|Table of Contents|

Analysis of differential genes and biological functions of radiosensitivity in prostate cancer:Based on GEO database

Journal Of Modern Oncology[ISSN:1672-4992/CN:61-1415/R]

Issue:
2022 06
Page:
1056-1059
Research Field:
Publishing date:

Info

Title:
Analysis of differential genes and biological functions of radiosensitivity in prostate cancer:Based on GEO database
Author(s):
HUANG WenlinXU YongQU GenyiDUAN GuangjunZHANG YulongLIU Ziwei
The Second Department of Urology,Zhuzhou Hospital Affiliated to Xiangya School of Medicine,Central South University,Hunan Zhuzhou 412007,China.
Keywords:
prostate cancerradiosensitivitybioinformatics analysis
PACS:
R737.25
DOI:
10.3969/j.issn.1672-4992.2022.06.021
Abstract:
Objective:To explore the potential relationship between differential gene expression,biological function enrichment and disease prognosis affecting the sensitivity of prostate cancer radiotherapy using bioinformatics.Methods:Retrieve and obtain data on differential gene expression of prostate cancer radiosensitivity in the GEO database (GSM3954350,GSM3954351,GSM3954352).GER2 tool was used to screen and analyze the differential genes.Enrichr database performed enrichment analysis of GO and KEGG.Cytoscape software built protein-protein interaction (PPI) networks and analyzed key genes.Results:A total of 7 041 differentially expressed genes were screened,including 3 842 high expression genes and 3 199 low expression genes.The top 20 differentially expressed genes were selected for further analysis.Their biological functions were mainly enriched in the following aspects:Nuclease activity regulation,enzyme-linked receptor protein signaling pathway,nucleotide excision repair,DNA gap filling.Cytological components were mainly located outside the cell.Molecular functions were enriched in structural molecular activity,receptor binding,serine-type peptidase activity,etc.The analysis of KEGG signaling pathway showed that the differential genes were mainly enriched in the mismatch repair pathway,non-homologous terminal binding pathway and so on.Conclusion:Through the analysis of the differential genes related to the radiosensitivity of prostate cancer,the key differential genes found in this study can help to understand the potential molecular mechanism of prostate cancer radiotherapy resistance,and can provide a theoretical basis for further improving the effectiveness of radiation therapy of prostate cancer.

References:

[1]SIEGEL REBECCA L,MILLER KIMBERLY D,JEMAL AHMEDIN.Cancer statistics,2018[J] .CA Cancer J Clin,2018,68:7-30.
[2]MOTTET N,VAN DEN BERGH RCN,BRIERS E,et al.EAU-EANM-ESTRO-ESUR-SIOG guidelines on prostate cancer[J].Eur Assoc Urol,2019,75(6):889-890.
[3]BOLLA M,DE REIJKE TM,VAN TIENHOVEN G,et al.Duraton of androgen supresson n the treatment of prostate cancer[J].New England Journal of Medicine,2009,360(24):2516.
[4]THOMPSON IM,TANGEN CM,PARADELO J.Adjuvant radiotherapy for pathological T3N0M0 prostate cancer significantly reduces risk of metastases and improves survival:Long-term follow-up of a randomized clinical trial[J].J Urol,2009,181:956-962.
[5]POLKINGHORN WR,ZELEFSKY MJ.Improving outcomes in high-risk prostate cancer with radiotherapy[J].Reports of Practical Oncology & Radiotherapy,2013,18(6):333-337.
[6]CHANG L,GRAHAM P,HAO J,et al.Emerging roles of radioresistance in prostate cancer metastasis and radiation therapy[J].Cancer & Metastasis Reviews,2014,33(2-3):469-496.
[7]RUSSO G,ZEGAR C,GIORDANO A.Advantages and limitations of microarray technology in human cancer[J].Oncogene,2003,22(42):6497-6507.
[8]SZKLARCZYK DAMIAN,FRANCESCHINI ANDREA,KUHN MICHAEL,et al.The STRING database in 2011:functional interaction networks of proteins,globally integrated and scored[J].Nuclc Acids Research,2010,39(Database issue):D561-D568.
[9]JOHANSSON SILVIA,ASTRMLENNART,SANDIN FREDRIK,et al.Hypofractionated proton boost combined with external beam radiotherapy for treatment of localized prostate cancer[J].Prostate Cancer,2012,2012:654861.
[10]PAHLAJANI NIRAJ,RUTH KAREN J,BUYYOUNOUSKI MARK K,et al.Radiotherapy doses of 80 Gy and higher are associated with lower mortality in men with Gleason score 8 to 10 prostate cancer.[J] .Int J Radiat Oncol Biol Phys,2012,82:1949-1956.
[11]BARKER HOLLY E,PAGET JAMES TE,KHAN AADIL A,et al.The tumour microenvironment after radiotherapy:mechanisms of resistance and recurrence[J] .Nat Rev Cancer,2015,15:409-425.
[12]SEIFERT M,PEITZSCH C,GORODETSKA I,et al.Network-based analysis of prostate cancer cell lines reveals novel marker gene candidates associated with radioresistance and patient relapse[J].PLoS Computational Biology,2019,15(11):e1007460.
[13]BONKHOFF H.Factors implicated in radiation therapy failure and radiosensitization of prostate cancer[J].Australasian Radiology,2012,2012(6):584.
[14]CHAISWING L,WEISS HL,JAYSWAL RD,et al.Profiles of radioresistance mechanisms in prostate cancer[J].Critical Reviews in Oncogenesis,2018,23(1-2):39.
[15]MARWITZ S,HEINBOCKEL L,SCHEUFELE S,et al.Epigenetic modifications of the VGF gene in human non-small cell lung cancer tissues pave the way towards enhanced expression[J].Clinical Epigenetics,2017,9(1):123.
[16]WANG Xiuxing,PRAGER BRIANA C,WU Qiulian,et al.Reciprocal signaling between glioblastoma stem cells and differentiated tumor cells promotes malignant progression[J].Cell Stem Cell,2018,22:514-528.

Memo

Memo:
湖南省自然科学基金(编号:2020JJ8054)
Last Update: 1900-01-01