TERT Promoter Mutation c.-124C>T Commonly Occurs in Low-Grade Fibromatosis-like Metaplastic Breast Carcinoma
Low-grade fibromatosis-like metaplastic carcinoma (FLMC) is a very rare subtype of triple-negative metaplastic (spindle cell) breast carcinoma. It is characterized by the proliferation of spindle cells closely resembling fibromatosis, which represents a benign fibroblastic/myofibroblastic breast pro...
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Veröffentlicht in: | Archives of pathology & laboratory medicine (1976) 2023-12, Vol.147 (12), p.1451-1457 |
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container_title | Archives of pathology & laboratory medicine (1976) |
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creator | Webersinke, Gerald Burghofer, Jonathan Malli, Theodora Rammer, Melanie Jahn, Stephan Wenzel Niendorf, Axel Tavassoli, Fattaneh A Moinfar, Farid |
description | Low-grade fibromatosis-like metaplastic carcinoma (FLMC) is a very rare subtype of triple-negative metaplastic (spindle cell) breast carcinoma. It is characterized by the proliferation of spindle cells closely resembling fibromatosis, which represents a benign fibroblastic/myofibroblastic breast proliferation. Unlike most triple-negative and basal-like breast cancers, FLMC has a very low potential for metastases, but demonstrates frequent local recurrences.
To genetically characterize FLMC.
To this end, we analyzed 7 cases by targeted next-generation sequencing for 315 cancer-related genes and performed comparative microarray copy number analysis in 5 of these cases.
All cases shared TERT alterations (6 patients with recurrent c.-124C>T TERT promoter mutation and 1 patient with copy number gain encompassing the TERT locus), had oncogenic PIK3CA/PIK3R1 mutations (activation of the PI3K/AKT/mTOR pathway), and lacked mutations in TP53. TERT was overexpressed in all FLMCs. CDKN2A/B loss or mutation was observed in 4 of 7 cases (57%). Furthermore, tumors displayed chromosomal stability with only few copy number variations and a low tumor mutational burden.
We conclude that FLMCs typically show the recurrent TERT promoter mutation c.-124C>T, activation of the PI3K/AKT/mTOR pathway, low genomic instability, and wild-type TP53. In conjunction with previous data of metaplastic (spindle cell) carcinoma with and without fibromatosis-like morphology, FLMC is most likely distinguished by TERT promoter mutation. Thus, our data support the notion of a distinct subgroup within low-grade metaplastic breast cancer with spindle cell morphology and associated TERT mutations. |
doi_str_mv | 10.5858/arpa.2022-0159-OA |
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To genetically characterize FLMC.
To this end, we analyzed 7 cases by targeted next-generation sequencing for 315 cancer-related genes and performed comparative microarray copy number analysis in 5 of these cases.
All cases shared TERT alterations (6 patients with recurrent c.-124C>T TERT promoter mutation and 1 patient with copy number gain encompassing the TERT locus), had oncogenic PIK3CA/PIK3R1 mutations (activation of the PI3K/AKT/mTOR pathway), and lacked mutations in TP53. TERT was overexpressed in all FLMCs. CDKN2A/B loss or mutation was observed in 4 of 7 cases (57%). Furthermore, tumors displayed chromosomal stability with only few copy number variations and a low tumor mutational burden.
We conclude that FLMCs typically show the recurrent TERT promoter mutation c.-124C>T, activation of the PI3K/AKT/mTOR pathway, low genomic instability, and wild-type TP53. In conjunction with previous data of metaplastic (spindle cell) carcinoma with and without fibromatosis-like morphology, FLMC is most likely distinguished by TERT promoter mutation. Thus, our data support the notion of a distinct subgroup within low-grade metaplastic breast cancer with spindle cell morphology and associated TERT mutations.</description><identifier>ISSN: 0003-9985</identifier><identifier>EISSN: 1543-2165</identifier><identifier>DOI: 10.5858/arpa.2022-0159-OA</identifier><identifier>PMID: 36897999</identifier><language>eng</language><publisher>United States: College of American Pathologists</publisher><subject>Actin ; Breast cancer ; Breast carcinoma ; Calponin ; Cell morphology ; Cloning ; Collagen ; Connective tissue diseases ; Cytology ; ErbB-2 protein ; Estrogen receptors ; Genes ; Genomes ; Microsatellite instability ; Morphology ; Mutation ; Next-generation sequencing ; Progesterone ; Software ; Stroma ; Tumors</subject><ispartof>Archives of pathology & laboratory medicine (1976), 2023-12, Vol.147 (12), p.1451-1457</ispartof><rights>2023 College of American Pathologists.</rights><rights>Copyright College of American Pathologists Dec 2023</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1269-7dc2710c90e70baad6438225662dca33cc01c9396cedc39c0624f79389fbee703</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/36897999$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Webersinke, Gerald</creatorcontrib><creatorcontrib>Burghofer, Jonathan</creatorcontrib><creatorcontrib>Malli, Theodora</creatorcontrib><creatorcontrib>Rammer, Melanie</creatorcontrib><creatorcontrib>Jahn, Stephan Wenzel</creatorcontrib><creatorcontrib>Niendorf, Axel</creatorcontrib><creatorcontrib>Tavassoli, Fattaneh A</creatorcontrib><creatorcontrib>Moinfar, Farid</creatorcontrib><title>TERT Promoter Mutation c.-124C>T Commonly Occurs in Low-Grade Fibromatosis-like Metaplastic Breast Carcinoma</title><title>Archives of pathology & laboratory medicine (1976)</title><addtitle>Arch Pathol Lab Med</addtitle><description>Low-grade fibromatosis-like metaplastic carcinoma (FLMC) is a very rare subtype of triple-negative metaplastic (spindle cell) breast carcinoma. It is characterized by the proliferation of spindle cells closely resembling fibromatosis, which represents a benign fibroblastic/myofibroblastic breast proliferation. Unlike most triple-negative and basal-like breast cancers, FLMC has a very low potential for metastases, but demonstrates frequent local recurrences.
