Department of BioMedicine, Neurosciences and Advanced Diagnostics (Bi.N.D), Via Divisi 83, 90133 Palermo, Italy.
IRCCS ISTITUTO ORTOPEDICO RIZZOLI, 40138 Bologna, Italy.
Int J Mol Sci. 2019 Feb 13;20(4):801. doi: 10.3390/ijms20040801.
The long non-coding RNA H19 (lncH19) is broadly transcribed in the first stage of development and silenced in most cells of an adult organism; it appears again in several tumors where, through different molecular mediators, promotes cell proliferation, motility and metastases. LncH19 has been associated with hypoxia-inducible factor 1-alpha (HIF-1α) activation and, in some tumors, it has proved to be necessary and required to sustain hypoxic responses. Here we propose to investigate a putative role for the lncH19 in hypoxia induced multiple myeloma (MM) progression. Transcriptional analysis of MM cell lines (RPMI and MM1.S) exposed to normoxia or hypoxia (1% O₂) was done in order to evaluate lncH19 levels under hypoxic stimulation. Then, to investigate the role of lncH19 in hypoxia mediated MM progression, transcriptional, protein and functional assays have been performed on hypoxia stimulated MM cell lines, silenced or not for lncH19. Our data demonstrated that hypoxic stimulation in MM cell lines induced the overexpression of lncH19, which, in turn, is required for the expression of the hypoxia induced genes involved in MM dissemination, such as C-X-C Motif Chemokine Receptor 4 (CXCR4) and Snail. Moreover, adhesion assays demonstrated that lncH19 silencing abrogates the increased adhesion on stromal cells induced by the hypoxic condition. Finally, Western blot analysis indicated that lncH19 silencing impaired HIF1α nuclear translocation. The LncH19, required for the induction of hypoxic responses in MM cells, could represent a new therapeutic target for MM.
长链非编码 RNA H19(lncH19)在发育的早期广泛转录,在成年生物体的大多数细胞中沉默;它在几种肿瘤中再次出现,通过不同的分子介质,促进细胞增殖、运动和转移。lncH19 与缺氧诱导因子 1-α(HIF-1α)的激活有关,在一些肿瘤中,它被证明是维持缺氧反应所必需和必需的。在这里,我们提出研究 lncH19 在缺氧诱导多发性骨髓瘤(MM)进展中的潜在作用。为了评估缺氧刺激下 lncH19 的水平,对暴露于常氧或缺氧(1% O₂)的 MM 细胞系(RPMI 和 MM1.S)进行了转录分析。然后,为了研究 lncH19 在缺氧介导的 MM 进展中的作用,对缺氧刺激的 MM 细胞系进行了转录、蛋白和功能测定,这些细胞系被沉默或未沉默 lncH19。我们的数据表明,MM 细胞系中的缺氧刺激诱导了 lncH19 的过表达,而 lncH19 的过表达又需要缺氧诱导的与 MM 扩散相关的基因的表达,如 C-X-C 基序趋化因子受体 4(CXCR4)和 Snail。此外,粘附实验表明,lncH19 沉默可消除缺氧条件下诱导的基质细胞粘附增加。最后,Western blot 分析表明,lncH19 沉默可损害 HIF1α 的核易位。lncH19 是 MM 细胞中诱导缺氧反应所必需的,它可能成为 MM 的一个新的治疗靶点。