Loading…

Cysteinyl-tRNA Synthetase 1 Promotes Ferroptosis-Induced Cell Death via Regulating GPX4 Expression

Esophageal squamous cell carcinoma (ESCC) has still been considered to be the most common malignant tumors in China. Emerging evidence indicates that cysteinyl-tRNA synthetase 1 (CARS1) has been considered as a ferroptosis-related gene in ESCC. However, the roles and molecular mechanisms of CARS1 in...

Full description

Saved in:
Bibliographic Details
Published in:Journal of oncology 2022-09, Vol.2022, p.1-16
Main Authors: Zhang, Wanfei, Lin, Xianzuan, Chen, Shaogeng
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c453t-2c5cdfd4d309e9801b3092a60ade12ec1adb51f39c0d542a5eb34a8af4b42dde3
cites cdi_FETCH-LOGICAL-c453t-2c5cdfd4d309e9801b3092a60ade12ec1adb51f39c0d542a5eb34a8af4b42dde3
container_end_page 16
container_issue
container_start_page 1
container_title Journal of oncology
container_volume 2022
creator Zhang, Wanfei
Lin, Xianzuan
Chen, Shaogeng
description Esophageal squamous cell carcinoma (ESCC) has still been considered to be the most common malignant tumors in China. Emerging evidence indicates that cysteinyl-tRNA synthetase 1 (CARS1) has been considered as a ferroptosis-related gene in ESCC. However, the roles and molecular mechanisms of CARS1 in ferroptosis-induced cell death of ESCC are still largely unknown. In our study, we investigated an aberrantly upregulated gene in ESCC tumor tissues CARS1 significantly inhibited cell proliferation, and the ability of migration and invasion promoted the relative level of MDA and ROS and decreased GPX4 expression level in two ESCC cell lines. Mechanistically, both the ferroptosis inhibitor ferrostatin-1 and its inducer erastin were further used and indicated that CARS1 participated in the ferroptosis-induced cell death. Together, these results revealed that CARS1 has a critical function in the progression of ESCC by promoting ferroptosis-induced cell death.
doi_str_mv 10.1155/2022/4849174
format article
fullrecord <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9534673</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A721690926</galeid><sourcerecordid>A721690926</sourcerecordid><originalsourceid>FETCH-LOGICAL-c453t-2c5cdfd4d309e9801b3092a60ade12ec1adb51f39c0d542a5eb34a8af4b42dde3</originalsourceid><addsrcrecordid>eNp9kc1rFEEQxQdRMEZv_gENXgQd05_zcRGWNYmBEENU8NbUdNfsdpjtXrt7ovvfO8MuiXrIqR7Uj1f1eEXxmtEPjCl1winnJ7KRLavlk-KIVU1dNlLRp3_p58WLlG4prSRtq6OiW-5SRud3Q5lvrhbk687nNWZISBi5jmETMiZyhjGGbQ7JpfLC29GgJUscBvIJIa_JnQNyg6txgOz8ipxf_5Dk9Pc2Ykou-JfFsx6GhK8O87j4fnb6bfm5vPxyfrFcXJZGKpFLbpSxvZVW0BbbhrJuEhwqChYZR8PAdor1ojXUKslBYSckNNDLTnJrURwXH_e-27HboDXoc4RBb6PbQNzpAE7_u_FurVfhTrdKyKoWk8Hbg0EMP0dMWW9cMlNM8BjGpHnNhWwEUzP65j_0NozRT_Fmirc1a3jzQK1gQO18H6a7ZjbVi5qzqp0CVhP1fk-ZGFKK2N-_zKiee9Vzr_rQ64S_2-Nr5y38co_TfwBh5aKC</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2722971828</pqid></control><display><type>article</type><title>Cysteinyl-tRNA Synthetase 1 Promotes Ferroptosis-Induced Cell Death via Regulating GPX4 Expression</title><source>Wiley Online Library</source><source>Publicly Available Content (ProQuest)</source><source>PubMed Central</source><creator>Zhang, Wanfei ; Lin, Xianzuan ; Chen, Shaogeng</creator><contributor>Xu, Yingkun ; Yingkun Xu</contributor><creatorcontrib>Zhang, Wanfei ; Lin, Xianzuan ; Chen, Shaogeng ; Xu, Yingkun ; Yingkun Xu</creatorcontrib><description>Esophageal squamous cell carcinoma (ESCC) has still been considered to be the most common malignant tumors in China. Emerging evidence indicates that cysteinyl-tRNA synthetase 1 (CARS1) has been considered as a ferroptosis-related gene in ESCC. However, the roles and molecular mechanisms of CARS1 in ferroptosis-induced cell death of ESCC are still largely unknown. In our study, we investigated an aberrantly upregulated gene in ESCC tumor tissues CARS1 significantly inhibited cell proliferation, and the ability of migration and invasion promoted the relative level of MDA and ROS and decreased GPX4 expression level in two ESCC cell lines. Mechanistically, both the ferroptosis inhibitor ferrostatin-1 and its inducer erastin were further used and indicated that CARS1 participated in the ferroptosis-induced cell death. Together, these results revealed that CARS1 has a critical function in the progression of ESCC by promoting ferroptosis-induced cell death.