METTL7B Is Required for Cancer Cell Proliferation and Tumorigenesis in Non-Small Cell Lung Cancer

Lung cancer remains a leading cause of cancer-associated mortality worldwide, however, molecular mechanisms underlying lung cancer tumorigenesis and progression remain unknown. Here, we report evidence showing that one member of the mammalian methyltransferase-like family (METTL), METTL7B, is a pote...

Full description

Bibliographic Details
Main Authors: Dongcheng Liu, Wei Li, Fuhua Zhong, Jianhua Yin, Wei Zhou, Shixuan Li, Xuefeng Sun, Jing Xu, Guofeng Li, Yuxin Wen, Jiaqing Wang, Malin Hong, Zhiqiang Cheng, Jimin Yuan, Lingyun Dai, Jichao Sun, Jigang Wang, Chen Qiu, Guangsuo Wang, Chang Zou
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-02-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fphar.2020.00178/full
id doaj-5e044c708762482fafa302eaaab71631
record_format Article
collection DOAJ
language English
format Article
sources DOAJ
author Dongcheng Liu
Dongcheng Liu
Wei Li
Wei Li
Fuhua Zhong
Jianhua Yin
Wei Zhou
Shixuan Li
Xuefeng Sun
Jing Xu
Guofeng Li
Yuxin Wen
Jiaqing Wang
Malin Hong
Zhiqiang Cheng
Zhiqiang Cheng
Jimin Yuan
Lingyun Dai
Jichao Sun
Jigang Wang
Chen Qiu
Guangsuo Wang
Chang Zou
Chang Zou
spellingShingle Dongcheng Liu
Dongcheng Liu
Wei Li
Wei Li
Fuhua Zhong
Jianhua Yin
Wei Zhou
Shixuan Li
Xuefeng Sun
Jing Xu
Guofeng Li
Yuxin Wen
Jiaqing Wang
Malin Hong
Zhiqiang Cheng
Zhiqiang Cheng
Jimin Yuan
Lingyun Dai
Jichao Sun
Jigang Wang
Chen Qiu
Guangsuo Wang
Chang Zou
Chang Zou
METTL7B Is Required for Cancer Cell Proliferation and Tumorigenesis in Non-Small Cell Lung Cancer
Frontiers in Pharmacology
METTL7B
non-small cell lung cancer
proliferation
tumorigenesis
cell cycle
author_facet Dongcheng Liu
Dongcheng Liu
Wei Li
Wei Li
Fuhua Zhong
Jianhua Yin
Wei Zhou
Shixuan Li
Xuefeng Sun
Jing Xu
Guofeng Li
Yuxin Wen
Jiaqing Wang
Malin Hong
Zhiqiang Cheng
Zhiqiang Cheng
Jimin Yuan
Lingyun Dai
Jichao Sun
Jigang Wang
Chen Qiu
Guangsuo Wang
Chang Zou
Chang Zou
author_sort Dongcheng Liu
title METTL7B Is Required for Cancer Cell Proliferation and Tumorigenesis in Non-Small Cell Lung Cancer
title_short METTL7B Is Required for Cancer Cell Proliferation and Tumorigenesis in Non-Small Cell Lung Cancer
title_full METTL7B Is Required for Cancer Cell Proliferation and Tumorigenesis in Non-Small Cell Lung Cancer
title_fullStr METTL7B Is Required for Cancer Cell Proliferation and Tumorigenesis in Non-Small Cell Lung Cancer
title_full_unstemmed METTL7B Is Required for Cancer Cell Proliferation and Tumorigenesis in Non-Small Cell Lung Cancer
title_sort mettl7b is required for cancer cell proliferation and tumorigenesis in non-small cell lung cancer
publisher Frontiers Media S.A.
