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Methylation Profiling of Benign and Malignant Breast Lesions and Its Application to Cytopathology
Methylation of tumor suppressor genes has been implicated in breast cancer development. However, methylation profiles of different breast lesions, subtypes of carcinoma in particular, have not been examined in detail. In this study, we use methylation-specific PCR (MSP) to generate gene methylation...
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Published in: | Modern pathology 2003-11, Vol.16 (11), p.1095-1101 |
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description | Methylation of tumor suppressor genes has been implicated in breast cancer development. However, methylation profiles of different breast lesions, subtypes of carcinoma in particular, have not been examined in detail. In this study, we use methylation-specific PCR (MSP) to generate gene methylation profiles of different breast lesions and to test the clinical utility of such profiles. We examined the methylation status of three genes, RARβ2, RASSF1A, and cyclin D2, on 102 samples of breast tissue, from benign (n = 36), to in situ carcinoma (n = 21), to invasive carcinoma (n = 45). We found that almost all cases of invasive carcinoma (96%) contained at least one methylated gene from our panel, whereas gene methylation was less common among benign lesions (42%) and in situ carcinoma (76%). Of the three genes, cyclin D2 methylation was most specific for malignancy because only 1 of 35 benign cases was methylated at this gene (1 case was not informative). The major histologic subtypes of invasive carcinoma show similar methylation profiles in the genes examined. We next performed MSP analysis on archival breast fine-needle aspiration (FNA) biopsy samples and corresponding surgical biopsy specimens and found a high concordance between the two types of specimens. We then analyzed 17 breast FNA biopsy samples with an indeterminate diagnosis. In this setting, MSP had a high specificity (100%) and modest sensitivity (67%) for identifying malignancy. |
doi_str_mv | 10.1097/01.MP.0000095782.79895.E2 |
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However, methylation profiles of different breast lesions, subtypes of carcinoma in particular, have not been examined in detail. In this study, we use methylation-specific PCR (MSP) to generate gene methylation profiles of different breast lesions and to test the clinical utility of such profiles. We examined the methylation status of three genes, RARβ2, RASSF1A, and cyclin D2, on 102 samples of breast tissue, from benign (n = 36), to in situ carcinoma (n = 21), to invasive carcinoma (n = 45). We found that almost all cases of invasive carcinoma (96%) contained at least one methylated gene from our panel, whereas gene methylation was less common among benign lesions (42%) and in situ carcinoma (76%). Of the three genes, cyclin D2 methylation was most specific for malignancy because only 1 of 35 benign cases was methylated at this gene (1 case was not informative). The major histologic subtypes of invasive carcinoma show similar methylation profiles in the genes examined. We next performed MSP analysis on archival breast fine-needle aspiration (FNA) biopsy samples and corresponding surgical biopsy specimens and found a high concordance between the two types of specimens. We then analyzed 17 breast FNA biopsy samples with an indeterminate diagnosis. In this setting, MSP had a high specificity (100%) and modest sensitivity (67%) for identifying malignancy.</description><identifier>ISSN: 0893-3952</identifier><identifier>EISSN: 1530-0285</identifier><identifier>DOI: 10.1097/01.MP.0000095782.79895.E2</identifier><identifier>PMID: 14614048</identifier><identifier>CODEN: MODPEO</identifier><language>eng</language><publisher>New York: Elsevier Inc</publisher><subject>Biopsy ; Biopsy, Needle ; Breast cancer ; Breast Diseases - genetics ; Breast Diseases - pathology ; Breast lesions ; Breast Neoplasms - genetics ; Breast Neoplasms - pathology ; Carcinoma - genetics ; Carcinoma - pathology ; Carcinoma in Situ - genetics ; Carcinoma in Situ - pathology ; Cellular biology ; Cyclin D2 ; DNA Fingerprinting ; DNA Methylation ; Female ; Fine needle aspiration biopsy ; Gene Frequency ; Genes ; Humans ; Laboratory Medicine ; Medicine ; Medicine & Public Health ; Methylation