Polymerase Chain Reaction-Based Microsatellite Analysis of Fine-Needle Aspirations from Hürthle Cell Neoplasms
Fine-needle aspiration (FNA) of the thyroid is the sine qua non in the preoperative evaluation of thyroid nodules. Despite this, cytological examination of FNA cannot differentiate malignant from benign Hürthle cell neoplasms. We have previously shown that Hürthle cell carcinomas harbor more genetic...
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Veröffentlicht in: | Thyroid (New York, N.Y.) N.Y.), 1997-12, Vol.7 (6), p.853-857 |
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creator | Takiyama, Y Saji, M Clark, D P Phillips, G S Segev, D L Smallridge, R C Westra, W H Udelsman, R Zeiger, M A |
description | Fine-needle aspiration (FNA) of the thyroid is the
sine qua non
in the preoperative evaluation of thyroid nodules. Despite this, cytological examination of FNA cannot differentiate malignant from benign Hürthle cell neoplasms. We have previously shown that Hürthle cell carcinomas harbor more genetic alterations on chromosomal arms lq and 2p than Hürthle cell adenomas, and that all Hürthle cell neoplasms have a significantly higher frequency of alterations on chromosomal arm lp compared with normal thyroid. To determine if these genetic alterations could be detected in FNA samples, we examined DNA from FNAs that were available from eight Hürthle cell neoplasms. Polymerase chain reaction (PCR) amplification of DNA demonstrated either direct correlation with alterations seen in the tumor samples or in some instances, additional chromosomal alterations. We conclude that PCR-based microsatellite DNA analysis of preoperative FNA samples from Hürthle cell neoplasms can potentially distinguish Hürthle cell carcinomas from adenomas and that with further validation and perfection, this technique may allow more optimal surgical management of patients with these lesions. |
doi_str_mv | 10.1089/thy.1997.7.853 |
format | Article |
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sine qua non
in the preoperative evaluation of thyroid nodules. Despite this, cytological examination of FNA cannot differentiate malignant from benign Hürthle cell neoplasms. We have previously shown that Hürthle cell carcinomas harbor more genetic alterations on chromosomal arms lq and 2p than Hürthle cell adenomas, and that all Hürthle cell neoplasms have a significantly higher frequency of alterations on chromosomal arm lp compared with normal thyroid. To determine if these genetic alterations could be detected in FNA samples, we examined DNA from FNAs that were available from eight Hürthle cell neoplasms. Polymerase chain reaction (PCR) amplification of DNA demonstrated either direct correlation with alterations seen in the tumor samples or in some instances, additional chromosomal alterations. We conclude that PCR-based microsatellite DNA analysis of preoperative FNA samples from Hürthle cell neoplasms can potentially distinguish Hürthle cell carcinomas from adenomas and that with further validation and perfection, this technique may allow more optimal surgical management of patients with these lesions.</description><identifier>ISSN: 1050-7256</identifier><identifier>EISSN: 1557-9077</identifier><identifier>DOI: 10.1089/thy.1997.7.853</identifier><identifier>PMID: 9459628</identifier><language>eng</language><publisher>United States</publisher><subject>Adenocarcinoma - genetics ; Alleles ; Biopsy, Needle ; Chromosomes, Human, Pair 1 - genetics ; DNA - analysis ; DNA - genetics ; DNA, Neoplasm - analysis ; DNA, Neoplasm - genetics ; Gene Deletion ; Humans ; Microsatellite Repeats - genetics ; Polymerase Chain Reaction ; Thyroid Neoplasms - genetics</subject><ispartof>Thyroid (New York, N.Y.), 1997-12, Vol.7 (6), p.853-857</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c335t-c763b1eb9d5068ae157eef4f28584ba3b8c0fe4d975b940be23e375345d4f7823</citedby><cites>FETCH-LOGICAL-c335t-c763b1eb9d5068ae157eef4f28584ba3b8c0fe4d975b940be23e375345d4f7823</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.liebertpub.com/doi/epdf/10.1089/thy.1997.7.853$$EPDF$$P50$$Gmaryannliebert$$H</linktopdf><linktohtml>$$Uhttps://www.liebertpub.com/doi/full/10.1089/thy.1997.7.853$$EHTML$$P50$$Gmaryannliebert$$H</linktohtml><link.rule.ids>314,777,781,3029,21704,27905,27906,55272,55284</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9459628$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Takiyama, Y</creatorcontrib><creatorcontrib>Saji, M</creatorcontrib><creatorcontrib>Clark, D P</creatorcontrib><creatorcontrib>Phillips, G S</creatorcontrib><creatorcontrib>Segev, D L</creatorcontrib><creatorcontrib>Smallridge, R C</creatorcontrib><creatorcontrib>Westra, W H</creatorcontrib><creatorcontrib>Udelsman, R</creatorcontrib><creatorcontrib>Zeiger, M A</creatorcontrib><title>Polymerase Chain Reaction-Based Microsatellite Analysis of Fine-Needle Aspirations from Hürthle Cell Neoplasms</title><title>Thyroid (New York, N.Y.)</title><addtitle>Thyroid</addtitle><description>Fine-needle aspiration (FNA) of the thyroid is the
sine qua non
in the preoperative evaluation of thyroid nodules. Despite this, cytological examination of FNA cannot differentiate malignant from benign Hürthle cell neoplasms. We have previously shown that Hürthle cell carcinomas harbor more genetic alterations on chromosomal arms lq and 2p than Hürthle cell adenomas, and that all Hürthle cell neoplasms have a significantly higher frequency of alterations on chromosomal arm lp compared with normal thyroid. To determine if these genetic alterations could be detected in FNA samples, we examined DNA from FNAs that were available from eight Hürthle cell neoplasms. Polymerase chain reaction (PCR) amplification of DNA demonstrated either direct correlation with alterations seen in the tumor samples or in some instances, additional chromosomal alterations. We conclude that PCR-based microsatellite DNA analysis of preoperative FNA samples from Hürthle cell neoplasms can potentially distinguish Hürthle cell carcinomas from adenomas and that with further validation and perfection, this technique may allow more optimal surgical management of patients with these lesions.</description><subject>Adenocarcinoma - genetics</subject><subject>Alleles</subject><subject>Biopsy, Needle</subject><subject>Chromosomes, Human, Pair 1 - genetics</subject><subject>DNA - analysis</subject><subject>DNA - genetics</subject><subject>DNA, Neoplasm - analysis</subject><subject>DNA, Neoplasm - genetics</subject><subject>Gene Deletion</subject><subject>Humans</subject><subject>Microsatellite Repeats - genetics</subject><subject>Polymerase Chain Reaction</subject><subject>Thyroid Neoplasms - genetics</subject><issn>1050-7256</issn><issn>1557-9077</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE9PwyAchonRTJ1evZlw8tZKCxQ4zsU5E53G6JnQ9tcM05YJ3WHfzZtfTJotXj1B3n-BB6GrjKQZkep2WO_STCmRilRyeoTOMs5FoogQx_FOOElEzotTdB7CJyFZIQWdoIliXBW5PEPu1bW7DrwJgOdrY3v8BqYarOuTu6jV-NlW3gUzQNvaAfCsN-0u2IBdgxe2h2QFULdRDxvrzdgLuPGuw8ufbz-sozOPTbwCt2lN6MIFOmlMG-DycE7Rx-L-fb5Mnl4eHuezp6SilA9JJQpaZlCqmpNCGsi4AGhYk0suWWloKSvSAKuV4KVipIScAhWcMl6zRsicTtHNfnfj3dcWwqA7G6r4FNOD2wYtFGeUShqD6T44fjN4aPTG2874nc6IHgnrSFiPhLXQkXAsXB-Wt2UH9V_8gDT6bO-Pqun71kIJfvhv9hdp64tS</recordid><startdate>19971201</startdate><enddate>19971201</enddate><creator>Takiyama, Y</creator><creator>Saji, M</creator><creator>Clark, D P</creator><creator>Phillips, G S</creator><creator>Segev, D L</creator><creator>Smallridge, R C</creator><creator>Westra, W H</creator><creator>Udelsman, R</creator><creator>Zeiger, M A</creator><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></search><sort><creationdate>19971201</creationdate><title>Polymerase Chain Reaction-Based