To genetically characterize FLMC.
To this end, we analyzed 7 cases by targeted next-generation sequencing for 315 cancer-related genes and performed comparative microarray copy number analysis in 5 of these cases.
All cases shared TERT alterations (6 patients with recurrent c.-124C>T TERT promoter mutation and 1 patient with copy number gain encompassing the TERT locus), had oncogenic PIK3CA/PIK3R1 mutations (activation of the PI3K/AKT/mTOR pathway), and lacked mutations in TP53. TERT was overexpressed in all FLMCs. CDKN2A/B loss or mutation was observed in 4 of 7 cases (57%). Furthermore, tumors displayed chromosomal stability with only few copy number variations and a low tumor mutational burden.
We conclude that FLMCs typically show the recurrent TERT promoter mutation c.-124C>T, activation of the PI3K/AKT/mTOR pathway, low genomic instability, and wild-type TP53. In conjunction with previous data of metaplastic (spindle cell) carcinoma with and without fibromatosis-like morphology, FLMC is most likely distinguished by TERT promoter mutation. Thus, our data support the notion of a distinct subgroup within low-grade metaplastic breast cancer with spindle cell morphology and associated TERT mutations.</description><subject>Actin</subject><subject>Breast cancer</subject><subject>Breast carcinoma</subject><subject>Calponin</subject><subject>Cell morphology</subject><subject>Cloning</subject><subject>Collagen</subject><subject>Connective tissue diseases</subject><subject>Cytology</subject><subject>ErbB-2 protein</subject><subject>Estrogen receptors</subject><subject>Genes</subject><subject>Genomes</subject><subject>Microsatellite instability</subject><subject>Morphology</subject><subject>Mutation</subject><subject>Next-generation sequencing</subject><subject>Progesterone</subject><subject>Software</subject><subject>Stroma</subject><subject>Tumors</subject><issn>0003-9985</issn><issn>1543-2165</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNpdkc1rGzEQxUVoSVynf0AuRdBLLnL1savduRTcJR8FG5fgnoU8K4OS3ZUr7VL830fGaQ85zQz83mN4j5AbwRdlXdbfbDzYheRSMi5KYJvlBZmJslBMCl1-IDPOuWIAdXlFPqX0nE-QUlySK6VrqABgRrrt3dOW_oqhD6OLdD2NdvRhoLhgQhbN9y1tQt-HoTvSDeIUE_UDXYW_7CHa1tF7v8tSO4bkE-v8i6NrN9pDZ9Pokf6ILi-0sRH9kLFr8nFvu-Q-v805-X1_t20e2Wrz8LNZrhgKqYFVLcpKcATuKr6zttWFqqUstZYtWqUQuUBQoNG1qAC5lsW-AlXDfueyRM3J7dn3EMOfyaXR9D6h6zo7uDAlI6tai5yGLDL69R36HKY45O-MBF5x0GWtMyXOFMaQUnR7c4i-t_FoBDenKsypCnOqwpyqMJtl1nx5c552vWv_K_5lr14B0KCD-w</recordid><startdate>20231201</startdate><enddate>20231201</enddate><creator>Webersinke, Gerald</creator><creator>Burghofer, Jonathan</creator><creator>Malli, Theodora</creator><creator>Rammer, Melanie</creator><creator>Jahn, Stephan Wenzel</creator><creator>Niendorf, Axel</creator><creator>Tavassoli, Fattaneh A</creator><creator>Moinfar, Farid</creator><general>College of American Pathologists</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>4T-</scope><scope>4U-</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</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>M2P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20231201</creationdate><title>TERT Promoter Mutation c.-124C>T Commonly Occurs in Low-Grade Fibromatosis-like Metaplastic Breast Carcinoma</title><author>Webersinke, Gerald ; Burghofer, Jonathan ; Malli, Theodora ; Rammer, Melanie ; Jahn, Stephan Wenzel ; Niendorf, Axel ; Tavassoli, Fattaneh A ; Moinfar, Farid</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1269-7dc2710c90e70baad6438225662dca33cc01c9396cedc39c0624f79389fbee703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Actin</topic><topic>Breast cancer</topic><topic>Breast carcinoma</topic><topic>Calponin</topic><topic>Cell morphology</topic><topic>Cloning</topic><topic>Collagen</topic><topic>Connective tissue diseases</topic><topic>Cytology</topic><topic>ErbB-2 protein</topic><topic>Estrogen receptors</topic><topic>Genes</topic><topic>Genomes</topic><topic>Microsatellite instability</topic><topic>Morphology</topic><topic>Mutation</topic><topic>Next-generation