Laboratory of Experimental Endocrinology-LEEx, Institute of Biomedical Science, Federal University of Rio de Janeiro, Rio de Janeiro 21941-902, Brazil.
Postgraduate Program in Endocrinology, Faculty of Medicine, Federal University of Rio de Janeiro, Rio de Janeiro 21941-902, Brazil.
Genes (Basel). 2022 Apr 12;13(4):674. doi: 10.3390/genes13040674.
Gap junction intercellular communication (GJIC) is considered a key mechanism in the regulation of tissue homeostasis. GJIC structures are organized in two transmembrane channels, with each channel formed by connexins (Cxs). GJIC and Cxs expression alterations are related to the process of tumorigenesis in different cell types. Pituitary neuroendocrine tumors (PitNETs) represent 15-20% of intracranial neoplasms, and usually display benign behavior. Nevertheless, some may have aggressive behavior, invading adjacent tissues, and featuring a high proliferation rate. We aimed to assess the expression and relevance of GJIC and Cxs proteins in PitNETs. We evaluated the mRNA expression levels of Cx26, 32, and 43, and the protein expression of Cx43 in a series of PitNETs. In addition, we overexpressed Cx43 in pituitary tumor cell lines. At the mRNA level, we observed variable expression of all the connexins in the tumor samples. Cx43 protein expression was absent in most of the pituitary tumor samples that were studied. Moreover, in vitro studies revealed that the overexpression of Cx43 decreases cell growth and induces apoptosis in pituitary tumor cell lines. Our results indicate that the downregulation of Cx43 protein might be involved in the tumorigenesis of most pituitary adenomas and have a potential therapeutic value for pituitary tumor therapy.
缝隙连接细胞间通讯(GJIC)被认为是调节组织动态平衡的关键机制。GJIC 结构组织在两个跨膜通道中,每个通道由连接蛋白(Cx)形成。GJIC 和 Cx 的表达改变与不同细胞类型的肿瘤发生过程有关。垂体神经内分泌肿瘤(PitNETs)占颅内肿瘤的 15-20%,通常表现为良性行为。然而,有些可能具有侵袭性行为,侵犯邻近组织,并具有高增殖率。我们旨在评估缝隙连接和 Cx 蛋白在 PitNETs 中的表达和相关性。我们评估了一系列 PitNETs 中 Cx26、32 和 43 的 mRNA 表达水平以及 Cx43 的蛋白表达。此外,我们在垂体瘤细胞系中过表达了 Cx43。在 mRNA 水平上,我们观察到肿瘤样本中所有连接蛋白的表达存在差异。在大多数研究的垂体肿瘤样本中,Cx43 蛋白表达缺失。此外,体外研究表明,Cx43 的过表达可降低垂体瘤细胞系的细胞生长并诱导细胞凋亡。我们的结果表明,Cx43 蛋白的下调可能参与了大多数垂体腺瘤的肿瘤发生,并且对垂体瘤的治疗具有潜在的治疗价值。