Tracking the Clonal Evolution of Adenosquamous Carcinoma, a Rare Variant of Intraductal Papillary Mucinous Neoplasm of the Pancreas
Adenosquamous carcinoma (ASC) is an uncommon variant of pancreatic neoplasm. We sought to trace the mode of tumor progression using specimens of ASC associated with intraductal papillary mucinous neoplasm (IPMN) of the pancreas. A resected specimen of the primary pancreatic ASC, developed in a 72-ye...
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Veröffentlicht in: | Pancreas 2016-07, Vol.45 (6), p.915-918 |
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creator | Matsuzaka, Suguru Karasaki, Hidenori Ono, Yusuke Ogata, Munehiko Oikawa, Kensuke Tamakawa, Susumu Chiba, Shin-Ichi Muraki, Miho Yokochi, Tomoki Funakoshi, Hiroshi Kono, Toru Nagashima, Kazuo Mizukami, Yusuke |
description | Adenosquamous carcinoma (ASC) is an uncommon variant of pancreatic neoplasm. We sought to trace the mode of tumor progression using specimens of ASC associated with intraductal papillary mucinous neoplasm (IPMN) of the pancreas. A resected specimen of the primary pancreatic ASC, developed in a 72-year-old man, was subjected to mutation profiling using amplicon-targeted sequencing and digital polymerase chain reaction. DNA was isolated from each histological compartment including noninvasive IPMN, squamous cell carcinoma (SCC), and adenocarcinoma (AC). Histologically, an IPMN with a large mural nodule was identified. The invasive tumor predominantly consisted of SCC, and a smaller AC was found around the lesion. Squamous metaplasias were sporadically distributed within benign IPMNs. Mutation alleles KRAS and GNAS were identified in all specimens of IPMN including the areas of squamous metaplasia. In addition, these mutations were found in SCC and AC. Clear transition from flat/low-papillary IPMN to SCC indicated a potent invasion front, and the SCC compartment was genetically unique, because the area has a higher frequency of mutation KRAS. The invasive tumors with distinct histological appearances shared the form of noninvasive IPMN as a common precursor, rather than de novo cancer, suggesting the significance of a genetic profiling scheme of tumors associated with IPMN. |
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We sought to trace the mode of tumor progression using specimens of ASC associated with intraductal papillary mucinous neoplasm (IPMN) of the pancreas. A resected specimen of the primary pancreatic ASC, developed in a 72-year-old man, was subjected to mutation profiling using amplicon-targeted sequencing and digital polymerase chain reaction. DNA was isolated from each histological compartment including noninvasive IPMN, squamous cell carcinoma (SCC), and adenocarcinoma (AC). Histologically, an IPMN with a large mural nodule was identified. The invasive tumor predominantly consisted of SCC, and a smaller AC was found around the lesion. Squamous metaplasias were sporadically distributed within benign IPMNs. Mutation alleles KRAS and GNAS were identified in all specimens of IPMN including the areas of squamous metaplasia. In addition, these mutations were found in SCC and AC. Clear transition from flat/low-papillary IPMN to SCC indicated a potent invasion front, and the SCC compartment was genetically unique, because the area has a higher frequency of mutation KRAS. The invasive tumors with distinct histological appearances shared the form of noninvasive IPMN as a common precursor, rather than de novo cancer, suggesting the significance of a genetic profiling scheme of tumors associated with IPMN.