HNMT Upregulation Induces Cancer Stem Cell Formation and Confers Protection against Oxidative Stress through Interaction with HER2 in Non-Small-Cell Lung Cancer

Background: The treatment of non‐small‐cell lung cancer (NSCLC) involves platinum-based chemotherapy. It is typically accompanied by chemoresistance resulting from antioxidant properties conferred by cancer stem cells (CSCs). Human epidermal growth factor receptor 2 (HER2) enhances CSCs and antioxid...

Full description

Bibliographic Details
Main Authors: Kuo, Kuang-Tai, Lin, Cheng-Hsin, Wang, Chun-Hua, Pikatan, Narpati Wesa, Yadav, Vijesh Kumar, Fong, Iat-Hang, Yeh, Chi-Tai, Lee, Wei-Hwa, Huang, Wen-Chien
Format: Article
Language:English
Published: MDPI 2022
Subjects:
Online Access:https://repository.ugm.ac.id/279058/1/HNMT-Upregulation-Induces-Cancer-Stem-Cell-Formation-and-Confers-Protection-against-Oxidative-Stress-through-Interaction-with-HER2-in-NonSmallCell-Lung-CancerInternational-Journal-of-Molecular-Sciences.pdf
_version_ 1826050371972235264
author Kuo, Kuang-Tai
Lin, Cheng-Hsin
Wang, Chun-Hua
Pikatan, Narpati Wesa
Yadav, Vijesh Kumar
Fong, Iat-Hang
Yeh, Chi-Tai
Lee, Wei-Hwa
Huang, Wen-Chien
author_facet Kuo, Kuang-Tai
Lin, Cheng-Hsin
Wang, Chun-Hua
Pikatan, Narpati Wesa
Yadav, Vijesh Kumar
Fong, Iat-Hang
Yeh, Chi-Tai
Lee, Wei-Hwa
Huang, Wen-Chien
author_sort Kuo, Kuang-Tai
collection UGM
description Background: The treatment of non‐small‐cell lung cancer (NSCLC) involves platinum-based chemotherapy. It is typically accompanied by chemoresistance resulting from antioxidant properties conferred by cancer stem cells (CSCs). Human epidermal growth factor receptor 2 (HER2) enhances CSCs and antioxidant properties in cancers, including NSCLC. Methods: Here, we elucidated the role of histamine N‐methyltransferase (HNMT), a histamine metabolism enzyme significantly upregulated in NSCLC and coexpressed with HER2. HNMT expression in lung cancer tissues was determined using quantitative reverse transcription PCR (RT‐qPCR). A publicly available dataset was used to determine HNMT’s potential as an NSCLC target molecule. Immunohisto-chemistry and coimmunoprecipitation were used to determine HNMT–HER2 correlations and in-teractions, respectively. HNMT shRNA and overexpression plasmids were used to explore HNMT functions in vitro and in vivo. We also examined miRNAs that may target HNMT and investigated HNMT/HER2′s role on NSCLC cells’ antioxidant properties. Finally, how HNMT loss affects NSCLC cells’ sensitivity to cisplatin was investigated. Results: HNMT was significantly upregu-lated in human NSCLC tissues, conferred a worse prognosis, and was coexpressed with HER2. HNMT depletion and overexpression respectively decreased and increased cell proliferation, colony formation, tumorsphere formation, and CSCs marker expression. Coimmunoprecipitation analysis indicated that HNMT directly interacts with HER2. TARGETSCAN analysis revealed that HNMT is a miR‐223 and miR‐3065‐5p target. TBHp treatment increased HER2 expression, whereas shHNMT disrupted the Nuclear factor erythroid 2‐related factor 2 (Nrf2)/ hemeoxygenase‐1 (HO‐ 1)/HER2 axis and increased reactive oxygen species accumulation in NSCLC cells. Finally, shHNMT sensitized H441 cells to cisplatin treatment in vitro and in vivo. Conclusions: Therefore, HNMT up-regulation in NSCLC cells may upregulate HER2 expression, increasing tumorigenicity and chemo-resistance through CSCs maintenance and antioxidant properties. This newly discovered regulatory axis may aid in retarding NSCLC progression and chemoresistance.
