CNOT7 depletion reverses natural killer cell resistance by modulating the tumor immune microenvironment of hepatocellular carcinoma

A major obstacle to effective cancer immunotherapy is the tumor immune microenvironment. Natural killer (NK) cell resistance has been suggested as a primary cause of poor prognosis in hepatocellular carcinoma (HCC), which seemingly correlates with CNOT7 overexpression. CNOT7, a cytoplasmic mRNA dead...

Full description

Bibliographic Details
Main Authors: Chongren Ren, Xiaojing Ren, Dujuan Cao, Haichao Zhao, Zhensheng Zhai, Huiyu Li, Yanjun Li, Xifeng Fu, Jiefeng He, Haoliang Zhao
Format: Article
Language:English
Published: Wiley 2020-05-01
Series:FEBS Open Bio
Subjects:
Online Access:https://doi.org/10.1002/2211-5463.12836
_version_ 1818162070458204160
author Chongren Ren
Xiaojing Ren
Dujuan Cao
Haichao Zhao
Zhensheng Zhai
Huiyu Li
Yanjun Li
Xifeng Fu
Jiefeng He
Haoliang Zhao
author_facet Chongren Ren
Xiaojing Ren
Dujuan Cao
Haichao Zhao
Zhensheng Zhai
Huiyu Li
Yanjun Li
Xifeng Fu
Jiefeng He
Haoliang Zhao
author_sort Chongren Ren
collection DOAJ
description A major obstacle to effective cancer immunotherapy is the tumor immune microenvironment. Natural killer (NK) cell resistance has been suggested as a primary cause of poor prognosis in hepatocellular carcinoma (HCC), which seemingly correlates with CNOT7 overexpression. CNOT7, a cytoplasmic mRNA deadenylase that is highly expressed in HCC, may regulate cytokine transforming growth factor‐β1 (TGF‐β1) secretion by controlling nuclear factor‐κB subunit p65 trafficking. CNOT7 depletion suppresses TGF‐β1 secretion in HCC and promotes interferon‐γ (IFN‐γ) secretion by NK cells, and we previously demonstrated that CNOT7 depletion reversed IFN‐γ resistance in HCC cells. Therefore, we hypothesized that CNOT7 depletion might reverse NK cell resistance by influencing the tumor immune microenvironment of HCC. To test this hypothesis, we examined the correlation between CNOT7, STAT1, TGF‐β1 and IFN‐γ expression with hepatitis B virus‐related cirrhosis and HCC with hepatitis B virus‐related cirrhosis. We found that modulation of CNOT7 expression alters TGF‐β1 secretion in HCC and IFN‐γ secretion in NK cells. We also examined the effects of NK cells in HepG2 cells with CNOT7 knockdown, which showed that NK cell surface CD107a expression is up‐regulated and caspase‐3 expression is significantly enhanced in CNOT7‐deficient HepG2 cells. Overall, our results show that knockdown of CNOT7 expression reverses NK cell resistance in HCC cells. Therefore, CNOT7 depletion has potential as a new adjuvant therapy in immunotherapy for HCC.
first_indexed 2024-12-11T16:27:49Z
format Article
id doaj.art-473946f2ee9c4bdeab315dc7280e8cc7
institution Directory Open Access Journal
issn 2211-5463
language English
last_indexed 2024-12-11T16:27:49Z
publishDate 2020-05-01
publisher Wiley
record_format Article
series FEBS Open Bio
spelling doaj.art-473946f2ee9c4bdeab315dc7280e8cc72022-12-22T00:58:40ZengWileyFEBS Open Bio2211-54632020-05-0110584786010.1002/2211-5463.12836CNOT7 depletion reverses natural killer cell resistance by modulating the tumor immune microenvironment of hepatocellular carcinomaChongren Ren0Xiaojing Ren1Dujuan Cao2Haichao Zhao3Zhensheng Zhai4Huiyu Li5Yanjun Li6Xifeng Fu7Jiefeng He8Haoliang Zhao9Shanxi Bethune Hospital TaiYuan ChinaGraduate College of Shanxi Medical University TaiYuan ChinaShanxi Bethune Hospital TaiYuan ChinaGraduate College of Shanxi Medical University TaiYuan ChinaShanxi Bethune Hospital TaiYuan ChinaShanxi Bethune Hospital TaiYuan ChinaShanxi Bethune Hospital TaiYuan ChinaShanxi Bethune Hospital TaiYuan ChinaShanxi Bethune Hospital TaiYuan ChinaShanxi Bethune Hospital TaiYuan ChinaA major obstacle to effective cancer immunotherapy is the tumor immune microenvironment. Natural killer (NK) cell resistance has been suggested as a primary cause of poor prognosis in hepatocellular carcinoma (HCC), which seemingly correlates with CNOT7 