<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>34</volume><submitter>Lin DI</submitter><pubmed_abstract>Mesonephric carcinoma is a rare cancer that most often arises within the cervix, and less frequently, in the ovary and endometrium. A retrospective search of our CLIA-certified and CAP-accredited reference molecular laboratory database (Foundation Medicine, Inc.) identified 20 mesonephric or mesonephric-like, cervical (n = 10), endometrial (n = 5), ovarian (n = 4) or peri-bladder (n = 1) carcinomas that had undergone comprehensive genomic profiling via next generation sequencing. Activating &lt;i>KRAS&lt;/i> mutations were present in 90%, 18 of 20 cases, including G12V (n = 7), G12D (n = 6), G12A (n = 3) and G12C (n = 2). Other recurrent alterations were identified in &lt;i>ARID1A&lt;/i> (25%), &lt;i>PIK3CA&lt;/i> (20%), &lt;i>CTNNB1&lt;/i> (15%), &lt;i>TP53&lt;/i> (10%), &lt;i>MLL2&lt;/i> (10%) and &lt;i>CDKN2A&lt;/i> (10%). One </pubmed_abstract><journal>Gynecologic oncology reports</journal><pagination>100652</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7529833</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Molecular profiling of mesonephric and mesonephric-like carcinomas of cervical, endometrial and ovarian origin.</pubmed_title><pmcid>PMC7529833</pmcid><pubmed_authors>Killian JK</pubmed_authors><pubmed_authors>Shah N</pubmed_authors><pubmed_authors>Hemmerich A</pubmed_authors><pubmed_authors>Severson EA</pubmed_authors><pubmed_authors>Huang RSP</pubmed_authors><pubmed_authors>Elvin JA</pubmed_authors><pubmed_authors>Haberberger J</pubmed_authors><pubmed_authors>Tse JY</pubmed_authors><pubmed_authors>Edgerly C</pubmed_authors><pubmed_authors>Ramkissoon SH</pubmed_authors><pubmed_authors>Lin DI</pubmed_authors><pubmed_authors>Vergilio JA</pubmed_authors><pubmed_authors>Ross JS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Molecular profiling of mesonephric and mesonephric-like carcinomas of cervical, endometrial and ovarian origin.</name><description>Mesonephric carcinoma is a rare cancer that most often arises within the cervix, and less frequently, in the ovary and endometrium. A retrospective search of our CLIA-certified and CAP-accredited reference molecular laboratory database (Foundation Medicine, Inc.) identified 20 mesonephric or mesonephric-like, cervical (n = 10), endometrial (n = 5), ovarian (n = 4) or peri-bladder (n = 1) carcinomas that had undergone comprehensive genomic profiling via next generation sequencing. Activating &lt;i>KRAS&lt;/i> mutations were present in 90%, 18 of 20 cases, including G12V (n = 7), G12D (n = 6), G12A (n = 3) and G12C (n = 2). Other recurrent alterations were identified in &lt;i>ARID1A&lt;/i> (25%), &lt;i>PIK3CA&lt;/i> (20%), &lt;i>CTNNB1&lt;/i> (15%), &lt;i>TP53&lt;/i> (10%), &lt;i>MLL2&lt;/i> (10%) and &lt;i>CDKN2A&lt;/i> (10%). One </description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Nov</publication><modification>2025-04-18T19:38:24.412Z</modification><creation>2020-11-07T09:59:44Z</creation></dates><accession>S-EPMC7529833</accession><cross_references><pubmed>33024807</pubmed><doi>10.1016/j.gore.2020.100652</doi></cross_references></HashMap>