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Establishment and characterization of 12 uterine cervical‐carcinoma cell lines: Common sequence variation in the E7 gene of HPV‐16‐positive cell lines
A total of 12 carcinoma cell lines of the human uterine cervix were established from 5 keratinizing and 5 non‐keratinizing squamous‐cell carcinomas, and 2 small‐cell carcinomas. Of these, 10 lines grew as adherent cells and 2 as floating aggregates. All lines showed (i) similarity in morphology to t...
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Published in: | International journal of cancer 1997-07, Vol.72 (2), p.313-320 |
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container_title | International journal of cancer |
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creator | Ku, Ja‐Lok Kim, Woo‐Ho Park, Hyun‐Sook Kang, Soon‐Beom Park, Jae‐Gahb |
description | A total of 12 carcinoma cell lines of the human uterine cervix were established from 5 keratinizing and 5 non‐keratinizing squamous‐cell carcinomas, and 2 small‐cell carcinomas. Of these, 10 lines grew as adherent cells and 2 as floating aggregates. All lines showed (i) similarity in morphology to the primary tumor from which they were derived; (ii) high viability with relatively long doubling times (48–96 hr); (iii) absence of Mycoplasma and other bacteria, apart from one Mycoplasma‐contaminated line; (iv) genetic heterogeneity by DNA‐fingerprinting analysis; (v) absence of p53 mutation from exon 4 through 9; and (vi) the presence of HPV DNA sequence. Among the lines, 7 were infected by HPV‐16, 3 by HPV‐18, 1 by HPV‐31, and 1 by HPV‐33; the 2 cell lines derived from small‐cell carcinomas contained HPV‐18. Interestingly, 6 of the 7 cell lines containing HPV‐16‐type DNA harbored the same alteration of E7 at nucleotide position 647 (amino acid 29, AAT |iO AGT, Asn |iO Ser), whereas the 3 HPV‐18‐positive lines did not; 3 cell lines proved to have intact E1/E2 of HPV, suggesting the presence of episomally replicating HPV DNA as well as the integrated form, whereas the other 9 lines were shown to have integrated HPV. Taken together, these cell lines would be very useful for studying the biology of uterine cervical carcinoma. Int. J. Cancer 72:313–320, 1997. © 1997 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/(SICI)1097-0215(19970717)72:2<313::AID-IJC19>3.0.CO;2-G |
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Of these, 10 lines grew as adherent cells and 2 as floating aggregates. All lines showed (i) similarity in morphology to the primary tumor from which they were derived; (ii) high viability with relatively long doubling times (48–96 hr); (iii) absence of Mycoplasma and other bacteria, apart from one Mycoplasma‐contaminated line; (iv) genetic heterogeneity by DNA‐fingerprinting analysis; (v) absence of p53 mutation from exon 4 through 9; and (vi) the presence of HPV DNA sequence. Among the lines, 7 were infected by HPV‐16, 3 by HPV‐18, 1 by HPV‐31, and 1 by HPV‐33; the 2 cell lines derived from small‐cell carcinomas contained HPV‐18. Interestingly, 6 of the 7 cell lines containing HPV‐16‐type DNA harbored the same alteration of E7 at nucleotide position 647 (amino acid 29, AAT |iO AGT, Asn |iO Ser), whereas the 3 HPV‐18‐positive lines did not; 3 cell lines proved to have intact E1/E2 of HPV, suggesting the presence of episomally replicating HPV DNA as well as the integrated form, whereas the other 9 lines were shown to have integrated HPV. Taken together, these cell lines would be very useful for studying the biology of uterine cervical carcinoma. Int. J. Cancer 72:313–320, 1997. © 1997 Wiley‐Liss, Inc.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/(SICI)1097-0215(19970717)72:2<313::AID-IJC19>3.0.CO;2-G</identifier><identifier>PMID: 9219839</identifier><identifier>CODEN: IJCNAW</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Biological and medical sciences ; Carcinoma - genetics ; Carcinoma - pathology ; Carcinoma - virology ; Female ; Female genital diseases ; Genes, Viral ; Gynecology. Andrology. Obstetrics ; human papillomavirus 16 ; Humans ; Medical sciences ; Oncogene Proteins, Viral - genetics ; Papillomaviridae ; Papillomavirus E7 Proteins ; Sequence Analysis ; Tumor Cells, Cultured ; Tumors ; Uterine Cervical Neoplasms - genetics ; Uterine Cervical Neoplasms - pathology ; Uterine Cervical Neoplasms - virology</subject><ispartof>International journal of cancer, 1997-07, Vol.72 (2), p.313-320</ispartof><rights>Copyright © 1997 Wiley‐Liss, Inc.