Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Modern pathology 2003-11, Vol.16 (11), p.1095-1101
Main Authors: Pu, Robert T, Laitala, Lauren E, Alli, Patricia M, Fackler, Mary Jo, Sukumar, Saraswati, Clark, Douglas P
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-c524t-e6583e718306fab02d68e09e2b565541a220c4bd13b128315dc0947d7f3219cc3
cites cdi_FETCH-LOGICAL-c524t-e6583e718306fab02d68e09e2b565541a220c4bd13b128315dc0947d7f3219cc3
container_end_page 1101
container_issue 11
container_start_page 1095
container_title Modern pathology
container_volume 16
creator Pu, Robert T
Laitala, Lauren E
Alli, Patricia M
Fackler, Mary Jo
Sukumar, Saraswati
Clark, Douglas P
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
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_71369077</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0893395222046919</els_id><sourcerecordid>984911991</sourcerecordid><originalsourceid>FETCH-LOGICAL-c524t-e6583e718306fab02d68e09e2b565541a220c4bd13b128315dc0947d7f3219cc3</originalsourceid><addsrcrecordid>eNqNkU9v1DAQxS0EokvhI4ACB24J_hMnNrd2tYVKu2IPcLYcZ7J1lbWD7a203x63WXUlTvVlLL3fvBnNQ-gzwRXBsv2GSbXZVvjxSd4KWrVSSF6t6Cu0IJzhElPBX6MFFpKVTHJ6gd7FeI8xqbmgb9EFqRtS41oskN5AujuOOlnvim3wgx2t2xV-KK7B2Z0rtOuLjR7zV7tUXAfQMRVriJmPT-JtisXVNI3WzCbJF8tj8pNOd370u-N79GbQY4QPp3qJ_tysfi9_lutfP26XV-vScFqnEhouGLREMNwMusO0bwRgCbTjDec10ZRiU3c9YR2hghHeGyzrtm8HRok0hl2ir7PvFPzfA8Sk9jYaGEftwB-iaglrJG7bDH75D7z3h-DybopSQjiWjGdIzpAJPsYAg5qC3etwVASrxxAUJmqzVecQ1FMIakVz76fTgEO3h_7cebp6Br7PQMyS20E4b_AS949zs9PpEODZnQmR8yZZX8465GM_2GwejQVnoLcBTFK9ty-Y8g_F7LKs</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>221150935</pqid></control><display><type>article</type><title>Methylation Profiling of Benign and Malignant Breast Lesions and Its Application to Cytopathology</title><source>Nature</source><creator>Pu, Robert T ; Laitala, Lauren E ; Alli, Patricia M ; Fackler, Mary Jo ; Sukumar, Saraswati ; Clark, Douglas P</creator><creatorcontrib>Pu, Robert T ; Laitala, Lauren E ; Alli, Patricia M ; Fackler, Mary Jo ; Sukumar, Saraswati ; Clark, Douglas P</creatorcontrib><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><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 &amp; 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 &amp; 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 &amp; 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 - genetics</subject><subject>RARβ2</subject><subject>RASSF1A</subject><subject>Surgical and cytopathology specimens</subject><issn>0893-3952</issn><issn>1530-0285</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNqNkU9v1DAQxS0EokvhI4ACB24J_hMnNrd2tYVKu2IPcLYcZ7J1lbWD7a203x63WXUlTvVlLL3fvBnNQ-gzwRXBsv2GSbXZVvjxSd4KWrVSSF6t6Cu0IJzhElPBX6MFFpKVTHJ6gd7FeI8xqbmgb9EFqRtS41oskN5AujuOOlnvim3wgx2t2xV-KK7B2Z0rtOuLjR7zV7tUXAfQMRVriJmPT-JtisXVNI3WzCbJF8tj8pNOd370u-N79GbQY4QPp3qJ_tysfi9_lutfP26XV-vScFqnEhouGLREMNwMusO0bwRgCbTjDec10ZRiU3c9YR2hghHeGyzrtm8HRok0hl2ir7PvFPzfA8Sk9jYaGEftwB-iaglrJG7bDH75D7z3h-DybopSQjiWjGdIzpAJPsYAg5qC3etwVASrxxAUJmqzVecQ1FMIakVz76fTgEO3h_7cebp6Br7PQMyS20E4b_AS949zs9PpEODZnQmR8yZZX8465GM_2GwejQVnoLcBTFK9ty-Y8g_F7LKs</recordid><startdate>20031101</startdate><enddate>20031101</enddate><creator>Pu, Robert T</creator><creator>Laitala, Lauren E</creator><creator>Alli, Patricia M</creator><creator>Fackler, Mary Jo</creator><creator>Sukumar, Saraswati</creator><creator>Clark, Douglas P</creator><general>Elsevier Inc</general><general>Nature Publishing Group US</general><general>Elsevier Limited</general><scope>6I.</scope><scope>AAFTH</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>3V.</scope><scope>7QP</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</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>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope></search><sort><creationdate>20031101</creationdate><title>Methylation Profiling of Benign and Malignant Breast Lesions and Its Application to Cytopathology</title><author>Pu, Robert T ; Laitala, Lauren E ; Alli, Patricia M ; Fackler, Mary Jo ; Sukumar, Saraswati ; Clark, Douglas P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c524t-e6583e718306fab02d68e09e2b565541a220c4bd13b128315dc0947d7f3219cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Biopsy</topic><topic>Biopsy, Needle</topic><topic>Breast cancer</topic><topic>Breast Diseases - 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 &amp; 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 &amp; Calcified Tissue Abstracts</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; 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 &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing &amp; 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>
fulltext fulltext
identifier ISSN: 0893-3952
ispartof Modern pathology, 2003-11, Vol.16 (11), p.1095-1101
issn 0893-3952
1530-0285
language eng
recordid cdi_proquest_miscellaneous_71369077
source Nature
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T03%3A15%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Methylation%20Profiling%20of%20Benign%20and%20Malignant%20Breast%20Lesions%20and%20Its%20Application%20to%20Cytopathology&rft.jtitle=Modern%20pathology&rft.au=Pu,%20Robert%20T&rft.date=2003-11-01&rft.volume=16&rft.issue=11&rft.spage=1095&rft.epage=1101&rft.pages=1095-1101&rft.issn=0893-3952&rft.eissn=1530-0285&rft.coden=MODPEO&rft_id=info:doi/10.1097/01.MP.0000095782.79895.E2&rft_dat=%3Cproquest_cross%3E984911991%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c524t-e6583e718306fab02d68e09e2b565541a220c4bd13b128315dc0947d7f3219cc3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=221150935&rft_id=info:pmid/14614048&rfr_iscdi=true