<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Persson M</submitter><funding>the Swedish state under the agreement between the Swedish government and the country councils, the ALF-agreement</funding><funding>The Sjöberg Foundation</funding><funding>Assar Gabrielsson Foundation</funding><funding>Swedish Cancer Society</funding><pagination>3691</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9367430</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(15)</volume><pubmed_abstract>Adenoid cystic carcinoma (ACC) is an aggressive head and neck malignancy characterized by a t (6;9) translocation resulting in an &lt;i>MYB-NFIB&lt;/i> gene fusion or, more rarely, an &lt;i>MYBL1&lt;/i> fusion. The true frequency and clinical significance of these alterations are still unclear. Here, we have used tissue microarrays and analyzed 391 ACCs and 647 non-ACC salivary neoplasms to study the prevalence, expression, and clinical significance of &lt;i>MYB/MYBL1&lt;/i> alterations by FISH and immunohistochemistry. Alterations of &lt;i>MYB&lt;/i> or &lt;i>MYBL1&lt;/i> were found in 78% of the cases, of which 62% had &lt;i>MYB&lt;/i> alterations and 16% had &lt;i>MYBL1&lt;/i> rearrangements. Overexpression of MYB/MYBL1 oncoproteins was detected in 93% of the cases. &lt;i>MYB&lt;/i> split signal, seen in 39% of the cases, was specifi</pubmed_abstract><journal>Cancers</journal><pubmed_title>Rearrangements, Expression, and Clinical Significance of MYB and MYBL1 in Adenoid Cystic Carcinoma: A Multi-Institutional Study.</pubmed_title><pmcid>PMC9367430</pmcid><funding_grant_id>AG-Fond FB17-22, FB20-91</funding_grant_id><funding_grant_id>ALFGBG-965537</funding_grant_id><funding_grant_id>2021-01-14:4</funding_grant_id><funding_grant_id>CAN 21 1773</funding_grant_id><pubmed_authors>Frierson HF</pubmed_authors><pubmed_authors>El-Naggar AK</pubmed_authors><pubmed_authors>Loening T</pubmed_authors><pubmed_authors>Brandwein-Weber MS</pubmed_authors><pubmed_authors>Ferrarotto R</pubmed_authors><pubmed_authors>Andersson MK</pubmed_authors><pubmed_authors>Stenman G</pubmed_authors><pubmed_authors>Mitani Y</pubmed_authors><pubmed_authors>Boecker W</pubmed_authors><pubmed_authors>Persson M</pubmed_authors><pubmed_authors>Moskaluk C</pubmed_authors><pubmed_authors>Fonseca I</pubmed_authors></additional><is_claimable>false</is_claimable><name>Rearrangements, Expression, and Clinical Significance of MYB and MYBL1 in Adenoid Cystic Carcinoma: A Multi-Institutional Study.</name><description>Adenoid cystic carcinoma (ACC) is an aggressive head and neck malignancy characterized by a t (6;9) translocation resulting in an &lt;i>MYB-NFIB&lt;/i> gene fusion or, more rarely, an &lt;i>MYBL1&lt;/i> fusion. The true frequency and clinical significance of these alterations are still unclear. Here, we have used tissue microarrays and analyzed 391 ACCs and 647 non-ACC salivary neoplasms to study the prevalence, expression, and clinical significance of &lt;i>MYB/MYBL1&lt;/i> alterations by FISH and immunohistochemistry. Alterations of &lt;i>MYB&lt;/i> or &lt;i>MYBL1&lt;/i> were found in 78% of the cases, of which 62% had &lt;i>MYB&lt;/i> alterations and 16% had &lt;i>MYBL1&lt;/i> rearrangements. Overexpression of MYB/MYBL1 oncoproteins was detected in 93% of the cases. &lt;i>MYB&lt;/i> split signal, seen in 39% of the cases, was specifi</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jul</publication><modification>2025-04-22T11:29:46.927Z</modification><creation>2025-04-06T00:00:34.909Z</creation></dates><accession>S-EPMC9367430</accession><cross_references><pubmed>35954356</pubmed><doi>10.3390/cancers14153691</doi></cross_references></HashMap>