: Esophageal adenocarcinoma (EAC) is a severe malignancy with increasing incidence, poorly understood pathogenesis, and low survival rates. We sequenced 164 EAC samples of naïve patients (without chemo-radiotherapy) with high coverage using next-generation sequencing technologies. A total of 337 variants were identified across the whole cohort, with TP53 as the most frequently altered gene (67.27%). Missense mutations in TP53 correlated with worse cancer-specific survival (log-rank p = 0.001). In seven cases, we found disruptive mutations in HNF1alpha associated with other gene alterations. Moreover, we detected gene fusions through massive parallel sequencing of RNA, indicating that it is not a rare event in EAC. In conclusion, we report that a specific type of TP53 mutation (missense changes) negatively affected cancer-specific survival in EAC. HNF1alpha was identified as a new EAC-mutated gene.

Correlations between Molecular Alterations, Histopathological Characteristics, and Poor Prognosis in Esophageal Adenocarcinoma / Orsini, Arianna; Mastracci, Luca; Bozzarelli, Isotta; Ferrari, Anna; Isidori, Federica; Fiocca, Roberto; Lugaresi, Marialuisa; D'Errico, Antonietta; Malvi, Deborah; Cataldi-Stagetti, Erica; Spaggiari, Paola; Tomezzoli, Anna; Albarello, Luca; Ristimäki, Ari; Bottiglieri, Luca; Krishnadath, Kausilia K; Rosati, Riccardo; Fumagalli Romario, Uberto; De Manzoni, Giovanni; Räsänen, Jari; Martinelli, Giovanni; Mattioli, Sandro; Bonora, Elena; On Behalf Of The Eacsge Consortium, Null. - In: CANCERS. - ISSN 2072-6694. - 15:5(2023). [10.3390/cancers15051408]

Correlations between Molecular Alterations, Histopathological Characteristics, and Poor Prognosis in Esophageal Adenocarcinoma

Rosati, Riccardo;
2023-01-01

Abstract

: Esophageal adenocarcinoma (EAC) is a severe malignancy with increasing incidence, poorly understood pathogenesis, and low survival rates. We sequenced 164 EAC samples of naïve patients (without chemo-radiotherapy) with high coverage using next-generation sequencing technologies. A total of 337 variants were identified across the whole cohort, with TP53 as the most frequently altered gene (67.27%). Missense mutations in TP53 correlated with worse cancer-specific survival (log-rank p = 0.001). In seven cases, we found disruptive mutations in HNF1alpha associated with other gene alterations. Moreover, we detected gene fusions through massive parallel sequencing of RNA, indicating that it is not a rare event in EAC. In conclusion, we report that a specific type of TP53 mutation (missense changes) negatively affected cancer-specific survival in EAC. HNF1alpha was identified as a new EAC-mutated gene.
2023
HNF1alpha
SMAD4
TP53
esophageal adenocarcinoma
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11768/137816
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