of β-catenin could be shown in tumors with β-catenin mutations. In the vast majority of tumors with PTEN mutations, a regular staining pattern of the cytoplasmic and membranous compartments was found. We therefore conclude that, in contrast to prostate cancer, mutations in the PTEN gene seem not to affect cellular distribution of the β-catenin protein in endometrial carcinomas.