profile ; Middle Aged ; MSP ; Neoplasm Invasiveness ; original-article ; Pathology ; Polymerase Chain Reaction ; Promoter Regions, Genetic - genetics ; RARβ2 ; RASSF1A ; Surgical and cytopathology specimens</subject><ispartof>Modern pathology, 2003-11, Vol.16 (11), p.1095-1101</ispartof><rights>2003 United States & Canadian Academy of Pathology</rights><rights>The United States and Canadian Academy of Pathology, Inc. 2003</rights><rights>Copyright Nature Publishing Group Nov 2003</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c524t-e6583e718306fab02d68e09e2b565541a220c4bd13b128315dc0947d7f3219cc3</citedby><cites>FETCH-LOGICAL-c524t-e6583e718306fab02d68e09e2b565541a220c4bd13b128315dc0947d7f3219cc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,2727,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14614048$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pu, Robert T</creatorcontrib><creatorcontrib>Laitala, Lauren E</creatorcontrib><creatorcontrib>Alli, Patricia M</creatorcontrib><creatorcontrib>Fackler, Mary Jo</creatorcontrib><creatorcontrib>Sukumar, Saraswati</creatorcontrib><creatorcontrib>Clark, Douglas P</creatorcontrib><title>Methylation Profiling of Benign and Malignant Breast Lesions and Its Application to Cytopathology</title><title>Modern pathology</title><addtitle>Mod Pathol</addtitle><addtitle>Mod Pathol</addtitle><description>Methylation of tumor suppressor genes has been implicated in breast cancer development. However, methylation profiles of different breast lesions, subtypes of carcinoma in particular, have not been examined in detail. In this study, we use methylation-specific PCR (MSP) to generate gene methylation profiles of different breast lesions and to test the clinical utility of such profiles. We examined the methylation status of three genes, RARβ2, RASSF1A, and cyclin D2, on 102 samples of breast tissue, from benign (n = 36), to in situ carcinoma (n = 21), to invasive carcinoma (n = 45). We found that almost all cases of invasive carcinoma (96%) contained at least one methylated gene from our panel, whereas gene methylation was less common among benign lesions (42%) and in situ carcinoma (76%). Of the three genes, cyclin D2 methylation was most specific for malignancy because only 1 of 35 benign cases was methylated at this gene (1 case was not informative). The major histologic subtypes of invasive carcinoma show similar methylation profiles in the genes examined. We next performed MSP analysis on archival breast fine-needle aspiration (FNA) biopsy samples and corresponding surgical biopsy specimens and found a high concordance between the two types of specimens. We then analyzed 17 breast FNA biopsy samples with an indeterminate diagnosis. In this setting, MSP had a high specificity (100%) and modest sensitivity (67%) for identifying malignancy.</description><subject>Biopsy</subject><subject>Biopsy, Needle</subject><subject>Breast cancer</subject><subject>Breast Diseases - genetics</subject><subject>Breast Diseases - pathology</subject><subject>Breast lesions</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - pathology</subject><subject>Carcinoma - genetics</subject><subject>Carcinoma - pathology</subject><subject>Carcinoma in Situ - genetics</subject><subject>Carcinoma in Situ - pathology</subject><subject>Cellular biology</subject><subject>Cyclin D2</subject><subject>DNA Fingerprinting</subject><subject>DNA Methylation</subject><subject>Female</subject><subject>Fine needle aspiration biopsy</subject><subject>Gene Frequency</subject><subject>Genes</subject><subject>Humans</subject><subject>Laboratory Medicine</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Methylation profile</subject><subject>Middle Aged</subject><subject>MSP</subject><subject>Neoplasm Invasiveness</subject><subject>original-article</subject><subject>Pathology</subject><subject>Polymerase Chain Reaction</subject><subject>Promoter Regions, Genetic - 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genetics</topic><topic>Breast Diseases - pathology</topic><topic>Breast lesions</topic><topic>Breast Neoplasms - genetics</topic><topic>Breast Neoplasms - pathology</topic><topic>Carcinoma - genetics</topic><topic>Carcinoma - pathology</topic><topic>Carcinoma in Situ - genetics</topic><topic>Carcinoma in Situ - pathology</topic><topic>Cellular biology</topic><topic>Cyclin D2</topic><topic>DNA