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Verfasst von:Nepal, Chirag [VerfasserIn]   i
 Zhu, Bin [VerfasserIn]   i
 O’Rourke, Colm J. [VerfasserIn]   i
 Bhatt, Deepak Kumar [VerfasserIn]   i
 Lee, Donghyuk [VerfasserIn]   i
 Song, Lei [VerfasserIn]   i
 Wang, Difei [VerfasserIn]   i
 Van Dyke, Alison L. [VerfasserIn]   i
 Choo-Wosoba, Hyoyoung [VerfasserIn]   i
 Liu, Zhiwei [VerfasserIn]   i
 Hildesheim, Allan [VerfasserIn]   i
 Goldstein, Alisa M. [VerfasserIn]   i
 Dean, Michael [VerfasserIn]   i
 LaFuente-Barquero, Juan [VerfasserIn]   i
 Lawrence, Scott [VerfasserIn]   i
 Mutreja, Karun [VerfasserIn]   i
 Olanich, Mary E. [VerfasserIn]   i
 Lorenzo Bermejo, Justo [VerfasserIn]   i
 Ferreccio, Catterina [VerfasserIn]   i
 Roa, Juan Carlos [VerfasserIn]   i
 Rashid, Asif [VerfasserIn]   i
 Hsing, Ann W. [VerfasserIn]   i
 Gao, Yu-Tang [VerfasserIn]   i
 Chanock, Stephen J. [VerfasserIn]   i
 Araya, Juan Carlos [VerfasserIn]   i
 Andersen, Jesper B. [VerfasserIn]   i
 Koshiol, Jill [VerfasserIn]   i
Titel:Integrative molecular characterisation of gallbladder cancer reveals micro-environment-associated subtypes
Verf.angabe:Chirag Nepal, Bin Zhu, Colm J. O’Rourke, Deepak Kumar Bhatt, Donghyuk Lee, Lei Song, Difei Wang, Alison L. Van Dyke, Hyoyoung Choo-Wosoba, Zhiwei Liu, Allan Hildesheim, Alisa M. Goldstein, Michael Dean, Juan LaFuente-Barquero, Scott Lawrence, Karun Mutreja, Mary E. Olanich, Justo Lorenzo Bermejo, Catterina Ferreccio, Juan Carlos Roa, Asif Rashid, Ann W. Hsing, Yu-Tang Gao, Stephen J. Chanock, Juan Carlos Araya, Jesper B. Andersen, Jill Koshiol
Jahr:2021
Umfang:13 S.
Fussnoten:Online 1 December 2020 ; Gesehen am 16.06.2021
Titel Quelle:Enthalten in: Journal of hepatology
Ort Quelle:Amsterdam [u.a.] : Elsevier Science, 1985
Jahr Quelle:2021
Band/Heft Quelle:74(2021), 5, Seite 1132-1144
ISSN Quelle:1600-0641
Abstract:Background & Aims - Gallbladder cancer (GBC) is the most common type of biliary tract cancer, but the molecular mechanisms involved in gallbladder carcinogenesis remain poorly understood. In this study, we applied integrative genomics approaches to characterise GBC and explore molecular subtypes associated with patient survival. - Methods - We profiled the mutational landscape of GBC tumours (whole-exome sequencing on 92, targeted sequencing on 98, in total 190 patients). In a subset (n = 45), we interrogated the matched transcriptomes, DNA methylomes, and somatic copy number alterations. We explored molecular subtypes identified through clustering tumours by genes whose expression was associated with survival in 47 tumours and validated subtypes on 34 publicly available GBC cases. - Results - Exome analysis revealed TP53 was the most mutated gene. The overall mutation rate was low (median 0.82 Mut/Mb). APOBEC-mediated mutational signatures were more common in tumours with higher mutational burden. Aflatoxin-related signatures tended to be highly clonal (present in ≥50% of cancer cells). Transcriptome-wide survival association analysis revealed a 95-gene signature that stratified all GBC patients into 3 subtypes that suggested an association with overall survival post-resection. The 2 poor-survival subtypes were associated with adverse clinicopathologic features (advanced stage, pN1, pM1), immunosuppressive micro-environments (myeloid-derived suppressor cell accumulation, extensive desmoplasia, hypoxia) and T cell dysfunction, whereas the good-survival subtype showed the opposite features. - Conclusion - These data suggest that the tumour micro-environment and immune profiles could play an important role in gallbladder carcinogenesis and should be evaluated in future clinical studies, along with mutational profiles. - Lay summary - Gallbladder cancer is highly fatal, and its causes are poorly understood. We evaluated gallbladder tumours to see if there were differences between tumours in genetic information such as DNA and RNA. We found evidence of aflatoxin exposure in these tumours, and immune cells surrounding the tumours were associated with survival.
DOI:doi:10.1016/j.jhep.2020.11.033
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1016/j.jhep.2020.11.033
 Volltext: https://www.sciencedirect.com/science/article/pii/S0168827820338204
 DOI: https://doi.org/10.1016/j.jhep.2020.11.033
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Aflatoxin
 Gallbladder cancer
 Immunogenomics
 Micro-environment
 Molecular subgroups
K10plus-PPN:1760543934
Verknüpfungen:→ Zeitschrift

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