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Overexpression of the SMYD3 Promotes Proliferation, Migration, and Invasion of Pancreatic Cancer

机译:SMYD3的过度表达促进胰腺癌的增殖,迁移和侵袭

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Background The Suvar, Enhancer of zeste, and Trithorax (SET), myeloid-Nervy-DEAF-1 (MYND) domain-containing protein 3 (SMYD3), was reported to be upregulated in various tumors. However, its role in pancreatic cancer progression remains unclear. Aims To explore the role of SMYD3 in the pancreatic cancer. Methods The expressions of SMYD3, caspase-3, and matrix metallopeptidase-2 (MMP-2) were detected in pancreatic cancer and non-tumor tissues by immunohistochemistry. The CCK-8 and transwell assays were performed to test proliferation, migration, and invasion ability in short hairpin RNA (shRNA-SMYD3) pancreatic cancer cell line SW1190. RT-PCR and Western blot were used to detect the expressions of SMYD3, caspase-3, and MMP-2 in SW1990 cell line and shRNA-SMYD3 SW1990 cell line. Results The expressions of SMYD3, caspase-3, and MMP-2 were upregulated in pancreatic cancer. The SMYD3 was positively associated with caspase-3 and MMP-2 expressions in pancreatic cancer tissues. SMYD3, TNM stages, histological differentiation, and lymph node metastasis were identified as an independent prognostic factor. Moreover, interfered SMYD3 expression in SW1990 cell line significantly reduced the cell proliferation, migration, and invasion. RT-PCR and Western blot showed the expression of MMP-2 decreased in shRNA-SMYD3 SW1990 cell line, but no significant change was observed in the caspase-3 expression. Conclusions The overexpression of SMYD3 promoted proliferation, migration, and invasion of pancreatic cancer, and SMYD3 may affect the pancreatic cancer progression by regulating MMP-2 rather than caspase-3.
机译:背景技术据报道,据报道含有含有结构域蛋白3(SMYD3)的苏瓦尔,Zeste和Trithorax(Set),髓鞘蛋白3(MyND3)。然而,它在胰腺癌进展中的作用仍然不清楚。旨在探讨SMYD3在胰腺癌中的作用。方法通过免疫组织化学在胰腺癌和非肿瘤组织中检测到SMYD3,Caspase-3和基质金属肽酶-2(MMP-2)的表达。在短发夹RNA(SHRNA-SMYD3)胰腺癌细胞系SW1190中,进行CCK-8和Transwell测定以测试增殖,迁移和侵袭能力。 RT-PCR和Western印迹用于检测SW1990细胞系和SHRNA-SMYD3 SW1990细胞系中SMYD3,Caspase-3和MMP-2的表达。结果SMYD3,Caspase-3和MMP-2的表达在胰腺癌中令人抑制。 Smyd3在胰腺癌组织中与Caspase-3和MMP-2表达呈正相关。 SMYD3,TNM阶段,组织学分化和淋巴结转移被鉴定为独立的预后因子。此外,SW1990细胞系中干扰的SMYD3表达显着降低了细胞增殖,迁移和侵袭。 RT-PCR和Western印迹显示SCRNA-Smyd3 SW1990细胞中MMP-2的表达,但在Caspase-3表达中没有观察到显着变化。结论SMYD3的过表达促进胰腺癌的增殖,迁移和侵袭,SMYD3可以通过调节MMP-2而不是Caspase-3来影响胰腺癌进展。

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