</description><identifier>ISSN: 1687-8450</identifier><identifier>EISSN: 1687-8450</identifier><identifier>EISSN: 1687-8469</identifier><identifier>DOI: 10.1155/2022/4849174</identifier><language>eng</language><publisher>New York: Hindawi</publisher><subject>Antibiotics ; Apoptosis ; Biochemistry ; Cancer ; Care and treatment ; Cell culture ; Cell death ; Esophageal cancer ; Ferroptosis ; Investigations ; Ligases ; Lipid peroxidation ; Lipids ; Medical prognosis ; Reagents ; Squamous cell carcinoma ; Transfer RNA</subject><ispartof>Journal of oncology, 2022-09, Vol.2022, p.1-16</ispartof><rights>Copyright © 2022 Wanfei Zhang et al.</rights><rights>COPYRIGHT 2022 John Wiley &amp; Sons, Inc.</rights><rights>Copyright © 2022 Wanfei Zhang et al. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2022 Wanfei Zhang et al. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c453t-2c5cdfd4d309e9801b3092a60ade12ec1adb51f39c0d542a5eb34a8af4b42dde3</citedby><cites>FETCH-LOGICAL-c453t-2c5cdfd4d309e9801b3092a60ade12ec1adb51f39c0d542a5eb34a8af4b42dde3</cites><orcidid>0000-0001-9749-5940</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2722971828/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2722971828?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768,74869</link.rule.ids></links><search><contributor>Xu, Yingkun</contributor><contributor>Yingkun Xu</contributor><creatorcontrib>Zhang, Wanfei</creatorcontrib><creatorcontrib>Lin, Xianzuan</creatorcontrib><creatorcontrib>Chen, Shaogeng</creatorcontrib><title>Cysteinyl-tRNA Synthetase 1 Promotes Ferroptosis-Induced Cell Death via Regulating GPX4 Expression</title><title>Journal of oncology</title><description>Esophageal squamous cell carcinoma (ESCC) has still been considered to be the most common malignant tumors in China. Emerging evidence indicates that cysteinyl-tRNA synthetase 1 (CARS1) has been considered as a ferroptosis-related gene in ESCC. However, the roles and molecular mechanisms of CARS1 in ferroptosis-induced cell death of ESCC are still largely unknown. In our study, we investigated an aberrantly upregulated gene in ESCC tumor tissues CARS1 significantly inhibited cell proliferation, and the ability of migration and invasion promoted the relative level of MDA and ROS and decreased GPX4 expression level in two ESCC cell lines. Mechanistically, both the ferroptosis inhibitor ferrostatin-1 and its inducer erastin were further used and indicated that CARS1 participated in the ferroptosis-induced cell death. Together, these results revealed that CARS1 has a critical function in the progression of ESCC by promoting ferroptosis-induced cell death.</description><subject>Antibiotics</subject><subject>Apoptosis</subject><subject>Biochemistry</subject><subject>Cancer</subject><subject>Care and treatment</subject><subject>Cell culture</subject><subject>Cell death</subject><subject>Esophageal cancer</subject><subject>Ferroptosis</subject><subject>Investigations</subject><subject>Ligases</subject><subject>Lipid peroxidation</subject><subject>Lipids</subject><subject>Medical prognosis</subject><subject>Reagents</subject><subject>Squamous cell carcinoma</subject><subject>Transfer RNA</subject><issn>1687-8450</issn><issn>1687-8450</issn><issn>1687-8469</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNp9kc1rFEEQxQdRMEZv_gENXgQd05_zcRGWNYmBEENU8NbUdNfsdpjtXrt7ovvfO8MuiXrIqR7Uj1f1eEXxmtEPjCl1winnJ7KRLavlk-KIVU1dNlLRp3_p58WLlG4prSRtq6OiW-5SRud3Q5lvrhbk687nNWZISBi5jmETMiZyhjGGbQ7JpfLC29GgJUscBvIJIa_JnQNyg6txgOz8ipxf_5Dk9Pc2Ykou-JfFsx6GhK8O87j4fnb6bfm5vPxyfrFcXJZGKpFLbpSxvZVW0BbbhrJuEhwqChYZR8PAdor1ojXUKslBYSckNNDLTnJrURwXH_e-27HboDXoc4RBb6PbQNzpAE7_u_FurVfhTrdKyKoWk8Hbg0EMP0dMWW9cMlNM8BjGpHnNhWwEUzP65j_0NozRT_Fmirc1a3jzQK1gQO18H6a7ZjbVi5qzqp0CVhP1fk-ZGFKK2N-_zKiee9Vzr_rQ64S_2-Nr5y38co_TfwBh5aKC</recordid><startdate>20220928</startdate><enddate>20220928</enddate><creator>Zhang, Wanfei</creator><creator>Lin, Xianzuan</creator><creator>Chen, Shaogeng</creator><general>Hindawi</general><general>John Wiley &amp; Sons, Inc</general><general>Hindawi