</description><identifier>ISSN: 0885-3177</identifier><identifier>EISSN: 1536-4828</identifier><identifier>DOI: 10.1097/MPA.0000000000000556</identifier><identifier>PMID: 27295533</identifier><language>eng</language><publisher>United States</publisher><subject>Adenocarcinoma - genetics ; Adenocarcinoma - pathology ; Adenocarcinoma, Mucinous - genetics ; Adenocarcinoma, Mucinous - pathology ; Aged ; Carcinoma, Adenosquamous - genetics ; Carcinoma, Adenosquamous - pathology ; Carcinoma, Pancreatic Ductal - genetics ; Carcinoma, Pancreatic Ductal - pathology ; Carcinoma, Papillary - genetics ; Carcinoma, Papillary - pathology ; Carcinoma, Squamous Cell - genetics ; Carcinoma, Squamous Cell - pathology ; Chromogranins - genetics ; Clonal Evolution ; Disease Progression ; Gene Frequency ; GTP-Binding Protein alpha Subunits, Gs - genetics ; Humans ; Male ; Mutation ; Pancreatic Neoplasms - genetics ; Pancreatic Neoplasms - pathology ; Proto-Oncogene Proteins p21(ras) - genetics</subject><ispartof>Pancreas, 2016-07, Vol.45 (6), p.915-918</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c373t-4cfad236eb8c2b8ef3b7b861b478a384a568659a8b19e5e380ea27984206d0763</citedby><cites>FETCH-LOGICAL-c373t-4cfad236eb8c2b8ef3b7b861b478a384a568659a8b19e5e380ea27984206d0763</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27295533$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Matsuzaka, Suguru</creatorcontrib><creatorcontrib>Karasaki, Hidenori</creatorcontrib><creatorcontrib>Ono, Yusuke</creatorcontrib><creatorcontrib>Ogata, Munehiko</creatorcontrib><creatorcontrib>Oikawa, Kensuke</creatorcontrib><creatorcontrib>Tamakawa, Susumu</creatorcontrib><creatorcontrib>Chiba, Shin-Ichi</creatorcontrib><creatorcontrib>Muraki, Miho</creatorcontrib><creatorcontrib>Yokochi, Tomoki</creatorcontrib><creatorcontrib>Funakoshi, Hiroshi</creatorcontrib><creatorcontrib>Kono, Toru</creatorcontrib><creatorcontrib>Nagashima, Kazuo</creatorcontrib><creatorcontrib>Mizukami, Yusuke</creatorcontrib><title>Tracking the Clonal Evolution of Adenosquamous Carcinoma, a Rare Variant of Intraductal Papillary Mucinous Neoplasm of the Pancreas</title><title>Pancreas</title><addtitle>Pancreas</addtitle><description>Adenosquamous carcinoma (ASC) is an uncommon variant of pancreatic neoplasm. We sought to trace the mode of tumor progression using specimens of ASC associated with intraductal papillary mucinous neoplasm (IPMN) of the pancreas. A resected specimen of the primary pancreatic ASC, developed in a 72-year-old man, was subjected to mutation profiling using amplicon-targeted sequencing and digital polymerase chain reaction. DNA was isolated from each histological compartment including noninvasive IPMN, squamous cell carcinoma (SCC), and adenocarcinoma (AC). Histologically, an IPMN with a large mural nodule was identified. The invasive tumor predominantly consisted of SCC, and a smaller AC was found around the lesion. Squamous metaplasias were sporadically distributed within benign IPMNs. Mutation alleles KRAS and GNAS were identified in all specimens of IPMN including the areas of squamous metaplasia. In addition, these mutations were found in SCC and AC. Clear transition from flat/low-papillary IPMN to SCC indicated a potent invasion front, and the SCC compartment was genetically unique, because the area has a higher frequency of mutation KRAS. The invasive tumors with distinct histological appearances shared the form of noninvasive IPMN as a common precursor, rather than de novo cancer, suggesting the significance of a genetic profiling scheme of tumors associated with IPMN.