<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang LL</submitter><funding>NCI NIH HHS</funding><pagination>57-63</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4647535</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>113(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>MYCN amplification with subsequent MYCN protein overexpression is a powerful indicator of poor prognosis of neuroblastoma patients. Little is known regarding the prognostic significance of the homologous MYC protein expression in neuroblastoma.&lt;h4>Methods&lt;/h4>Immunostaining for MYCN and MYC protein was performed on 357 undifferentiated/poorly differentiated neuroblastomas. Results were analysed with other prognostic markers.&lt;h4>Results&lt;/h4>Sixty-seven (19%) tumours were MYCN(+), 38 (11%) were MYC(+), and one(0.3%) had both proteins(+). MYCN(+) tumours and MYC(+) tumours were more likely diagnosed in children>18months with stage4-disease. MYCN(+) tumours were associated with amplified MYCN, Unfavourable Histology (UH), and High-MKI (Mitosis-Karyorrhexis Index). MYC(+) tum</pubmed_abstract><journal>British journal of cancer</journal><pubmed_title>Augmented expression of MYC and/or MYCN protein defines highly aggressive MYC-driven neuroblastoma: a Children's Oncology Group study.</pubmed_title><pmcid>PMC4647535</pmcid><funding_grant_id>U10 CA098543</funding_grant_id><funding_grant_id>R01CA127571</funding_grant_id><funding_grant_id>P01 CA081403</funding_grant_id><funding_grant_id>P01CA081403</funding_grant_id><funding_grant_id>R01 CA127571</funding_grant_id><funding_grant_id>U10 CA180886</funding_grant_id><funding_grant_id>U10 CA180899</funding_grant_id><funding_grant_id>U10CA98413</funding_grant_id><funding_grant_id>U10CA98543</funding_grant_id><funding_grant_id>U10 CA098413</funding_grant_id><pubmed_authors>Maris JM</pubmed_authors><pubmed_authors>Asgharzadeh S</pubmed_authors><pubmed_authors>Look AT</pubmed_authors><pubmed_authors>London WB</pubmed_authors><pubmed_authors>Ikegaki N</pubmed_authors><pubmed_authors>Naranjo A</pubmed_authors><pubmed_authors>Hogarty MD</pubmed_authors><pubmed_authors>Park JR</pubmed_authors><pubmed_authors>Cohn SL</pubmed_authors><pubmed_authors>Teshiba R</pubmed_authors><pubmed_authors>Seeger RC</pubmed_authors><pubmed_authors>Shimada H</pubmed_authors><pubmed_authors>Tang XX</pubmed_authors><pubmed_authors>Gastier-Foster JM</pubmed_authors><pubmed_authors>Wang LL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Augmented expression of MYC and/or MYCN protein defines highly aggressive MYC-driven neuroblastoma: a Children's Oncology Group study.</name><description>&lt;h4>Background&lt;/h4>MYCN amplification with subsequent MYCN protein overexpression is a powerful indicator of poor prognosis of neuroblastoma patients. Little is known regarding the prognostic significance of the homologous MYC protein expression in neuroblastoma.&lt;h4>Methods&lt;/h4>Immunostaining for MYCN and MYC protein was performed on 357 undifferentiated/poorly differentiated neuroblastomas. Results were analysed with other prognostic markers.&lt;h4>Results&lt;/h4>Sixty-seven (19%) tumours were MYCN(+), 38 (11%) were MYC(+), and one(0.3%) had both proteins(+). MYCN(+) tumours and MYC(+) tumours were more likely diagnosed in children>18months with stage4-disease. MYCN(+) tumours were associated with amplified MYCN, Unfavourable Histology (UH), and High-MKI (Mitosis-Karyorrhexis Index). MYC(+) tum</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Jun</publication><modification>2025-04-22T15:10:46.857Z</modification><creation>2019-03-27T02:02:04Z</creation></dates><accession>S-EPMC4647535</accession><cross_references><pubmed>26035700</pubmed><doi>10.1038/bjc.2015.188</doi></cross_references></HashMap>