Department of Gastroenterology and Hepatology, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China (mainland).
Med Sci Monit. 2018 Mar 9;24:1424-1433. doi: 10.12659/msm.909186.
BACKGROUND Colorectal cancer (CRC) is the third most common cancer worldwide, making it is a serious threat to human health. It is imperative to develop new therapeutics to improve the CRC treatment efficiency. The aim of this study was to investigate the role of NPRL2 in improving sensitivity to CPT-11 in colon cancer cells. MATERIAL AND METHODS NPRL2 overexpression was established by transfecting the recombinant lentivirus-encoding NPRL2 gene into HCT116 colon cancer cells. Cell proliferation was identified using Cell Counting Kit-8 (CCK8) assay. Cell cycle and apoptosis were examined by flow cytometry. An immunofluorescence staining assay was conducted to examine the expression of γ-H2AX. Wound-healing and Transwell assays were utilized to show cell migration and invasion capability. The expression of apoptosis-related proteins (cleaved caspase-3, caspase-9, cleaved PARP, BAX, and Bcl-2), invasion-related proteins (MMP2, MMP9, p-PI3K, and p-AKT), and DNA damage checkpoint pathway proteins (p-ATM, p-Chk2, Cdc25C, Cdc2, and Cyclin B1) were quantified by Western blotting. RESULTS A CCK8 assay revealed that the overexpression of NPRL2 improved the sensitivity of CPT-11 in HCT116 cells (P<0.05). Functionally, NPRL2 overexpression elevated the sensitivity of CPT-11 by preventing colon cancer cell proliferation, cell movement, and invasion, and promoting cell apoptosis and G2/M cell cycle arrest. Mechanistically, NPRL2 overexpression enhanced CPT-11 sensitivity by activating the DNA damage checkpoint pathway. CONCLUSIONS NPRL2 overexpression enhances sensitivity to CPT-11 treatment in colon cancer cells, and it may serve as a molecular therapeutic agent to treat patients with CRC.
结直肠癌(CRC)是全球第三大常见癌症,严重威胁人类健康。开发新的治疗方法以提高 CRC 治疗效率势在必行。本研究旨在探讨 NPRL2 在提高结肠癌细胞对 CPT-11 敏感性中的作用。
通过转染编码 NPRL2 基因的重组慢病毒,建立 NPRL2 过表达。使用细胞计数试剂盒-8(CCK8)测定细胞增殖。通过流式细胞术检测细胞周期和凋亡。免疫荧光染色检测γ-H2AX 的表达。通过划痕愈合和 Transwell 测定评估细胞迁移和侵袭能力。通过 Western blot 测定定量检测凋亡相关蛋白(cleaved caspase-3、caspase-9、cleaved PARP、BAX 和 Bcl-2)、侵袭相关蛋白(MMP2、MMP9、p-PI3K 和 p-AKT)和 DNA 损伤检查点通路蛋白(p-ATM、p-Chk2、Cdc25C、Cdc2 和 Cyclin B1)的表达。
CCK8 测定显示 NPRL2 过表达可提高 CPT-11 在 HCT116 细胞中的敏感性(P<0.05)。功能上,NPRL2 过表达通过抑制结肠癌细胞增殖、运动和侵袭,促进细胞凋亡和 G2/M 细胞周期阻滞,提高 CPT-11 的敏感性。机制上,NPRL2 过表达通过激活 DNA 损伤检查点通路增强 CPT-11 的敏感性。
NPRL2 过表达增强了结肠癌细胞对 CPT-11 治疗的敏感性,可能成为治疗 CRC 患者的分子治疗剂。