Gene expression analysis of early and advanced gastric cancers

被引:69
作者
Vecchi, M.
Nuciforo, P.
Romagnoli, S.
Confalonieri, S.
Pellegrini, C.
Serio, G.
Quarto, M.
Capra, M.
Roviaro, G. C.
Contessini Avesani, E.
Corsi, C.
Coggi, G.
Di Fiore, P. P.
Bosari, S. [1 ]
机构
[1] Univ Milan, Dipartimento Med Chirurgia & Odontoiatria, Osped San Paolo & Fdn IRCCS Osped Maggiore Policl, Pathol Unit, I-20142 Milan, Italy
[2] IFOM Fdn, Ist FIRC Oncol Mol, Milan, Italy
[3] Univ Milan, Fdn IRCCS Osped Maggiore Policlin Mangiagalli & R, Dipartimento Sci Chirurg, Milan, Italy
[4] AO San Paolo, Dipartimento Chirurg & Special Chirurg, Milan, Italy
[5] Ist Europeo Oncol, Dipartimento Oncol Sperimentale, Milan, Italy
[6] Univ Milan, Dipartimento Med Chirurg & Odontoiatria, Milan, Italy
关键词
gastric cancer; early gastric cancer; advanced gastric cancer; gene expression profiling; tissue microarrays; LONG-TERM; MUCOSA; CARCINOGENESIS; METASTASIS; PROFILES; INVASION; CLAUDINS;
D O I
10.1038/sj.onc.1210208
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gastric carcinoma is one of the major causes of cancer mortality worldwide. Early detection results in excellent prognosis for patients with early cancer (EGC), whereas the prognosis of advanced cancer (AGC) patients remains poor. It is not clear whether EGC and AGC are molecularly distinct, and whether they represent progressive stages of the same tumor or different entities ab initio. Gene expression profiles of EGC and AGC were determined by Affymetrix technology and quantitative polymerase chain reaction. Representative regulated genes were further analysed by in situ hybridization (ISH) on tissue microarrays. Expression analysis allowed the identification of a signature that differentiates AGC from EGC. In addition, comparison with normal gastric mucosa indicated that the majority of alterations associated with EGC are retained in AGC, and that further expression changes mark the transition from EGC to AGC. Finally, ISH analysis showed that representative genes, differentially expressed in the invasive areas of EGC and AGC, are not differentially expressed in the non-invasive areas of the same tumors. Our data are more directly compatible with a progression model of gastric carcinogenesis, whereby EGC and AGC may represent different molecular stages of the same tumor. Finally, the identification of an AGC-specific signature might help devising novel therapeutic strategies for advanced gastric cancer.
引用
收藏
页码:4284 / 4294
页数:11
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