Comprehensive genetic and epigenetic characterization of Lynch‐like syndrome patients

Lynch-like syndrome (LLS) presents very similar clinicopathological characteristics to Lynch syndrome (LS) but the mechanism for cancer predisposition remains unknown. The present study aims to investigate the causal mechanism of LLS by a comprehensive genetic and epigenetic approach. Thirty-two LLS and 34 LS patients with colorectal cancer (CRC) fitting the Amsterdam and Bethesda criteria were included, along with 29 CRC sporadic patients, and analyzed for the presence of pathogenic variants in 94 genes associated with hereditary tumors. The cohorts were also characterized for the methylation profile and examined through a sample group analysis and a Stochastic Epigenetic Mutations (SEMs) analysis in comparison with 29 age-matched healthy controls. The multigene panel analysis revealed the presence of pathogenic variants in non-mismatch repair (MMR) genes and three variants classified as pathogenic/likely pathogenic possibly predisposing to LLS. The epigenetic analysis showed epivariations targeting genes associated with LS or DNA repair, most of them associated with the Fanconi Anemia pathway, which could explain the susceptibility to cancer. Our results highlight the need for using extended genetic and epigenetic analyses to understand the causal mechanism of LLS.

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Publication Details

Journal
International Journal of Cancer
Published
2025-04-21
DOI
https://doi.org/10.1002/ijc.35451
Citations
2
Primary Topic
Genetic factors in colorectal cancer
Type
article
Field-Weighted Citation Impact
2.94

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article

Comprehensive genetic and epigenetic characterization of Lynch‐like syndrome patients

Rita Danesi, Daniela Barana, Valentina Zampiga, Francesca Pirini et al.
2 citations
International Journal of Cancer
Genetic factors in colorectal cancer
2.94
article

Comprehensive genetic and epigenetic characterization of Lynch‐like syndrome patients

Rita Danesi, Daniela Barana, Valentina Zampiga, Francesca Pirini, Valentina Arcangeli, Elisabetta Petracci, Sara Bravaccini, Giorgia Marisi, Gianluca Tedaldi, Michela Tebaldi, Ilaria Cangini, Luca Roncucci, Davide Gentilini, Monica Pedroni, Luciano Calzari, Mila Ravegnani, Alessandro Passardi, Daniele Calistri, Alessandra Viel
article en
2 citations

Abstract

Lynch-like syndrome (LLS) presents very similar clinicopathological characteristics to Lynch syndrome (LS) but the mechanism for cancer predisposition remains unknown. The present study aims to investigate the causal mechanism of LLS by a comprehensive genetic and epigenetic approach. Thirty-two LLS and 34 LS patients with colorectal cancer (CRC) fitting the Amsterdam and Bethesda criteria were included, along with 29 CRC sporadic patients, and analyzed for the presence of pathogenic variants in 94 genes associated with hereditary tumors. The cohorts were also characterized for the methylation profile and examined through a sample group analysis and a Stochastic Epigenetic Mutations (SEMs) analysis in comparison with 29 age-matched healthy controls. The multigene panel analysis revealed the presence of pathogenic variants in non-mismatch repair (MMR) genes and three variants classified as pathogenic/likely pathogenic possibly predisposing to LLS. The epigenetic analysis showed epivariations targeting genes associated with LS or DNA repair, most of them associated with the Fanconi Anemia pathway, which could explain the susceptibility to cancer. Our results highlight the need for using extended genetic and epigenetic analyses to understand the causal mechanism of LLS.

International Journal of CancerVol. 157(4)
University of Modena and Reggio Emilia (IT), Università degli Studi di Enna Kore (IT), University of Pavia (IT), Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IT), Centro di Riferimento Oncologico (IT), IRCCS Istituto Auxologico Italiano (IT), Istituti di Ricovero e Cura a Carattere Scientifico (IT)
Ministero della Salute
Good health and well-being
Openalex Percentile: Top 10%
Genetic factors in colorectal cancer
2.94
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