Early Hepatic Lesions Display Immature Tertiary Lymphoid Structures and Show Elevated Expression of Immune Inhibitory and Immunosuppressive Molecules.
Aged
B-Lymphocytes
/ immunology
Biomarkers, Tumor
/ immunology
Carcinogenesis
/ genetics
Carcinoma, Hepatocellular
/ genetics
Female
Gene Expression Profiling
Gene Expression Regulation, Neoplastic
/ genetics
Humans
Liver
/ immunology
Liver Neoplasms
/ genetics
Male
Middle Aged
T-Lymphocytes
/ immunology
Tertiary Lymphoid Structures
/ genetics
Journal
Clinical cancer research : an official journal of the American Association for Cancer Research
ISSN: 1557-3265
Titre abrégé: Clin Cancer Res
Pays: United States
ID NLM: 9502500
Informations de publication
Date de publication:
15 08 2020
15 08 2020
Historique:
received:
07
09
2019
revised:
24
01
2020
accepted:
03
04
2020
pubmed:
10
4
2020
medline:
28
10
2021
entrez:
10
4
2020
Statut:
ppublish
Résumé
The impact of tertiary lymphoid structures (TLS) in hepatocellular carcinoma (HCC) progression is being extensively investigated. However, their presence during the early steps of human liver carcinogenesis remains unknown. We thus aimed to determine whether TLS are induced in preneoplastic/early hepatic lesions (EHL), and whether they are associated with a particular immune profile. A series of 127 EHLs (low/high-grade dysplastic nodules, early HCC, and small and progressed HCC) was included in the study. TLSs were investigated by pathologic reviewing. Densities of immune cells were assessed using IHC. A subset of lesions was microdissected and gene expression profiling was performed with a custom NanoString panel. Compared with surrounding cirrhotic nodules, EHL of all stages displayed increased densities of T cells, B cells, and dendritic cells. Immature TLSs were identified in 24% of EHL. Gene expression profiling identified a subset of EHL with elevated mRNA levels of various cytokines involved in immune cells' recruitment and TLS induction. This subgroup of EHL also showed overexpression of genes related to T- and B-cells' activation and antigen presentation, as well as those related to immunosuppression and immune exhaustion. Local immune activation occurs in the very early steps of liver carcinogenesis; however, it may not be fully efficient and paradoxically favor immune evasion and progression to full-blown HCC. These results have implications for the development of anti-HCC chemopreventive strategies in cirrhotic patients.
Identifiants
pubmed: 32269054
pii: 1078-0432.CCR-19-2929
doi: 10.1158/1078-0432.CCR-19-2929
doi:
Substances chimiques
Biomarkers, Tumor
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
4381-4389Informations de copyright
©2020 American Association for Cancer Research.