sequencing</topic><topic>Progesterone</topic><topic>Software</topic><topic>Stroma</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Webersinke, Gerald</creatorcontrib><creatorcontrib>Burghofer, Jonathan</creatorcontrib><creatorcontrib>Malli, Theodora</creatorcontrib><creatorcontrib>Rammer, Melanie</creatorcontrib><creatorcontrib>Jahn, Stephan Wenzel</creatorcontrib><creatorcontrib>Niendorf, Axel</creatorcontrib><creatorcontrib>Tavassoli, Fattaneh A</creatorcontrib><creatorcontrib>Moinfar, Farid</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>University Readers</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</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 Edition)</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>Science 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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Archives of pathology & laboratory medicine (1976)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Webersinke, Gerald</au><au>Burghofer, Jonathan</au><au>Malli, Theodora</au><au>Rammer, Melanie</au><au>Jahn, Stephan Wenzel</au><au>Niendorf, Axel</au><au>Tavassoli, Fattaneh A</au><au>Moinfar, Farid</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>TERT Promoter Mutation c.-124C>T Commonly Occurs in Low-Grade Fibromatosis-like Metaplastic Breast Carcinoma</atitle><jtitle>Archives of pathology & laboratory medicine (1976)</jtitle><addtitle>Arch Pathol Lab Med</addtitle><date>2023-12-01</date><risdate>2023</risdate><volume>147</volume><issue>12</issue><spage>1451</spage><epage>1457</epage><pages>1451-1457</pages><issn>0003-9985</issn><eissn>1543-2165</eissn><abstract>Low-grade fibromatosis-like metaplastic carcinoma (FLMC) is a very rare subtype of triple-negative metaplastic (spindle cell) breast carcinoma. It is characterized by the proliferation of spindle cells closely resembling fibromatosis, which represents a benign fibroblastic/myofibroblastic breast proliferation. Unlike most triple-negative and basal-like breast cancers, FLMC has a very low potential for metastases, but demonstrates frequent local recurrences.
To genetically characterize FLMC.
To this end, we analyzed 7 cases by targeted next-generation sequencing for 315 cancer-related genes and performed comparative microarray copy number analysis in 5 of these cases.
All cases shared TERT alterations (6 patients with recurrent c.-124C>T TERT promoter mutation and 1 patient with copy number gain encompassing the TERT locus), had oncogenic PIK3CA/PIK3R1 mutations (activation of the PI3K/AKT/mTOR pathway), and lacked mutations in TP53. TERT was overexpressed in all FLMCs. CDKN2A/B loss or mutation was observed in 4 of 7 cases (57%). Furthermore, tumors displayed chromosomal stability with only few copy number variations and a low tumor mutational burden.
We conclude that FLMCs typically show the recurrent TERT promoter mutation c.-124C>T, activation of the PI3K/AKT/mTOR pathway, low genomic instability, and wild-type TP53. In conjunction with previous data of metaplastic (spindle cell) carcinoma with and without fibromatosis-like morphology, FLMC is most likely distinguished by TERT promoter mutation. Thus, our data support the notion of a distinct subgroup within low-grade metaplastic breast cancer with spindle cell morphology and associated TERT mutations.</abstract><cop>United States</cop><pub>College of American Pathologists</pub><pmid>36897999</pmid><doi>10.5858/arpa.2022-0159-OA</doi><tpages>7</tpages></addata></record> |
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source | Allen Press Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Actin Breast cancer Breast carcinoma Calponin Cell morphology Cloning Collagen Connective tissue diseases Cytology ErbB-2 protein Estrogen receptors Genes Genomes Microsatellite instability Morphology Mutation Next-generation sequencing Progesterone Software Stroma Tumors |
title | TERT Promoter Mutation c.-124C>T Commonly Occurs in Low-Grade Fibromatosis-like Metaplastic Breast Carcinoma |
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