</description><subject>Adenocarcinoma - genetics</subject><subject>Adenocarcinoma - pathology</subject><subject>Adenocarcinoma, Mucinous - genetics</subject><subject>Adenocarcinoma, Mucinous - pathology</subject><subject>Aged</subject><subject>Carcinoma, Adenosquamous - genetics</subject><subject>Carcinoma, Adenosquamous - pathology</subject><subject>Carcinoma, Pancreatic Ductal - genetics</subject><subject>Carcinoma, Pancreatic Ductal - pathology</subject><subject>Carcinoma, Papillary - genetics</subject><subject>Carcinoma, Papillary - pathology</subject><subject>Carcinoma, Squamous Cell - genetics</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Chromogranins - genetics</subject><subject>Clonal Evolution</subject><subject>Disease Progression</subject><subject>Gene Frequency</subject><subject>GTP-Binding Protein alpha Subunits, Gs - genetics</subject><subject>Humans</subject><subject>Male</subject><subject>Mutation</subject><subject>Pancreatic Neoplasms - genetics</subject><subject>Pancreatic Neoplasms - pathology</subject><subject>Proto-Oncogene Proteins p21(ras) - genetics</subject><issn>0885-3177</issn><issn>1536-4828</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkD1PwzAQhi0EglL4Bwh5ZCDFjuPYGauqfEgUKlRYo4vjQCCxWztBYuaP44iCELfc8n7cPQidUDKhJBMXi-V0Qv4O5-kOGlHO0iiRsdxFIyIljxgV4gAdev9KCBWMZ_voIBZxxjljI_S5cqDeavOMuxeNZ4010OD5u236rrYG2wpPS22s3_TQ2t7jGThVG9vCOQb8AE7jJ3A1mG6Q3pjOQdmrLmQsYV03DbgPvOgHR_DeabtuwLeDdGhbglFOgz9CexU0Xh9v9xg9Xs5Xs-vo9v7qZja9jRQTrIsSVUEZs1QXUsWF1BUrRCFTWiRCApMJ8FSmPANZ0ExzzSTREItMJjFJSyJSNkZn37lrZze99l3e1l7pcKXR4b6cikzEPAl0gzT5lipnvXe6yteubsM3OSX5gD8P-PP_-IPtdNvQF60uf00_vNkX49iBNA</recordid><startdate>201607</startdate><enddate>201607</enddate><creator>Matsuzaka, Suguru</creator><creator>Karasaki, Hidenori</creator><creator>Ono, Yusuke</creator><creator>Ogata, Munehiko</creator><creator>Oikawa, Kensuke</creator><creator>Tamakawa, Susumu</creator><creator>Chiba, Shin-Ichi</creator><creator>Muraki, Miho</creator><creator>Yokochi, Tomoki</creator><creator>Funakoshi, Hiroshi</creator><creator>Kono, Toru</creator><creator>Nagashima, Kazuo</creator><creator>Mizukami, Yusuke</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>201607</creationdate><title>Tracking the Clonal Evolution of Adenosquamous Carcinoma, a Rare Variant of Intraductal Papillary Mucinous Neoplasm of the Pancreas</title><author>Matsuzaka, Suguru ; Karasaki, Hidenori ; Ono, Yusuke ; Ogata, Munehiko ; Oikawa, Kensuke ; Tamakawa, Susumu ; Chiba, Shin-Ichi ; Muraki, Miho ; Yokochi, Tomoki ; Funakoshi, Hiroshi ; Kono, Toru ; Nagashima, Kazuo ; Mizukami, Yusuke</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c373t-4cfad236eb8c2b8ef3b7b861b478a384a568659a8b19e5e380ea27984206d0763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adenocarcinoma - genetics</topic><topic>Adenocarcinoma - pathology</topic><topic>Adenocarcinoma, Mucinous - genetics</topic><topic>Adenocarcinoma, Mucinous - pathology</topic><topic>Aged</topic><topic>Carcinoma, Adenosquamous - genetics</topic><topic>Carcinoma, Adenosquamous - pathology</topic><topic>Carcinoma, Pancreatic Ductal - genetics</topic><topic>Carcinoma, Pancreatic Ductal - pathology</topic><topic>Carcinoma, Papillary - genetics</topic><topic>Carcinoma, Papillary - pathology</topic><topic>Carcinoma, Squamous Cell - genetics</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Chromogranins - genetics</topic><topic>Clonal Evolution</topic><topic>Disease Progression</topic><topic>Gene Frequency</topic><topic>GTP-Binding Protein alpha Subunits, Gs - genetics</topic><topic>Humans</topic><topic>Male</topic><topic>Mutation</topic><topic>Pancreatic Neoplasms - genetics</topic><topic>Pancreatic Neoplasms - pathology</topic><topic>Proto-Oncogene Proteins