Loading…
Isolation and Characterization of a Novel Bladder Cancer Cell Line: Inhibition by Epidermal Growth Factor
A novel continuous cell line, designated BC3c, was established from a surgical biopsy of an invasive solid transitional cell carcinoma of the bladder derived from an 82-yr-old Caucasian female. BC3c cells were near-triploid bearing multiple structural and numerical chromosome anomalies. The epitheli...
Saved in:
Published in: | In vitro cellular & developmental biology. Animal 1998-10, Vol.34 (9), p.722-728 |
---|---|
Main Authors: | , , , |
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-c441t-68b24f1ff86fbe91eabf04187a49207790ce5357184c4d7c342f25d924d48a093 |
---|---|
cites | cdi_FETCH-LOGICAL-c441t-68b24f1ff86fbe91eabf04187a49207790ce5357184c4d7c342f25d924d48a093 |
container_end_page | 728 |
container_issue | 9 |
container_start_page | 722 |
container_title | In vitro cellular & developmental biology. Animal |
container_volume | 34 |
creator | Pratsinis, H Saetta, A Gagos, S Davaris, P |
description | A novel continuous cell line, designated BC3c, was established from a surgical biopsy of an invasive solid transitional cell carcinoma of the bladder derived from an 82-yr-old Caucasian female. BC3c cells were near-triploid bearing multiple structural and numerical chromosome anomalies. The epithelial origin of the cancer cells was indicated by the expression of cytokeratins 8 and 19 as well as by the absence of mesenchymal markers. Polymerase chain reaction-restriction-fragment length polymorphisms and single-strand conformation polymorphism mutation detection assays did not reveal any mutations in H-ras codon 12 and K-ras codons 12 and 13. In addition, no mutation in specific hot-spot codons of the p53 gene and no accumulation of the p53 protein were observed. BC3c cells grew rapidly in vitro, even in the absence of exogenous growth factors, because they were found to stimulate their growth in an autocrine manner. BC3c cells were found to express the epidermal growth factor-receptor (EGF-r) abundantly, but in contrast to other established bladder cancer cell lines, human recombinant epidermal growth factor inhibited the cells' proliferation in vitro. These features render the newly established bladder cancer cell line BC3c a useful tool for further experimentation. |
doi_str_mv | 10.1007/s11626-998-0068-z |
format | article |
fullrecord | <record><control><sourceid>jstor_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_70004555</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>4294855</jstor_id><sourcerecordid>4294855</sourcerecordid><originalsourceid>FETCH-LOGICAL-c441t-68b24f1ff86fbe91eabf04187a49207790ce5357184c4d7c342f25d924d48a093</originalsourceid><addsrcrecordid>eNqFkU9r3DAQxUVpSdKkHyCQgOihNzcaeSxZvTVL_iwszSWF3oRsS6wWr7WRvA3ZT19tvOSQS3UZofebh2YeIefAvgNj8ioBCC4KpeqCMVEXuw_kBCosC8nEn4_5ziQUXCh2TD6ntGL5KBBH5EhJhZzjCfHzFHoz-jBQM3R0tjTRtKONfjc9BkcN_RX-2p5e96brbKQzM7T7YvueLvxgf9D5sPSNf-WbF3qz8Rlbm57exfA8LultdgzxjHxypk_2y6Gekt-3N4-z-2LxcDef_VwULSKMhagbjg6cq4VrrAJrGscQamlQcSalYq2tykpCjS12si2RO151imOHtWGqPCXfJt9NDE9bm0a99qnNnzWDDdukZV4CVlX1XxAkAAoFGfz6DlyFbRzyEJqXqFQpyz0EE9TGkFK0Tm-iX5v4ooHpfVh6CkvnsPQ-LL3LPZcH422ztt1bxyGdrF9M-irlBb7JyBXWeYB_8DCX6w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>234993731</pqid></control><display><type>article</type><title>Isolation and Characterization of a Novel Bladder Cancer Cell Line: Inhibition by Epidermal Growth Factor</title><source>JSTOR Archival Journals and Primary Sources Collection</source><source>Springer Nature</source><creator>Pratsinis, H ; Saetta, A ; Gagos, S ; Davaris, P</creator><creatorcontrib>Pratsinis, H ; Saetta, A ; Gagos, S ; Davaris, P</creatorcontrib><description>A novel continuous cell line, designated BC3c, was established from a surgical biopsy of an invasive solid transitional cell carcinoma of the bladder derived from an 82-yr-old Caucasian female. BC3c cells were near-triploid