Jin Y, Yu L L, Zhang B, Liu C F, Chen Y
Department of General Surgery, Tongde Hospital of Zhejiang Province, Zhejiang, China.
Department of Anesthesiology, the Children's Hospital, Zhejiang University School of Medicine, Zhejiang, China.
Braz J Med Biol Res. 2018 Nov 1;51(12):e7811. doi: 10.1590/1414-431X20187811.
Among the novel class of endogenous long non-coding RNAs, circular RNA (circRNA) is known as a key regulator in the development and progression of different cancers. Its function and mechanism in the tumorigenesis of colorectal cancer, however, has not been well studied. This study thus aimed to investigate potential regulation of colorectal cancer by circRNAs and the corresponding regulatory mechanism. We demonstrated that the expression of circRNA hsa_circ_0000523 (also known as circ_006229) was down-regulated in different colorectal cancer cell lines. It was also found that interference of hsa_circ_0000523 induced proliferation and suppressed apoptosis of colorectal cancer cells, the proliferation rate of which was reduced by the overexpression of hsa_circ_0000523. In addition, we found that miR-31 could recognize hsa_circ_0000523 sequence and that it acted as a "sponge" of miR-31, indirectly regulating Wnt/β-catenin signaling pathway, which was involved in the progression of colorectal cancer. The results suggested that the expression of hsa_circ_0000523 correlated to the tumorigenesis of colorectal cancer cells. In addition, as a sponge of miR-31, the low level of hsa_circ_0000523 led to activation of Wnt/β-catenin signaling pathway, inducing the subsequent progress of colorectal cancer.
在新型内源性长链非编码RNA中,环状RNA(circRNA)被认为是不同癌症发生发展过程中的关键调节因子。然而,其在结直肠癌发生中的功能和机制尚未得到充分研究。因此,本研究旨在探讨circRNA对结直肠癌的潜在调控作用及其相应的调控机制。我们发现,环状RNA hsa_circ_0000523(也称为circ_006229)在不同的结直肠癌细胞系中表达下调。还发现干扰hsa_circ_0000523可诱导结直肠癌细胞增殖并抑制其凋亡,而过表达hsa_circ_0000523可降低其增殖率。此外,我们发现miR-31可以识别hsa_circ_0000523序列,并且它作为miR-31的“海绵”,间接调节参与结直肠癌进展的Wnt/β-连环蛋白信号通路。结果表明,hsa_circ_0000523的表达与结直肠癌细胞的肿瘤发生相关。此外,作为miR-31的海绵,hsa_circ_0000523的低水平导致Wnt/β-连环蛋白信号通路的激活,从而诱导结直肠癌的后续进展。