Molecular pathological epidemiology of colorectal neoplasia: an emerging transdisciplinary and interdisciplinary field

被引:448
作者
Ogino, Shuji [1 ,2 ,3 ,4 ]
Chan, Andrew T. [3 ,4 ,5 ]
Fuchs, Charles S. [2 ,3 ,4 ,6 ]
Giovannucci, Edward [3 ,4 ,7 ]
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dana Farber Canc Inst,Dept Pathol, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[3] Canc Epidemiol Program, Boston, MA USA
[4] Dana Farber Harvard Canc Ctr, Gastrointestinal Malignancies Program, Boston, MA USA
[5] Massachusetts Gen Hosp, Gastrointestinal Unit, Boston, MA 02114 USA
[6] Harvard Univ, Sch Med, Brigham & Womens Hosp, Dept Med,Channing Lab, Boston, MA 02115 USA
[7] Harvard Univ, Sch Publ Hlth, Dept Epidemiol & Nutr, Boston, MA 02115 USA
关键词
ISLAND METHYLATOR PHENOTYPE; BODY-MASS INDEX; TUMOR MICROSATELLITE INSTABILITY; LIFE-STYLE FACTORS; III COLON-CANCER; K-RAS MUTATIONS; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; MGMT PROMOTER METHYLATION; ONE-CARBON METABOLISM; FOLIC-ACID SUPPLEMENTATION;
D O I
10.1136/gut.2010.217182
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Colorectal cancer is a complex disease resulting from somatic genetic and epigenetic alterations, including locus-specific CpG island methylation and global DNA or LINE-1 hypomethylation. Global molecular characteristics such as microsatellite instability (MSI), CpG island methylator phenotype (CIMP), global DNA hypomethylation, and chromosomal instability cause alterations of gene function on a genome-wide scale. Activation of oncogenes including KRAS, BRAF and PIK3CA affects intracellular signalling pathways and has been associated with CIMP and MSI. Traditional epidemiology research has investigated various factors in relation to an overall risk of colon and/or rectal cancer. However, colorectal cancers comprise a heterogeneous group of diseases with different sets of genetic and epigenetic alterations. To better understand how a particular exposure influences the carcinogenic and pathologic process, somatic molecular changes and tumour biomarkers have been studied in relation to the exposure of interest. Moreover, an investigation of interactive effects of tumour molecular changes and the exposures of interest on tumour behaviour (prognosis or clinical outcome) can lead to a better understanding of tumour molecular changes, which may be prognostic or predictive tissue biomarkers. These new research efforts represent 'molecular pathologic epidemiology', which is a multidisciplinary field of investigations of the interrelationship between exogenous and endogenous (eg, genetic) factors, tumoural molecular signatures and tumour progression. Furthermore, integrating genome-wide association studies (GWAS) with molecular pathological investigation is a promising area (GWAS-MPE approach). Examining the relationship between susceptibility alleles identified by GWAS and specific molecular alterations can help elucidate the function of these alleles and provide insights into whether susceptibility alleles are truly causal. Although there are challenges, molecular pathological epidemiology has unique strengths, and can provide insights into the pathogenic process and help optimise personalised prevention and therapy. In this review, we overview this relatively new field of research and discuss measures to overcome challenges and move this field forward.
引用
收藏
页码:397 / 411
页数:15
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