Oncogene alterations in endometrial carcinosarcomas
| Autor: | José Palacios Calvo, Juan Díaz-Martín, Koen Van de Vijver, Laura Romero-Pérez, María Ángeles López-García, Esther Oliva, Michele Biscuola, María Ángeles Castilla, Xavier Matias-Guiu |
|---|---|
| Přispěvatelé: | Pathologie, RS: GROW - School for Oncology and Reproduction |
| Jazyk: | angličtina |
| Rok vydání: | 2013 |
| Předmět: |
Neuroblastoma RAS viral oncogene homolog
Adult Receptor ErbB-2 PDGFRA medicine.disease_cause Predictive markers Proto-Oncogene Mas Pathology and Forensic Medicine Uterine serous carcinoma Phosphatidylinositol 3-Kinases Growth factor receptor Carcinosarcoma medicine Anaplastic lymphoma kinase Humans Anaplastic Lymphoma Kinase Epidermal growth factor receptor Protein kinase B Aged Aged 80 and over biology Gene Amplification Receptor Protein-Tyrosine Kinases Endometrial carcinosarcomas Oncogenes Middle Aged medicine.disease Endometrial Neoplasms ErbB Receptors Proto-Oncogene Proteins c-kit Mixed Tumor Malignant Cancer research biology.protein Female KRAS Proto-Oncogene Proteins c-akt |
| Zdroj: | Human Pathology, 44(5), 852-859. W B Saunders Co-Elsevier Inc |
| ISSN: | 0046-8177 |
| Popis: | Endometrial carcinosarcomas are aggressive neoplasias composed of high-grade carcinomatous and sarcomatous elements. The pathogenesis and specific genetic alterations underlying these tumors are still not well known. We analyzed alterations in oncogenes involved in the pathogenesis of endometrial carcinomas that might represent predictive markers for specific therapies. Immunohistochemistry for HER2 (tyrosine kinase-type cell surface receptor HER2) and c-KIT (tyrosine-protein kinase Kit) and fluorescence in situ hybridization for EGFR (epidermal growth factor receptor) and ALK (anaplastic lymphoma receptor tyrosine kinase) were carried out for 76 endometrial carcinosarcoma samples on sequential tissue microarray sections. Analysis of 238 mutations across 19 common oncogenes was performed on 34 samples using the Sequenom OncoCarta Panel (Sequenom, Hamburg, Germany). We observed EGFR, HER2, and c-KIT expression in 71%, 1.5%, and 2.7% of tumors, respectively. EGFR amplification was detected in 11 of 76 endometrial carcinosarcomas (14.5%). Four samples showed both amplification and aneuploidy (5.2%). ALK amplification together with chromosome 2 polysomy was found in 1.3% of endometrial carcinosarcomas. In total, 23 mutations in 9 different oncogenes were detected in 15 (44.1%) of 34 endometrial carcinosarcomas. Five endometrial carcinosarcomas (14.7%) had 2 or more mutations. Eleven tumors (32.3%) had mutations affecting the PI3K (phosphoinositide-3-kinase)/AKT (v-akt murine thymoma viral oncogene homolog 1) (6 mutations in PIK3CA (PI3K catalytic alpha polypeptide) and 1 in AKT) and/or RAS/BRAF (serine/threonine-protein kinase B-raf) pathway (3 KRAS [kirsten RAS oncogene homolog], 2 NRAS [neuroblastoma RAS viral oncogene homolog], and 1 BRAF). Mutations in PDGFRA (platelet-derived growth factor receptor, alpha polypeptide) and/or KIT were found in 5 endometrial carcinosarcomas (14.7%). Finally, we found mutations in MET (met proto-oncogene [hepatocyte growth factor receptor]) in 2 tumors (5.9%) and in EGFR in one (2.9%). Our study evidences mutations in oncogenes in endometrial carcinosarcomas that are targets or modulators of response to specific therapies in other human cancers, with PI3K/AKT being the most frequently altered pathway. |
| Databáze: | OpenAIRE |
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