</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2719489$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9219839$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ku, Ja‐Lok</creatorcontrib><creatorcontrib>Kim, Woo‐Ho</creatorcontrib><creatorcontrib>Park, Hyun‐Sook</creatorcontrib><creatorcontrib>Kang, Soon‐Beom</creatorcontrib><creatorcontrib>Park, Jae‐Gahb</creatorcontrib><title>Establishment and characterization of 12 uterine cervical‐carcinoma cell lines: Common sequence variation in the E7 gene of HPV‐16‐positive cell lines</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>A total of 12 carcinoma cell lines of the human uterine cervix were established from 5 keratinizing and 5 non‐keratinizing squamous‐cell carcinomas, and 2 small‐cell carcinomas. Of these, 10 lines grew as adherent cells and 2 as floating aggregates. All lines showed (i) similarity in morphology to the primary tumor from which they were derived; (ii) high viability with relatively long doubling times (48–96 hr); (iii) absence of Mycoplasma and other bacteria, apart from one Mycoplasma‐contaminated line; (iv) genetic heterogeneity by DNA‐fingerprinting analysis; (v) absence of p53 mutation from exon 4 through 9; and (vi) the presence of HPV DNA sequence. Among the lines, 7 were infected by HPV‐16, 3 by HPV‐18, 1 by HPV‐31, and 1 by HPV‐33; the 2 cell lines derived from small‐cell carcinomas contained HPV‐18. Interestingly, 6 of the 7 cell lines containing HPV‐16‐type DNA harbored the same alteration of E7 at nucleotide position 647 (amino acid 29, AAT |iO AGT, Asn |iO Ser), whereas the 3 HPV‐18‐positive lines did not; 3 cell lines proved to have intact E1/E2 of HPV, suggesting the presence of episomally replicating HPV DNA as well as the integrated form, whereas the other 9 lines were shown to have integrated HPV. Taken together, these cell lines would be very useful for studying the biology of uterine cervical carcinoma. Int. J. Cancer 72:313–320, 1997. © 1997 Wiley‐Liss, Inc.</description><subject>Biological and medical sciences</subject><subject>Carcinoma - genetics</subject><subject>Carcinoma - pathology</subject><subject>Carcinoma - virology</subject><subject>Female</subject><subject>Female genital diseases</subject><subject>Genes, Viral</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>human papillomavirus 16</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>Oncogene Proteins, Viral - genetics</subject><subject>Papillomaviridae</subject><subject>Papillomavirus E7 Proteins</subject><subject>Sequence Analysis</subject><subject>Tumor Cells, Cultured</subject><subject>Tumors</subject><subject>Uterine Cervical Neoplasms - genetics</subject><subject>Uterine Cervical Neoplasms - pathology</subject><subject>Uterine Cervical Neoplasms - virology</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNqFkt2O0zAQhS0EWroLj4DkC4R2L1LGP4nrglitQukGrVQkfsSd5TgONUqcEqdFyxWPwAPwdDwJDi0Vd9zY0pkzn0YzB6FLAlMCQJ-evy3y4oKAFAlQkp4TKQUIIi4EndPnjLD5_Kp4mRSvcyJfsClM89UzmizvoMmx5y6aRBIkgrDsPjoN4TMAISnwE3QiKZEzJifo5yIMumxcWLfWD1j7Cpu17rUZbO--6cF1Hnc1JhRvR8VbbGy_c0Y3v77_MLo3znetjmLT4CaWwxznXdvGrmC_bK03Fu907_Yg5_Gwtngh8CcbSZF7_eZD5JAsPpsuuMHt7D-sB-herZtgHx7-M_T-1eJdfp3crJZFfnWTbBgXMjE6BQsgOYBhpayMsTMQdVmb0gjKM80qybk2oooiN6bSZZmams9YVVtZaXaGnuy5m76LQ4dBtS6MY2hvu21QQhKapYz-10gyApRziMZHB-O2bG2lNr1rdX-rDnuP9ceHug5xl3WvvXHhaKOCSD4bbR_3tq-usbfHMgE1hkSNGVHjvdV4b_U3I0pQRVXMiIoRUX8iopgCla-ivNwL7DcC7bm_</recordid><startdate>19970717</startdate><enddate>19970717</enddate><creator>Ku, Ja‐Lok</creator><creator>Kim, Woo‐Ho</creator><creator>Park, Hyun‐Sook</creator><creator>Kang, Soon‐Beom</creator><creator>Park, Jae‐Gahb</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7TO</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19970717</creationdate><title>Establishment and characterization of 12 uterine cervical‐carcinoma cell lines: Common sequence