Department of Respiratory, The Third People's Hospital of Linyi , Linyi, China.
Department of Oncology, The Third People's Hospital of Linyi , Linyi, China.
Bioengineered. 2021 Dec;12(1):414-425. doi: 10.1080/21655979.2021.1872191.
As a type of non-coding RNA, circular RNA (circRNA) figures prominently in human cancer progression. Nonetheless, the expression, function, and regulatory mechanism of circ_0001287 in non-small cell lung cancer (NSCLC) remain obscure. In this work, quantitative real-time polymerase chain reaction (qRT-PCR) was implemented to quantify circ_0001287 and miR-21 expressions in NSCLC tissues and cells. The relationship between circ_0001287 expression and the clinicopathological parameters of NSCLC patients was examined. Cell counting kit-8 (CCK-8), 5-bromo-2©-deoxyuridine (BrdU), and Transwell experiments were conducted to detect the multiplication, migration, and invasion of NSCLC cells after circ_0001287 was overexpressed or knocked down. The survival of NSCLC cells was studied using colony formation experiment under different doses of radiation. RNA immunoprecipitation (RIP) experiment and luciferase reporter gene experiment verified the binding relationship between circ_0001287 and miR-21. Western blot was employed to examine the regulatory effects of circ_0001287 and miR-21 on phosphatase and tensin homolog (PTEN) expression. We reported that circ_0001287 expression was down-modulated in NSCLC tissues and cell lines. Besides, circ_0001287 low expression was associated with low differentiation and positive lymph node invasion of NSCLC. Circ_0001287 overexpression suppressed the multiplication, migration, invasion, and radioresistance of NSCLC cells, whereas circ_0001287 knockdown promoted the above phenotypes. Circ_0001287 could adsorb miR-21 and repress its expression, and indirectly up-modulate PTEN expression in NSCLC cells. Taken together, circ_0001287/miR-21/PTEN axis is probably involved in regulating NSCLC cell multiplication, metastasis, and radioresistance.
环状 RNA(circRNA)作为一种非编码 RNA,在人类癌症进展中起着重要作用。然而,circ_0001287 在非小细胞肺癌(NSCLC)中的表达、功能和调控机制仍不清楚。在本研究中,采用实时定量聚合酶链反应(qRT-PCR)检测 NSCLC 组织和细胞中 circ_0001287 和 miR-21 的表达。分析 circ_0001287 表达与 NSCLC 患者临床病理参数的关系。通过细胞计数试剂盒-8(CCK-8)、5-溴-2©-脱氧尿苷(BrdU)和 Transwell 实验检测过表达或敲低 circ_0001287 后 NSCLC 细胞的增殖、迁移和侵袭。采用不同剂量辐射下的集落形成实验研究 NSCLC 细胞的存活情况。通过 RNA 免疫沉淀(RIP)实验和荧光素酶报告基因实验验证 circ_0001287 与 miR-21 的结合关系。采用 Western blot 检测 circ_0001287 和 miR-21 对磷酸酶和张力蛋白同源物(PTEN)表达的调控作用。我们报道 circ_0001287 在 NSCLC 组织和细胞系中表达下调。此外,circ_0001287 低表达与 NSCLC 低分化和阳性淋巴结浸润有关。circ_0001287 过表达抑制 NSCLC 细胞的增殖、迁移、侵袭和放射抵抗,而 circ_0001287 敲低则促进上述表型。circ_0001287 可以吸附 miR-21 并抑制其表达,从而间接上调 NSCLC 细胞中 PTEN 的表达。综上所述,circ_0001287/miR-21/PTEN 轴可能参与调节 NSCLC 细胞的增殖、转移和放射抵抗。