Microsatellite Analysis of Fine-Needle Aspirations from Hürthle Cell Neoplasms</title><author>Takiyama, Y ; Saji, M ; Clark, D P ; Phillips, G S ; Segev, D L ; Smallridge, R C ; Westra, W H ; Udelsman, R ; Zeiger, M A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c335t-c763b1eb9d5068ae157eef4f28584ba3b8c0fe4d975b940be23e375345d4f7823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Adenocarcinoma - genetics</topic><topic>Alleles</topic><topic>Biopsy, Needle</topic><topic>Chromosomes, Human, Pair 1 - genetics</topic><topic>DNA - analysis</topic><topic>DNA - genetics</topic><topic>DNA, Neoplasm - analysis</topic><topic>DNA, Neoplasm - genetics</topic><topic>Gene Deletion</topic><topic>Humans</topic><topic>Microsatellite Repeats - genetics</topic><topic>Polymerase Chain Reaction</topic><topic>Thyroid Neoplasms - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Takiyama, Y</creatorcontrib><creatorcontrib>Saji, M</creatorcontrib><creatorcontrib>Clark, D P</creatorcontrib><creatorcontrib>Phillips, G S</creatorcontrib><creatorcontrib>Segev, D L</creatorcontrib><creatorcontrib>Smallridge, R C</creatorcontrib><creatorcontrib>Westra, W H</creatorcontrib><creatorcontrib>Udelsman, R</creatorcontrib><creatorcontrib>Zeiger, M A</creatorcontrib><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><jtitle>Thyroid (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Takiyama, Y</au><au>Saji, M</au><au>Clark, D P</au><au>Phillips, G S</au><au>Segev, D L</au><au>Smallridge, R C</au><au>Westra, W H</au><au>Udelsman, R</au><au>Zeiger, M A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polymerase Chain Reaction-Based Microsatellite Analysis of Fine-Needle Aspirations from Hürthle Cell Neoplasms</atitle><jtitle>Thyroid (New York, N.Y.)</jtitle><addtitle>Thyroid</addtitle><date>1997-12-01</date><risdate>1997</risdate><volume>7</volume><issue>6</issue><spage>853</spage><epage>857</epage><pages>853-857</pages><issn>1050-7256</issn><eissn>1557-9077</eissn><abstract>Fine-needle aspiration (FNA) of the thyroid is the
sine qua non
in the preoperative evaluation of thyroid nodules. Despite this, cytological examination of FNA cannot differentiate malignant from benign Hürthle cell neoplasms. We have previously shown that Hürthle cell carcinomas harbor more genetic alterations on chromosomal arms lq and 2p than Hürthle cell adenomas, and that all Hürthle cell neoplasms have a significantly higher frequency of alterations on chromosomal arm lp compared with normal thyroid. To determine if these genetic alterations could be detected in FNA samples, we examined DNA from FNAs that were available from eight Hürthle cell neoplasms. Polymerase chain reaction (PCR) amplification of DNA demonstrated either direct correlation with alterations seen in the tumor samples or in some instances, additional chromosomal alterations. We conclude that PCR-based microsatellite DNA analysis of preoperative FNA samples from Hürthle cell neoplasms can potentially distinguish Hürthle cell carcinomas from adenomas and that with further validation and perfection, this technique may allow more optimal surgical management of patients with these lesions.</abstract><cop>United States</cop><pmid>9459628</pmid><doi>10.1089/thy.1997.7.853</doi><tpages>5</tpages></addata></record> |
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source | Mary Ann Liebert Online Subscription; MEDLINE |
subjects | Adenocarcinoma - genetics Alleles Biopsy, Needle Chromosomes, Human, Pair 1 - genetics DNA - analysis DNA - genetics DNA, Neoplasm - analysis DNA, Neoplasm - genetics Gene Deletion Humans Microsatellite Repeats - genetics Polymerase Chain Reaction Thyroid Neoplasms - genetics |
title | Polymerase Chain Reaction-Based Microsatellite Analysis of Fine-Needle Aspirations from Hürthle Cell Neoplasms |
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