RETRACTED: Cell Division Cycle-Associated Protein 3 (CDCA3) Is a Potential Biomarker for Clinical Prognosis and Immunotherapy in Pan-Cancer (Retracted Article)

被引:6
作者
Xu, Yingkun [1 ]
Shen, Meiying [1 ]
Peng, Yang [1 ]
Liu, Li [1 ]
Tang, Lingfeng [1 ]
Yang, Ting [2 ]
Pu, Dongyao [1 ]
Tan, Wenhao [1 ]
Zhang, Wenjie [1 ]
Liu, Shengchun [1 ]
机构
[1] Chongqing Med Univ, Affiliated Hosp 1, Dept Breast & Thyroid Surg, Chongqing 400042, Peoples R China
[2] Chongqing Med Univ, Women & Childrens Hosp, Dept Breast & Thyroid Surg, Chongqing 401120, Peoples R China
基金
中国国家自然科学基金;
关键词
EXPRESSION; DYSPLASIA; TOME-1;
D O I
10.1155/2022/4632453
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
CDCA3 is an essential regulator in cell mitosis and can regulate many physiological and pathological processes in the human body by stimulating certain proteins such as cell cycle regulatory proteins, transcription factors, and signal transduction molecules. Although several studies have shown that dysregulation of CDCA3 is a common phenomenon in human cancers, no systematic pan-cancer analysis has been performed. In this study, we comprehensively investigated the role of CDCA3 in 33 human cancer types by utilizing multiple cancer-related databases and bioinformatics analysis tools, including TCGA, GTEx, GEPIA, TIMER, STRING, Metascape, and Cytoscape. Evidence from bioinformatics databases shows that CDCA3 is overexpressed in almost all human cancer types, and its overexpression is significantly associated with survival in patients with more than ten cancer types. CDCA3 expression positively correlates with immune cell infiltration levels in multiple human cancer types. Furthermore, the results of the GSEA analysis revealed that overexpression of CDCA3 may promote the malignant progression of cancer by activating various oncogenic signaling pathways in human cancers. In conclusion, our pan-cancer analysis provides a comprehensive overview of the oncogenic role of CDCA3 in multiple human cancer types, suggesting that CDCA3 may serve as a potential therapeutic target and prognostic biomarker in multiple human cancer types.
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页数:28
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共 49 条
  • [1] Expression of CDCA3 Is a Prognostic Biomarker and Potential Therapeutic Target in Non-Small Cell Lung Cancer
    Adams, Mark N.
    Burgess, Joshua T.
    He, Yaowu
    Gately, Kathy
    Snell, Cameron
    Zhang, Shu-Dong
    Hooper, John D.
    Richard, Derek J.
    O'Byrne, Kenneth J.
    [J]. JOURNAL OF THORACIC ONCOLOGY, 2017, 12 (07) : 1071 - 1084
  • [2] Recent Advances in Theranostic Applications of Nanomaterials in Cancer
    Ahmed, Faraha
    Khan, Mohammad Ahmed
    Haider, Nafis
    Ahmad, Mohammad Zaki
    Ahmad, Javed
    [J]. CURRENT PHARMACEUTICAL DESIGN, 2022, 28 (02) : 133 - 150
  • [3] Tome-1, a trigger of mitotic entry, is degraded during G1 via the APC
    Ayad, NG
    Rankin, S
    Murakami, M
    Jebanathirajah, J
    Gygi, S
    Kirschner, MW
    [J]. CELL, 2003, 113 (01) : 101 - 113
  • [4] A novel miR-375-HOXB3-CDCA3/DNMT3B regulatory circuitry contributes to leukemogenesis in acute myeloid leukemia
    Bi, Laixi
    Zhou, Bin
    Li, Haiying
    He, Licai
    Wang, Chunjing
    Wang, Zhonggai
    Zhu, Liqing
    Chen, Mengqian
    Gao, Shenmeng
    [J]. BMC CANCER, 2018, 18
  • [5] Landscape of Microsatellite Instability Across 39 Cancer Types
    Bonneville, Russell
    Krook, Melanie A.
    Kautto, Esko A.
    Miya, Jharna
    Wing, Michele R.
    Chen, Hui-Zi
    Reeser, Julie W.
    Yu, Lianbo
    Roychowdhury, Sameek
    [J]. JCO PRECISION ONCOLOGY, 2017, 1 : 1 - 15
  • [6] Current and future cancer staging after neoadjuvant treatment for solid tumors
    Byrd, David R.
    Brierley, James D.
    Baker, Thomas P.
    Sullivan, Daniel C.
    Gress, Donna M.
    [J]. CA-A CANCER JOURNAL FOR CLINICIANS, 2021, 71 (02) : 140 - 148
  • [7] HoxB3 promotes prostate cancer cell progression by transactivating CDCA3
    Chen, Jing
    Zhu, Shimiao
    Jiang, Ning
    Shang, Zhiqun
    Quan, Changyi
    Niu, Yuanjie
    [J]. CANCER LETTERS, 2013, 330 (02) : 217 - 224
  • [8] Suppression of CDCA3 inhibits prostate cancer progression via NF-κB/cyclin D1 signaling inactivation and p21 accumulation
    Gu, Peng
    Zhang, Minhao
    Zhu, Jin
    He, Xiaoliang
    Yang, Dongrong
    [J]. ONCOLOGY REPORTS, 2022, 47 (02)
  • [9] OY-TES-1 may regulate the malignant behavior of liver cancer via NANOG, CD9, CCND2 and CDCA3: A bioinformatic analysis combine with RNAi and oligonucleotide microarray
    Hu, Qiping
    Fu, Jun
    Luo, Bin
    Huang, Miao
    Guo, Wenwen
    Lin, Yongda
    Xie, Xiaoxun
    Xiao, Shaowen
    [J]. ONCOLOGY REPORTS, 2015, 33 (04) : 1965 - 1975
  • [10] Translating bioinformatics in oncology: guilt-by-profiling analysis and identification of KIF18B and CDCA3 as novel driver genes in carcinogenesis
    Itzel, Timo
    Scholz, Peter
    Maass, Thorsten
    Krupp, Markus
    Marquardt, Jens U.
    Strand, Susanne
    Becker, Diana
    Staib, Frank
    Binder, Harald
    Roessler, Stephanie
    Wang, Xin Wei
    Thorgeirsson, Snorri
    Mueller, Martina
    Galle, Peter R.
    Teufel, Andreas
    [J]. BIOINFORMATICS, 2015, 31 (02) : 216 - 224