series Frontiers in Pharmacology
issn 1663-9812
publishDate 2020-02-01
description Lung cancer remains a leading cause of cancer-associated mortality worldwide, however, molecular mechanisms underlying lung cancer tumorigenesis and progression remain unknown. Here, we report evidence showing that one member of the mammalian methyltransferase-like family (METTL), METTL7B, is a potential molecular target for treatment of non-small cell lung cancer (NSCLC). METTL7B expression was elevated in the majority of NSCLC comparing to normal tissues. Increased expression of METTL7B contributed to advanced stages of tumor development and poor survival in NSCLC patients. Lentivirus-mediated shRNA silencing of METTL7B suppressed proliferation and tumorigenesis of cancer cells in vitro and in vivo. Investigation on gene expression profiles of NSCLC cells revealed that abundant cell cycle related genes were downregulated in the absence of METTL7B. Pathway enrichment analysis indicated that METTL7B participated in cell cycle regulation. Notably, CCND1, a key regulator for G1/S transition, was significantly decreased with the depletion of METTL7B, resulting in G0/G1 arrest, indicating that METTL7B is critical for cell cycle progression. Taken together, our findings implicate that METTL7B is essential for NSCLC development and progression. METTL7B might serve as a potential therapeutic target for NSCLC.
topic METTL7B
non-small cell lung cancer
proliferation
tumorigenesis
cell cycle
url https://www.frontiersin.org/article/10.3389/fphar.2020.00178/full
work_keys_str_mv AT dongchengliu mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT dongchengliu mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT weili mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT weili mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT fuhuazhong mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT jianhuayin mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT weizhou mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT shixuanli mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT xuefengsun mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT jingxu mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT guofengli mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT yuxinwen mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT jiaqingwang mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT malinhong mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT zhiqiangcheng mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT zhiqiangcheng mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT jiminyuan mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT lingyundai mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT jichaosun mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT jigangwang mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT chenqiu mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT guangsuowang mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT changzou mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
AT changzou mettl7bisrequiredforcancercellproliferationandtumorigenesisinnonsmallcelllungcancer
_version_ 1724664118142566400
spelling doaj-5e044c708762482fafa302eaaab716312020-11-25T03:08:48ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122020-02-011110.3389/fphar.2020.00178518090METTL7B Is Required for Cancer Cell Proliferation and Tumorigenesis in Non-Small Cell Lung CancerDongcheng Liu0Dongcheng Liu1Wei Li2Wei Li3Fuhua Zhong4Jianhua Yin5Wei Zhou6Shixuan Li7Xuefeng Sun8Jing Xu9Guofeng Li10Yuxin Wen11Jiaqing Wang12Malin Hong13Zhiqiang Cheng14Zhiqiang Cheng15Jimin Yuan16Lingyun Dai17Jichao Sun18Jigang Wang19Chen Qiu20Guangsuo Wang21Chang Zou22Chang Zou23Department of Clinical Medical Research Center, The Second Clinical Medical College of Jinan University, the First Affiliated Hospital of Southern University of Science and Technology, Shenzhen People’s Hospital, Shenzhen, ChinaIntegrated Chinese and Western Medicine Postdoctoral Research Station, Jinan University, Guangzhou, ChinaDepartment of Clinical Medical Research Center, The Second Clinical Medical College of Jinan University, the First Affiliated Hospital of Southern University of Science and Technology, Shenzhen People’s Hospital, Shenzhen, ChinaShenzhen Public Service Platform on Tumor Precision Medicine and Molecular Diagnosis, the Second Clinical Medical College of Jinan University, Shenzhen People’s Hospital, Shenzhen, ChinaDepartment of Clinical Medical Research Center, The Second Clinical Medical College of Jinan University, the First Affiliated Hospital of Southern University of Science and Technology, Shenzhen People’s Hospital, Shenzhen, ChinaLaboratory