Integrated genomic analysis reveals mutated ELF3 as a potential gallbladder cancer vaccine candidate
Gallbladder cancer (GBC) is an aggressive gastrointestinal malignancy with no approved targeted therapy. Here, we analyze exomes ( n = 160), transcriptomes ( n = 115), and low pass whole genomes ( n = 146) from 167 gallbladder cancers (GBCs) from patients in Korea, India and Chile. In addition, w...
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Veröffentlicht in: | Nature communications 2020-08, Vol.11 (1), p.4225-4225, Article 4225 |
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Sprache: | eng |
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Zusammenfassung: | Gallbladder cancer (GBC) is an aggressive gastrointestinal malignancy with no approved targeted therapy. Here, we analyze exomes (
n
= 160), transcriptomes (
n
= 115), and low pass whole genomes (
n
= 146) from 167 gallbladder cancers (GBCs) from patients in Korea, India and Chile. In addition, we also sequence samples from 39 GBC high-risk patients and detect evidence of early cancer-related genomic lesions. Among the several significantly mutated genes not previously linked to GBC are ETS domain genes
ELF3
and
EHF
,
CTNNB1
,
APC
,
NSD1
,
KAT8
,
STK11
and
NFE2L2
. A majority of
ELF3
alterations are frame-shift mutations that result in several cancer-specific neoantigens that activate T-cells indicating that they are cancer vaccine candidates. In addition, we identify recurrent alterations in KEAP1/NFE2L2 and WNT pathway in GBC. Taken together, these define multiple targetable therapeutic interventions opportunities for GBC treatment and management.
Gallbladder cancer incidence shows characteristic geographic patterns. Here the authors perform a genomic analysis of gallbladder cancers in patients from countries with high incidence (South Korea, India and Chile) and identify ELF3 and other significantly mutated genes not previously associated with gallbladder cancer. |
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ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/s41467-020-17880-4 |