Progress and Opportunities in Molecular Pathological Epidemiology of Colorectal Premalignant Lesions

被引:48
作者
Lochhead, Paul [1 ]
Chan, Andrew T. [2 ,3 ,4 ]
Giovannucci, Edward [3 ,4 ,5 ,6 ]
Fuchs, Charles S. [3 ,4 ,7 ]
Wu, Kana [6 ]
Nishihara, Reiko [4 ,6 ,7 ]
O'Brien, Michael [8 ]
Ogino, Shuji [4 ,5 ,7 ,9 ]
机构
[1] Univ Aberdeen, Inst Med Sci, Aberdeen AB25 2ZD, Scotland
[2] Massachusetts Gen Hosp, Div Gastroenterol, Boston, MA 02114 USA
[3] Brigham & Womens Hosp, Dept Med, Channing Div Network Med, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Boston, MA USA
[5] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[6] Harvard Univ, Sch Publ Hlth, Dept Nutr, Boston, MA 02115 USA
[7] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[8] Boston Univ, Med Ctr, Dept Pathol, Boston, MA USA
[9] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
关键词
ISLAND METHYLATOR PHENOTYPE; RAS PROTOONCOGENE MUTATION; BETA-CATENIN ALTERATIONS; LIFE-STYLE FACTORS; BODY-MASS INDEX; KRAS CODONS 12; MICROSATELLITE INSTABILITY; COLON-CANCER; CHROMOSOMAL INSTABILITY; BRAF MUTATION;
D O I
10.1038/ajg.2014.153
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Molecular pathological epidemiology (MPE) is an integrative molecular and population health science that addresses the molecular pathogenesis and heterogeneity of disease processes. The MPE of colonic and rectal premalignant lesions (including hyperplastic polyps, tubular adenomas, tubulovillous adenomas, villous adenomas, traditional serrated adenomas, sessile serrated adenomas/sessile serrated polyps, and hamartomatous polyps) can provide unique opportunities for examining the influence of diet, lifestyle, and environmental exposures on specific pathways of carcinogenesis. Colorectal neoplasia can provide a practical model by which both malignant epithelial tumor (carcinoma) and its precursor are subjected to molecular pathological analyses. KRAS, BRAF, and PIK3CA oncogene mutations, microsatellite instability, CpG island methylator phenotype, and LINE-1 methylation are commonly examined tumor biomarkers. Future opportunities include interrogation of comprehensive genomic, epigenomic, or panomic datasets, and the adoption of in vivo pathology techniques. Considering the colorectal continuum hypothesis and emerging roles of gut microbiota and host immunity in tumorigenesis, detailed information on tumor location is important. There are unique strengths and caveats, especially with regard to case ascertainment by colonoscopy. The MPE of colorectal premalignant lesions can identify etiologic exposures associated with neoplastic initiation and progression, help us better understand colorectal carcinogenesis, and facilitate personalized prevention, screening, and therapy.
引用
收藏
页码:1205 / 1214
页数:10
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