Mixed epithelial mesenchymal phenotype tumor cell model based on Keratin 5 bidirectional regulation and control function and construction method of mixed epithelial mesenchymal phenotype tumor cell model
The invention discloses a mixed epithelial mesenchymal phenotype tumor cell model based on a keratin5 bidirectional regulation function, belongs to the technical field of tumor models, the model is a stable mixed E/M phenotype cell model obtained after keratin5 gene knock-down is carried out on epit...
Gespeichert in:
Hauptverfasser: | , , , , , |
---|---|
Format: | Patent |
Sprache: | chi ; eng |
Schlagworte: | |
Online-Zugang: | Volltext bestellen |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | |
container_start_page | |
container_title | |
container_volume | |
creator | CHEN DAN GU CUIRONG LI DONGXU LIU HUIFEN CAO BANGRONG MI KUN |
description | The invention discloses a mixed epithelial mesenchymal phenotype tumor cell model based on a keratin5 bidirectional regulation function, belongs to the technical field of tumor models, the model is a stable mixed E/M phenotype cell model obtained after keratin5 gene knock-down is carried out on epithelial cells, and the invention further discloses a construction method of the model. The mixed E/M phenotype cell stemness, the in-vitro migration and invasion ability and the drug resistance to the chemotherapeutic drug cis-platinum of the cell model are all remarkably enhanced, so that convenience can be provided for research on tumor invasion and metastasis.
本发明公开了一种基于keratin5双向调控功能的混合上皮间充质表型肿瘤细胞模型,属于肿瘤模型技术领域,所述模型为对上皮型细胞进行keratin5的基因敲降后获得的稳定的混合E/M表型细胞模型,本发明还公开了上述模型的构建方法;本发明的细胞模型的混合E/M表型细胞干性、体外迁移及侵袭能力、以及对化疗药物顺铂的耐药性均显著增强,从而能够对肿瘤侵袭转移研究提供便利。 |
format | Patent |
fullrecord | <record><control><sourceid>epo_EVB</sourceid><recordid>TN_cdi_epo_espacenet_CN115975948A</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CN115975948A</sourcerecordid><originalsourceid>FETCH-epo_espacenet_CN115975948A3</originalsourceid><addsrcrecordid>eNqdTktqwzAU9CaLkvQOrwfIwqSmzbKYhEBIV90bRR7HAuk9IT1DfMZcqirtosuQ1XyYGeapup3cFT0hOh3hnfEUkMF2nEPhcQSLzhGkU5BEFr4EpIens8mlJ0xHJKOOqaGz612CVSdcugmXyZsfQYZ7ssKaxNMwsf1vZk3TrxGgo5TJgcJjn1bVYjA-4_kPl9XLfvfVHtaI0iFHY8HQrv2s62b71mxf3z8292S-AUhnZtg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>patent</recordtype></control><display><type>patent</type><title>Mixed epithelial mesenchymal phenotype tumor cell model based on Keratin 5 bidirectional regulation and control function and construction method of mixed epithelial mesenchymal phenotype tumor cell model</title><source>esp@cenet</source><creator>CHEN DAN ; GU CUIRONG ; LI DONGXU ; LIU HUIFEN ; CAO BANGRONG ; MI KUN</creator><creatorcontrib>CHEN DAN ; GU CUIRONG ; LI DONGXU ; LIU HUIFEN ; CAO BANGRONG ; MI KUN</creatorcontrib><description>The invention discloses a mixed epithelial mesenchymal phenotype tumor cell model based on a keratin5 bidirectional regulation function, belongs to the technical field of tumor models, the model is a stable mixed E/M phenotype cell model obtained after keratin5 gene knock-down is carried out on epithelial cells, and the invention further discloses a construction method of the model. The mixed E/M phenotype cell stemness, the in-vitro migration and invasion ability and the drug resistance to the chemotherapeutic drug cis-platinum of the cell model are all remarkably enhanced, so that convenience can be provided for research on tumor invasion and metastasis.
