Further Study on Field Cancerization in the Human Colon

被引:1
作者
Rubio, Carlos A. [1 ,2 ,4 ,5 ]
Lang-Schwarz, Corinna [3 ]
Vieth, Michael [3 ]
机构
[1] Karolinska Inst, Dept Pathol, Stockholm, Sweden
[2] Univ Hosp, Stockholm, Sweden
[3] Friedrich Alexander Univ, Inst Pathol, Klinikum Bayreuth, Bayreuth, Germany
[4] Karolinska Inst, Dept Pathol, S-17176 Stockholm, Sweden
[5] Univ Hosp, S-17176 Stockholm, Sweden
关键词
Field cancerization; colon; nondysplastic crypts; crypt branching; tubular adenomas; SMALL-INTESTINE; CRYPT FISSION; ADJACENT; CARCINOMA; TRACT;
D O I
10.21873/anticanres.16098
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: Nearly 70 years ago, Slaughter launched the hypothesis of field cancerization for oral carcinomas; that hypothesis was subsequently also claimed for carcinomas in other organs. We previously found in the colon mucosa adjacent to nonpolypoid adenomas, branching crypts lined by normal epithelium (BCNE). Here, we explored whether BCNE could also be found in the colon mucosa adjacent to sporadic polypoid tubular adenomas (TA), the most prevalent of all colon adenomas. Patients and Methods: Nondysplastic mucosa adjacent to TA was found in 103 out of 131 TA. All BCNE adjacent to TA were recorded. Results: In 98 (95.1%) out of 103 TA having nondysplastic adjacent mucosa, 645 BCNE were registered: 82.6% were in asymmetric branching and 17.4% in symmetric branching. Thus, BCNE in asymmetric branching predominated. The frequency of BCNE adjacent to TA was influenced by the adenoma size and degree of dysplasia severity. Contrarywise, the frequency of BCNE adjacent to TA was neither influenced by the age or sex of the patients, nor by the colon localization of TA. Conclusion: BCNE often occur in the normal mucosa adjacent to TA. BCNE emerge as integral components of TA. The majority of the BCNE were in asymmetric branching, considered as aberrations of cryptogenesis. We propose that the accretion of asymmetric BCNE adjacent to TA supports Slaughter's hypothesis of field cancerization.
引用
收藏
页码:5891 / 5895
页数:5
相关论文
共 34 条
[1]  
BENNER SE, 1992, CANCER RES, V52, pS2758
[2]   Second primary tumors and field cancerization in oral and oropharyngeal cancer: Molecular techniques provide new insights and definitions [J].
Braakhuis, BJM ;
Tabor, MP ;
Leemans, CR ;
van der Waal, I ;
Snow, GB ;
Brakenhoff, RH .
HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK, 2002, 24 (02) :198-206
[3]  
Braakhuis BJM, 2003, CANCER RES, V63, P1727
[4]   Risk factors for right colon, left colon and rectal cancers differ between men and women: the population-based HUNT study in Norway [J].
Brenne, Siv S. ;
Ness-Jensen, Eivind ;
Edna, Tom-Harald ;
Lydersen, Stian ;
Laugsand, Eivor A. .
COLORECTAL DISEASE, 2023, 25 (01) :44-55
[5]   Nanoscale changes in chromatin organization represent the initial steps of tumorigenesis: a transmission electron microscopy study [J].
Cherkezyan, Lusik ;
Stypula-Cyrus, Yolanda ;
Subramanian, Hariharan ;
White, Craig ;
Dela Cruz, Mart ;
Wali, Ramesh K. ;
Goldberg, Michael J. ;
Bianchi, Laura K. ;
Roy, Hemant K. ;
Backman, Vadim .
BMC CANCER, 2014, 14
[6]   TURNOVER AND SHEDDING OF EPITHELIAL CELLS .1. TURNOVER IN GASTRO-INTESTINAL TRACT [J].
CREAMER, B ;
SHORTER, RG ;
BAMFORTH, J .
GUT, 1961, 2 (02) :110-&
[7]   Crypt fission peaks early during infancy and crypt hyperplasia broadly peaks during infancy and childhood in the small intestine of humans [J].
Cummins, Adrian G. ;
Catto-Smith, Anthony G. ;
Cameron, Donald J. ;
Couper, Richard T. ;
Davidson, Geoffrey P. ;
Day, Andrew S. ;
Hammond, Paul D. ;
Moore, David J. ;
Thompson, Fiona M. .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 2008, 47 (02) :153-157
[8]  
Dahl J., 2007, HISTOLOGY PATHOLOGIS, VThird, P629
[9]  
Dampier CH, 2020, CLIN TRANSL GASTROEN, V11
[10]   Molecular evidence of field cancerization initiated by diabetes in colon cancer patients [J].
Del Puerto-Nevado, Laura ;
Minguez, Pablo ;
Corton, Marta ;
Solanes-Casado, Sonia ;
Prieto, Isabel ;
Mass, Sebastian ;
Belen Sanz, Ana ;
Gonzalez-Alonso, Paula ;
Villaverde, Cristina ;
Portal-Nunez, Sergio ;
Aguilera, Oscar ;
Gomez-Guerrero, Carmen ;
Esbrit, Pedro ;
Vivanco, Fernando ;
Gonzalez, Nieves ;
Ayuso, Carmen ;
Ortiz, Alberto ;
Rojo, Federico ;
Egido, Jesus ;
Alvarez-Llamas, Gloria ;
Garcia-Foncillas, Jesus .
MOLECULAR ONCOLOGY, 2019, 13 (04) :857-872