Field cancerisation in colorectal cancer: A new frontier or pastures past?

被引:34
作者
Patel, Abhilasha [1 ]
Tripathi, Gyanendra [2 ]
Gopalakrishnan, Kishore [3 ]
Williams, Nigel [1 ]
Arasaradnam, Ramesh P. [2 ]
机构
[1] Univ Hosp Coventry & Warwickshire NHS Trust, Dept Colorectal Surg, Coventry CV2 2DX, W Midlands, England
[2] Univ Warwick, Coventry CV4 7AL, W Midlands, England
[3] Univ Hosp Coventry & Warwickshire NHS Trust, Dept Pathol, Coventry CV2 2DX, W Midlands, England
关键词
Colorectal cancer; Carcinogenesis; Biomarkers; Epigenetics; Synchronous; NORMAL COLONIC-MUCOSA; TRANSITIONAL MUCOSA; CELL-PROLIFERATION; CLINICAL-IMPLICATIONS; TUMOR PROGRESSION; CLONAL EVOLUTION; GENE-EXPRESSION; CRYPT FISSION; IN-VIVO; ADJACENT;
D O I
10.3748/wjg.v21.i13.3763
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Despite considerable advances in our understanding of cancer biology, early diagnosis of colorectal cancer remains elusive. Based on the adenoma-carcinoma sequence, cancer develops through the progressive accumulation of mutations in key genes that regulate cell growth. However, recent mathematical modelling suggests that some of these genetic events occur prior to the development of any discernible histological abnormality. Cells acquire pro-tumourigenic mutations that are not able to produce morphological change but predispose to cancer formation. These cells can grow to form large patches of mucosa from which a cancer arises. This process has been termed "field cancerisation". It has received little attention in the scientific literature until recently. Several studies have now demonstrated cellular, genetic and epigenetic alterations in the macroscopically normal mucosa of colorectal cancer patients. In some reports, these changes were effectively utilised to identify patients with a neoplastic lesion suggesting potential application in the clinical setting. In this article, we present the scientific evidence to support field cancerisation in colorectal cancer and discuss important limitations that require further investigation. Characterisation of the field defect is necessary to enable early diagnosis of colorectal cancer and identify molecular targets for chemoprevention. Field cancerisation offers a promising prospect for experimental cancer research and has potential to improve patient outcomes in the clinical setting.
引用
收藏
页码:3763 / 3772
页数:10
相关论文
共 84 条
[1]   Karyometry of the colonic mucosa [J].
Alberts, David S. ;
Einspahr, Janine G. ;
Krouse, Robert S. ;
Prasad, Anil ;
Ranger-Moore, James ;
Hamilton, Peter ;
Ismail, Ayaaz ;
Lance, Peter ;
Goldschmid, Steven ;
Hess, Lisa M. ;
Yozwiak, Michael ;
Bartels, Hubert G. ;
Bartels, Peter H. .
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2007, 16 (12) :2704-2716
[2]  
Amerongen AVN, 1998, BIOL CHEM, V379, P1
[3]   RECTAL EPITHELIAL-CELL PROLIFERATION PATTERNS AS PREDICTORS OF ADENOMATOUS COLORECTAL POLYP RECURRENCE [J].
ANTI, M ;
MARRA, G ;
ARMELAO, F ;
PERCESEPE, A ;
FICARELLI, R ;
RICCIUTO, GM ;
VALENTI, A ;
RAPACCINI, GL ;
DEVITIS, I ;
DAGOSTINO, G ;
BRIGHI, S ;
VECCHIO, FM .
GUT, 1993, 34 (04) :525-530
[4]   Severe imbalance of cell proliferation and apoptosis in the left colon and in the rectosigmoid tract in subjects with a history of large adenomas [J].
Anti, M ;
Armuzzi, A ;
Morini, S ;
Iascone, E ;
Pignataro, G ;
Coco, C ;
Lorenzetti, R ;
Paolucci, M ;
Covino, M ;
Gasbarrini, A ;
Vecchio, FM ;
Gasbarrini, G .
GUT, 2001, 48 (02) :238-246
[5]   Advances in Biophotonics Detection of Field Carcinogenesis for Colon Cancer Risk Stratification [J].
Backman, Vadim ;
Roy, Hemant K. .
JOURNAL OF CANCER, 2013, 4 (03) :251-261
[6]   A "field change" of inhibited apoptosis occurs in colorectal mucosa adjacent to colorectal adenocarcinoma [J].
Badvie, S. ;
Hanna-Morris, A. ;
Andreyev, H. J. N. ;
Cohen, P. ;
Saini, S. ;
Allen-Mersh, T. G. .
JOURNAL OF CLINICAL PATHOLOGY, 2006, 59 (09) :942-946
[7]   Epigenetic Silencing of miR-137 Is an Early Event in Colorectal Carcinogenesis [J].
Balaguer, Francesc ;
Link, Alexander ;
Lozano, Juan Jose ;
Cuatrecasas, Miriam ;
Nagasaka, Takeshi ;
Boland, C. Richard ;
Goel, Ajay .
CANCER RESEARCH, 2010, 70 (16) :6609-6618
[8]  
Bedi GC, 1996, CANCER RES, V56, P2484
[9]   Profiling CpG island field methylation in both morphologically normal and neoplastic human colonic mucosa [J].
Belshaw, N. J. ;
Elliott, G. O. ;
Foxall, R. J. ;
Dainty, J. R. ;
Pal, N. ;
Coupe, A. ;
Garg, D. ;
Bradburn, D. M. ;
Mathers, J. C. ;
Johnson, I. T. .
BRITISH JOURNAL OF CANCER, 2008, 99 (01) :136-142
[10]  
Bernstein C, 1999, CANCER RES, V59, P2353