Your browser doesn't support javascript.
loading
Chromosome 7 Multiplication in EGFR-positive Lung Carcinomas Based on Tissue Microarray Analysis.
Tsiambas, Evangelos; Mastronikolis, Nicholas S; Lefas, Alicia Y; Georgiannos, Stavros N; Ragos, Vasileios; Fotiades, Panagiotis P; Tsoukalas, Nikolaos; Kavantzas, Nikolaos; Karameris, Andreas; Peschos, Dimitrios; Patsouris, Efstratios; Syrigos, Konstantinos.
Affiliation
  • Tsiambas E; Department of IHC & Molecular Biology, 401 GAH, Athens, Greece tsiambasecyto@yahoo.gr.
  • Mastronikolis NS; Department of Pathology, Medical School, University of Athens, Athens, Greece.
  • Lefas AY; Department of ENT, Head and Neck Surgery, Medical School, University of Patras, Patras, Greece.
  • Georgiannos SN; Faculty of Medicine, University of Southampton, Southampton, U.K.
  • Ragos V; Department of Breast Surgery, Blue Cross Hospital Breast Cancer Action Fund, London, U.K.
  • Fotiades PP; Department of Maxillofacial, School of Medicine, University of Ioannina, Ioannina, Greece.
  • Tsoukalas N; Department of Surgery, Leicester General Hospital, Leicester, U.K.
  • Kavantzas N; Department of Oncology, 417 VA Hospital (NIMTS), Athens, Greece.
  • Karameris A; Department of Pathology, Medical School, University of Athens, Athens, Greece.
  • Peschos D; Department of Pathology, 417 VA Hospital (NIMTS), Athens, Greece.
  • Patsouris E; Department of Physiology, Medical School, University of Ioannina, Ioannina, Greece.
  • Syrigos K; Department of Pathology, Medical School, University of Athens, Athens, Greece.
In Vivo ; 31(4): 641-648, 2017.
Article in En | MEDLINE | ID: mdl-28652432
BACKGROUND/AIM: Epidermal growth factor receptor (EGFR) over-activation is observed in significant proportions of non-small cell lung carcinomas (NSCLC). Our aim was to investigate the role of chromosome 7 multiplication with regard to its influence in EGFR expression, combined or not with gene amplification. MATERIALS AND METHODS: Using tissue microarray technology, fifty (n=50) primary NSCLCs were cored and re-embedded into the final recipient block. Immunohistochemistry (IHC) and also chromogenic in situ hybridization (CISH) were performed. RESULTS: EGFR expression at any level was detected in 40/50 (80%) cores. Over-expression was observed in 23/40 (57.5%) cases. Gene amplification was identified in 11/50 (22%) cases whereas chromosome 7 polysomy in 8/50 (16%) cases. Pure chromosome 7 multiplication alone led to low or moderate levels of expression. Overall EGFR expression was correlated with gene (p=0.001) and interestingly with chromosome 7 centromere numerical imbalances (p=0.004). CONCLUSION: EGFR expression is associated not only with amplification, but also with chromosome 7 centromere multiple copies. Chromosome 7 multiplication -due to centromere region amplification or true polysomy- is critical for applying monoclonal antibody targeted therapeutic strategies excluding the pure non-amplified cases.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 7 / Carcinoma, Non-Small-Cell Lung / ErbB Receptors / Aneuploidy Type of study: Prognostic_studies Limits: Aged / Humans / Middle aged Language: En Journal: In Vivo Journal subject: NEOPLASIAS Year: 2017 Document type: Article Affiliation country: Greece Country of publication: Greece

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, Pair 7 / Carcinoma, Non-Small-Cell Lung / ErbB Receptors / Aneuploidy Type of study: Prognostic_studies Limits: Aged / Humans / Middle aged Language: En Journal: In Vivo Journal subject: NEOPLASIAS Year: 2017 Document type: Article Affiliation country: Greece Country of publication: Greece