| Literature DB >> 28421464 |
Daniel Bulzico1,2, Davi Coe Torres3, Gerson Moura Ferreira4, Bruno Ricardo Barreto Pires4, Paulo Antônio Silvestre de Faria5, Rocio Hassan3, Eliana Abdelhay4, Mario Vaisman6, Leonardo Vieira Neto7,6.
Abstract
Adrenocortical carcinomas (ACC) are very rare tumors related to TP53 mutations mostly in childhood onset cases. Epithelial-mesenchymal transition (EMT) transcription factors TWIST1 and Smad interacting protein 1 (SIP1) are related to poorer outcomes in other malignancies, but their role in ACC is unknown. We describe a case of an advanced metastatic ACC (Weiss-score of 9) in a patient at age 76. After primary tumor resection, mitotane therapy was started as palliation to low-volume liver metastasis. After a 2-year period of stable disease, the patient died due to brain metastasis. Somatic gene sequencing revealed a novel TP53 mutation in DNA extracted from paraffin-embedded tissue, a deletion of 8bp in exon 8 (c.811_818del8; GAGGTGCG/-) in homo or hemizygosis causing a subsequent frameshift and premature stop codon at position 302. Immunohistochemistry of P53 and p-Ser-15 P53 showed absent tumoral staining. In addition, immunohistochemical analysis showed an increased expression of the mesenchymal markers vimentin and fibronectin. At last, EMT transcription factors TWIST1 and SIP1 were also overexpressed in tumoral cells. This case report describes an aggressive ACC with not only a novel somatic mutation, but also a novel International Agency for Research on Cancer database 8 base-pair deletion in TP53 exon 8. In addition, the expression of EMT inducers TWIST1 and SIP1 have been reported for the first time in an ACC case. Further investigation is needed to clarify the biologic significance of this new TP53 mutation and its role in the EMT process.Entities:
Keywords: Adrenocortical carcinoma; Mutation; SIP1; TP53; TWIST1
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Year: 2017 PMID: 28421464 DOI: 10.1007/s12022-017-9482-7
Source DB: PubMed Journal: Endocr Pathol ISSN: 1046-3976 Impact factor: 3.943