Serveur d'exploration Chloroquine

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Knockdown of TRIM65 inhibits autophagy and cisplatin resistance in A549/DDP cells by regulating miR-138-5p/ATG7

Identifieur interne : 000702 ( Main/Exploration ); précédent : 000701; suivant : 000703

Knockdown of TRIM65 inhibits autophagy and cisplatin resistance in A549/DDP cells by regulating miR-138-5p/ATG7

Auteurs : Xufeng Pan ; Yong Chen ; Yuzhou Shen ; Jicheng Tantai

Source :

RBID : PMC:6546683

Abstract

Cisplatin resistance is the main cause of treatment failure in patients with non-small-cell lung cancer (NSCLC). Autophagy is a key mechanism of resistance to chemotherapy. Given that tripartite motif (TRIM)-containing proteins are involved in the regulation of autophagy and chemoresistance, we aimed to study the functions of TRIM protein members in autophagy-mediated chemoresistance of NSCLC. We found that TRIM65 was significantly increased in cisplatin-resistant NSCLC cell line (A549/DDP) as compared to the parental cell line (A549). Knockdown of TRIM65 can enhance cisplatin-induced apoptosis and inhibit autophagy in A549/DDP cells, as indicated by Annexin V/PI staining, caspase3 activity test, and LC3-II immunofluorescence staining. Additionally, knockdown of TRIM65 significantly decreased the expression of an important autophagy mediator, ATG7, which was a potential target of miR-138-5p. miR-138-5p inhibitor significantly abolished the effects of TRIM65 knockdown on autophagy and cisplatin-induced apoptosis. Moreover, TRIM65 induced the ubiquitination and degradation of TNRC6A, resulting in the suppressed expression of miR-138-5p. TRIM65 knockdown inhibited the growth of tumors derived from A549/DDP cells. Furthermore, cisplatin-resistant NSCLC tissues displayed higher expression of TRIM65 mRNA and lower expression of miR-138-5p as compared to cisplatin non-resistant ones. miR-138-5p expression was negatively correlated with TRIM65 mRNA in NSCLC tissues. Collectively, the present study indicates that TRIM65 knockdown attenuates autophagy and cisplatin resistance in A549/DDP cells via regulating miR-138-5p.


