Investigation of the influence of high-risk human papillomavirus on the biochemical composition of cervical cancer cells using vibrational spectroscopy
The main aetiology of cervical cancer is infection with high-risk human papillomavirus (HPV). Cervical cancer is almost 100% curable if detected in the early stages. Thus, information about the presence and levels of HPV in patient samples has high clinical value. As current screening methods, such...
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description | The main aetiology of cervical cancer is infection with high-risk human papillomavirus (HPV). Cervical cancer is almost 100% curable if detected in the early stages. Thus, information about the presence and levels of HPV in patient samples has high clinical value. As current screening methods, such as the Pap smear test, are highly subjective and in many cases show low sensitivity and specificity, new supportive techniques are desirable to improve the quality of cervical cancer screening. In this study, vibrational spectroscopic techniques (Raman and Fourier Transform Infra Red absorption) have been applied to the investigation of four cervical cancer cell lines: HPV negative C33A, HPV-18 positive HeLa with 20-50 integrated HPV copies per cell, HPV-16 positive SiHa with 1-2 integrated HPV strands per cell and HPV-16 positive CaSki containing 60-600 integrated HPV copies per cell. Results show that vibrational spectroscopic techniques can discriminate between the cell lines and elucidate cellular differences originating from proteins, nucleic acids and lipids. Similarities between C33A and SiHa cells were exhibited in the Raman and infrared spectra and were confirmed by Principal Component Analysis (PCA). Analysis of the biochemical composition of the investigated cells, with the aid of PCA, showed a clear discrimination between the C33A-SiHa group and HeLa and CaSki cell lines indicating the potential of vibrational spectroscopic techniques as a support to current methods for cervical cancer screening. |
doi_str_mv | 10.1039/c0an00571a |
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Cervical cancer is almost 100% curable if detected in the early stages. Thus, information about the presence and levels of HPV in patient samples has high clinical value. As current screening methods, such as the Pap smear test, are highly subjective and in many cases show low sensitivity and specificity, new supportive techniques are desirable to improve the quality of cervical cancer screening. In this study, vibrational spectroscopic techniques (Raman and Fourier Transform Infra Red absorption) have been applied to the investigation of four cervical cancer cell lines: HPV negative C33A, HPV-18 positive HeLa with 20-50 integrated HPV copies per cell, HPV-16 positive SiHa with 1-2 integrated HPV strands per cell and HPV-16 positive CaSki containing 60-600 integrated HPV copies per cell. Results show that vibrational spectroscopic techniques can discriminate between the cell lines and elucidate cellular differences originating from proteins, nucleic acids and lipids. Similarities between C33A and SiHa cells were exhibited in the Raman and infrared spectra and were confirmed by Principal Component Analysis (PCA). Analysis of the biochemical composition of the investigated cells, with the aid of PCA, showed a clear discrimination between the C33A-SiHa group and HeLa and CaSki cell lines indicating the potential of vibrational spectroscopic techniques as a support to current methods for cervical cancer screening.</description><identifier>ISSN: 0003-2654</identifier><identifier>EISSN: 1364-5528</identifier><identifier>DOI: 10.1039/c0an00571a</identifier><identifier>PMID: 20967345</identifier><identifier>CODEN: ANALAO</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Analytical chemistry ; Cell Line, Tumor ; Chemistry ; Exact sciences and technology ; Female ; HeLa Cells ; Human papillomavirus ; Human papillomavirus 18 - pathogenicity ; Humans ; Mass Screening - methods ; Multivariate Analysis ; Papillomavirus Infections - complications ; Sensitivity and Specificity ; Spectrometric and optical methods ; Spectroscopy, Fourier Transform Infrared - methods ; Spectrum Analysis, Raman - methods ; Tumor Virus Infections ; Uterine Cervical Neoplasms - chemistry ; Uterine Cervical Neoplasms - etiology ; Uterine Cervical Neoplasms - virology</subject><ispartof>Analyst (London), 2010-12, Vol.135 (12), p.3087-3093</ispartof><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c348t-3379b827c6d1dcd590ea27f554a19f7c3e6828e24df8a4e618259f994bbf01d13</citedby><cites>FETCH-LOGICAL-c348t-3379b827c6d1dcd590ea27f554a19f7c3e6828e24df8a4e618259f994bbf01d13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>309,310,314,776,780,785,786,2818,23909,23910,25118,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23693283$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20967345$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>OSTROWSKA, Kamila Magdalena</creatorcontrib><creatorcontrib>MALKIN, Alison</creatorcontrib><creatorcontrib>MEADE, Aidan</creatorcontrib><creatorcontrib>O'LEARY, John</creatorcontrib><creatorcontrib>MARTIN, Cara</creatorcontrib><creatorcontrib>SPILLANE, Cathy</creatorcontrib><creatorcontrib>BYME, Hugh James</creatorcontrib><creatorcontrib>LYNG, Fiona Maria</creatorcontrib><title>Investigation of the influence of high-risk human papillomavirus on the biochemical composition of cervical cancer cells using vibrational spectroscopy</title><title>Analyst (London)</title><addtitle>Analyst</addtitle><description>The main aetiology of cervical cancer is infection with high-risk human papillomavirus (HPV). Cervical cancer is almost 100% curable if detected in the early stages. Thus, information about the presence and levels of HPV in patient samples has high clinical value. As current screening methods, such as the Pap smear test, are highly subjective and in many cases show low sensitivity and specificity, new supportive techniques are desirable to improve the quality of cervical cancer screening. In this study, vibrational spectroscopic techniques (Raman and Fourier Transform Infra Red absorption) have been applied to the investigation of four cervical cancer cell lines: HPV negative C33A, HPV-18 positive HeLa with 20-50 integrated HPV copies per cell, HPV-16 positive SiHa with 1-2 integrated HPV strands per cell and HPV-16 positive CaSki containing 60-600 integrated HPV copies per cell. Results show that vibrational spectroscopic techniques can discriminate between the cell lines and elucidate cellular differences originating from proteins, nucleic acids and lipids. Similarities between C33A and SiHa cells were exhibited in the Raman and infrared spectra and were confirmed by Principal Component Analysis (PCA). Analysis of the biochemical composition of the investigated cells, with the aid of PCA, showed a clear discrimination between the C33A-SiHa group and HeLa and CaSki cell lines indicating the potential of vibrational spectroscopic techniques as a support to current methods for cervical cancer screening.</description><subject>Analytical chemistry</subject><subject>Cell Line, Tumor</subject><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>Female</subject><subject>HeLa Cells</subject><subject>Human papillomavirus</subject><subject>Human papillomavirus 18 - pathogenicity</subject><subject>Humans</subject><subject>Mass Screening - methods</subject><subject>Multivariate Analysis</subject><subject>Papillomavirus Infections - complications</subject><subject>Sensitivity and Specificity</subject><subject>Spectrometric and optical methods</subject><subject>Spectroscopy, Fourier Transform Infrared - methods</subject><subject>Spectrum Analysis, Raman - methods</subject><subject>Tumor Virus Infections</subject><subject>Uterine Cervical Neoplasms - chemistry</subject><subject>Uterine Cervical Neoplasms - etiology</subject><subject>Uterine Cervical Neoplasms - virology</subject><issn>0003-2654</issn><issn>1364-5528</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkctKxDAUhoMoznjZ-ACSjQhCNdc2WYp4GRDc6LqkaTKNtk1N2gGfxNc144y6dBXOyXf-k_w_ACcYXWJE5ZVGqkeIF1jtgDmmOcs4J2IXzBFCNCM5ZzNwEONrKjHiaB_MCJJ5QRmfg89FvzJxdEs1Ot9Db-HYGOh6206m12bdaNyyyYKLb7CZOtXDQQ2ubX2nVi5MEaap9UjlvG5M57Rqofbd4KP7UdQmrDZ9lSRDqts2wim6fglXrgrfq9N1HIweg4_aDx9HYM-qNprj7XkIXu5un28essen-8XN9WOmKRNjRmkhK0EKnde41jWXyChSWM6ZwtIWmppcEGEIq61QzORYEC6tlKyqLMI1pofgfKM7BP8-JSfKzsX1A1Vv_BRLwXmR3GLifxIJlmBRJPJiQ-r0mRiMLYfgOhU-SozKdWLlX2IJPt3KTlVn6l_0J6IEnG0BFZOJNiQTXfzjaC4pEZR-Adx6oeY</recordid><startdate>201012</startdate><enddate>201012</enddate><creator>OSTROWSKA, Kamila Magdalena</creator><creator>MALKIN, Alison</creator><creator>MEADE, Aidan</creator><creator>O'LEARY, John</creator><creator>MARTIN, Cara</creator><creator>SPILLANE, Cathy</creator><creator>BYME, Hugh James</creator><creator>LYNG, Fiona Maria</creator><general>Royal Society of Chemistry</general><scope>IQODW</scope><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>7X8</scope><scope>7U9</scope><scope>H94</scope></search><sort><creationdate>201012</creationdate><title>Investigation of the influence of high-risk human papillomavirus on the biochemical composition of cervical cancer cells using vibrational spectroscopy</title><author>OSTROWSKA, Kamila Magdalena ; MALKIN, Alison ; MEADE, Aidan ; O'LEARY, John ; MARTIN, Cara ; SPILLANE, Cathy ; BYME, Hugh James ; LYNG, Fiona Maria</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c348t-3379b827c6d1dcd590ea27f554a19f7c3e6828e24df8a4e618259f994bbf01d13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Analytical chemistry</topic><topic>Cell Line, Tumor</topic><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>Female</topic><topic>HeLa Cells</topic><topic>Human papillomavirus</topic><topic>Human papillomavirus 18 - pathogenicity</topic><topic>Humans</topic><topic>Mass Screening - methods</topic><topic>Multivariate Analysis</topic><topic>Papillomavirus Infections - complications</topic><topic>Sensitivity and Specificity</topic><topic>Spectrometric and optical methods</topic><topic>Spectroscopy, Fourier Transform Infrared - methods</topic><topic>Spectrum Analysis, Raman - methods</topic><topic>Tumor Virus Infections</topic><topic>Uterine Cervical Neoplasms - chemistry</topic><topic>Uterine Cervical Neoplasms - etiology</topic><topic>Uterine Cervical Neoplasms - virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>OSTROWSKA, Kamila Magdalena</creatorcontrib><creatorcontrib>MALKIN, Alison</creatorcontrib><creatorcontrib>MEADE, Aidan</creatorcontrib><creatorcontrib>O'LEARY, John</creatorcontrib><creatorcontrib>MARTIN, Cara</creatorcontrib><creatorcontrib>SPILLANE, Cathy</creatorcontrib><creatorcontrib>BYME, Hugh James</creatorcontrib><creatorcontrib>LYNG, Fiona Maria</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>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Analyst (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>OSTROWSKA, Kamila Magdalena</au><au>MALKIN, Alison</au><au>MEADE, Aidan</au><au>O'LEARY, John</au><au>MARTIN, Cara</au><au>SPILLANE, Cathy</au><au>BYME, Hugh James</au><au>LYNG, Fiona Maria</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigation of the influence of high-risk human papillomavirus on the biochemical composition of cervical cancer cells using vibrational spectroscopy</atitle><jtitle>Analyst (London)</jtitle><addtitle>Analyst</addtitle><date>2010-12</date><risdate>2010</risdate><volume>135</volume><issue>12</issue><spage>3087</spage><epage>3093</epage><pages>3087-3093</pages><issn>0003-2654</issn><eissn>1364-5528</eissn><coden>ANALAO</coden><abstract>The main aetiology of cervical cancer is infection with high-risk human papillomavirus (HPV). Cervical cancer is almost 100% curable if detected in the early stages. Thus, information about the presence and levels of HPV in patient samples has high clinical value. As current screening methods, such as the Pap smear test, are highly subjective and in many cases show low sensitivity and specificity, new supportive techniques are desirable to improve the quality of cervical cancer screening. In this study, vibrational spectroscopic techniques (Raman and Fourier Transform Infra Red absorption) have been applied to the investigation of four cervical cancer cell lines: HPV negative C33A, HPV-18 positive HeLa with 20-50 integrated HPV copies per cell, HPV-16 positive SiHa with 1-2 integrated HPV strands per cell and HPV-16 positive CaSki containing 60-600 integrated HPV copies per cell. Results show that vibrational spectroscopic techniques can discriminate between the cell lines and elucidate cellular differences originating from proteins, nucleic acids and lipids. Similarities between C33A and SiHa cells were exhibited in the Raman and infrared spectra and were confirmed by Principal Component Analysis (PCA). Analysis of the biochemical composition of the investigated cells, with the aid of PCA, showed a clear discrimination between the C33A-SiHa group and HeLa and CaSki cell lines indicating the potential of vibrational spectroscopic techniques as a support to current methods for cervical cancer screening.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><pmid>20967345</pmid><doi>10.1039/c0an00571a</doi><tpages>7</tpages></addata></record> |
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subjects | Analytical chemistry Cell Line, Tumor Chemistry Exact sciences and technology Female HeLa Cells Human papillomavirus Human papillomavirus 18 - pathogenicity Humans Mass Screening - methods Multivariate Analysis Papillomavirus Infections - complications Sensitivity and Specificity Spectrometric and optical methods Spectroscopy, Fourier Transform Infrared - methods Spectrum Analysis, Raman - methods Tumor Virus Infections Uterine Cervical Neoplasms - chemistry Uterine Cervical Neoplasms - etiology Uterine Cervical Neoplasms - virology |
title | Investigation of the influence of high-risk human papillomavirus on the biochemical composition of cervical cancer cells using vibrational spectroscopy |
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