bearing multiple structural and numerical chromosome anomalies. The epithelial origin of the cancer cells was indicated by the expression of cytokeratins 8 and 19 as well as by the absence of mesenchymal markers. Polymerase chain reaction-restriction-fragment length polymorphisms and single-strand conformation polymorphism mutation detection assays did not reveal any mutations in H-ras codon 12 and K-ras codons 12 and 13. In addition, no mutation in specific hot-spot codons of the p53 gene and no accumulation of the p53 protein were observed. BC3c cells grew rapidly in vitro, even in the absence of exogenous growth factors, because they were found to stimulate their growth in an autocrine manner. BC3c cells were found to express the epidermal growth factor-receptor (EGF-r) abundantly, but in contrast to other established bladder cancer cell lines, human recombinant epidermal growth factor inhibited the cells' proliferation in vitro. These features render the newly established bladder cancer cell line BC3c a useful tool for further experimentation.</description><identifier>ISSN: 1071-2690</identifier><identifier>EISSN: 1543-706X</identifier><identifier>DOI: 10.1007/s11626-998-0068-z</identifier><identifier>PMID: 9794224</identifier><identifier>CODEN: IVCAED</identifier><language>eng</language><publisher>Germany: Society for In Vitro Biology</publisher><subject>Aged ; Aged, 80 and over ; Cancer ; Carcinoma, Transitional Cell - genetics ; Carcinoma, Transitional Cell - pathology ; Cell culture techniques ; Cell Division - drug effects ; Cell growth ; Cell lines ; Codons ; Cultured cells ; Epidermal Growth Factor - pharmacology ; Female ; Genetic mutation ; Growth, Differentiation, and Senescence ; Humans ; Karyotyping ; Transitional cell carcinoma ; Tumor cell line ; Tumor Cells, Cultured ; Urinary bladder ; Urinary Bladder Neoplasms - genetics ; Urinary Bladder Neoplasms - pathology</subject><ispartof>In vitro cellular & developmental biology. Animal, 1998-10, Vol.34 (9), p.722-728</ispartof><rights>Copyright 1998 Society for In Vitro Biology</rights><rights>Copyright Society for In Vitro Biology Oct 1998</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-68b24f1ff86fbe91eabf04187a49207790ce5357184c4d7c342f25d924d48a093</citedby><cites>FETCH-LOGICAL-c441t-68b24f1ff86fbe91eabf04187a49207790ce5357184c4d7c342f25d924d48a093</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/4294855$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/4294855$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,58238,58471</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9794224$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pratsinis, H</creatorcontrib><creatorcontrib>Saetta, A</creatorcontrib><creatorcontrib>Gagos, S</creatorcontrib><creatorcontrib>Davaris, P</creatorcontrib><title>Isolation and Characterization of a Novel Bladder Cancer Cell Line: Inhibition by Epidermal Growth Factor</title><title>In vitro cellular & developmental biology. Animal</title><addtitle>In Vitro Cell Dev Biol Anim</addtitle><description>A novel continuous cell line, designated BC3c, was established from a surgical biopsy of an invasive solid transitional cell carcinoma of the bladder derived from an 82-yr-old Caucasian female. BC3c cells were near-triploid bearing multiple structural and numerical chromosome anomalies. The epithelial origin of the cancer cells was indicated by the expression of cytokeratins 8 and 19 as well as by the absence of mesenchymal markers. Polymerase chain reaction-restriction-fragment length polymorphisms and single-strand conformation polymorphism mutation detection assays did not reveal any mutations in H-ras codon 12 and K-ras codons 12 and 13. In addition, no mutation in specific hot-spot codons of the p53 gene and no accumulation of the p53 protein were observed. BC3c cells grew rapidly in vitro, even in the absence of exogenous growth factors, because they were found to stimulate their growth in an autocrine manner. BC3c cells were found to express the epidermal growth factor-receptor (EGF-r) abundantly, but in contrast to other established bladder cancer cell lines, human recombinant epidermal growth factor inhibited the cells' proliferation in vitro. These features render the newly established bladder cancer cell line BC3c a useful tool for further experimentation.