Limited</general><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9749-5940</orcidid></search><sort><creationdate>20220928</creationdate><title>Cysteinyl-tRNA Synthetase 1 Promotes Ferroptosis-Induced Cell Death via Regulating GPX4 Expression</title><author>Zhang, Wanfei ; Lin, Xianzuan ; Chen, Shaogeng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c453t-2c5cdfd4d309e9801b3092a60ade12ec1adb51f39c0d542a5eb34a8af4b42dde3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Antibiotics</topic><topic>Apoptosis</topic><topic>Biochemistry</topic><topic>Cancer</topic><topic>Care and treatment</topic><topic>Cell culture</topic><topic>Cell death</topic><topic>Esophageal cancer</topic><topic>Ferroptosis</topic><topic>Investigations</topic><topic>Ligases</topic><topic>Lipid peroxidation</topic><topic>Lipids</topic><topic>Medical prognosis</topic><topic>Reagents</topic><topic>Squamous cell carcinoma</topic><topic>Transfer RNA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Wanfei</creatorcontrib><creatorcontrib>Lin, Xianzuan</creatorcontrib><creatorcontrib>Chen, Shaogeng</creatorcontrib><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access Journals</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Wanfei</au><au>Lin, Xianzuan</au><au>Chen, Shaogeng</au><au>Xu, Yingkun</au><au>Yingkun Xu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cysteinyl-tRNA Synthetase 1 Promotes Ferroptosis-Induced Cell Death via Regulating GPX4 Expression</atitle><jtitle>Journal of oncology</jtitle><date>2022-09-28</date><risdate>2022</risdate><volume>2022</volume><spage>1</spage><epage>16</epage><pages>1-16</pages><issn>1687-8450</issn><eissn>1687-8450</eissn><eissn>1687-8469</eissn><abstract>Esophageal squamous cell carcinoma (ESCC) has still been considered to be the most common malignant tumors in China. Emerging evidence indicates that cysteinyl-tRNA synthetase 1 (CARS1) has been considered as a ferroptosis-related gene in ESCC. However, the roles and molecular mechanisms of CARS1 in ferroptosis-induced cell death of ESCC are still largely unknown. In our study, we investigated an aberrantly upregulated gene in ESCC tumor tissues CARS1 significantly inhibited cell proliferation, and the ability of migration and invasion promoted the relative level of MDA and ROS and decreased GPX4 expression level in two ESCC cell lines. Mechanistically, both the ferroptosis inhibitor ferrostatin-1 and its inducer erastin were further used and indicated that CARS1 participated in the ferroptosis-induced cell death. Together, these results revealed that CARS1 has a critical function in the progression of ESCC by promoting ferroptosis-induced cell death.</abstract><cop>New York</cop><pub>Hindawi</pub><doi>10.1155/2022/4849174</doi><tpages>16</tpages><orcidid>https://orcid.org/0000-0001-9749-5940</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1687-8450
ispartof Journal of oncology, 2022-09, Vol.2022, p.1-16
issn 1687-8450
1687-8450
1687-8469
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9534673
source Wiley Online Library; Publicly Available Content (ProQuest); PubMed Central
subjects Antibiotics
Apoptosis
Biochemistry
Cancer
Care and treatment
Cell culture
Cell death
Esophageal cancer
Ferroptosis
Investigations
Ligases
Lipid peroxidation
Lipids
Medical prognosis
Reagents
Squamous cell carcinoma
Transfer RNA
title Cysteinyl-tRNA Synthetase 1 Promotes Ferroptosis-Induced Cell Death via Regulating GPX4 Expression
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-04T19%3A22%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cysteinyl-tRNA%20Synthetase%201%20Promotes%20Ferroptosis-Induced%20Cell%20Death%20via%20Regulating%20GPX4%20Expression&rft.jtitle=Journal%20of%20oncology&rft.au=Zhang,%20Wanfei&rft.date=2022-09-28&rft.volume=2022&rft.spage=1&rft.epage=16&rft.pages=1-16&rft.issn=1687-8450&rft.eissn=1687-8450&rft_id=info:doi/10.1155/2022/4849174&rft_dat=%3Cgale_pubme%3EA721690926%3C/gale_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c453t-2c5cdfd4d309e9801b3092a60ade12ec1adb51f39c0d542a5eb34a8af4b42dde3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2722971828&rft_id=info:pmid/&rft_galeid=A721690926&rfr_iscdi=true