first_indexed 2024-03-14T00:02:55Z
format Article
id oai:generic.eprints.org:279058
institution Universiti Gadjah Mada
language English
last_indexed 2024-03-14T00:02:55Z
publishDate 2022
publisher MDPI
record_format dspace
spelling oai:generic.eprints.org:2790582023-10-31T05:29:52Z https://repository.ugm.ac.id/279058/ HNMT Upregulation Induces Cancer Stem Cell Formation and Confers Protection against Oxidative Stress through Interaction with HER2 in Non-Small-Cell Lung Cancer Kuo, Kuang-Tai Lin, Cheng-Hsin Wang, Chun-Hua Pikatan, Narpati Wesa Yadav, Vijesh Kumar Fong, Iat-Hang Yeh, Chi-Tai Lee, Wei-Hwa Huang, Wen-Chien Surgery Oncology and Carcinogenesis Cancer Cell Biology Background: The treatment of non‐small‐cell lung cancer (NSCLC) involves platinum-based chemotherapy. It is typically accompanied by chemoresistance resulting from antioxidant properties conferred by cancer stem cells (CSCs). Human epidermal growth factor receptor 2 (HER2) enhances CSCs and antioxidant properties in cancers, including NSCLC. Methods: Here, we elucidated the role of histamine N‐methyltransferase (HNMT), a histamine metabolism enzyme significantly upregulated in NSCLC and coexpressed with HER2. HNMT expression in lung cancer tissues was determined using quantitative reverse transcription PCR (RT‐qPCR). A publicly available dataset was used to determine HNMT’s potential as an NSCLC target molecule. Immunohisto-chemistry and coimmunoprecipitation were used to determine HNMT–HER2 correlations and in-teractions, respectively. HNMT shRNA and overexpression plasmids were used to explore HNMT functions in vitro and in vivo. We also examined miRNAs that may target HNMT and investigated HNMT/HER2′s role on NSCLC cells’ antioxidant properties. Finally, how HNMT loss affects NSCLC cells’ sensitivity to cisplatin was investigated. Results: HNMT was significantly upregu-lated in human NSCLC tissues, conferred a worse prognosis, and was coexpressed with HER2. HNMT depletion and overexpression respectively decreased and increased cell proliferation, colony formation, tumorsphere formation, and CSCs marker expression. Coimmunoprecipitation analysis indicated that HNMT directly interacts with HER2. TARGETSCAN analysis revealed that HNMT is a miR‐223 and miR‐3065‐5p target. TBHp treatment increased HER2 expression, whereas shHNMT disrupted the Nuclear factor erythroid 2‐related factor 2 (Nrf2)/ hemeoxygenase‐1 (HO‐ 1)/HER2 axis and increased reactive oxygen species accumulation in NSCLC cells. Finally, shHNMT sensitized H441 cells to cisplatin treatment in vitro and in vivo. Conclusions: Therefore, HNMT up-regulation in NSCLC cells may upregulate HER2 expression, increasing tumorigenicity and chemo-resistance through CSCs maintenance and antioxidant properties. This newly discovered regulatory axis may aid in retarding NSCLC progression and chemoresistance. MDPI 2022-01-31 Article PeerReviewed application/pdf en https://repository.ugm.ac.id/279058/1/HNMT-Upregulation-Induces-Cancer-Stem-Cell-Formation-and-Confers-Protection-against-Oxidative-Stress-through-Interaction-with-HER2-in-NonSmallCell-Lung-CancerInternational-Journal-of-Molecular-Sciences.pdf Kuo, Kuang-Tai and Lin, Cheng-Hsin and Wang, Chun-Hua and Pikatan, Narpati Wesa and Yadav, Vijesh Kumar and Fong, Iat-Hang and Yeh, Chi-Tai and Lee, Wei-Hwa and Huang, Wen-Chien (2022) HNMT Upregulation Induces Cancer Stem Cell Formation and Confers Protection against Oxidative Stress through Interaction with HER2 in Non-Small-Cell Lung Cancer. International Journal of Molecular Sciences, 23 (3). pp. 1-19. ISSN 16616596 https://www.mdpi.com/1422-0067/23/3/1663 https://doi.org/10.3390/ijms23031663
