基于生物信息学探究CXCL3在结肠腺癌中的临床价值
Exploration of the Clinical Value of CXCL3 in Colon Adenocarcinoma Based on Bioinformatics
DOI: 10.12677/acm.2024.1472015, PDF,    科研立项经费支持
作者: 陶俊安, 宋政烨, 张 云*, 胡慧娴*:皖南医学院医学工程学教研室,安徽 芜湖
关键词: CXCL3结肠腺癌临床价值CXCL3 Colon Adenocarcinoma Clinical Value
摘要: 目的:通过生物信息学方法分析趋化因子CXCL3在结肠腺癌(Colon adenocircinoma, COAD)中的临床价值。方法:从TCGA数据库中提取出趋化因子CXCL3在COAD患者组织中的基因表达谱,通过R语言进行数据整理,并在COAD患者肿瘤组织与癌旁正常组织中进行差异表达分析,再对CXCL3进行相关性分析。为了进一步探讨CXCL3在COAD中可能参与的分子机制,通过DAVID平台展开CXCL3的功能富集分析,并呈现可视化结果,再结合临床病理因素分析,最后通过GEO外部数据库进行验证。结果:经分析发现CXCL3及其共表达基因集在肿瘤组织中高表达(p < 0.05),且对患者生存有不良的潜在影响。结论:CXCL3基因结肠腺癌患者中高表达,对患者的预后有一定影响。
Abstract: Objective: To analyze the clinical value of chemokine CXCL3 in colon adenocarcinoma (COAD) by bioinformatics methods. Methods: The gene expression profile of chemokine CXCL3 in the tissues of COAD patients was extracted from the TCGA database, and the data were collated by R language, and the differential expression analysis was carried out in the tumor tissues of COAD patients and adjacent normal tissues, and then the correlation analysis of CXCL3 was carried out. To further explore the possible molecular mechanisms of CXCL3 involvement in COAD, the functional enrichment analysis of CXCL3 was expanded by the DAVID platform and the visual results were presented. After that, it was combined with clinic pathological factor analysis. Finally, it is verified through the GEO external database. Results: The analysis showed that CXCL3 and its co-expressed gene sets were highly expressed in tumor tissues (p < 0.05), and had a potential adverse effect on the survival of patients. Conclusion: The high expression of CXCL3 gene in patients with colon adenocarcinoma has a certain impact on the prognosis of patients.
文章引用:陶俊安, 宋政烨, 张云, 胡慧娴. 基于生物信息学探究CXCL3在结肠腺癌中的临床价值[J]. 临床医学进展, 2024, 14(7): 305-312. https://doi.org/10.12677/acm.2024.1472015

参考文献

[1] Xi, Y. and Xu, P. (2021) Global Colorectal Cancer Burden in 2020 and Projections to 2040. Translational Oncology, 14, Article 101174. [Google Scholar] [CrossRef] [PubMed]
[2] 郭士祥. 结直肠癌的发病因素及高危人群的预防对策[J]. 求医问药(下半月), 2012, 10(6): 239-240.
[3] 邢洁, 李鹏, 张澍田. 中国结直肠癌防治现状[J]. 中华结直肠疾病电子杂志, 2013, 2(6): 288-291.
[4] Harris, R., Sawaya, G.F., Moyer, V.A., et al. (2011) Reconsidering the Criteria for Evaluating Proposed Screening Programs: Reflections from 4 Current and Former Members of the U.S. Preventive Services Task Force. Epidemiologic Reviews, 33, 20-35. [Google Scholar] [CrossRef] [PubMed]
[5] Dobrow, M.J., Hagens, V., Chafe, R., et al. (2018) Consolidated Principles for Screening Based on a Systematic Review and Consensus Process. Canadian Medical Association Journal, 190, E422-E429. [Google Scholar] [CrossRef] [PubMed]
[6] Dekker, E. and Rex, D.K. (2018) Advances in CRC Prevention: Screening and Surveillance. Gastroenterology, 154, 1970-1984. [Google Scholar] [CrossRef] [PubMed]
[7] Fitzpatrick-Lewis, D., Ali, M.U., Warren, R., Kenny, M., Sherifali, D. and Raina, P. (2016) Screening for Colorectal Cancer: A Systematic Review and Meta-Analysis. Clinical Colorectal Cancer, 15, 298-313. [Google Scholar] [CrossRef] [PubMed]
[8] 杜晓帆, 沙如拉, 李文新. 趋化因子在结肠癌中的研究进展[J]. 内蒙古医学杂志, 2023, 55(10): 1194-1196.
