Literature DB >> 30565747

Coexpression network analysis linked H2AFJ to chemoradiation resistance in colorectal cancer.

Xiaojie Wang1, Waleed M Ghareeb1,2, Xingrong Lu1, Ying Huang1, Shenghui Huang1, Pan Chi1.   

Abstract

Neoadjuvant chemoradiotherapy (CRT) resistance is a complex phenomenon and it remains a major problem for patients with a priori resistant tumor. Therefore, there is a strong need to investigate molecular biomarkers which may guide for treatment decision-making. In our study, weighted gene coexpression network analysis was applied to identify CRT-resistance hub modules in 12 colorectal cancer (CRC) cell lines with different CRT sensitivities from GSE20298 data set. The green module and purple module had the highest correlations with CRT resistance. Gene ontology enrichment analysis indicated that the function of these two modules focused on interferon-mediated signaling pathway, immune response, chromatin modulation, Rho GTPases activities, and regulation of apoptotic process. Then, 15 hub genes in both the coexpression and protein-protein interaction networks were selected. Among these hub genes, higher H2A histone family member J (H2AFJ) expression was independently validated in patient cohorts from two testing data sets of GSE46862 and GSE68204 to be related to CRT resistance. The receiver operating characteristic curve showed that H2AFJ could efficiently distinguish CRT-resistance cases from CRT-sensitive cases in another two testing data sets. Furthermore, meta-analysis of 12 Gene Expression Omnibus-sourced data sets showed that H2AFJ messenger RNA levels were significantly higher in CRC tissues than in normal colon tissues. High H2AFJ expression was correlated with a significant worse event- and relapse-free survival by analyzing the data from the R2: Genomics Analysis and Visualization Platform. Gene set enrichment analysis determined that the mechanism of H2AFJ-mediated CRT resistance might involve the ERK5 (MAPK7), human immunodeficiency virus Nef (HIV Nef), and inflammatory pathways. This study is the first, to the best of our knowledge, to implicate and verify H2AFJ as an effective new marker for CRT response prediction.
© 2018 Wiley Periodicals, Inc.

Entities:  

Keywords:  H2AFJ; colorectal cancer; neoadjuvant chemoradiotherapy; resistance; weighted gene coexpression network analysis

Year:  2018        PMID: 30565747     DOI: 10.1002/jcb.28319

Source DB:  PubMed          Journal:  J Cell Biochem        ISSN: 0730-2312            Impact factor:   4.429


  6 in total

1.  Identification of Key Gene Targets for Sensitizing Colorectal Cancer to Chemoradiation: an Integrative Network Analysis on Multiple Transcriptomics Data.

Authors:  Hamed Manoochehri; Akram Jalali; Hamid Tanzadehpanah; Amir Taherkhani; Massoud Saidijam
Journal:  J Gastrointest Cancer       Date:  2021-08-25

2.  A Four Gene-Based Risk Score System Associated with Chemoradiotherapy Response and Tumor Recurrence in Rectal Cancer by Co-Expression Network Analysis.

Authors:  Yanwu Sun; Yiyi Zhang; Xuejing Wu; Pan Chi
Journal:  Onco Targets Ther       Date:  2020-07-08       Impact factor: 4.147

3.  Stromal Cell Signature Associated with Response to Neoadjuvant Chemotherapy in Locally Advanced Breast Cancer.

Authors:  Maria Lucia Hirata Katayama; René Aloísio da Costa Vieira; Victor Piana Andrade; Rosimeire Aparecida Roela; Luiz Guilherme Cernaglia Aureliano Lima; Ligia Maria Kerr; Adriano Polpo de Campos; Carlos Alberto de Bragança Pereira; Pedro Adolpho de Menezes Pacheco Serio; Giselly Encinas; Simone Maistro; Matheus de Almeida Leite Petroni; Maria Mitzi Brentani; Maria Aparecida Azevedo Koike Folgueira
Journal:  Cells       Date:  2019-12-04       Impact factor: 6.600

4.  Hypermethylation and Downregulation of UTP6 Are Associated With Stemness Properties, Chemoradiotherapy Resistance, and Prognosis in Rectal Cancer: A Co-expression Network Analysis.

Authors:  Yiyi Zhang; Qiao Gao; Yong Wu; Yong Peng; Jinfu Zhuang; Yuanfeng Yang; Weizhong Jiang; Xing Liu; Guoxian Guan
Journal:  Front Cell Dev Biol       Date:  2021-08-18

5.  Histone Variant H2A.J Is Enriched in Luminal Epithelial Gland Cells.

Authors:  Christophe E Redon; Zoe Schmal; Gargi Tewary; Adèle Mangelinck; Régis Courbeyrette; Jean-Yves Thuret; Mirit I Aladjem; William M Bonner; Claudia E Rübe; Carl Mann
Journal:  Genes (Basel)       Date:  2021-10-22       Impact factor: 4.096

6.  FBXW4 Acts as a Protector of FOLFOX-Based Chemotherapy in Metastatic Colorectal Cancer Identified by Co-Expression Network Analysis.

Authors:  Yiyi Zhang; Lijun Sun; Xiaojie Wang; Yanwu Sun; Ying Chen; Meifang Xu; Pan Chi; Xingrong Lu; Zongbin Xu
Journal:  Front Genet       Date:  2020-03-11       Impact factor: 4.599

  6 in total

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