variation in the E7 gene of HPV‐16‐positive cell lines</title><author>Ku, Ja‐Lok ; Kim, Woo‐Ho ; Park, Hyun‐Sook ; Kang, Soon‐Beom ; Park, Jae‐Gahb</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p3479-ca50e009400c3b9dcce807fbfcbc7246a3d944ac7d7fb4ccdabb5cf483dfe9da3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Biological and medical sciences</topic><topic>Carcinoma - genetics</topic><topic>Carcinoma - pathology</topic><topic>Carcinoma - virology</topic><topic>Female</topic><topic>Female genital diseases</topic><topic>Genes, Viral</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>human papillomavirus 16</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>Oncogene Proteins, Viral - genetics</topic><topic>Papillomaviridae</topic><topic>Papillomavirus E7 Proteins</topic><topic>Sequence Analysis</topic><topic>Tumor Cells, Cultured</topic><topic>Tumors</topic><topic>Uterine Cervical Neoplasms - genetics</topic><topic>Uterine Cervical Neoplasms - pathology</topic><topic>Uterine Cervical Neoplasms - virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ku, Ja‐Lok</creatorcontrib><creatorcontrib>Kim, Woo‐Ho</creatorcontrib><creatorcontrib>Park, Hyun‐Sook</creatorcontrib><creatorcontrib>Kang, Soon‐Beom</creatorcontrib><creatorcontrib>Park, Jae‐Gahb</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ku, Ja‐Lok</au><au>Kim, Woo‐Ho</au><au>Park, Hyun‐Sook</au><au>Kang, Soon‐Beom</au><au>Park, Jae‐Gahb</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Establishment and characterization of 12 uterine cervical‐carcinoma cell lines: Common sequence variation in the E7 gene of HPV‐16‐positive cell lines</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>1997-07-17</date><risdate>1997</risdate><volume>72</volume><issue>2</issue><spage>313</spage><epage>320</epage><pages>313-320</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><coden>IJCNAW</coden><abstract>A total of 12 carcinoma cell lines of the human uterine cervix were established from 5 keratinizing and 5 non‐keratinizing squamous‐cell carcinomas, and 2 small‐cell carcinomas. Of these, 10 lines grew as adherent cells and 2 as floating aggregates. All lines showed (i) similarity in morphology to the primary tumor from which they were derived; (ii) high viability with relatively long doubling times (48–96 hr); (iii) absence of Mycoplasma and other bacteria, apart from one Mycoplasma‐contaminated line; (iv) genetic heterogeneity by DNA‐fingerprinting analysis; (v) absence of p53 mutation from exon 4 through 9; and (vi) the presence of HPV DNA sequence. Among the lines, 7 were infected by HPV‐16, 3 by HPV‐18, 1 by HPV‐31, and 1 by HPV‐33; the 2 cell lines derived from small‐cell carcinomas contained HPV‐18. Interestingly, 6 of the 7 cell lines containing HPV‐16‐type DNA harbored the same alteration of E7 at nucleotide position 647 (amino acid 29, AAT |iO AGT, Asn |iO Ser), whereas the 3 HPV‐18‐positive lines did not; 3 cell lines proved to have intact E1/E2 of HPV, suggesting the presence of episomally replicating HPV DNA as well as the integrated form, whereas the other 9 lines were shown to have integrated HPV. Taken together, these cell lines would be very useful for studying the biology of uterine cervical carcinoma. Int. J. Cancer 72:313–320, 1997. © 1997 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>9219839</pmid><doi>10.1002/(SICI)1097-0215(19970717)72:2<313::AID-IJC19>3.0.CO;2-G</doi><tpages>8</tpages></addata></record> |
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subjects | Biological and medical sciences Carcinoma - genetics Carcinoma - pathology Carcinoma - virology Female Female genital diseases Genes, Viral Gynecology. Andrology. Obstetrics human papillomavirus 16 Humans Medical sciences Oncogene Proteins, Viral - genetics Papillomaviridae Papillomavirus E7 Proteins Sequence Analysis Tumor Cells, Cultured Tumors Uterine Cervical Neoplasms - genetics Uterine Cervical Neoplasms - pathology Uterine Cervical Neoplasms - virology |
title | Establishment and characterization of 12 uterine cervical‐carcinoma cell lines: Common sequence variation in the E7 gene of HPV‐16‐positive cell lines |
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