PMID- 25203430 OWN - NLM STAT- MEDLINE DCOM- 20151117 LR - 20161020 IS - 1533-4058 (Electronic) IS - 1533-4058 (Linking) VI - 23 IP - 2 DP - 2015 Feb TI - The HER2 gene and HER2 protein status and chromosome 17 polysomy in gastric cancer cells in own material. PG - 113-7 LID - 10.1097/PAI.0000000000000070 [doi] AB - BACKGROUND: The aims of the study were to assess the expression of HER2 protein, the amplification of the HER2 gene, and the occurrence of chromosome 17 polysomy in gastric cancer cells and to analyze the relation between the results of such a determination and the selected clinicopathologic parameters in patients treated for gastric cancer. METHODS: Tissue samples of primary tumor from 83 consecutive patients who underwent gastric cancer resection were analyzed by immunohistochemical (IHC) analysis and fluorescence in situ hybridization (FISH). RESULTS: A positive result of the IHC test, with a minimum score +, was obtained among 22.8% patients. The FISH test was carried out successfully among 58 patients, including 10.3% cases with a positive result, whereas the presence of chromosome 17 polysomy was confirmed among 13.8% patients. A statistically significant dependence was found between the presence of HER2 overexpression and: the lower stage of tumor infiltration, the higher grade of cancer differentiation, no mucinous component, and the intestinal type according to the Lauren classification. Statistically significant relation was found between chromosome 17 polysomy and the tumor location in the proximal part of the stomach, the performance of the palliative procedure, the presence of distant metastases, and a higher frequency of postoperative complications. CONCLUSIONS: There is no complete coincidence in gastric cancer between the occurrence of the HER2 gene amplification and the HER2 receptor expression. The impact of the HER2 gene status and HER2 protein on prognosis in gastric cancer remains unclear. Chromosome 17 polysomy may be an important negative prognostic factor in gastric cancer. FAU - Ciesielski, Maciej AU - Ciesielski M AD - *Department of Oncological Surgery double daggerDivision of Pathomorphology, Gdynia Oncology Centre, Red Cross Maritime Hospital, Gdynia daggerDivision of Propedeutics of Oncology, Medical University of Gdansk, Gdansk, Poland. FAU - Kruszewski, Wieslaw Janusz AU - Kruszewski WJ FAU - Smialek, Urszula AU - Smialek U FAU - Walczak, Jakub AU - Walczak J FAU - Szajewski, Mariusz AU - Szajewski M FAU - Szefel, Jaroslaw AU - Szefel J FAU - Wydra, Jacek AU - Wydra J FAU - Kawecki, Krzysztof AU - Kawecki K LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - Appl Immunohistochem Mol Morphol JT - Applied immunohistochemistry & molecular morphology : AIMM JID - 100888796 RN - 0 (Biomarkers, Tumor) RN - EC 2.7.10.1 (ERBB2 protein, human) RN - EC 2.7.10.1 (Receptor, ErbB-2) SB - IM MH - Adult MH - Aged MH - Aged, 80 and over MH - Biomarkers, Tumor/metabolism MH - Chromosome Duplication MH - Chromosomes, Human, Pair 17/*genetics MH - Female MH - Gene Amplification MH - Humans MH - Immunohistochemistry MH - In Situ Hybridization, Fluorescence MH - Male MH - Middle Aged MH - Neoplasm Metastasis MH - Neoplasm Staging MH - Prognosis MH - Receptor, ErbB-2/genetics/*metabolism MH - Stomach Neoplasms/*diagnosis/pathology EDAT- 2014/09/10 06:00 MHDA- 2015/11/18 06:00 CRDT- 2014/09/10 06:00 PHST- 2014/09/10 06:00 [entrez] PHST- 2014/09/10 06:00 [pubmed] PHST- 2015/11/18 06:00 [medline] AID - 10.1097/PAI.0000000000000070 [doi] PST - ppublish SO - Appl Immunohistochem Mol Morphol. 2015 Feb;23(2):113-7. doi: 10.1097/PAI.0000000000000070.