Role of the CBX Molecular Family in Lung Adenocarcinoma Tumorigenesis and Immune Infiltration

被引:7
作者
Zhang, Chun [1 ]
Chang, Lisha [2 ]
Yao, Yizhen [3 ]
Chao, Ce [4 ]
Ge, Zhongchun [5 ]
Fan, Chengfeng [1 ]
Yu, Hualin [6 ]
Wang, Bin [4 ]
Yang, Jingsong [1 ]
机构
[1] Nanjing Med Univ, Dept Oncol, Nanjing First Hosp, Nanjing, Peoples R China
[2] Nanjing Med Univ, Dept Oncol, Affiliated Hosp 2, Nanjing, Peoples R China
[3] Nanjing First Hosp, Dept Resp Med, Nanjing Yuhua Hosp, Yuhua Branch, Nanjing, Peoples R China
[4] Soochow Univ, Dept Cardiothorac Surg, Affiliated Hosp 3, Changzhou, Jiangsu, Peoples R China
[5] Peoples Hosp Xuyi, Dept Cardiol, Xuyi, Peoples R China
[6] Nantong Univ, Nantong Third Peoples Hosp, Dept Radiotherapy, Nantong, Peoples R China
基金
中国国家自然科学基金;
关键词
lung adenocarcinoma; CBX molecular family; immune infiltration; tumorigenesis; prognosis; CELL-CYCLE CONTROL; TUMOR MICROENVIRONMENT; GENE-EXPRESSION; CANCER; PROGRESSION; RESPONSES; SURVIVAL; LNCRNAS;
D O I
10.3389/fgene.2021.771062
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: The members of the Chromobox (CBX) family are important epigenetic regulatory molecules with critical biological roles in many tumors. However, no study has analyzed or verified their role in lung adenocarcinoma (LUAD).Methods: UALCAN and Oncomine databases were used to analyze CBX expression in LUAD, and the cBioPortal database was used to analyze CBX genetic variations. The Kaplan-Meier plotter and UALCAN databases were used to identify molecules with prognostic value. Gene Ontology pathway, receiver operating characteristic curves, and tumor-infiltrating immune cell analyses were used to clarify the biological function of the CBX hub molecules. Paired tumor samples and lung adenocarcinoma cell lines were collected for molecular functional assays to validate the results of the bioinformatics analysis.Results: CBX3/5 may have a cancer-promoting effect and its expression is associated with a poor patient prognosis, while CBX7 shows an opposite trend. CBX3/5/7 can regulate signaling pathways, regulate tumor immune cell infiltration, and has diagnostic value. Molecular biology experiments show that CBX3/5 is highly expressed in LUAD patients; in vitro it promotes the proliferation and migration of the LUAD cell line and can regulate the expression of the corresponding cytokines. CBX7 has opposite effects.Conclusion: Our bioinformatics analysis and subsequent experimental verification confirmed the CBX family members acted as hub signaling molecules in LUAD. The results provide new potential targets for the diagnosis and treatment of this cancer.
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页数:15
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共 44 条
  • [1] HP1γ Promotes Lung Adenocarcinoma by Downregulating the Transcription-Repressive Regulators NCOR2 and ZBTB7A
    Alam, Hunain
    Li, Na
    Dhar, Shilpa S.
    Wu, Sarah J.
    Lv, Jie
    Chen, Kaifu
    Flores, Elsa R.
    Baseler, Laura
    Lee, Min Gyu
    [J]. CANCER RESEARCH, 2018, 78 (14) : 3834 - 3848
  • [2] UALCAN: A Portal for Facilitating Tumor Subgroup Gene Expression and Survival Analyses
    Chandrashekar, Darshan S.
    Bashel, Bhuwan
    Balasubramanya, Sai Akshaya Hodigere
    Creighton, Chad J.
    Ponce-Rodriguez, Israel
    Chakravarthi, Balabhadrapatruni V. S. K.
    Varambally, Sooryanarayana
    [J]. NEOPLASIA, 2017, 19 (08): : 649 - 658
  • [3] Cancer Statistics in China, 2015
    Chen, Wanqing
    Zheng, Rongshou
    Baade, Peter D.
    Zhang, Siwei
    Zeng, Hongmei
    Bray, Freddie
    Jemal, Ahmedin
    Yu, Xue Qin
    He, Jie
    [J]. CA-A CANCER JOURNAL FOR CLINICIANS, 2016, 66 (02) : 115 - 132
  • [4] Cytokines in the Treatment of Cancer
    Conlon, Kevin C.
    Miljkovic, Milos D.
    Waldmann, Thomas A.
    [J]. JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 2019, 39 (01) : 6 - 21
  • [5] Identification of Potential Crucial Genes and Key Pathways in Breast Cancer Using Bioinformatic Analysis
    Deng, Jun-Li
    Xu, Yun-hua
    Wang, Guo
    [J]. FRONTIERS IN GENETICS, 2019, 10
  • [6] Antitumor Responses in the Absence of Toxicity in Solid Tumors by Targeting B7-H3 via Chimeric Antigen Receptor T Cells
    Du, Hongwei
    Hirabayashi, Koichi
    Ahn, Sarah
    Kren, Nancy Porterfield
    Montgomery, Stephanie Ann
    Wang, Xinhui
    Tiruthani, Karthik
    Mirlekar, Bhalchandra
    Michaud, Daniel
    Greene, Kevin
    Herrera, Silvia Gabriela
    Xu, Yang
    Sun, Chuang
    Chen, Yuhui
    Ma, Xingcong
    Ferrone, Cristina Rosa
    Pylayeva-Gupta, Yuliya
    Yeh, Jen Jen
    Liu, Rihe
    Savoldo, Barbara
    Ferrone, Soldano
    Dotti, Gianpietro
    [J]. CANCER CELL, 2019, 35 (02) : 221 - +
  • [7] Immune and Inflammatory Cells in Thyroid Cancer Microenvironment
    Ferrari, Silvia Martina
    Fallahi, Poupak
    Galdiero, Maria Rosaria
    Ruffilli, Ilaria
    Elia, Giusy
    Ragusa, Francesca
    Paparo, Sabrina Rosaria
    Patrizio, Armando
    Mazzi, Valeria
    Varricchi, Gilda
    Marone, Gianni
    Antonelli, Alessandro
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (18)
  • [8] Integrative Analysis of Complex Cancer Genomics and Clinical Profiles Using the cBioPortal
    Gao, Jianjiong
    Aksoy, Buelent Arman
    Dogrusoz, Ugur
    Dresdner, Gideon
    Gross, Benjamin
    Sumer, S. Onur
    Sun, Yichao
    Jacobsen, Anders
    Sinha, Rileen
    Larsson, Erik
    Cerami, Ethan
    Sander, Chris
    Schultz, Nikolaus
    [J]. SCIENCE SIGNALING, 2013, 6 (269) : pl1
  • [9] Melanoma-derived factors alter the maturation and activation of differentiated tissue-resident dendritic cells
    Hargadon, Kristian M.
    Bishop, Johnathan D.
    Brandt, John P.
    Hand, Zachary C.
    Ararso, Yonathan T.
    Forrest, Osric A.
    [J]. IMMUNOLOGY AND CELL BIOLOGY, 2016, 94 (01) : 24 - 38
  • [10] Lung cancer: current therapies and new targeted treatments
    Hirsch, Fred R.
    Scagliotti, Giorgio V.
    Mulshine, James L.
    Kwon, Regina
    Curran, Walter J.
    Wu, Yi-Long
    Paz-Ares, Luis
    [J]. LANCET, 2017, 389 (10066) : 299 - 311