Author:
Møller Pål,Haupt Saskia,Ahadova Aysel,Kloor Matthias,Sampson Julian R.,Sunde Lone,Seppälä Toni,Burn John,Bernstein Inge,Capella Gabriel,Evans D. Gareth,Lindblom Annika,Winship Ingrid,Macrae Finlay,Katz Lior,Laish Ido,Vainer Elez,Monahan Kevin,Half Elizabeth,Horisberger Karoline,da Silva Leandro Apolinário,Heuveline Vincent,Therkildsen Christina,Lautrup Charlotte,Klarskov Louise L,Cavestro Giulia Martina,Möslein Gabriela,Hovig Eivind,Dominguez-Valentin Mev
Abstract
Abstract
Background
Colorectal cancers (CRCs) in the Lynch syndromes have been assumed to emerge through an accelerated adenoma-carcinoma pathway. In this model adenomas with deficient mismatch repair have an increased probability of acquiring additional cancer driver mutation(s) resulting in more rapid progression to malignancy. If this model was accurate, the success of colonoscopy in preventing CRC would be a function of the intervals between colonoscopies and mean sojourn time of detectable adenomas. Contrary to expectations, colonoscopy did not decrease incidence of CRC in the Lynch syndromes and shorter colonoscopy intervals have not been effective in reducing CRC incidence. The prospective Lynch Syndrome Database (PLSD) was designed to examine these issues in carriers of pathogenic variants of the mis-match repair (path_MMR) genes.
Materials and methods
We examined the CRC and colorectal adenoma incidences in 3,574 path_MLH1, path_MSH2, path_MSH6 and path_PMS2 carriers subjected to regular colonoscopy with polypectomy, and considered the results based on sojourn times and stochastic probability paradigms.
Results
Most of the path_MMR carriers in each genetic group had no adenomas. There was no association between incidences of CRC and the presence of adenomas. There was no CRC observed in path_PMS2 carriers.
Conclusions
Colonoscopy prevented CRC in path_PMS2 carriers but not in the others. Our findings are consistent with colonoscopy surveillance blocking the adenoma-carcinoma pathway by removing identified adenomas which might otherwise become CRCs. However, in the other carriers most CRCs likely arised from dMMR cells in the crypts that have an increased mutation rate with increased stochastic chaotic probabilities for mutations. Therefore, this mechanism, that may be associated with no or only a short sojourn time of MSI tumours as adenomas, could explain the findings in our previous and current reports.
Funder
The Norwegian Cancer Society
Manchester National Institute for Health Research (NIHR) Biomedical Research Centre
Cancer Society Finland
Sigrid Juselius Foundation
Jane and Aatos Erkko Foundation
Relander Foundation
Academy of Finland
Publisher
Springer Science and Business Media LLC