Mezzomo Lisiane Cervieri, Pesce Frederico Giacomoni, Marçal Josenel Maria Barcelos, Haag Taiana, Ferreira Nelson Pires, Lima Julia Fernanda Semmelmann Pereira, Leães Carolina Garcia Soares, Oliveira Miriam Costa, da Fonte Kohek Maria Beatriz
Post Graduation Program of Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, RS, Brazil.
Laboratory of Molecular Biology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, RS, Brazil.
Endocr Pathol. 2017 Mar;28(1):13-21. doi: 10.1007/s12022-016-9463-2.
Despite recent advances in molecular genetics, the pituitary adenoma initiation, development, progress, and the molecular basis of their unique features are still poorly understood. In this sense, it is proposed that stem cell could be involved in pituitary adenoma tumorigenesis. It is suggested that TP63 has important functions in stem cells, and it may have interplay of TP63 and Notch and its ligand Jagged in this process. This study aimed to evaluate the distinct expression of TP63 isoforms (TAp63 and ΔNp63), as well as its correlation with Notch3 receptor and its ligand Jagged1 in human pituitary adenomas at the messenger RNA (mRNA) level. We included 77 pituitary adenoma tumor samples from patients who underwent surgical resection. The expression levels of TP63 isoforms (TAp63 and ΔNp63) and Notch3 and its ligand Jagged1 were evaluated by qRT-PCR using isoform-specific primers. We also evaluated proliferation index immunohistochemically using KI-67 antibody. The expression levels were associated with clinical outcomes, as age, gender, tumor size, and tumor subtype. In summary, we found that mRNA expression of both TP63 isoforms decreased in pituitary adenomas compared with normal pituitary control. On the other hand, there was an increase of relative Notch3 and Jagged1 mRNA expression in the majority of examined samples. The mRNA expression of three genes evaluated was correlated and statistically significantly. There was no significant association between gene expression and the analyzed clinical data. The current study has provided the first time evidence that Tap63 and ΔNp63 isoforms are underexpressed in most pituitary adenomas. These results are correlated with Notch3 and its ligand Jagged1 overexpression, corroborating previous studies pointing its antagonistic interactions.
尽管分子遗传学最近取得了进展,但垂体腺瘤的起始、发展、进展及其独特特征的分子基础仍知之甚少。从这个意义上说,有人提出干细胞可能参与垂体腺瘤的肿瘤发生。有人认为TP63在干细胞中具有重要功能,并且在此过程中TP63可能与Notch及其配体Jagged存在相互作用。本研究旨在评估TP63异构体(TAp63和ΔNp63)在信使核糖核酸(mRNA)水平上在人垂体腺瘤中的不同表达,以及其与Notch3受体及其配体Jagged1的相关性。我们纳入了77例接受手术切除的垂体腺瘤肿瘤样本。使用异构体特异性引物通过qRT-PCR评估TP63异构体(TAp63和ΔNp63)以及Notch3及其配体Jagged1的表达水平。我们还使用KI-67抗体通过免疫组织化学评估增殖指数。表达水平与临床结果相关,如年龄、性别、肿瘤大小和肿瘤亚型。总之,我们发现与正常垂体对照相比,垂体腺瘤中两种TP63异构体的mRNA表达均降低。另一方面,在大多数检测样本中,相对Notch3和Jagged1的mRNA表达增加。所评估的三个基因的mRNA表达具有相关性且在统计学上具有显著意义。基因表达与分析的临床数据之间没有显著关联。本研究首次提供证据表明,在大多数垂体腺瘤中Tap63和ΔNp63异构体表达不足。这些结果与Notch3及其配体Jagged1的过表达相关,证实了先前指出其拮抗相互作用的研究。