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dc.contributor.authorMøller, Pål
dc.contributor.authorHaupt, Saskia
dc.contributor.authorAhadova, Aysel
dc.contributor.authorKloor, Matthias
dc.contributor.authorSampson, Julian R.
dc.contributor.authorSunde, Lone
dc.contributor.authorSeppälä, Toni
dc.contributor.authorBurn, John
dc.contributor.authorBernstein, Inge
dc.contributor.authorCapella, Gabriel
dc.contributor.authorEvans, D. G.
dc.contributor.authorLindblom, Annika
dc.contributor.authorWinship, Ingrid
dc.contributor.authorMacrae, Finlay
dc.contributor.authorKatz, Lior
dc.contributor.authorLaish, Ido
dc.contributor.authorVainer, Elez
dc.contributor.authorMonahan, Kevin
dc.contributor.authorHalf, Elizabeth
dc.contributor.authorHorisberger, Karoline
dc.contributor.authorda Silva, Leandro A.
dc.contributor.authorHeuveline, Vincent
dc.contributor.authorTherkildsen, Christina
dc.contributor.authorLautrup, Charlotte
dc.contributor.authorKlarskov, Louise L.
dc.contributor.authorCavestro, Giulia M.
dc.contributor.authorMöslein, Gabriela
dc.contributor.authorHovig, Eivind
dc.contributor.authorDominguez-Valentin, Mev
dc.date.accessioned2024-05-14T05:04:53Z
dc.date.available2024-05-14T05:04:53Z
dc.date.issued2024
dc.identifier.citationHereditary Cancer in Clinical Practice. 2024 May 13;22(1):6
dc.identifier.urihttp://hdl.handle.net/10852/110922
dc.description.abstractBackground 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.
dc.language.isoeng
dc.rightsThe Author(s); licensee Springer International Publishing Ltd.
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleIncidences of colorectal adenomas and cancers under colonoscopy surveillance suggest an accelerated “Big Bang” pathway to CRC in three of the four Lynch syndromes
dc.typeJournal article
dc.date.updated2024-05-14T05:04:54Z
dc.creator.authorMøller, Pål
dc.creator.authorHaupt, Saskia
dc.creator.authorAhadova, Aysel
dc.creator.authorKloor, Matthias
dc.creator.authorSampson, Julian R.
dc.creator.authorSunde, Lone
dc.creator.authorSeppälä, Toni
dc.creator.authorBurn, John
dc.creator.authorBernstein, Inge
dc.creator.authorCapella, Gabriel
dc.creator.authorEvans, D. G.
dc.creator.authorLindblom, Annika
dc.creator.authorWinship, Ingrid
dc.creator.authorMacrae, Finlay
dc.creator.authorKatz, Lior
dc.creator.authorLaish, Ido
dc.creator.authorVainer, Elez
dc.creator.authorMonahan, Kevin
dc.creator.authorHalf, Elizabeth
dc.creator.authorHorisberger, Karoline
dc.creator.authorda Silva, Leandro A.
dc.creator.authorHeuveline, Vincent
dc.creator.authorTherkildsen, Christina
dc.creator.authorLautrup, Charlotte
dc.creator.authorKlarskov, Louise L.
dc.creator.authorCavestro, Giulia M.
dc.creator.authorMöslein, Gabriela
dc.creator.authorHovig, Eivind
dc.creator.authorDominguez-Valentin, Mev
dc.identifier.doihttps://doi.org/10.1186/s13053-024-00279-3
dc.type.documentTidsskriftartikkel
dc.type.peerreviewedPeer reviewed
dc.type.versionPublishedVersion
cristin.articleid6


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