Fingerprinting</topic><topic>DNA Methylation</topic><topic>Female</topic><topic>Fine needle aspiration biopsy</topic><topic>Gene Frequency</topic><topic>Genes</topic><topic>Humans</topic><topic>Laboratory Medicine</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Methylation profile</topic><topic>Middle Aged</topic><topic>MSP</topic><topic>Neoplasm Invasiveness</topic><topic>original-article</topic><topic>Pathology</topic><topic>Polymerase Chain Reaction</topic><topic>Promoter Regions, Genetic - genetics</topic><topic>RARβ2</topic><topic>RASSF1A</topic><topic>Surgical and cytopathology specimens</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pu, Robert T</creatorcontrib><creatorcontrib>Laitala, Lauren E</creatorcontrib><creatorcontrib>Alli, Patricia M</creatorcontrib><creatorcontrib>Fackler, Mary Jo</creatorcontrib><creatorcontrib>Sukumar, Saraswati</creatorcontrib><creatorcontrib>Clark, Douglas P</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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>Calcium & Calcified Tissue Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences 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>ProQuest Pharma Collection</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 UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>Modern pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pu, Robert T</au><au>Laitala, Lauren E</au><au>Alli, Patricia M</au><au>Fackler, Mary Jo</au><au>Sukumar, Saraswati</au><au>Clark, Douglas P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Methylation Profiling of Benign and Malignant Breast Lesions and Its Application to Cytopathology</atitle><jtitle>Modern pathology</jtitle><stitle>Mod Pathol</stitle><addtitle>Mod Pathol</addtitle><date>2003-11-01</date><risdate>2003</risdate><volume>16</volume><issue>11</issue><spage>1095</spage><epage>1101</epage><pages>1095-1101</pages><issn>0893-3952</issn><eissn>1530-0285</eissn><coden>MODPEO</coden><abstract>Methylation of tumor suppressor genes has been implicated in breast cancer development. However, methylation profiles of different breast lesions, subtypes of carcinoma in particular, have not been examined in detail. In this study, we use methylation-specific PCR (MSP) to generate gene methylation profiles of different breast lesions and to test the clinical utility of such profiles. We examined the methylation status of three genes, RARβ2, RASSF1A, and cyclin D2, on 102 samples of breast tissue, from benign (n = 36), to in situ carcinoma (n = 21), to invasive carcinoma (n = 45). We found that almost all cases of invasive carcinoma (96%) contained at least one methylated gene from our panel, whereas gene methylation was less common among benign lesions (42%) and in situ carcinoma (76%). Of the three genes, cyclin D2 methylation was most specific for malignancy because only 1 of 35 benign cases was methylated at this gene (1 case was not informative). The major histologic subtypes of invasive carcinoma show similar methylation profiles in the genes examined. We next performed MSP analysis on archival breast fine-needle aspiration (FNA) biopsy samples and corresponding surgical biopsy specimens and found a high concordance between the two types of specimens. We then analyzed 17 breast FNA biopsy samples with an indeterminate diagnosis. In this setting, MSP had a high specificity (100%) and modest sensitivity (67%) for identifying malignancy.</abstract><cop>New York</cop><pub>Elsevier Inc</pub><pmid>14614048</pmid><doi>10.1097/01.MP.0000095782.79895.E2</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biopsy Biopsy, Needle Breast cancer Breast Diseases - genetics Breast Diseases - pathology Breast lesions Breast Neoplasms - genetics Breast Neoplasms - pathology Carcinoma - genetics Carcinoma - pathology Carcinoma in Situ - genetics Carcinoma in Situ - pathology Cellular biology Cyclin D2 DNA Fingerprinting DNA Methylation Female Fine needle aspiration biopsy Gene Frequency Genes Humans Laboratory Medicine Medicine Medicine & Public Health Methylation profile Middle Aged MSP Neoplasm Invasiveness original-article Pathology Polymerase Chain Reaction Promoter Regions, Genetic - genetics RARβ2 RASSF1A Surgical and cytopathology specimens |
title | Methylation Profiling of Benign and Malignant Breast Lesions and Its Application to Cytopathology |
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