Detailed Information on Publication Record
2020
Loss of histone macroH2A1 in hepatocellular carcinoma cells promotes paracrine-mediated chemoresistance and CD4(+)CD25(+)FoxP3(+) regulatory T cells activation
LO RE, Oriana, Tommaso MAZZA, Sebastiano GIALLONGO, Paola SANNA, Francesca RAPPA et. al.Basic information
Original name
Loss of histone macroH2A1 in hepatocellular carcinoma cells promotes paracrine-mediated chemoresistance and CD4(+)CD25(+)FoxP3(+) regulatory T cells activation
Authors
LO RE, Oriana (380 Italy, belonging to the institution), Tommaso MAZZA (380 Italy), Sebastiano GIALLONGO (380 Italy, belonging to the institution), Paola SANNA (380 Italy), Francesca RAPPA (380 Italy), Tu Vinh Luong LUONG (826 United Kingdom of Great Britain and Northern Ireland), Giovanni VOLTI (380 Italy), Adéla DVOŘÁKOVÁ (203 Czech Republic, belonging to the institution), Tania ROSKAMS (56 Belgium), Matthias VAN HAELE (56 Belgium), Emmanuel TSOCHATZIS (826 United Kingdom of Great Britain and Northern Ireland) and Manlio VINCIGUERRA (380 Italy, guarantor)
Edition
THERANOSTICS, LAKE HAVEN, IVYSPRING INT PUBL, 2020, 1838-7640
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10601 Cell biology
Country of publisher
Australia
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 11.556
RIV identification code
RIV/00216224:14110/20:00116196
Organization unit
Faculty of Medicine
UT WoS
000498874200028
Keywords in English
hepatocellular carcinoma; histone macroH2A1; adaptive immune system; chemoresistance
Tags
International impact, Reviewed
Změněno: 17/3/2021 13:47, Mgr. Tereza Miškechová
Abstract
V originále
Rationale: Loss of histone macroH2A1 induces appearance of cancer stem cells (CSCs)-like cells in hepatocellular carcinoma (HCC). How CSCs interact with the tumor microenvironment and the adaptive immune system is unclear. Methods: We screened aggressive human HCC for macroH2A1 and CD44 CSC marker expression. We also knocked down (KD) macroH2A1 in HCC cells, and performed integrated transcriptomic and secretomic analyses. Results: Human HCC showed low macroH2A1 and high CD44 expression compared to control tissues. MacroH2A1 KD CSC-like cells transferred paracrinally their chemoresistant properties to parental HCC cells. MacroH2A1 KD conditioned media transcriptionally reprogrammed parental HCC cells activated regulatory CD4(+)/CD25(+)/FoxP3(+) T cells (Tregs). Conclusions: Loss of macroH2A1 in HCC cells drives cancer stem-cell propagation and evasion from immune surveillance.
Links
LM2015091, research and development project |
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MUNI/A/0951/2019, interní kód MU |
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