Ming Zhixiang, Zhang Ruoyi, Xu Jianhua, Ding Wei, Qin Lei
Department of General Surgery, The First Affiliated Hospital of Soochow University, Suzhou, China.
Department of General Surgery, Nantong Hospital of Traditional Chinese Medicine, Nantong, China.
J Gastrointest Oncol. 2022 Dec;13(6):3278-3289. doi: 10.21037/jgo-22-1167.
We performed and experiments to observe the expression of long intergenic nonprotein coding RNA 1426 (LINC01426) in pancreatic cancer tissues and cells, investigate the impact of LINC01426 on the proliferation and migration of pancreatic cancer cells, and deduce the underlying molecular mechanism.
LINC01426 expression was measured by fluorescence-based quantitative polymerase chain reaction (PCR) in pancreatic cancer tissues and cell lines. The lentiviral vector was used to create shRNA-NC, shLINC01426#2, pcDNA-NC, and pcDNA-LINC01426 pancreatic cancer cell lines. Cell Counting Kit-8 (CCK-8), clonogenic, and scratch tests were used to measure the effects of LINC01426 knockdown or overexpression on the migration and proliferation of pancreatic cancer cells. The expression levels of genes involved in migration (E-cadherin, N-cadherin, and vimentin) were examined by Western blotting after LINC01426 was either knocked down or overexpressed. The effect of LINC01426 knockdown on the proliferation of pancreatic cancer cells was verified in nude mice.
LINC01426 was highly expressed in pancreatic cancer cells and tissues. Overexpression of LINC01426 might have promoted the proliferation, clonogenicity, and migration of pancreatic cancer cells, while knockdown of LINC01426 decreased these activities. In pancreatic cancer cells, knockdown of LINC01426 dramatically enhanced E-cadherin expression while lowering N-cadherin and vimentin expression, whereas overexpression of LINC01426 had the opposite effect. Knockdown of LINC01426 substantially decreased pancreatic cancer cell proliferation in an study.
Overexpression of LINC01426 was shown to increase the migration and proliferation of pancreatic cancer cells in both and experiments. LINC01426 could be a novel predictive biomarker and source of prospective therapeutic targets for patients with pancreatic cancer.
我们进行了实验以观察长链基因间非编码RNA 1426(LINC01426)在胰腺癌组织和细胞中的表达,研究LINC01426对胰腺癌细胞增殖和迁移的影响,并推断其潜在的分子机制。
采用基于荧光的定量聚合酶链反应(PCR)检测胰腺癌组织和细胞系中LINC01426的表达。使用慢病毒载体构建shRNA-NC、shLINC01426#2、pcDNA-NC和pcDNA-LINC01426胰腺癌细胞系。使用细胞计数试剂盒-8(CCK-8)、克隆形成试验和划痕试验来检测LINC01426敲低或过表达对胰腺癌细胞迁移和增殖的影响。在LINC01426敲低或过表达后,通过蛋白质印迹法检测参与迁移的基因(E-钙黏蛋白、N-钙黏蛋白和波形蛋白)的表达水平。在裸鼠中验证LINC01426敲低对胰腺癌细胞增殖的影响。
LINC01426在胰腺癌细胞和组织中高表达。LINC01426的过表达可能促进了胰腺癌细胞的增殖、克隆形成能力和迁移,而LINC01426的敲低则降低了这些活性。在胰腺癌细胞中,LINC01426的敲低显著增强了E-钙黏蛋白的表达,同时降低了N-钙黏蛋白和波形蛋白的表达,而LINC01426的过表达则产生相反的效果。在一项研究中,LINC01426的敲低显著降低了胰腺癌细胞增殖。
在体内和体外实验中均表明,LINC01426的过表达增加了胰腺癌细胞的迁移和增殖。LINC01426可能是胰腺癌患者一种新的预测生物标志物和潜在治疗靶点来源。