Comparison of gene-expression profiles between diffuse- and intestinal-type gastric cancers using a genome-wide cdna microarray

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ABSTRACT Gastric cancer is the fourth leading cause of cancer-related death in the world. Two histologically distinct types of gastric carcinoma, ‘intestinal’ and ‘diffuse’, have different


epidemiological and pathophysiological features that suggest different mechanisms of carcinogenesis. A number of studies have investigated intestinal-type gastric cancers at the molecular


level, but little is known about mechanisms involved in the diffuse type, which has a more invasive phenotype and poorer prognosis. To clarify the mechanisms that underlie its development


and/or progression, we compared the expression profiles of 20 laser-microbeam-microdissected diffuse-type gastric-cancer tissues with corresponding noncancerous mucosae by means of a cDNA


microarray containing 23 040 genes. We identified 153 genes that were commonly upregulated and more than 1500 that were commonly downregulated in the tumors. We also identified a number of


genes related to tumor progression. Furthermore, comparison of the expression profiles of diffuse-type with those of intestinal-type gastric cancers identified 46 genes that may represent


distinct molecular signatures of each histological type. The putative signature of diffuse-type cancer exhibited altered expression of genes related to cell–matrix interaction and


extracellular-matrix (ECM) components, whereas that of intestinal-type cancer represented enhancement of cell growth. These data provide insight into different mechanisms underlying gastric


carcinogenesis and may also serve as a starting point for identifying novel diagnostic markers and/or therapeutic targets for diffuse-type gastric cancers. Access through your institution


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BIOMARKERS AND REPURPOSED DRUGS FOR GASTRIC ADENOCARCINOMA-RELATED GASTRIC INTESTINAL METAPLASIA Article Open access 04 November 2024 REFERENCES * Balkwill F . (2003). _Semin. Immunol._, 15,


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144–148. Download references ACKNOWLEDGEMENTS We thank Ms Tae Makino for technical assistance, Ms Emi Ichihashi for data analysis, Dr Naoki Oyaizu for reviewing the pathological data of


samples, Dr Arimichi Takabayashi, Dr Koichi Matsuo, Dr Akira Togashi, Dr Kazutaka Obama, Dr Takefumi Kikuchi, Dr Toshihiko Nishidate and Dr Soji Kakiuchi for helpful discussions and Dr Meiko


Takahashi for preparation of the manuscript. This work was supported in part by Research for the Future Program Grant (00L01402) from the Japan Society for the Promotion of Science. AUTHOR


INFORMATION AUTHORS AND AFFILIATIONS * Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, The University of Tokyo, Tokyo, Japan Natini Jinawath, Yoichi


Furukawa, Suguru Hasegawa, Meihua Li & Yusuke Nakamura * SNP Research Center, RIKEN (Institute of Physical and Chemical Research), Tokyo, Japan Tatsuhiko Tsunoda * Department of


Gastroenterological Surgery, Kyoto University Graduate School of Medicine, Kyoto, Japan Seiji Satoh * Department of Surgery, Cancer Institute Hospital, Tokyo, Japan Toshiharu Yamaguchi *


Department of Surgery, Sakai City Hospital, Osaka, Japan Hiroshi Imamura * Department of Surgery, Nara Hospital, Kinki University, School of Medicine, Nara, Japan Masatomo Inoue * Department


of Surgery, Sayama Hospital, Kinki University, School of Medicine, Osaka, Japan Hitoshi Shiozaki Authors * Natini Jinawath View author publications You can also search for this author


inPubMed Google Scholar * Yoichi Furukawa View author publications You can also search for this author inPubMed Google Scholar * Suguru Hasegawa View author publications You can also search


for this author inPubMed Google Scholar * Meihua Li View author publications You can also search for this author inPubMed Google Scholar * Tatsuhiko Tsunoda View author publications You can


also search for this author inPubMed Google Scholar * Seiji Satoh View author publications You can also search for this author inPubMed Google Scholar * Toshiharu Yamaguchi View author


publications You can also search for this author inPubMed Google Scholar * Hiroshi Imamura View author publications You can also search for this author inPubMed Google Scholar * Masatomo


Inoue View author publications You can also search for this author inPubMed Google Scholar * Hitoshi Shiozaki View author publications You can also search for this author inPubMed Google


Scholar * Yusuke Nakamura View author publications You can also search for this author inPubMed Google Scholar CORRESPONDING AUTHOR Correspondence to Yusuke Nakamura. ADDITIONAL INFORMATION


Supplementary Information accompanies the paper on Oncogene website (http://www.nature.com/onc) SUPPLEMENTARY INFORMATION SUPPLEMENTARY MATERIAL: 1 (PDF 38 KB) SUPPLEMENTARY MATERIAL: 2 (PDF


239 KB) RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Jinawath, N., Furukawa, Y., Hasegawa, S. _et al._ Comparison of gene-expression profiles between


diffuse- and intestinal-type gastric cancers using a genome-wide cDNA microarray. _Oncogene_ 23, 6830–6844 (2004). https://doi.org/10.1038/sj.onc.1207886 Download citation * Received: 27


November 2003 * Revised: 12 May 2004 * Accepted: 14 May 2004 * Published: 26 July 2004 * Issue Date: 02 September 2004 * DOI: https://doi.org/10.1038/sj.onc.1207886 SHARE THIS ARTICLE Anyone


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the Springer Nature SharedIt content-sharing initiative KEYWORDS * diffuse-type gastric cancer * cDNA microarray * laser-microbeam microdissection * expression profile