Cheng Y, He X, Wang L, Xu Y, Shen M, Zhang W, Xia Y, Zhang J, Zhang M, Wang Y, Hu J, Hu J
Department of Blood Transfusion, First Affiliated Hospital of Bengbu Medical College, Bengbu 233004, China.
Bengbu Medical College, Bengbu 233000, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2023 Apr 20;43(4):544-551. doi: 10.12122/j.issn.1673-4254.2023.04.06.
To analyze the expression of hydroxysteroid dehydrogenase like 2 (HSDL2) in rectal cancer tissues and the effect of changes in HSDL2 expression level on proliferation of rectal cancer cells.
Clinical data and tissue samples of 90 patients with rectal cancer admitted to our hospital from January 2020 to June 2022 were collected from the prospective clinical database and biological specimen database. The expression level of HSDL2 in rectal cancer and adjacent tissues was detected by immunohistochemistry, and based on the median level of HSDL2 expression, the patients were divided into high expression group (=45) and low expression group (=45) for analysis the correlation between HSDL2 expression level and the clinicopathological parameters. GO and KEGG enrichment analyses were performed to explore the role of HSDL2 in rectal cancer progression. The effects of changes in HSDL2 expression levels on rectal cancer cell proliferation, cell cycle and protein expressions were investigated in SW480 cells with lentivirus-mediated HSDL2 silencing or HSDL2 overexpression using CCK-8 assay, flow cytometry and Western blotting.
The expressions of HSDL2 and Ki67 were significantly higher in rectal cancer tissues than in the adjacent tissues ( < 0.05). Spearman correlation analysis showed that the expression of HSDL2 protein was positively correlated with Ki67, CEA and CA19-9 expressions ( < 0.01). The rectal cancer patients with high HSDL2 expressions had significantly higher likelihood of having CEA ≥5 μg/L, CA19-9 ≥37 kU/L, T3-4 stage, and N2-3 stage than those with a low HSDL2 expression ( < 0.05). GO and KEGG analysis showed that HSDL2 was mainly enriched in DNA replication and cell cycle. In SW480 cells, HSDL2 overexpression significantly promoted cell proliferation, increased cell percentage in S phase, and enhanced the expression levels of CDK6 and cyclinD1 ( < 0.05), and HSDL2 silencing produced the opposite effects ( < 0.05).
The high expression of HSDL2 in rectal cancer participates in malignant progression of the tumor by promoting the proliferation and cell cycle progress of the cancer cells.
分析2型羟类固醇脱氢酶样蛋白(HSDL2)在直肠癌组织中的表达情况以及HSDL2表达水平变化对直肠癌细胞增殖的影响。
收集2020年1月至2022年6月我院收治的90例直肠癌患者的临床资料和组织样本,这些样本来自前瞻性临床数据库和生物标本数据库。采用免疫组织化学法检测直肠癌组织及癌旁组织中HSDL2的表达水平,并根据HSDL2表达的中位数水平将患者分为高表达组(=45)和低表达组(=45),分析HSDL2表达水平与临床病理参数之间的相关性。进行基因本体(GO)和京都基因与基因组百科全书(KEGG)富集分析,以探讨HSDL2在直肠癌进展中的作用。使用慢病毒介导的HSDL2沉默或HSDL2过表达的方法,通过细胞计数试剂盒(CCK-8)检测、流式细胞术和蛋白质免疫印迹法,研究HSDL2表达水平变化对SW480细胞中直肠癌细胞增殖、细胞周期及蛋白质表达的影响。
直肠癌组织中HSDL2和Ki67的表达明显高于癌旁组织(<0.05)。Spearman相关性分析显示,HSDL2蛋白表达与Ki67、癌胚抗原(CEA)和糖类抗原19-9(CA19-9)的表达呈正相关(<0.01)。HSDL2高表达的直肠癌患者血清CEA≥5μg/L、CA19-9≥37kU/L、T3-4期及N2-3期的可能性明显高于HSDL2低表达患者(<0.05)。GO和KEGG分析表明,HSDL2主要富集于DNA复制和细胞周期。在SW480细胞中,HSDL2过表达显著促进细胞增殖,增加S期细胞百分比,并增强细胞周期蛋白依赖性激酶6(CDK6)和细胞周期蛋白D1(cyclinD1)的表达水平(<0.05),而HSDL2沉默则产生相反的效果(<0.05)。
直肠癌中HSDL2的高表达通过促进癌细胞的增殖和细胞周期进程参与肿瘤的恶性进展。