Epidermal growth factor receptor domain II, IV, and kinase domain mutations in human solid tumors |
| |
Authors: | Harri Sihto Marjut Puputti Laura Pulli Olli Tynninen Walter Koskinen Leena-Maija Aaltonen Minna Tanner Tom Böhling Tapio Visakorpi Ralf Bützow Aija Knuuttila Nina N. Nupponen Heikki Joensuu |
| |
Affiliation: | (1) Laboratory of Molecular Oncology, Room B426B, 4th floor, Biomedicum, Haartmaninkatu 8, P.O. Box 700, 00029 Helsinki, Finland;(2) Department of Pathology, Helsinki University Central Hospital (HUSLAB) and University of Helsinki, Haartmaninkatu 3, 00014 Helsinki, Finland;(3) Otorhinolaryngology-Head and Neck Surgery, Helsinki University Central Hospital, P.O. Box 220, 00029 HUS, Finland;(4) Department of Pulmonary Medicine, Helsinki University Central Hospital, P.O. Box 220, 00029 HUS, Finland;(5) Department of Oncology, Tampere University Central Hospital, P.O. Box 2000, 33521 Tampere, Finland;(6) Institute of Medical Technology, University of Tampere and Tampere University Hospital, Biokatu 6, 33520 Tampere, Finland;(7) Department of Oncology, Helsinki University Central Hospital, Haartmaninkatu 4, P.O. Box 180, 00029 Helsinki, Finland |
| |
Abstract: | Mutations that may predict response to adenosine 5-triphosphate (ATP)-mimetic epidermal growth factor receptor (EGFR) inhibitors occur in the EGFR kinase domain in lung adenocarcinomas and bronchioloalveolar carcinomas (BACs). Data on the frequency of EGFR mutations are sparse in other human tumors. Apart from the deletion mutant EGFRvIII, little is known about the frequency of mutations that encode for the EGFR extracellular domains II and IV that participate in receptor dimerization and formation of the tethered (autoinhibited) receptor conformation. We investigated 566 human neoplasms consisting of various histological types for mutations in exons 6, 7 (encode domain II), 14, 15 (domain IV), 18, 19, and 21 (the kinase domain) using denaturing high-performance liquid chromatography (DHPLC). Approximately 4,500 EGFR exons were screened for the presence of a mutation, and samples with an abnormal finding in DHPLC were sequenced. Only one mutation was found in the extracellular domain IV (glioblastoma), and none in domain II. Eight (11%) out of the 40 lung adenocarcinomas, or 33 BACs, investigated had exon 19 or 21 mutation in the kinase domain, but no mutations were found in other tumor types. Most of the lung cancers with mutated EGFR had three to six copies of the mutated gene in fluorescence in situ hybridization. We conclude that mutations of the EGFR kinase domain and the cysteine-rich extracellular domains are infrequent in most types of human cancer apart from lung adenocarcinoma. Mutated EGFR is usually not amplified in lung cancer. |
| |
Keywords: | Epidermal growth factor receptor Tyrosine kinase receptors Lung neoplasms Glioblastoma Mutation |
本文献已被 PubMed SpringerLink 等数据库收录! |
|