Comprehensive analysis of PTPN family expression and prognosis in acute myeloid leukemia

被引:4
作者
Liu, Yong [1 ]
Zhang, Jing [2 ]
Du, Zefan [1 ]
Huang, Junbin [1 ]
Cheng, Yucai [1 ]
Yi, Wenfang [1 ]
Li, Tianwen [1 ]
Yang, Jing [1 ]
Chen, Chun [1 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 7, Dept Pediat, Div Hematol Oncol, Shenzhen, Peoples R China
[2] Guangzhou Women & Childrens Med Ctr, Dept Breast & Thyroid Surg, Guangzhou, Peoples R China
关键词
PTPNs; AML; bioinformatics; prognosis; biomarker; expression level; PROTEIN-TYROSINE PHOSPHATASES; CANCER STATISTICS; ACTIVATION; APOPTOSIS; P38-ALPHA; DISEASE; KINASE; SERVER;
D O I
10.3389/fgene.2022.1087938
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: Tyrosyl phosphorylation is carried out by a group of enzymes known as non-receptor protein tyrosine phosphatases (PTPNs). In the current investigation, it is hoped to shed light on the relationships between the expression patterns of PTPN family members and the prognosis of acute myeloid leukemia (AML).Methods: PTPN expression was examined using GEPIA and GEO databases. To investigate the connection between PTPN expression and survival in AML patients, we downloaded data from the Broad TCGA Firehose and Clinical Proteomic Tumor Analysis (CPTAC) of the Cancer Genome Atlas (TCGA). We used quantitative real-time PCR (qRT-PCR) to confirm that essential genes were performed in clinical samples and cell lines. We then used western blot to verify that the genes expressed in the above databases were positive in normal tissues, AML patient samples, and AML cell lines. Next, we investigated associations between genome-wide expression profiles and PTPN6 expression using the GEO datasets. We investigated the interactive exploration of multidimensional cancer genomics using the cBioPortal datasets. Using the DAVID database, a study of gene ontology enrichment was performed. The protein-protein interaction (PPI) network was created using the STRING portal, and the gene-gene interaction network was performed using GeneMANIA.Results: Data from GEO and GEPIA revealed that most PTPN family members were linked to AML. Patients with leukemia have elevated levels of several PTPN members. All of the AML patients' poor overall survival (OS, p < .05) was significantly linked with higher expression of PTPN1, PTPN6, and PTPN7. Additionally, clinical samples showed that the expression of PTPN 6, PTPN 7, PTPN 13, and PTPN 14 was higher than normal in AML patients (p = .0116, p = .0034, p = .0092, and p = .0057, respectively) and AML cell lines (p = .0004, p = .0035, p = .0357, and p = .0177, respectively). Western blotting results showed that the expression of PTPN6 in AML samples and AML cell lines was significantly higher than that in normal control samples.Conclusion: Differentially expressed PTPN family members were found in AML. The prognosis of patients and PTPN gene expression were shown to be correlated. PTPN6 is one of these members and may be used as an AML diagnostic and prognostic marker.
引用
收藏
页数:12
相关论文
共 50 条
  • [31] Methylation-independent CHFR expression is a potential biomarker affecting prognosis in acute myeloid leukemia
    Zhou, Jing-Dong
    Zhang, Ting-Juan
    Li, Xi-Xi
    Ma, Ji-Chun
    Guo, Hong
    Wen, Xiang-Mei
    Yao, Dong-Ming
    Zhang, Wei
    Lin, Jiang
    Qian, Jun
    JOURNAL OF CELLULAR PHYSIOLOGY, 2018, 233 (06) : 4707 - 4714
  • [32] Decreased SCIN expression, associated with promoter methylation, is a valuable predictor for prognosis in acute myeloid leukemia
    Zhang, Zhi-Hui
    Zhang, Wei
    Zhou, Jing-Dong
    Zhang, Ting-Juan
    Ma, Ji-Chun
    Xu, Zi-Jun
    Lian, Xin-Yue
    Wu, De-Hong
    Wen, Xiang-Mei
    Deng, Zhao-Qun
    Lin, Jiang
    Qian, Jun
    MOLECULAR CARCINOGENESIS, 2018, 57 (06) : 735 - 744
  • [33] High expression of bcl-2 mRNA as a determinant of poor prognosis in acute myeloid leukemia
    Karakas, T
    Maurer, U
    Weidmann, E
    Miething, CC
    Hoelzer, D
    Bergmann, L
    ANNALS OF ONCOLOGY, 1998, 9 (02) : 159 - 165
  • [34] Low miR-192 expression predicts poor prognosis in pediatric acute myeloid leukemia
    Tian, Chunmei
    Zhang, Lin
    Li, Xiaohua
    Zhang, Yanjun
    Li, Jianchang
    Chen, Liang
    CANCER BIOMARKERS, 2018, 22 (02) : 209 - 215
  • [35] Comprehensive Analysis of the Expression, Prognosis, and Biological Significance of PLOD Family in Bladder Cancer
    Chen, Ru
    Jiang, Ming
    Hu, Bing
    Fu, Bin
    Sun, Ting
    INTERNATIONAL JOURNAL OF GENERAL MEDICINE, 2023, 16 : 707 - 722
  • [36] HLA-G expression is irrelevant to prognosis in patients with acute myeloid leukemia
    Guo, Q. Y.
    Chen, B. G.
    Ruan, Y. Y.
    Lin, A.
    Yan, W. H.
    LEUKEMIA RESEARCH, 2011, 35 (10) : 1350 - 1354
  • [37] Application of omics in the diagnosis, prognosis, and treatment of acute myeloid leukemia
    Zhang, Zhiyu
    Huang, Jiayi
    Zhang, Zhibo
    Shen, Hongjie
    Tang, Xiaowen
    Wu, Depei
    Bao, Xiebing
    Xu, Guoqiang
    Chen, Suning
    BIOMARKER RESEARCH, 2024, 12 (01)
  • [38] Prognostic value of the PDLIM family in acute myeloid leukemia
    Cui, Longzhen
    Cheng, Zhiheng
    Hu, Kai
    Pang, Yifan
    Liu, Yan
    Qian, Tingting
    Quan, Liang
    Dai, Yifeng
    Pang, Ying
    Ye, Xu
    Shi, Jinlong
    Fu, Lin
    AMERICAN JOURNAL OF TRANSLATIONAL RESEARCH, 2019, 11 (09): : 6124 - 6131
  • [39] Methylation-independent CRIP1 expression is a potential biomarker affecting prognosis in cytogenetically normal acute myeloid leukemia
    Ma, Bei-Bei
    Zhang, Ting-Juan
    Wang, Cui-Zhu
    Xu, Zi-Jun
    Zhou, Jing-Dong
    Gu, Yu
    Ma, Ji-Chun
    Deng, Zhao-Qun
    Lin, Jiang
    Qian, Jun
    AMERICAN JOURNAL OF TRANSLATIONAL RESEARCH, 2020, 12 (09): : 4840 - 4852
  • [40] The immunophenotype of acute myeloid leukemia: is there a relationship with prognosis?
    Mason, KD
    Juneja, SK
    Szer, J
    BLOOD REVIEWS, 2006, 20 (02) : 71 - 82