本发明公开了一种基于keratin5双向调控功能的混合上皮间充质表型肿瘤细胞模型,属于肿瘤模型技术领域,所述模型为对上皮型细胞进行keratin5的基因敲降后获得的稳定的混合E/M表型细胞模型,本发明还公开了上述模型的构建方法;本发明的细胞模型的混合E/M表型细胞干性、体外迁移及侵袭能力、以及对化疗药物顺铂的耐药性均显著增强,从而能够对肿瘤侵袭转移研究提供便利。</description><language>chi ; eng</language><subject>BEER ; BIOCHEMISTRY ; CHEMISTRY ; COMPOSITIONS THEREOF ; CULTURE MEDIA ; ENZYMOLOGY ; METALLURGY ; MICROBIOLOGY ; MICROORGANISMS OR ENZYMES ; MUTATION OR GENETIC ENGINEERING ; PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS ; SPIRITS ; VINEGAR ; WINE</subject><creationdate>2023</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20230418&DB=EPODOC&CC=CN&NR=115975948A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20230418&DB=EPODOC&CC=CN&NR=115975948A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>CHEN DAN</creatorcontrib><creatorcontrib>GU CUIRONG</creatorcontrib><creatorcontrib>LI DONGXU</creatorcontrib><creatorcontrib>LIU HUIFEN</creatorcontrib><creatorcontrib>CAO BANGRONG</creatorcontrib><creatorcontrib>MI KUN</creatorcontrib><title>Mixed epithelial mesenchymal phenotype tumor cell model based on Keratin 5 bidirectional regulation and control function and construction method of mixed epithelial mesenchymal phenotype tumor cell model</title><description>The invention discloses a mixed epithelial mesenchymal phenotype tumor cell model based on a keratin5 bidirectional regulation function, belongs to the technical field of tumor models, the model is a stable mixed E/M phenotype cell model obtained after keratin5 gene knock-down is carried out on epithelial cells, and the invention further discloses a construction method of the model. The mixed E/M phenotype cell stemness, the in-vitro migration and invasion ability and the drug resistance to the chemotherapeutic drug cis-platinum of the cell model are all remarkably enhanced, so that convenience can be provided for research on tumor invasion and metastasis.
本发明公开了一种基于keratin5双向调控功能的混合上皮间充质表型肿瘤细胞模型,属于肿瘤模型技术领域,所述模型为对上皮型细胞进行keratin5的基因敲降后获得的稳定的混合E/M表型细胞模型,本发明还公开了上述模型的构建方法;本发明的细胞模型的混合E/M表型细胞干性、体外迁移及侵袭能力、以及对化疗药物顺铂的耐药性均显著增强,从而能够对肿瘤侵袭转移研究提供便利。</description><subject>BEER</subject><subject>BIOCHEMISTRY</subject><subject>CHEMISTRY</subject><subject>COMPOSITIONS THEREOF</subject><subject>CULTURE MEDIA</subject><subject>ENZYMOLOGY</subject><subject>METALLURGY</subject><subject>MICROBIOLOGY</subject><subject>MICROORGANISMS OR ENZYMES</subject><subject>MUTATION OR GENETIC ENGINEERING</subject><subject>PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS</subject><subject>SPIRITS</subject><subject>VINEGAR</subject><subject>WINE</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2023</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqdTktqwzAU9CaLkvQOrwfIwqSmzbKYhEBIV90bRR7HAuk9IT1DfMZcqirtosuQ1XyYGeapup3cFT0hOh3hnfEUkMF2nEPhcQSLzhGkU5BEFr4EpIens8mlJ0xHJKOOqaGz612CVSdcugmXyZsfQYZ7ssKaxNMwsf1vZk3TrxGgo5TJgcJjn1bVYjA-4_kPl9XLfvfVHtaI0iFHY8HQrv2s62b71mxf3z8292S-AUhnZtg</recordid><startdate>20230418</startdate><enddate>20230418</enddate><creator>CHEN DAN</creator><creator>GU CUIRONG</creator><creator>LI DONGXU</creator><creator>LIU HUIFEN</creator><creator>CAO BANGRONG</creator><creator>MI KUN</creator><scope>EVB</scope></search><sort><creationdate>20230418</creationdate><title>Mixed epithelial mesenchymal phenotype tumor cell model based on Keratin 5 bidirectional regulation and control function