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上调的有丝分裂相关基因 CENPE、CENPF 和 DLGAP5 预测急性髓系白血病的不良预后和化疗耐药性。

Upregulated mitosis-associated genes CENPE, CENPF, and DLGAP5 predict poor prognosis and chemotherapy resistance of Acute Myeloid Leukemia.

出版信息

Cancer Biomark. 2022;35(1):11-25. doi: 10.3233/CBM-203170.

Abstract

BACKGROUND

Mitosis-associated genes are dysregulated in many types of cancers and play important roles in disease progression and chemotherapy resistance. However, their expression and functions in chemotherapy-resistant Acute Myeloid Leukemia (AML) are still largely undetermined.

OBJECTIVE

This study aims to explore the roles of spindle assembly checkpoint (SAC) genes CENPE, CENPF, and DLGAP5 in chemotherapy-resistant AML.

METHODS

RNA-sequencing (RNA-seq) was performed in patients with chemotherapy-resistant AML and chemotherapy-sensitive AML. AML mRNA data from 151 patients with recurrence were downloaded from TCGA. Integrated analysis of the differentially expressed genes (DEGs), GO and KEGG pathways. CENPE, CENPF, or DLGAP5 knockdown cell lines were used to analyse proliferation, apoptosis and cell cycle alterations.

RESULTS

A total of 87 DEGs (48 upregulated and 39 downregulated) were obtained through gene analysis of R/R-AML and a total of 329 DEGs (202 upregulated and 127 downregulated) were obtained in refractory S-AML. Upregulated DEGs were mainly enriched in cell cycle (GO: 0007049, hsa04110) and mitotic cell cycle (GO: 0000278) processes and pathway. Venn diagram analysis identified the most upregulated DEGs (including CENPE, CENPF, and DLGAP5) in chemoresistant AML. The expression of CENPE, CENPF and DLGAP5 in R-AML (TCGA) was significantly higher than that of primary AML (GEO). The proliferation of K562 cells after CENPE and DLGAP5 knockdown was significantly decreased (P= 0.0001 and P= 0.0006). In THP-1 cells, the CCK-8 values after CENPE, CENPF and DLGAP5 knockdown were significantly decreased (P= 0.01, P= 0.0395 and P= 0.0362). Knockdown of CENPE, CENPF and DLGAP5 significantly increased cell apoptosis by regulating Caspase-9, BAX, TP-53 and bcl-2, and induced cell cycle arrested by regulating CDK1, CDK2, CDKN1A, and CyclinD1.

CONCLUSIONS

In conclusion, the mitotic cell cycle-associated genes CENPE, CENPF, and DLGAP5 were upregulated in chemotherapy-resistant AML patients and might be useful for predicting poor prognosis.

摘要

背景

有丝分裂相关基因在许多类型的癌症中失调,在疾病进展和化疗耐药中发挥重要作用。然而,它们在化疗耐药性急性髓系白血病(AML)中的表达和功能仍在很大程度上未被确定。

目的

本研究旨在探讨纺锤体组装检查点(SAC)基因 CENPE、CENPF 和 DLGAP5 在化疗耐药性 AML 中的作用。

方法

对化疗耐药性 AML 和化疗敏感性 AML 患者进行 RNA 测序(RNA-seq)。从 TCGA 下载了 151 例复发患者的 AML mRNA 数据。对差异表达基因(DEGs)、GO 和 KEGG 通路进行综合分析。使用 CENPE、CENPF 或 DLGAP5 敲低细胞系分析增殖、凋亡和细胞周期变化。

结果

通过对 R/R-AML 的基因分析,共获得 87 个 DEGs(48 个上调和 39 个下调),难治性 S-AML 中获得 329 个 DEGs(202 个上调和 127 个下调)。上调的 DEGs 主要富集在细胞周期(GO:0007049,hsa04110)和有丝分裂细胞周期(GO:0000278)过程和途径中。Venn 图分析鉴定了化疗耐药性 AML 中最上调的 DEGs(包括 CENPE、CENPF 和 DLGAP5)。R-AML(TCGA)中 CENPE、CENPF 和 DLGAP5 的表达明显高于原发性 AML(GEO)。CENPE 和 DLGAP5 敲低后 K562 细胞的增殖明显降低(P=0.0001 和 P=0.0006)。在 THP-1 细胞中,CENPE、CENPF 和 DLGAP5 敲低后 CCK-8 值明显降低(P=0.01、P=0.0395 和 P=0.0362)。CENPE、CENPF 和 DLGAP5 的敲低通过调节 Caspase-9、BAX、TP-53 和 bcl-2 显著增加细胞凋亡,并通过调节 CDK1、CDK2、CDKN1A 和 CyclinD1 诱导细胞周期停滞。

结论

总之,在化疗耐药性 AML 患者中,有丝分裂细胞周期相关基因 CENPE、CENPF 和 DLGAP5 上调,可能有助于预测不良预后。

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