[9] Miller, M.C. and Mayo, K.H. (2017) Chemokines from a Structural Perspective. International Journal of Molecular Sciences, 18, Article 2088. [Google Scholar] [CrossRef] [PubMed]
[10] Zhang, L., Zhang, L.X., Li, H., et al. (2016) CXCL3 Contributes to CD133+ CSCs Maintenance and Forms a Positive Feedback Regulation Loop with CD133 in HCC via Erk1/2 Phosphorylation. Scientific Reports, 6, Article No. 27426. [Google Scholar] [CrossRef] [PubMed]
[11] 田雨. 趋化因子CXCL3在结直肠癌诊断与预后判断中的相关研究[D]: [硕士学位论文]. 无锡: 江南大学, 2021.
[12] 龚艺贞. 结肠腺癌的发病机制探索及趋化因子CXC亚家族基因在结肠腺癌中的临床应用价值及机制研究[D]: [博士学位论文]. 南宁: 广西医科大学, 2020.
[13] 刘娇. 基于生物信息学途径研究结直肠癌中CXCL的表达及其对预后的影响[D]: [硕士学位论文]. 大连: 大连医科大学, 2023.
[14] 程瑶, 牟文博, 辛华. 趋化因子CXCL3与肿瘤的相关性研究进展[J]. 化工时刊, 2020, 34(4): 26-28.
[15] Liao, W.T., Overman, M.J., et al. (2019) KRAS-IRF2 Axis Drives Immune Suppression and Immune Therapy Resistance in Colorectal Cancer. Cancer Cell, 35, 559-572.E7. [Google Scholar] [CrossRef] [PubMed]
[16] Wu, T., Yang, W., Sun, A., Wei, Z. and Lin, Q. (2022) The Role of CXC Chemokines in Cancer Progression. Cancers, 15, Article 167. [Google Scholar] [CrossRef] [PubMed]
[17] Xiong, Y., You, W., Wang, R., Peng, L. and Fu, Z. (2017) Prediction and Validation of Hub Genes Associated with Colorectal Cancer by Integrating PPI Network and Gene Expression Data. BioMed Research International, 2017, Article ID: 2421459. [Google Scholar] [CrossRef] [PubMed]
[18] Ruan, G.T., Gong, Y.Z., Liao, X.W., Wang, S., Huang, W., Wang, X.K., Zhu, G.Z., Liao, C. and Gao, F. (2019) Diagnostic and Prognostic Values of C-X-C Motif Chemokine Ligand 3 in Patients with Colon Cancer. Oncology Reports, 42, 1996-2008. [Google Scholar] [CrossRef] [PubMed]
[19] 李文斌. IL-17A/G-CSF axis对于免疫细胞的调控及其在结肠炎相关结直肠癌发生发展中的作用研究[D]: [博士学位论文]. 北京: 北京协和医学院, 2013.
[20] Cui, C., Zhang, R., Gu, F., Pei, Y., Sun, L., Huang, Y., Niu, G. and Li, J. (2022) Plasma CXCL3 Levels Are Associated with Tumor Progression and an Unfavorable Colorectal Cancer Prognosis. Journal of Immunology Research, 2022, Article ID: 1336509. [Google Scholar] [CrossRef] [PubMed]
[21] Ershov, P., Poyarkov, S., Konstantinova, Y., Veselovsky, E. and Makarova, A. (2023) Transcriptomic Signatures in Colorectal Cancer Progression. Current Molecular Medicine, 23, 239-249. [Google Scholar] [CrossRef] [PubMed]