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Cancer</subject><subject>Carcinoma, Transitional Cell - genetics</subject><subject>Carcinoma, Transitional Cell - pathology</subject><subject>Cell culture techniques</subject><subject>Cell Division - drug effects</subject><subject>Cell growth</subject><subject>Cell lines</subject><subject>Codons</subject><subject>Cultured cells</subject><subject>Epidermal Growth Factor - pharmacology</subject><subject>Female</subject><subject>Genetic mutation</subject><subject>Growth, Differentiation, and Senescence</subject><subject>Humans</subject><subject>Karyotyping</subject><subject>Transitional cell carcinoma</subject><subject>Tumor cell line</subject><subject>Tumor Cells, Cultured</subject><subject>Urinary bladder</subject><subject>Urinary Bladder Neoplasms - genetics</subject><subject>Urinary Bladder Neoplasms - pathology</subject><issn>1071-2690</issn><issn>1543-706X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNqFkU9r3DAQxUVpSdKkHyCQgOihNzcaeSxZvTVL_iwszSWF3oRsS6wWr7WRvA3ZT19tvOSQS3UZofebh2YeIefAvgNj8ioBCC4KpeqCMVEXuw_kBCosC8nEn4_5ziQUXCh2TD6ntGL5KBBH5EhJhZzjCfHzFHoz-jBQM3R0tjTRtKONfjc9BkcN_RX-2p5e96brbKQzM7T7YvueLvxgf9D5sPSNf-WbF3qz8Rlbm57exfA8LultdgzxjHxypk_2y6Gekt-3N4-z-2LxcDef_VwULSKMhagbjg6cq4VrrAJrGscQamlQcSalYq2tykpCjS12si2RO151imOHtWGqPCXfJt9NDE9bm0a99qnNnzWDDdukZV4CVlX1XxAkAAoFGfz6DlyFbRzyEJqXqFQpyz0EE9TGkFK0Tm-iX5v4ooHpfVh6CkvnsPQ-LL3LPZcH422ztt1bxyGdrF9M-irlBb7JyBXWeYB_8DCX6w</recordid><startdate>19981001</startdate><enddate>19981001</enddate><creator>Pratsinis, H</creator><creator>Saetta, A</creator><creator>Gagos, S</creator><creator>Davaris, P</creator><general>Society for In Vitro Biology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>4T-</scope><scope>7QL</scope><scope>7T7</scope><scope>7TK</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7QO</scope><scope>7X8</scope></search><sort><creationdate>19981001</creationdate><title>Isolation and Characterization of a Novel Bladder Cancer Cell Line: Inhibition by Epidermal Growth Factor</title><author>Pratsinis, H ; Saetta, A ; Gagos, S ; Davaris, P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-68b24f1ff86fbe91eabf04187a49207790ce5357184c4d7c342f25d924d48a093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Cancer</topic><topic>Carcinoma, Transitional Cell - genetics</topic><topic>Carcinoma, Transitional Cell - pathology</topic><topic>Cell culture techniques</topic><topic>Cell Division - drug effects</topic><topic>Cell growth</topic><topic>Cell lines</topic><topic>Codons</topic><topic>Cultured cells</topic><topic>Epidermal Growth Factor - pharmacology</topic><topic>Female</topic><topic>Genetic mutation</topic><topic>Growth, Differentiation, and Senescence</topic><topic>Humans</topic><topic>Karyotyping</topic><topic>Transitional cell carcinoma</topic><topic>Tumor cell line</topic><topic>Tumor Cells, Cultured</topic><topic>Urinary bladder</topic><topic>Urinary Bladder Neoplasms - genetics</topic><topic>Urinary Bladder Neoplasms - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pratsinis, H</creatorcontrib><creatorcontrib>Saetta, A</creatorcontrib><creatorcontrib>Gagos, S</creatorcontrib><creatorcontrib>Davaris, P</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database (Proquest)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Science Database (ProQuest)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</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>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>Biotechnology Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>In