p21(ras) - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Matsuzaka, Suguru</creatorcontrib><creatorcontrib>Karasaki, Hidenori</creatorcontrib><creatorcontrib>Ono, Yusuke</creatorcontrib><creatorcontrib>Ogata, Munehiko</creatorcontrib><creatorcontrib>Oikawa, Kensuke</creatorcontrib><creatorcontrib>Tamakawa, Susumu</creatorcontrib><creatorcontrib>Chiba, Shin-Ichi</creatorcontrib><creatorcontrib>Muraki, Miho</creatorcontrib><creatorcontrib>Yokochi, Tomoki</creatorcontrib><creatorcontrib>Funakoshi, Hiroshi</creatorcontrib><creatorcontrib>Kono, Toru</creatorcontrib><creatorcontrib>Nagashima, Kazuo</creatorcontrib><creatorcontrib>Mizukami, Yusuke</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>Pancreas</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Matsuzaka, Suguru</au><au>Karasaki, Hidenori</au><au>Ono, Yusuke</au><au>Ogata, Munehiko</au><au>Oikawa, Kensuke</au><au>Tamakawa, Susumu</au><au>Chiba, Shin-Ichi</au><au>Muraki, Miho</au><au>Yokochi, Tomoki</au><au>Funakoshi, Hiroshi</au><au>Kono, Toru</au><au>Nagashima, Kazuo</au><au>Mizukami, Yusuke</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tracking the Clonal Evolution of Adenosquamous Carcinoma, a Rare Variant of Intraductal Papillary Mucinous Neoplasm of the Pancreas</atitle><jtitle>Pancreas</jtitle><addtitle>Pancreas</addtitle><date>2016-07</date><risdate>2016</risdate><volume>45</volume><issue>6</issue><spage>915</spage><epage>918</epage><pages>915-918</pages><issn>0885-3177</issn><eissn>1536-4828</eissn><abstract>Adenosquamous carcinoma (ASC) is an uncommon variant of pancreatic neoplasm. We sought to trace the mode of tumor progression using specimens of ASC associated with intraductal papillary mucinous neoplasm (IPMN) of the pancreas. A resected specimen of the primary pancreatic ASC, developed in a 72-year-old man, was subjected to mutation profiling using amplicon-targeted sequencing and digital polymerase chain reaction. DNA was isolated from each histological compartment including noninvasive IPMN, squamous cell carcinoma (SCC), and adenocarcinoma (AC). Histologically, an IPMN with a large mural nodule was identified. The invasive tumor predominantly consisted of SCC, and a smaller AC was found around the lesion. Squamous metaplasias were sporadically distributed within benign IPMNs. Mutation alleles KRAS and GNAS were identified in all specimens of IPMN including the areas of squamous metaplasia. In addition, these mutations were found in SCC and AC. Clear transition from flat/low-papillary IPMN to SCC indicated a potent invasion front, and the SCC compartment was genetically unique, because the area has a higher frequency of mutation KRAS. The invasive tumors with distinct histological appearances shared the form of noninvasive IPMN as a common precursor, rather than de novo cancer, suggesting the significance of a genetic profiling scheme of tumors associated with IPMN.</abstract><cop>United States</cop><pmid>27295533</pmid><doi>10.1097/MPA.0000000000000556</doi><tpages>4</tpages></addata></record> |
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subjects | Adenocarcinoma - genetics Adenocarcinoma - pathology Adenocarcinoma, Mucinous - genetics Adenocarcinoma, Mucinous - pathology Aged Carcinoma, Adenosquamous - genetics Carcinoma, Adenosquamous - pathology Carcinoma, Pancreatic Ductal - genetics Carcinoma, Pancreatic Ductal - pathology Carcinoma, Papillary - genetics Carcinoma, Papillary - pathology Carcinoma, Squamous Cell - genetics Carcinoma, Squamous Cell - pathology Chromogranins - genetics Clonal Evolution Disease Progression Gene Frequency GTP-Binding Protein alpha Subunits, Gs - genetics Humans Male Mutation Pancreatic Neoplasms - genetics Pancreatic Neoplasms - pathology Proto-Oncogene Proteins p21(ras) - genetics |
title | Tracking the Clonal Evolution of Adenosquamous Carcinoma, a Rare Variant of Intraductal Papillary Mucinous Neoplasm of the Pancreas |
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