Molecular alterations in gastric cancer with special reference to the early-onset subtype

Currently, gastric cancer(GC) is one of the most frequently diagnosed neoplasms, with a global burden of 723000 deaths in 2012. It is the third leading cause of cancer-related death worldwide. There are numerous possible factors that stimulate the procarcinogenic activity of important genes. These f...

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Bibliographic Details
Published in:World journal of gastroenterology : WJG Vol. 22; no. 8; pp. 2460 - 2474
Main Authors: Skierucha, Małgorzata, Milne, Anya Na, Offerhaus, G Johan A, Polkowski, Wojciech P, Maciejewski, Ryszard, Sitarz, Robert
Format: Journal Article
Language:English
Published: United States Baishideng Publishing Group Inc 28-02-2016
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Summary:Currently, gastric cancer(GC) is one of the most frequently diagnosed neoplasms, with a global burden of 723000 deaths in 2012. It is the third leading cause of cancer-related death worldwide. There are numerous possible factors that stimulate the procarcinogenic activity of important genes. These factors include genetic susceptibility expressed in a singlenucleotide polymorphism, various acquired mutations(chromosomal instability, microsatellite instability, somatic gene mutations, epigenetic alterations) and environmental circumstances(e.g., helicobcter pylori infection, EBV infection, diet, and smoking). Most of the aforementioned pathways overlap, and authors agree that a clear-cut pathway for GC may not exist. Thus, the categorization of carcinogenic events is complicated. Lately, it has been claimed that research on early-onset gastric carcinoma(EOGC) and hereditary GC may contribute towards unravelling some part of the mystery of the GC molecular pattern because young patients are less exposed to environmental carcinogens and because carcinogenesis in this setting may be more dependent on genetic factors. The comparison of various aspects that differ and coexist in EOGCs and conventional GCs might enable scientists to: distinguish which features in the pathway of gastric carcinogenesisare modifiable, discover specific GC markers and identify a specific target. This review provides a summary of the data published thus far concerning the molecular characteristics of GC and highlights the outstanding features of EOGC.
Bibliography:Ma?gorzata Skierucha;Anya NA Milne;G Johan A Offerhaus;Wojciech P Polkowski;Ryszard Maciejewski;Robert Sitarz;Department of Human Anatomy, Medical University of Lublin;Department of Pathology, Diakonessenhuis;Department of Pathology, H04-312, University Medical Centre Utrecht;Department of Surgical Oncology, Medical University of Lublin
Author contributions: Skierucha M and Sitarz R developed the concept of the research, collected the research data and wrote the paper; Offerhaus GJA, Milne ANA, Polkowski WP and Maciejewski R provided significant content and critically revised the manuscript.
Telephone: +48-661012882 Fax: +48-81-7406149
Correspondence to: Robert Sitarz, MD, PhD, Department of Surgical Oncology, Medical University of Lublin, S. Staszica 11, 20-081 Lublin, Poland. r.sitarz@umlub.pl
ISSN:1007-9327
2219-2840
DOI:10.3748/wjg.v22.i8.2460