Url:
DOI: 10.1038/s41419-019-1660-8
PubMed: 31160576
PubMed Central: 6546683


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">Knockdown of TRIM65 inhibits autophagy and cisplatin resistance in A549/DDP cells by regulating miR-138-5p/ATG7</title>
<author>
<name sortKey="Pan, Xufeng" sort="Pan, Xufeng" uniqKey="Pan X" first="Xufeng" last="Pan">Xufeng Pan</name>
<affiliation>
<nlm:aff id="Aff1"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Chen, Yong" sort="Chen, Yong" uniqKey="Chen Y" first="Yong" last="Chen">Yong Chen</name>
<affiliation>
<nlm:aff id="Aff1"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Shen, Yuzhou" sort="Shen, Yuzhou" uniqKey="Shen Y" first="Yuzhou" last="Shen">Yuzhou Shen</name>
<affiliation>
<nlm:aff id="Aff1"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Tantai, Jicheng" sort="Tantai, Jicheng" uniqKey="Tantai J" first="Jicheng" last="Tantai">Jicheng Tantai</name>
<affiliation>
<nlm:aff id="Aff1"></nlm:aff>
</affiliation>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">PMC</idno>
<idno type="pmid">31160576</idno>
<idno type="pmc">6546683</idno>
<idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6546683</idno>
<idno type="RBID">PMC:6546683</idno>
<idno type="doi">10.1038/s41419-019-1660-8</idno>
<date when="2019">2019</date>
<idno type="wicri:Area/Pmc/Corpus">000059</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000059</idno>
<idno type="wicri:Area/Pmc/Curation">000059</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Curation">000059</idno>
<idno type="wicri:Area/Pmc/Checkpoint">000649</idno>
<idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Checkpoint">000649</idno>
<idno type="wicri:Area/Ncbi/Merge">000671</idno>
<idno type="wicri:Area/Ncbi/Curation">000671</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">000671</idno>
<idno type="wicri:Area/Main/Merge">000702</idno>
<idno type="wicri:Area/Main/Curation">000702</idno>
<idno type="wicri:Area/Main/Exploration">000702</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en" level="a" type="main">Knockdown of TRIM65 inhibits autophagy and cisplatin resistance in A549/DDP cells by regulating miR-138-5p/ATG7</title>
<author>
<name sortKey="Pan, Xufeng" sort="Pan, Xufeng" uniqKey="Pan X" first="Xufeng" last="Pan">Xufeng Pan</name>
<affiliation>
<nlm:aff id="Aff1"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Chen, Yong" sort="Chen, Yong" uniqKey="Chen Y" first="Yong" last="Chen">Yong Chen</name>
<affiliation>
<nlm:aff id="Aff1"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Shen, Yuzhou" sort="Shen, Yuzhou" uniqKey="Shen Y" first="Yuzhou" last="Shen">Yuzhou Shen</name>
<affiliation>
<nlm:aff id="Aff1"></nlm:aff>
</affiliation>
</author>
<author>
<name sortKey="Tantai, Jicheng" sort="Tantai, Jicheng" uniqKey="Tantai J" first="Jicheng" last="Tantai">Jicheng Tantai</name>
<affiliation>
<nlm:aff id="Aff1"></nlm:aff>
</affiliation>
</author>
</analytic>
<series>
<title level="j">Cell Death & Disease</title>
<idno type="eISSN">2041-4889</idno>
<imprint>
<date when="2019">2019</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass></textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<p id="Par1">Cisplatin resistance is the main cause of treatment failure in patients with non-small-cell lung cancer (NSCLC). Autophagy is a key mechanism of resistance to chemotherapy. Given that tripartite motif (TRIM)-containing proteins are involved in the regulation of autophagy and chemoresistance, we aimed to study the functions of TRIM protein members in autophagy-mediated chemoresistance of NSCLC. We found that TRIM65 was significantly increased in cisplatin-resistant NSCLC cell line (A549/DDP) as compared to the parental cell line (A549). Knockdown of TRIM65 can enhance cisplatin-induced apoptosis and inhibit autophagy in A549/DDP cells, as indicated by Annexin V/PI staining, caspase3 activity test, and LC3-II immunofluorescence staining. Additionally, knockdown of TRIM65 significantly decreased the expression of an important autophagy mediator, ATG7, which was a potential target of miR-138-5p. miR-138-5p inhibitor significantly abolished the effects of TRIM65 knockdown on autophagy and cisplatin-induced apoptosis. Moreover, TRIM65 induced the ubiquitination and degradation of TNRC6A, resulting in the suppressed expression of miR-138-5p. TRIM65 knockdown inhibited the growth of tumors derived from A549/DDP cells. Furthermore, cisplatin-resistant NSCLC tissues displayed higher expression of TRIM65 mRNA and lower expression of miR-138-5p as compared to cisplatin non-resistant ones. miR-138-5p expression was negatively correlated with TRIM65 mRNA in NSCLC tissues. Collectively, the present study indicates that TRIM65 knockdown attenuates autophagy and cisplatin resistance in A549/DDP cells via regulating miR-138-5p.</p>
