EZH2对结直肠肿瘤行为学的影响及其机制OACSTPCD
Effect of EZH2 on colorectal tumor behavior and its mechanism
目的 探究EZH2对结直肠肿瘤行为学的影响及其作用机制.方法 ①将40只BALB/c-nu裸鼠随机分为4组:EZH2-NC 组、EZH2-OE 组、EZH2-NC+PD1 抑制剂组、EZH2-OE+PD1 抑制剂组.按照 LipofectamineTM2000 转染法将 SW480细胞稳定转染EZH2空载体质粒或EZH2过表达载体,取转染成功SW480细胞溶液分别注入小鼠右侧腋窝皮下构建皮下移植瘤模型,然后EZH2-NC+PD1抑制剂组和EZH2-OE+PD1抑制剂组小鼠尾静脉注射PD1抑制剂(150 μg/mL),21 d后观察肿瘤体积.②SW480稳转细胞分为4组:EZH2-NC组、EZH2-OE组、EZH2-NC+PD1抑制剂组(转染成功后加入1.5 ng/mL PD1抑制剂)、EZH2-OE+PD1抑制剂组(转染成功后加入1.5 ng/mL PD1抑制剂).将以上4组SW480细胞和THP-1细胞进行共培养,应用CCK-8实验、划痕实验、Transwell实验分别检测SW480细胞增殖、迁移和侵袭能力.应用Western blot实验检测THP-1细胞中XBP-1、Cat K、Cat L、IL-6和Arg-1的蛋白表达水平和SW480细胞中的EZH2、p-STAT3、PD-1蛋白的表达水平.结果 ①裸鼠成瘤结果显示,与EZH2-NC组相比,EZH2-OE组肿瘤体积增大(P<0.01);与EZH2-NC+PD-1组相比,EZH2-OE+PD-1抑制剂组肿瘤体积差异无统计学意义.②将SW480细胞和THP1细胞进行共培养后,与EZH2-NC组相比,EZH2-OE组SW480细胞增殖、迁移、侵袭能力增强(P<0.01);与EZH2-NC+PD-1抑制剂组相比,EZH2-OE+PD-1抑制剂组SW480细胞增殖、迁移、侵袭能力差异无统计学意义.与EZH2-NC组相比,EZH2-OE组THP-1细胞中IL-6和Arg-1蛋白水平升高(P<0.05);与EZH2-NC组相比,EZH2-NC+PD1抑制剂组IL-6和Arg-1蛋白水平下降(P<0.01);与EZH2-OE组相比较,EZH2-OE+PD1抑制剂组IL-6和Arg-1蛋白水平下降(P<0.01).与EZH2-NC组相比,EZH2-OE组THP-1细胞中XBP-1、Cat K和Cat L蛋白水平升高(P<0.01);与 EZH2-NC 组比,EZH2-NC+PD-1 抑制剂组 XBP-1、Cat K 和 Cat L 蛋白水平下降(P<0.01);与 EZH2-OE 组相比,EZH2-OE+PD-1抑制剂组XBP-1、Cat K和Cat L蛋白水平下降(P<0.01).与EZH2-NC组相比,EZH2-OE组SW480细胞中EZH2、p-STAT3和PD-1蛋白水平升高(P<0.01);与EZH2-NC+PD-1抑制剂组相比,EZH2-OE+PD-1抑制剂组EZH2和p-STAT3蛋白水平升高(P<0.05).结论 EZH2通过上调STAT3/PD-1通路进而影响肿瘤相关巨噬细胞产生对结直肠癌进展发挥促进作用.
Objective To explore the effect and mechanism of EZH2 on the behavior of colorectal tumors.Methods ①Forty BALB/c-nu nude mice were randomly divided into four groups:EZH2-NC group,EZH2-OE group,EZH2-NC+PD1 inhibitor group,and EZH2-OE+PD1 inhibitor group.Human colorectal adenocartinoma cells SW480 were transfected with EZH2 empty vector and EZH2 overexpression plasmid,and then subcutaneously injected into BALB/c-nu nude mice to construct a graft tumor model,respectively.After successful transfection,the nude mice were injected with PD1 inhibitor(150 μg/mL)via the tail vein in EZH2-NC+PD1 inhibitor group and EZH2-OE+PD1 inhibitor group.Then the tumor volume was calculated and compared at 21 d.②The stably transfected SW480 cells were divided into EZH2-NC group,EZH2-OE group,EZH2-NC+PD1 inhibitor group(adding 1.5 ng/mL PD1 inhibitor after transfec-tion),and EZH2-OE+PD1 inhibitor group(adding 1.5 ng/mL PD1 inhibitor after transfection),and then SW480 cells and THP-1 cells were co-cultured.CCK-8 test,Scratch test and Transwell test were used to detect the proliferation,migration and invasion abilities of SW480 cells,respectively.Western blot was used to detect the expression levels of XBP-1,Cat K,Cat L,IL-6 and Arg-1 proteins in THP-1 cells and EZH2,p-STAT3 and PD-1 proteins in SW480 cells.Results ①The tumor formation results of nude mice showed that the tumor volume was increased in EZH2-OE group compared with EZH2-NC group(P<0.01),while there was no significant difference between EZH2-OE+PD-1 inhibitor group and EZH2-NC+PD-1 group.②After co-culture of SW480 cells and THP1 cells,the proliferation,migration and invasion abilities of SW480 cells were enhanced in EZH2-OE group compared with EZH2-NC group(P<0.01),while there was no significant difference between EZH2-OE+PD-1 inhibitor group and EZH2-NC+PD-1 group.The levels of IL-6 and Arg-1 proteins in THP-1 cells were higher in EZH2-OE group than in EZH2-NC group(P<0.05),and IL-6 and Arg-1 protein levels were lower in EZH2-NC+PD1 inhibitor group than in EZH2-NC group(P<0.01),and in EZH2-OE+PD1 inhibitor group than in EZH2-OE group(P<0.01).The protein levels of XBP-1,Cat K and Cat L in THP-1 cells were significantly higher in EZH2-OE group than in EZH2-NC group(P<0.01),and the protein levels of XBP-1,Cat K and Cat L were lower in EZH2-NC+PD-1 inhibitor group than in EZH2-NC group(P<0.01),and in EZH2-OE+PD-1 inhibitor group than in EZH2-OE group(P<0.01).Compared with EZH2-NC group,EZH2,p-STAT3 and PD-1 protein levels in SW480 cells in EZH2-OE group were increased(P<0.01).Compared with EZH2-NC+PD-1 inhibitor group,EZH2 and p-STAT3 protein levels in EZH2-OE+PD-1 inhibitor group were increased(P<0.05).Conclusion EZH2 may promote the progression of colorectal cancer by upregulating STAT3/PD-1 pathway,thereby affecting the tumor-associated macrophages.
武雪亮;韩磊;樊建春;路永刚
河北北方学院附属第一医院普通外科,张家口 075000||河北北方学院附属第一医院肿瘤研究所河北北方学院附属第一医院普通外科,张家口 075000河北北方学院研究生院河北省人民医院中心实验室
临床医学
EZH2STAT3PD-1结直肠癌肿瘤相关巨噬细胞
EZH2STAT3PD-1colorectal cancertumor-associated macrophages
《山西医科大学学报》 2024 (006)
680-688 / 9
河北省卫计委医学科学研究重点课题计划项目(20211330)
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