of Molecular Pharmacology, Department of Pharmacology, School of Pharmacy, Southwest Medical University, Luzhou, ChinaDepartment of Clinical Medical Research Center, The Second Clinical Medical College of Jinan University, the First Affiliated Hospital of Southern University of Science and Technology, Shenzhen People’s Hospital, Shenzhen, ChinaDepartment of Thoracic Surgery, the First Affiliated Hospital of Southern University of Sciences and Technology, Shenzhen People’s Hospital, Shenzhen, ChinaDepartment of Thoracic Surgery, the First Affiliated Hospital of Southern University of Sciences and Technology, Shenzhen People’s Hospital, Shenzhen, ChinaDepartment of Pathology, the First Affiliated Hospital of Southern University of Sciences and Technology, Shenzhen People’s Hospital, Shenzhen, ChinaDepartment of Thoracic Surgery, the First Affiliated Hospital of Southern University of Sciences and Technology, Shenzhen People’s Hospital, Shenzhen, ChinaDepartment of Thoracic Surgery, the First Affiliated Hospital of Southern University of Sciences and Technology, Shenzhen People’s Hospital, Shenzhen, ChinaDepartment of Thoracic Surgery, the First Affiliated Hospital of Southern University of Sciences and Technology, Shenzhen People’s Hospital, Shenzhen, ChinaDepartment of Clinical Medical Research Center, The Second Clinical Medical College of Jinan University, the First Affiliated Hospital of Southern University of Science and Technology, Shenzhen People’s Hospital, Shenzhen, ChinaShenzhen Public Service Platform on Tumor Precision Medicine and Molecular Diagnosis, the Second Clinical Medical College of Jinan University, Shenzhen People’s Hospital, Shenzhen, ChinaDepartment of Pathology, the First Affiliated Hospital of Southern University of Sciences and Technology, Shenzhen People’s Hospital, Shenzhen, ChinaThe Second Clinical Medical College of Jinan University, the First Affiliated Hospital of Southern University of Science and Technology, Shenzhen People’s Hospital, Shenzhen, ChinaThe Second Clinical Medical College of Jinan University, the First Affiliated Hospital of Southern University of Science and Technology, Shenzhen People’s Hospital, Shenzhen, ChinaThe Second Clinical Medical College of Jinan University, the First Affiliated Hospital of Southern University of Science and Technology, Shenzhen People’s Hospital, Shenzhen, ChinaThe Second Clinical Medical College of Jinan University, the First Affiliated Hospital of Southern University of Science and Technology, Shenzhen People’s Hospital, Shenzhen, ChinaDepartment of Respiratory and Critical Medicine, Shenzhen People's Hospital, Second Clinical Medical College, Jinan University, Shenzhen, ChinaDepartment of Thoracic Surgery, the First Affiliated Hospital of Southern University of Sciences and Technology, Shenzhen People’s Hospital, Shenzhen, ChinaDepartment of Clinical Medical Research Center, The Second Clinical Medical College of Jinan University, the First Affiliated Hospital of Southern University of Science and Technology, Shenzhen People’s Hospital, Shenzhen, ChinaShenzhen Public Service Platform on Tumor Precision Medicine and Molecular Diagnosis, the Second Clinical Medical College of Jinan University, Shenzhen People’s Hospital, Shenzhen, ChinaLung cancer remains a leading cause of cancer-associated mortality worldwide, however, molecular mechanisms underlying lung cancer tumorigenesis and progression remain unknown. Here, we report evidence showing that one member of the mammalian methyltransferase-like family (METTL), METTL7B, is a potential molecular target for treatment of non-small cell lung cancer (NSCLC). METTL7B expression was elevated in the majority of NSCLC comparing to normal tissues. Increased expression of METTL7B contributed to advanced stages of tumor development and poor survival in NSCLC patients. Lentivirus-mediated shRNA silencing of METTL7B suppressed proliferation and tumorigenesis of cancer cells in vitro and in vivo. Investigation on gene expression profiles of NSCLC cells revealed that abundant cell cycle related genes were downregulated in the absence of METTL7B. Pathway enrichment analysis indicated that METTL7B participated in cell cycle regulation. Notably, CCND1, a key regulator for G1/S transition, was significantly decreased with the depletion of METTL7B, resulting in G0/G1 arrest, indicating that METTL7B is critical for cell cycle progression. Taken together, our findings implicate that METTL7B is essential for NSCLC development and progression. METTL7B might serve as a potential therapeutic target for NSCLC.https://www.frontiersin.org/article/10.3389/fphar.2020.00178/fullMETTL7Bnon-small cell lung cancerproliferationtumorigenesiscell cycle