</div>
</front>
<back>
<div1 type="bibliography">
<listBibl>
<biblStruct>
<analytic>
<author>
<name sortKey="Bray, F" uniqKey="Bray F">F Bray</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Howlader, N" uniqKey="Howlader N">N Howlader</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Wang, Mc" uniqKey="Wang M">MC Wang</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Kuribayashi, K" uniqKey="Kuribayashi K">K Kuribayashi</name>
</author>
<author>
<name sortKey="Funaguchi, N" uniqKey="Funaguchi N">N Funaguchi</name>
</author>
<author>
<name sortKey="Nakano, T" uniqKey="Nakano T">T Nakano</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Girones, R" uniqKey="Girones R">R Gironés</name>
</author>
<author>
<name sortKey="L Pez, P" uniqKey="L Pez P">P López</name>
</author>
<author>
<name sortKey="Chulvi, R" uniqKey="Chulvi R">R Chulvi</name>
</author>
<author>
<name sortKey="Ca Abate, M" uniqKey="Ca Abate M">M Cañabate</name>
</author>
<author>
<name sortKey="Dolores, T" uniqKey="Dolores T">T Dolores</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Chang, A" uniqKey="Chang A">A Chang</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Mizushima, N" uniqKey="Mizushima N">N Mizushima</name>
</author>
<author>
<name sortKey="Komatsu, M" uniqKey="Komatsu M">M Komatsu</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Kobayashi, S" uniqKey="Kobayashi S">S Kobayashi</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Wu, Wk" uniqKey="Wu W">WK Wu</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Sui, X" uniqKey="Sui X">X Sui</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Aredia, F" uniqKey="Aredia F">F Aredia</name>
</author>
<author>
<name sortKey="Scovassi, Ai" uniqKey="Scovassi A">AI Scovassi</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Goldberg, Sb" uniqKey="Goldberg S">SB Goldberg</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Lin, S" uniqKey="Lin S">S Lin</name>
</author>
<author>
<name sortKey="Gregory, Ri" uniqKey="Gregory R">RI Gregory</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Pink, Rc" uniqKey="Pink R">RC Pink</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Xia, L" uniqKey="Xia L">L Xia</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Liang, Z" uniqKey="Liang Z">Z Liang</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Wang, Q" uniqKey="Wang Q">Q Wang</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Seca, H" uniqKey="Seca H">H Seca</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Jin, F" uniqKey="Jin F">F Jin</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Xu, L" uniqKey="Xu L">L Xu</name>
</author>
</analytic>
</biblStruct>
<biblStruct></biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Ozato, K" uniqKey="Ozato K">K Ozato</name>
</author>
<author>
<name sortKey="Shin, D M" uniqKey="Shin D">D-M Shin</name>
</author>
<author>
<name sortKey="Chang, T H" uniqKey="Chang T">T-H Chang</name>
</author>
<author>
<name sortKey="Morse, Hc" uniqKey="Morse H">HC Morse</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Hatakeyama, S" uniqKey="Hatakeyama S">S Hatakeyama</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Hatakeyama, S" uniqKey="Hatakeyama S">S Hatakeyama</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Zhang, L" uniqKey="Zhang L">L Zhang</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Ni, M" uniqKey="Ni M">M Ni</name>
</author>
<author>
<name sortKey="Wang, Y" uniqKey="Wang Y">Y Wang</name>
</author>
<author>
<name sortKey="Xie, L" uniqKey="Xie L">L Xie</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Liu, Y" uniqKey="Liu Y">Y Liu</name>
</author>
<author>
<name sortKey="Zhang, B" uniqKey="Zhang B">B Zhang</name>
</author>
<author>
