Peptide nucleic acids arrest the growth of gastric cancer cells SGC7901

Background Peptide nucleic acid (PNA) has many characteristics useful in molecular biology. This paper described an effective way to raise the cell ingestion rate of PNA so as to kill gastric cancer cells.Methods Heteroduplexes of PNAs and oligonucleotides, wrapped by Lipofectamine 2000, were used t...

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Veröffentlicht in:Chinese medical journal 2004-04, Vol.117 (4), p.566-570
1. Verfasser: 王宽 张岂凡 王锡山 薛英威 庞达 傅松滨
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description Background Peptide nucleic acid (PNA) has many characteristics useful in molecular biology. This paper described an effective way to raise the cell ingestion rate of PNA so as to kill gastric cancer cells.Methods Heteroduplexes of PNAs and oligonucleotides, wrapped by Lipofectamine 2000, were used to infect SGC7901 cells. The inhibitive effect of heteroduplexes was evaluated by analyzing cell clone forming and cell growth rate. Telomerase activity of SGC7901 cells was detected by polymerase chain reaction enzyme-linked immunosorbent assay (PCR-ELISA) and silver staining assay.Results PNAs showed a dose-dependent inhibition of cell proliferation. The percentage of proliferation inhibition was 99. 4% after 7 days; the rate of cloning inhibition was 98.2% after 8 days;whereas for oligonucleotide groups, at the same concentration, the percentages were 50.1% and 67.5% respectively. Antisense PNA-DNA-Lipofectamine 2000 group ( AP-D-L group ) exhibited significantly different percentages from the control groups ( P < 0.05). The test result indicated that telomerase activity of the AP-D-L group was inhibited ( P < 0. 05). At the same time, the impact on cell morphology was observed.Conclusions The results showed that PNAs are potent antisense reagents. The telomeraseassociated therapies are very promising for the treatment of malignant tumours.
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This paper described an effective way to raise the cell ingestion rate of PNA so as to kill gastric cancer cells.Methods Heteroduplexes of PNAs and oligonucleotides, wrapped by Lipofectamine 2000, were used to infect SGC7901 cells. The inhibitive effect of heteroduplexes was evaluated by analyzing cell clone forming and cell growth rate. Telomerase activity of SGC7901 cells was detected by polymerase chain reaction enzyme-linked immunosorbent assay (PCR-ELISA) and silver staining assay.Results PNAs showed a dose-dependent inhibition of cell proliferation. The percentage of proliferation inhibition was 99. 4% after 7 days; the rate of cloning inhibition was 98.2% after 8 days;whereas for oligonucleotide groups, at the same concentration, the percentages were 50.1% and 67.5% respectively. Antisense PNA-DNA-Lipofectamine 2000 group ( AP-D-L group ) exhibited significantly different percentages from the control groups ( P &lt; 0.05). The test result indicated that telomerase activity of the AP-D-L group was inhibited ( P &lt; 0. 05). At the same time, the impact on cell morphology was observed.Conclusions The results showed that PNAs are potent antisense reagents. The telomeraseassociated therapies are very promising for the treatment of malignant tumours.</description><identifier>ISSN: 0366-6999</identifier><identifier>EISSN: 2542-5641</identifier><identifier>PMID: 15109451</identifier><language>eng</language><publisher>China: Department of Abdominal Surgery, Turmour Clinical Hospital of Harbin Medical University, Harbin 150040, China%Department of Genetics, Harbin Medical University, Harbin 150086, China</publisher><subject>Cell Division - drug effects ; Cell Line, Tumor ; DNA-Binding Proteins ; Humans ; Peptide Nucleic Acids - therapeutic use ; SGC7901细胞系 ; Stomach Neoplasms - pathology ; Stomach Neoplasms - therapy ; Telomerase - antagonists &amp; inhibitors ; Telomerase - metabolism ; Transfection ; 端粒酶 ; 缩氨酸核酸 ; 肿瘤生物学</subject><ispartof>Chinese medical journal, 2004-04, Vol.117 (4), p.566-570</ispartof><rights>Copyright © Wanfang Data Co. Ltd. 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This paper described an effective way to raise the cell ingestion rate of PNA so as to kill gastric cancer cells.Methods Heteroduplexes of PNAs and oligonucleotides, wrapped by Lipofectamine 2000, were used to infect SGC7901 cells. The inhibitive effect of heteroduplexes was evaluated by analyzing cell clone forming and cell growth rate. Telomerase activity of SGC7901 cells was detected by polymerase chain reaction enzyme-linked immunosorbent assay (PCR-ELISA) and silver staining assay.Results PNAs showed a dose-dependent inhibition of cell proliferation. The percentage of proliferation inhibition was 99. 4% after 7 days; the rate of cloning inhibition was 98.2% after 8 days;whereas for oligonucleotide groups, at the same concentration, the percentages were 50.1% and 67.5% respectively. Antisense PNA-DNA-Lipofectamine 2000 group ( AP-D-L group ) exhibited significantly different percentages from the control groups ( P &lt; 0.05). The test result indicated that telomerase activity of the AP-D-L group was inhibited ( P &lt; 0. 05). At the same time, the impact on cell morphology was observed.Conclusions The results showed that PNAs are potent antisense reagents. The telomeraseassociated therapies are very promising for the treatment of malignant tumours.