and construction method of mixed epithelial mesenchymal phenotype tumor cell model</title><author>CHEN DAN ; GU CUIRONG ; LI DONGXU ; LIU HUIFEN ; CAO BANGRONG ; MI KUN</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_CN115975948A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>chi ; eng</language><creationdate>2023</creationdate><topic>BEER</topic><topic>BIOCHEMISTRY</topic><topic>CHEMISTRY</topic><topic>COMPOSITIONS THEREOF</topic><topic>CULTURE MEDIA</topic><topic>ENZYMOLOGY</topic><topic>METALLURGY</topic><topic>MICROBIOLOGY</topic><topic>MICROORGANISMS OR ENZYMES</topic><topic>MUTATION OR GENETIC ENGINEERING</topic><topic>PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS</topic><topic>SPIRITS</topic><topic>VINEGAR</topic><topic>WINE</topic><toplevel>online_resources</toplevel><creatorcontrib>CHEN DAN</creatorcontrib><creatorcontrib>GU CUIRONG</creatorcontrib><creatorcontrib>LI DONGXU</creatorcontrib><creatorcontrib>LIU HUIFEN</creatorcontrib><creatorcontrib>CAO BANGRONG</creatorcontrib><creatorcontrib>MI KUN</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>CHEN DAN</au><au>GU CUIRONG</au><au>LI DONGXU</au><au>LIU HUIFEN</au><au>CAO BANGRONG</au><au>MI KUN</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Mixed epithelial mesenchymal phenotype tumor cell model based on Keratin 5 bidirectional regulation and control function and construction method of mixed epithelial mesenchymal phenotype tumor cell model</title><date>2023-04-18</date><risdate>2023</risdate><abstract>The invention discloses a mixed epithelial mesenchymal phenotype tumor cell model based on a keratin5 bidirectional regulation function, belongs to the technical field of tumor models, the model is a stable mixed E/M phenotype cell model obtained after keratin5 gene knock-down is carried out on epithelial cells, and the invention further discloses a construction method of the model. The mixed E/M phenotype cell stemness, the in-vitro migration and invasion ability and the drug resistance to the chemotherapeutic drug cis-platinum of the cell model are all remarkably enhanced, so that convenience can be provided for research on tumor invasion and metastasis.
本发明公开了一种基于keratin5双向调控功能的混合上皮间充质表型肿瘤细胞模型,属于肿瘤模型技术领域,所述模型为对上皮型细胞进行keratin5的基因敲降后获得的稳定的混合E/M表型细胞模型,本发明还公开了上述模型的构建方法;本发明的细胞模型的混合E/M表型细胞干性、体外迁移及侵袭能力、以及对化疗药物顺铂的耐药性均显著增强,从而能够对肿瘤侵袭转移研究提供便利。</abstract><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | |
ispartof | |
issn | |
language | chi ; eng |
recordid | cdi_epo_espacenet_CN115975948A |
source | esp@cenet |
subjects | BEER BIOCHEMISTRY CHEMISTRY COMPOSITIONS THEREOF CULTURE MEDIA ENZYMOLOGY METALLURGY MICROBIOLOGY MICROORGANISMS OR ENZYMES MUTATION OR GENETIC ENGINEERING PROPAGATING, PRESERVING OR MAINTAINING MICROORGANISMS SPIRITS VINEGAR WINE |
title | Mixed epithelial mesenchymal phenotype tumor cell model based on Keratin 5 bidirectional regulation and control function and construction method of mixed epithelial mesenchymal phenotype tumor cell model |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T04%3A19%3A52IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-epo_EVB&rft_val_fmt=info:ofi/fmt:kev:mtx:patent&rft.genre=patent&rft.au=CHEN%20DAN&rft.date=2023-04-18&rft_id=info:doi/&rft_dat=%3Cepo_EVB%3ECN115975948A%3C/epo_EVB%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |