ARV-771 Acts as an Inducer of Cell Cycle Arrest and Apoptosis to Suppress Hepatocellular Carcinoma Progression

Hepatocellular carcinoma (HCC) is the most commonly diagnosed liver cancer with limited treatment options and extremely poor prognosis worldwide. Recently, the proteolysis targeting chimeras (PROTACs), which aim to induce proteasome-mediated degradation of interesting proteins via recruiting E3 liga...

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Main Authors: Yuanfei Deng, Cuifu Yu, Lushi Chen, Xin Zhang, Qiucheng Lei, Qing Liu, Gengxi Cai, Fang Liu
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-05-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphar.2022.858901/full
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author Yuanfei Deng
Cuifu Yu
Lushi Chen
Xin Zhang
Qiucheng Lei
Qing Liu
Gengxi Cai
Fang Liu
author_facet Yuanfei Deng
Cuifu Yu
Lushi Chen
Xin Zhang
Qiucheng Lei
Qing Liu
Gengxi Cai
Fang Liu
author_sort Yuanfei Deng
collection DOAJ
description Hepatocellular carcinoma (HCC) is the most commonly diagnosed liver cancer with limited treatment options and extremely poor prognosis worldwide. Recently, the proteolysis targeting chimeras (PROTACs), which aim to induce proteasome-mediated degradation of interesting proteins via recruiting E3 ligases, have become the advanced tools and attractive molecules for cancer treatment. However, the anticancer effects of PROTACs in HCC remain to be clarified. Here, we evaluate the anticancer activity of ARV-771, a previously reported PROTAC compound designed for bromodomain and extra-terminal domain (BET) proteins, in HCC. We show that ARV-771 suppresses the cell viability and colony formation of HCC cells via arresting cell cycle progression and triggering apoptosis. Further investigations reveal that ARV-771 notably downregulates multiple non-proteasomal deubiquitinases which are critical to the development of cancers. Additionally, HCC cells can decrease their sensitivity to ARV-771 via activating the MEK/ERK and p38 MAPKs. ARV-771 also inhibits HCC progression in vivo. Moreover, we show that ARV-771 and sorafenib, a Raf inhibitor that clinically used for targeted therapy of liver cancer, can synergistically inhibit the growth of HCC cells. Overall, this study not only explores the anticancer activity of ARV-771 and its underlying mechanisms in HCC, but also deepens our understanding of deubiquitinases, MAPKs, cell cycle, and apoptosis induction in cancer therapy.
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spelling doaj.art-1013ef9a6aa9461fa6aa13dea4fb300a2022-12-22T03:36:40ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122022-05-011310.3389/fphar.2022.858901858901ARV-771 Acts as an Inducer of Cell Cycle Arrest and Apoptosis to Suppress Hepatocellular Carcinoma ProgressionYuanfei Deng0Cuifu Yu1Lushi Chen2Xin Zhang3Qiucheng Lei4Qing Liu5Gengxi Cai6Fang Liu7Department of Pathology, The First People’s Hospital of Foshan, Foshan, ChinaGuangzhou Municipal and Guangdong Provincial Key Laboratory of Protein Modification and Degradation, School of Basic Medical Sciences, Guangzhou Medical University, Guangzhou, ChinaHealth Management Center, The First People’s Hospital of Foshan, Foshan, ChinaDepartment of Pathology, The First People’s Hospital of Foshan, Foshan, ChinaDepartment of Hepatopancreatic Surgery, The First People’s Hospital of Foshan, Foshan, ChinaDepartment of Pathology, The First People’s Hospital of Foshan, Foshan, ChinaDepartment of Breast Surgery, The First People’s Hospital of Foshan, Foshan, ChinaDepartment of Pathology, The First People’s Hospital of Foshan, Foshan, ChinaHepatocellular carcinoma (HCC) is the most commonly diagnosed liver cancer with limited treatment options and extremely poor prognosis worldwide. Recently, the proteolysis targeting chimeras (PROTACs), which aim to induce proteasome-mediated degradation of interesting proteins via recruiting E3 ligases, have become the advanced tools and attractive molecules for cancer treatment. However, the anticancer effects of PROTACs in HCC remain to be clarified. Here, we evaluate the anticancer activity of ARV-771, a previously reported PROTAC compound designed for bromodomain and extra-terminal domain (BET) proteins, in HCC. We show that ARV-771 suppresses the cell viability and colony formation of HCC cells via arresting cell cycle progression and triggering apoptosis. Further investigations reveal that ARV-771 notably downregulates multiple non-proteasomal deubiquitinases which are critical to the development of cancers. Additionally, HCC cells can decrease their sensitivity to ARV-771 via activating the MEK/ERK and p38 MAPKs. ARV-771 also inhibits HCC progression in vivo. Moreover, we show that ARV-771 and sorafenib, a Raf inhibitor that clinically used for targeted therapy of liver cancer, can synergistically inhibit the growth of HCC cells. Overall, this study not only explores the anticancer activity of ARV-771 and its underlying mechanisms in HCC, but also deepens our understanding of deubiquitinases, MAPKs, cell cycle, and apoptosis induction in cancer therapy.https://www.frontiersin.org/articles/10.3389/fphar.2022.858901/fullhepatocellular carcinomaPROTACsARV-771deubiquitinasesMAPKs
spellingShingle Yuanfei Deng
Cuifu Yu
Lushi Chen
Xin Zhang
Qiucheng Lei
Qing Liu
Gengxi Cai
Fang Liu
ARV-771 Acts as an Inducer of Cell Cycle Arrest and Apoptosis to Suppress Hepatocellular Carcinoma Progression
Frontiers in Pharmacology
hepatocellular carcinoma
PROTACs
ARV-771
deubiquitinases
MAPKs
title ARV-771 Acts as an Inducer of Cell Cycle Arrest and Apoptosis to Suppress Hepatocellular Carcinoma Progression
title_full ARV-771 Acts as an Inducer of Cell Cycle Arrest and Apoptosis to Suppress Hepatocellular Carcinoma Progression
title_fullStr ARV-771 Acts as an Inducer of Cell Cycle Arrest and Apoptosis to Suppress Hepatocellular Carcinoma Progression
title_full_unstemmed ARV-771 Acts as an Inducer of Cell Cycle Arrest and Apoptosis to Suppress Hepatocellular Carcinoma Progression
title_short ARV-771 Acts as an Inducer of Cell Cycle Arrest and Apoptosis to Suppress Hepatocellular Carcinoma Progression
title_sort arv 771 acts as an inducer of cell cycle arrest and apoptosis to suppress hepatocellular carcinoma progression
topic hepatocellular carcinoma
PROTACs
ARV-771
deubiquitinases
MAPKs
url https://www.frontiersin.org/articles/10.3389/fphar.2022.858901/full
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