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Finkin, S.* ; Yuan, D.T. ; Stein, I.* ; Taniguchi, K.* ; Weber, A.* ; Unger, K. ; Browning, J.L.* ; Goossens, N.* ; Nakagawa, S.* ; Gunasekaran, G.* ; Schwartz, M.E.* ; Kobayashi, M.* ; Kumada, H.* ; Berger, M.* ; Pappo, O.* ; Rajewsky, K.* ; Hoshida, Y.* ; Karin, M.* ; Heikenwälder, M. ; Ben-Neriah, Y.* ; Pikarsky, E.*

Ectopic lymphoid structures function as microniches for tumor progenitor cells in hepatocellular carcinoma.

Nat. Immunol. 16, 1235-1244 (2015)
DOI PMC
Open Access Green as soon as Postprint is submitted to ZB.
Ectopic lymphoid-like structures (ELSs) are often observed in cancer, yet their function is obscure. Although ELSs signify good prognosis in certain malignancies, we found that hepatic ELSs indicated poor prognosis for hepatocellular carcinoma (HCC). We studied an HCC mouse model that displayed abundant ELSs and found that they constituted immunopathological microniches wherein malignant hepatocyte progenitor cells appeared and thrived in a complex cellular and cytokine milieu until gaining self-sufficiency. The egress of progenitor cells and tumor formation were associated with the autocrine production of cytokines previously provided by the niche. ELSs developed via cooperation between the innate immune system and adaptive immune system, an event facilitated by activation of the transcription factor NF-κB and abolished by depletion of T cells. Such aberrant immunological foci might represent new targets for cancer therapy.
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Publication type Article: Journal article
Document type Scientific Article
Language english
Publication Year 2015
HGF-reported in Year 2015
ISSN (print) / ISBN 1529-2908
e-ISSN 1529-2916
Quellenangaben Volume: 16, Issue: 12, Pages: 1235-1244 Article Number: , Supplement: ,
Publisher Nature Publishing Group
Reviewing status Peer reviewed
POF-Topic(s) 30504 - Mechanisms of Genetic and Environmental Influences on Health and Disease
30203 - Molecular Targets and Therapies
Research field(s) Immune Response and Infection
Radiation Sciences
PSP Element(s) G-551600-001
G-501000-001
PubMed ID 26502405
Scopus ID 84947863720
Erfassungsdatum 2015-11-11