spellingShingle Surgery
Oncology and Carcinogenesis
Cancer Cell Biology
Kuo, Kuang-Tai
Lin, Cheng-Hsin
Wang, Chun-Hua
Pikatan, Narpati Wesa
Yadav, Vijesh Kumar
Fong, Iat-Hang
Yeh, Chi-Tai
Lee, Wei-Hwa
Huang, Wen-Chien
HNMT Upregulation Induces Cancer Stem Cell Formation and Confers Protection against Oxidative Stress through Interaction with HER2 in Non-Small-Cell Lung Cancer
title HNMT Upregulation Induces Cancer Stem Cell Formation and Confers Protection against Oxidative Stress through Interaction with HER2 in Non-Small-Cell Lung Cancer
title_full HNMT Upregulation Induces Cancer Stem Cell Formation and Confers Protection against Oxidative Stress through Interaction with HER2 in Non-Small-Cell Lung Cancer
title_fullStr HNMT Upregulation Induces Cancer Stem Cell Formation and Confers Protection against Oxidative Stress through Interaction with HER2 in Non-Small-Cell Lung Cancer
title_full_unstemmed HNMT Upregulation Induces Cancer Stem Cell Formation and Confers Protection against Oxidative Stress through Interaction with HER2 in Non-Small-Cell Lung Cancer
title_short HNMT Upregulation Induces Cancer Stem Cell Formation and Confers Protection against Oxidative Stress through Interaction with HER2 in Non-Small-Cell Lung Cancer
title_sort hnmt upregulation induces cancer stem cell formation and confers protection against oxidative stress through interaction with her2 in non small cell lung cancer
topic Surgery
Oncology and Carcinogenesis
Cancer Cell Biology
url https://repository.ugm.ac.id/279058/1/HNMT-Upregulation-Induces-Cancer-Stem-Cell-Formation-and-Confers-Protection-against-Oxidative-Stress-through-Interaction-with-HER2-in-NonSmallCell-Lung-CancerInternational-Journal-of-Molecular-Sciences.pdf
work_keys_str_mv AT kuokuangtai hnmtupregulationinducescancerstemcellformationandconfersprotectionagainstoxidativestressthroughinteractionwithher2innonsmallcelllungcancer
AT linchenghsin hnmtupregulationinducescancerstemcellformationandconfersprotectionagainstoxidativestressthroughinteractionwithher2innonsmallcelllungcancer
AT wangchunhua hnmtupregulationinducescancerstemcellformationandconfersprotectionagainstoxidativestressthroughinteractionwithher2innonsmallcelllungcancer
AT pikatannarpatiwesa hnmtupregulationinducescancerstemcellformationandconfersprotectionagainstoxidativestressthroughinteractionwithher2innonsmallcelllungcancer
AT yadavvijeshkumar hnmtupregulationinducescancerstemcellformationandconfersprotectionagainstoxidativestressthroughinteractionwithher2innonsmallcelllungcancer
AT fongiathang hnmtupregulationinducescancerstemcellformationandconfersprotectionagainstoxidativestressthroughinteractionwithher2innonsmallcelllungcancer
AT yehchitai hnmtupregulationinducescancerstemcellformationandconfersprotectionagainstoxidativestressthroughinteractionwithher2innonsmallcelllungcancer
AT leeweihwa hnmtupregulationinducescancerstemcellformationandconfersprotectionagainstoxidativestressthroughinteractionwithher2innonsmallcelllungcancer
AT huangwenchien hnmtupregulationinducescancerstemcellformationandconfersprotectionagainstoxidativestressthroughinteractionwithher2innonsmallcelllungcancer