</description><subject>Cell Division - drug effects</subject><subject>Cell Line, Tumor</subject><subject>DNA-Binding Proteins</subject><subject>Humans</subject><subject>Peptide Nucleic Acids - therapeutic use</subject><subject>SGC7901细胞系</subject><subject>Stomach Neoplasms - pathology</subject><subject>Stomach Neoplasms - therapy</subject><subject>Telomerase - antagonists &amp; inhibitors</subject><subject>Telomerase - metabolism</subject><subject>Transfection</subject><subject>端粒酶</subject><subject>缩氨酸核酸</subject><subject>肿瘤生物学</subject><issn>0366-6999</issn><issn>2542-5641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpF0E1LAzEQBuAgiq3VvyDx4m0hySbZzVGKtkJBQT2HJDv7UfejTXYp-uuNtCJzmMvDvDNzhuZMcJYIyek5mpNUykQqpWboKoQtIUyITF6iGRWUKC7oHK1eYTc2BeB-ci00DhvXFAEb7yGMeKwBV344jDUeSlyZMPpInOkdeOygbQN-Wy0zReg1uihNG-Dm1Bfo4-nxfblONi-r5-XDJnFM8jFxIC1lihsoOZTKOgssBcqyvFAcgDNeWC5daZjIC5nlMrMpFYwpZimXUqQLdH-cezB9afpKb4fJ9zFRf9eu2zJCeCya_8OdH_ZTPEZ3Tfhd2fQwTEFnNJcyIyTC2xOcbAeF3vmmM_5L__0ogrsjcPXQV_smhlrjPsumBa3yVBAi0h_GR2yn</recordid><startdate>20040401</startdate><enddate>20040401</enddate><creator>王宽 张岂凡 王锡山 薛英威 庞达 傅松滨</creator><general>Department of Abdominal Surgery, Turmour Clinical Hospital of Harbin Medical University, Harbin 150040, China%Department of Genetics, Harbin Medical University, Harbin 150086, China</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>2B.</scope><scope>4A8</scope><scope>92I</scope><scope>93N</scope><scope>PSX</scope><scope>TCJ</scope></search><sort><creationdate>20040401</creationdate><title>Peptide nucleic acids arrest the growth of gastric cancer cells SGC7901</title><author>王宽 张岂凡 王锡山 薛英威 庞达 傅松滨</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c264t-ce6b1294aef4ef9bcbe23e1278d94ee424db46cfa258d67867b3152292b146653</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Cell Division - drug effects</topic><topic>Cell Line, Tumor</topic><topic>DNA-Binding Proteins</topic><topic>Humans</topic><topic>Peptide Nucleic Acids - therapeutic use</topic><topic>SGC7901细胞系</topic><topic>Stomach Neoplasms - pathology</topic><topic>Stomach Neoplasms - therapy</topic><topic>Telomerase - antagonists &amp; inhibitors</topic><topic>Telomerase - metabolism</topic><topic>Transfection</topic><topic>端粒酶</topic><topic>缩氨酸核酸</topic><topic>肿瘤生物学</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>王宽 张岂凡 王锡山 薛英威 庞达 傅松滨</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>Wanfang Data Journals - Hong Kong</collection><collection>WANFANG Data Centre</collection><collection>Wanfang Data Journals</collection><collection>万方数据期刊 - 香港版</collection><collection>China Online Journals (COJ)</collection><collection>China Online Journals (COJ)</collection><jtitle>Chinese medical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>王宽 张岂凡 王锡山 薛英威 庞达 傅松滨</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Peptide nucleic acids arrest the growth of gastric cancer cells SGC7901</atitle><jtitle>Chinese medical journal</jtitle><addtitle>Chinese Medical Journal</addtitle><date>2004-04-01</date><risdate>2004</risdate><volume>117</volume><issue>4</issue><spage>566</spage><epage>570</epage><pages>566-570</pages><issn>0366-6999</issn><eissn>2542-5641</eissn><abstract>Background Peptide nucleic acid (PNA) has many characteristics useful in molecular biology. This paper described an effective way to raise the cell ingestion rate of PNA so as to kill gastric cancer cells.Methods Heteroduplexes of PNAs and oligonucleotides, wrapped by Lipofectamine 2000, were used to infect SGC7901 cells. The inhibitive effect of heteroduplexes was evaluated by analyzing cell clone forming and cell growth rate. Telomerase activity of SGC7901 cells was detected by polymerase chain reaction enzyme-linked immunosorbent assay (PCR-ELISA) and silver staining assay.Results PNAs showed a dose-dependent inhibition of cell proliferation. The percentage of proliferation inhibition was 99. 4% after 7 days; the rate of cloning inhibition was 98.2% after 8 days;whereas for oligonucleotide groups, at the same concentration, the percentages were 50.1% and 67.5% respectively. Antisense PNA-DNA-Lipofectamine 2000 group ( AP-D-L group ) exhibited significantly different percentages from the control groups ( P &lt; 0.05). The test result indicated that telomerase activity of the AP-D-L group was inhibited ( P &lt; 0. 05). At the same time, the impact on cell morphology was observed.Conclusions The results showed that PNAs are potent antisense reagents. The telomeraseassociated therapies are very promising for the treatment of malignant tumours.</abstract><cop>China</cop><pub>Department of Abdominal Surgery, Turmour Clinical Hospital of Harbin Medical University, Harbin 150040, China%Department of Genetics, Harbin Medical University, Harbin 150086, China</pub><pmid>15109451</pmid><tpages>5</tpages></addata></record>
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subjects Cell Division - drug effects
Cell Line, Tumor
DNA-Binding Proteins
Humans
Peptide Nucleic Acids - therapeutic use
SGC7901细胞系
Stomach Neoplasms - pathology
Stomach Neoplasms - therapy
Telomerase - antagonists & inhibitors
Telomerase - metabolism
Transfection
端粒酶
缩氨酸核酸
肿瘤生物学
title Peptide nucleic acids arrest the growth of gastric cancer cells SGC7901
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