<name sortKey="Shi, T" uniqKey="Shi T">T Shi</name>
</author>
<author>
<name sortKey="Qin, H" uniqKey="Qin H">H Qin</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Zhao, T T" uniqKey="Zhao T">T-T Zhao</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Tan, Z" uniqKey="Tan Z">Z Tan</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Yu, C" uniqKey="Yu C">C Yu</name>
</author>
<author>
<name sortKey="Chen, S" uniqKey="Chen S">S Chen</name>
</author>
<author>
<name sortKey="Guo, Y" uniqKey="Guo Y">Y Guo</name>
</author>
<author>
<name sortKey="Sun, C" uniqKey="Sun C">C Sun</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Li, S" uniqKey="Li S">S Li</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Tanida, I" uniqKey="Tanida I">I Tanida</name>
</author>
<author>
<name sortKey="Ueno, T" uniqKey="Ueno T">T Ueno</name>
</author>
<author>
<name sortKey="Kominami, E" uniqKey="Kominami E">E Kominami</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Qin, X" uniqKey="Qin X">X Qin</name>
</author>
<author>
<name sortKey="Yu, S" uniqKey="Yu S">S Yu</name>
</author>
<author>
<name sortKey="Xu, X" uniqKey="Xu X">X Xu</name>
</author>
<author>
<name sortKey="Shen, B" uniqKey="Shen B">B Shen</name>
</author>
<author>
<name sortKey="Feng, J" uniqKey="Feng J">J Feng</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Wang, Xl" uniqKey="Wang X">XL Wang</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Yang, Zj" uniqKey="Yang Z">ZJ Yang</name>
</author>
<author>
<name sortKey="Chee, Ce" uniqKey="Chee C">CE Chee</name>
</author>
<author>
<name sortKey="Huang, S" uniqKey="Huang S">S Huang</name>
</author>
<author>
<name sortKey="Sinicrope, Fa" uniqKey="Sinicrope F">FA Sinicrope</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Zhang, N" uniqKey="Zhang N">N Zhang</name>
</author>
<author>
<name sortKey="Yang, G" uniqKey="Yang G">G Yang</name>
</author>
<author>
<name sortKey="Shao, X" uniqKey="Shao X">X Shao</name>
</author>
<author>
<name sortKey="Wei, L" uniqKey="Wei L">L Wei</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Jin, Z" uniqKey="Jin Z">Z Jin</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Zhao, X" uniqKey="Zhao X">X Zhao</name>
</author>
<author>
<name sortKey="Yang, L" uniqKey="Yang L">L Yang</name>
</author>
<author>
<name sortKey="Hu, J" uniqKey="Hu J">J Hu</name>
</author>
<author>
<name sortKey="Ruan, J" uniqKey="Ruan J">J Ruan</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Tian, S" uniqKey="Tian S">S Tian</name>
</author>
<author>
<name sortKey="Guo, X" uniqKey="Guo X">X Guo</name>
</author>
<author>
<name sortKey="Yu, C" uniqKey="Yu C">C Yu</name>
</author>
<author>
<name sortKey="Sun, C" uniqKey="Sun C">C Sun</name>
</author>
<author>
<name sortKey="Jiang, J" uniqKey="Jiang J">J Jiang</name>
</author>
</analytic>
</biblStruct>
<biblStruct>
<analytic>
<author>
<name sortKey="Deng, X S" uniqKey="Deng X">X-S Deng</name>
</author>
</analytic>
</biblStruct>
</listBibl>
</div1>
</back>
</TEI>
<affiliations>
<list></list>
<tree>
<noCountry>
<name sortKey="Chen, Yong" sort="Chen, Yong" uniqKey="Chen Y" first="Yong" last="Chen">Yong Chen</name>
<name sortKey="Pan, Xufeng" sort="Pan, Xufeng" uniqKey="Pan X" first="Xufeng" last="Pan">Xufeng Pan</name>
<name sortKey="Shen, Yuzhou" sort="Shen, Yuzhou" uniqKey="Shen Y" first="Yuzhou" last="Shen">Yuzhou Shen</name>
<name sortKey="Tantai, Jicheng" sort="Tantai, Jicheng" uniqKey="Tantai J" first="Jicheng" last="Tantai">Jicheng Tantai</name>
</noCountry>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Sante/explor/ChloroquineV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000702 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 000702 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Sante
   |area=    ChloroquineV1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     PMC:6546683
   |texte=   Knockdown of TRIM65 inhibits autophagy and cisplatin resistance in A549/DDP cells by regulating miR-138-5p/ATG7
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i   -Sk "pubmed:31160576" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd   \
       | NlmPubMed2Wicri -a ChloroquineV1 

Wicri

This area was generated with Dilib version V0.6.33.
Data generation: Wed Mar 25 22:43:59 2020. Site generation: Sun Jan 31 12:44:45 2021