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Upregulation of DLC-1 inhibits pancreatic cancer progression: Studies with clinical samples and a pancreatic cancer model

机译:DLC-1的上调抑制胰腺癌的进展:临床样品和胰腺癌模型的研究

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摘要

Deleted in liver cancer 1 (DLC-1) serves a vital role in the progression of multiple cancers, including those of the pancreas. Numerous studies have aimed to reveal the anti-cancer mechanisms of the DLC-1 gene, though few have focused on its impact on the development of pancreatic cancer. Using clinical pancreatic cancer samples and pancreatic cancer cell lines, the present study aimed to reveal the role of DLC-1 in this disease. The expression levels of DLC-1 were determined in pancreatic cancer and adjacent normal tissues from patients with pancreatic cancer, indicating a decreased expression level of DLC-1 in cancerous tissues. Using the pancreatic cancer cell line SW1990, the effect of DLC overexpression on cell proliferation, invasive capacity and the cell cycle and were assessed. Using a mouse tumor model, the tumor-progression capacity of transfected and untransfected SW1990 cells was investigated, indicating that DLC-1 transfection reduced the capacity for tumor progression. Thus, the present study indicated that the overexpression of DLC-1 inhibited the proliferation and reduced the invasive capacity of SW1990 cells both in vitro and in vivo, and that it may have significant inhibitory effects on the development of pancreatic cancer.
机译:肝癌1(DLC-1)中的缺失在多种癌症(包括胰腺癌)的进展中起着至关重要的作用。许多研究旨在揭示DLC-1基因的抗癌机制,尽管很少有人关注其对胰腺癌发展的影响。本研究使用临床胰腺癌样本和胰腺癌细胞系,旨在揭示DLC-1在该疾病中的作用。测定了胰腺癌患者的胰腺癌和邻近正常组织中DLC-1的表达水平,表明癌组织中DLC-1的表达水平降低。使用胰腺癌细胞系SW1990,评估了DLC过表达对细胞增殖,侵袭能力和细胞周期的影响,并进行了评估。使用小鼠肿瘤模型,研究了转染和未转染的SW1990细胞的肿瘤进展能力,这表明DLC-1转染降低了肿瘤进展的能力。因此,本研究表明DLC-1的过量表达在体外和体内均抑制SW1990细胞的增殖并降低其侵袭能力,并且其可能对胰腺癌的发展具有显着的抑制作用。

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