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miR-324-5p Contributes to Cell Proliferation and Apoptosis in Pancreatic Cancer by Targeting KLF3

机译:MiR-324-5P通过靶向KLF3有助于细胞增殖和胰腺癌细胞凋亡

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Pancreatic cancer cells are characterized by high cell proliferation and low cell apoptosis, but the factors involved in these processes remain to be further studied. In this study, we report that miR-324-5p regulates the proliferation and apoptosis of pancreatic cancer cells through regulating the expression of Krüppel-like factor 3 (KLF3). In both pancreatic cancer tissues and cell lines, the levels of miR-324-5p are significantly increased. Inhibition of miR-324-5p represses cell proliferation but promotes cell apoptosis, whereas overexpression of miR-324-5p exerts the opposite effect. Furthermore, we identified KLF3, a factor regulating pancreatic cancer cell proliferation and apoptosis, as a new direct downstream target of miR-324-5p. Our results suggest that miR-324-5p plays an important role in pancreatic cancer cell proliferation and apoptosis via downregulating the expression of KLF3.
机译:胰腺癌细胞的特征在于细胞增殖和低细胞凋亡,但仍然进一步研究参与这些过程的因素。在这项研究中,我们通过调节Krüppel样因子3(KLF3)的表达来调节胰腺癌细胞的增殖和凋亡。在胰腺癌组织和细胞系中,miR-324-5p的水平显着增加。抑制miR-324-5p抑制细胞增殖,但促进细胞凋亡,而MiR-324-5p的过度表达施加相反的效果。此外,我们鉴定了KLF3,该因子调节胰腺癌细胞增殖和凋亡,作为MIR-324-5P的新直下游靶标。我们的研究结果表明,MIR-324-5P在胰腺癌细胞增殖和凋亡中发挥着重要作用,通过下调KLF3的表达。

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