overexpression. CNOT7, a cytoplasmic mRNA deadenylase that is highly expressed in HCC, may regulate cytokine transforming growth factor‐β1 (TGF‐β1) secretion by controlling nuclear factor‐κB subunit p65 trafficking. CNOT7 depletion suppresses TGF‐β1 secretion in HCC and promotes interferon‐γ (IFN‐γ) secretion by NK cells, and we previously demonstrated that CNOT7 depletion reversed IFN‐γ resistance in HCC cells. Therefore, we hypothesized that CNOT7 depletion might reverse NK cell resistance by influencing the tumor immune microenvironment of HCC. To test this hypothesis, we examined the correlation between CNOT7, STAT1, TGF‐β1 and IFN‐γ expression with hepatitis B virus‐related cirrhosis and HCC with hepatitis B virus‐related cirrhosis. We found that modulation of CNOT7 expression alters TGF‐β1 secretion in HCC and IFN‐γ secretion in NK cells. We also examined the effects of NK cells in HepG2 cells with CNOT7 knockdown, which showed that NK cell surface CD107a expression is up‐regulated and caspase‐3 expression is significantly enhanced in CNOT7‐deficient HepG2 cells. Overall, our results show that knockdown of CNOT7 expression reverses NK cell resistance in HCC cells. Therefore, CNOT7 depletion has potential as a new adjuvant therapy in immunotherapy for HCC.https://doi.org/10.1002/2211-5463.12836CNOT7hepatocellular carcinomaHepG2STAT1TGF‐β1
spellingShingle Chongren Ren
Xiaojing Ren
Dujuan Cao
Haichao Zhao
Zhensheng Zhai
Huiyu Li
Yanjun Li
Xifeng Fu
Jiefeng He
Haoliang Zhao
CNOT7 depletion reverses natural killer cell resistance by modulating the tumor immune microenvironment of hepatocellular carcinoma
FEBS Open Bio
CNOT7
hepatocellular carcinoma
HepG2
STAT1
TGF‐β1
title CNOT7 depletion reverses natural killer cell resistance by modulating the tumor immune microenvironment of hepatocellular carcinoma
title_full CNOT7 depletion reverses natural killer cell resistance by modulating the tumor immune microenvironment of hepatocellular carcinoma
title_fullStr CNOT7 depletion reverses natural killer cell resistance by modulating the tumor immune microenvironment of hepatocellular carcinoma
title_full_unstemmed CNOT7 depletion reverses natural killer cell resistance by modulating the tumor immune microenvironment of hepatocellular carcinoma
title_short CNOT7 depletion reverses natural killer cell resistance by modulating the tumor immune microenvironment of hepatocellular carcinoma
title_sort cnot7 depletion reverses natural killer cell resistance by modulating the tumor immune microenvironment of hepatocellular carcinoma
topic CNOT7
hepatocellular carcinoma
HepG2
STAT1
TGF‐β1
url https://doi.org/10.1002/2211-5463.12836
work_keys_str_mv AT chongrenren cnot7depletionreversesnaturalkillercellresistancebymodulatingthetumorimmunemicroenvironmentofhepatocellularcarcinoma
AT xiaojingren cnot7depletionreversesnaturalkillercellresistancebymodulatingthetumorimmunemicroenvironmentofhepatocellularcarcinoma
AT dujuancao cnot7depletionreversesnaturalkillercellresistancebymodulatingthetumorimmunemicroenvironmentofhepatocellularcarcinoma
AT haichaozhao cnot7depletionreversesnaturalkillercellresistancebymodulatingthetumorimmunemicroenvironmentofhepatocellularcarcinoma
AT zhenshengzhai cnot7depletionreversesnaturalkillercellresistancebymodulatingthetumorimmunemicroenvironmentofhepatocellularcarcinoma
AT huiyuli cnot7depletionreversesnaturalkillercellresistancebymodulatingthetumorimmunemicroenvironmentofhepatocellularcarcinoma
AT yanjunli cnot7depletionreversesnaturalkillercellresistancebymodulatingthetumorimmunemicroenvironmentofhepatocellularcarcinoma
AT xifengfu cnot7depletionreversesnaturalkillercellresistancebymodulatingthetumorimmunemicroenvironmentofhepatocellularcarcinoma
AT jiefenghe cnot7depletionreversesnaturalkillercellresistancebymodulatingthetumorimmunemicroenvironmentofhepatocellularcarcinoma
AT haoliangzhao cnot7depletionreversesnaturalkillercellresistancebymodulatingthetumorimmunemicroenvironmentofhepatocellularcarcinoma