vitro cellular & developmental biology. Animal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pratsinis, H</au><au>Saetta, A</au><au>Gagos, S</au><au>Davaris, P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Isolation and Characterization of a Novel Bladder Cancer Cell Line: Inhibition by Epidermal Growth Factor</atitle><jtitle>In vitro cellular & developmental biology. Animal</jtitle><addtitle>In Vitro Cell Dev Biol Anim</addtitle><date>1998-10-01</date><risdate>1998</risdate><volume>34</volume><issue>9</issue><spage>722</spage><epage>728</epage><pages>722-728</pages><issn>1071-2690</issn><eissn>1543-706X</eissn><coden>IVCAED</coden><abstract>A novel continuous cell line, designated BC3c, was established from a surgical biopsy of an invasive solid transitional cell carcinoma of the bladder derived from an 82-yr-old Caucasian female. BC3c cells were near-triploid bearing multiple structural and numerical chromosome anomalies. The epithelial origin of the cancer cells was indicated by the expression of cytokeratins 8 and 19 as well as by the absence of mesenchymal markers. Polymerase chain reaction-restriction-fragment length polymorphisms and single-strand conformation polymorphism mutation detection assays did not reveal any mutations in H-ras codon 12 and K-ras codons 12 and 13. In addition, no mutation in specific hot-spot codons of the p53 gene and no accumulation of the p53 protein were observed. BC3c cells grew rapidly in vitro, even in the absence of exogenous growth factors, because they were found to stimulate their growth in an autocrine manner. BC3c cells were found to express the epidermal growth factor-receptor (EGF-r) abundantly, but in contrast to other established bladder cancer cell lines, human recombinant epidermal growth factor inhibited the cells' proliferation in vitro. These features render the newly established bladder cancer cell line BC3c a useful tool for further experimentation.</abstract><cop>Germany</cop><pub>Society for In Vitro Biology</pub><pmid>9794224</pmid><doi>10.1007/s11626-998-0068-z</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1071-2690 |
ispartof | In vitro cellular & developmental biology. Animal, 1998-10, Vol.34 (9), p.722-728 |
issn | 1071-2690 1543-706X |
language | eng |
recordid | cdi_proquest_miscellaneous_70004555 |
source | JSTOR Archival Journals and Primary Sources Collection; Springer Nature |
subjects | Aged Aged, 80 and over Cancer Carcinoma, Transitional Cell - genetics Carcinoma, Transitional Cell - pathology Cell culture techniques Cell Division - drug effects Cell growth Cell lines Codons Cultured cells Epidermal Growth Factor - pharmacology Female Genetic mutation Growth, Differentiation, and Senescence Humans Karyotyping Transitional cell carcinoma Tumor cell line Tumor Cells, Cultured Urinary bladder Urinary Bladder Neoplasms - genetics Urinary Bladder Neoplasms - pathology |
title | Isolation and Characterization of a Novel Bladder Cancer Cell Line: Inhibition by Epidermal Growth Factor |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-23T13%3A23%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-jstor_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Isolation%20and%20Characterization%20of%20a%20Novel%20Bladder%20Cancer%20Cell%20Line:%20Inhibition%20by%20Epidermal%20Growth%20Factor&rft.jtitle=In%20vitro%20cellular%20&%20developmental%20biology.%20Animal&rft.au=Pratsinis,%20H&rft.date=1998-10-01&rft.volume=34&rft.issue=9&rft.spage=722&rft.epage=728&rft.pages=722-728&rft.issn=1071-2690&rft.eissn=1543-706X&rft.coden=IVCAED&rft_id=info:doi/10.1007/s11626-998-0068-z&rft_dat=%3Cjstor_proqu%3E4294855%3C/jstor_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c441t-68b24f1ff86fbe91eabf04187a49207790ce5357184c4d7c342f25d924d48a093%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=234993731&rft_id=info:pmid/9794224&rft_jstor_id=4294855&rfr_iscdi=true |