Advanced Search
Volume 42 Issue 6
Jun.  2020
Turn off MathJax
Article Contents
Peng XU, Bing WANG, Gang FANG, Xiaolong SHI, Wenbin LIU. Analysis of Breast Cancer Subtypes Prediction Based on Alternative Splicing Disorders[J]. Journal of Electronics & Information Technology, 2020, 42(6): 1348-1354. doi: 10.11999/JEIT190871
Citation: Peng XU, Bing WANG, Gang FANG, Xiaolong SHI, Wenbin LIU. Analysis of Breast Cancer Subtypes Prediction Based on Alternative Splicing Disorders[J]. Journal of Electronics & Information Technology, 2020, 42(6): 1348-1354. doi: 10.11999/JEIT190871

Analysis of Breast Cancer Subtypes Prediction Based on Alternative Splicing Disorders

doi: 10.11999/JEIT190871
Funds:  The National Key R&D Program of China (2019YFA0706402), The National Natural Science Foundation of China (61572367, 61573017, 61972107, 61972109)
  • Received Date: 2019-11-01
  • Rev Recd Date: 2020-05-10
  • Available Online: 2020-05-23
  • Publish Date: 2020-06-22
  • Alternative splicing is closely related to the occurrence and development of a variety of complex diseases, the emergence of various diseases including tumors is often accompanied by the occurrence of alternative splicing disorders. The existing analysis of breast cancer subtypes is mainly based on single splicing isoform, and the difference in the overall distribution of splicing isoforms caused by alternative splicing disorders among subtypes is not considered. Therefore, a prediction method of breast cancer subtypes based on alternative splicing disorders is proposed, which mainly uses Jensen-Shannon(JS) divergence to find genes with large differences in alternative splicing disorders between subtypes, then constructes Back Propagation(BP) neural network model to classify breast cancer subtypes. The results show that this method could not only effectively detect tumor heterogeneous molecules, but also had good identification results in the classification of breast cancer subtypes, with an average F1-score of 0.89, and could provide personalized drug recommendations for patients with breast cancer subtypes. This study will effectively promote the development of breast cancer subtypes based on alternative splicing disorders.
  • loading
  • ULE J and BLENCOWE B J. Alternative splicing regulatory networks: Functions, mechanisms, and evolution[J]. Molecular Cell, 2019, 76(2): 329–345. doi: 10.1016/j.molcel.2019.09.017
    PAN Qun, SHAI O, LEE L J, et al. Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing[J]. Nature Genetics, 2008, 40(12): 1413–1415. doi: 10.1038/ng.259
    HIRSCH C L, AKDEMIR Z C, WANG Li, et al. Myc and SAGA rewire an alternative splicing network during early somatic cell reprogramming[J]. Genes & Development, 2015, 29(8): 803–816. doi: 10.1101/gad.255109.114
    VENABLES J P. Aberrant and alternative splicing in cancer[J]. Cancer Research, 2004, 64(21): 7647–7654. doi: 10.1158/0008-5472.CAN-04-1910
    NARYSHKIN N A, WEETALL M, DAKKA A, et al. SMN2 splicing modifiers improve motor function and longevity in mice with spinal muscular atrophy[J]. Science, 2014, 345(6197): 688–693. doi: 10.1126/science.1250127
    GILLINGS A S, BALMANNO K, WIGGINS C M, et al. Apoptosis and autophagy: BIM as a mediator of tumour cell death in response to oncogene-targeted therapeutics[J]. The FEBS Journal, 2009, 276(21): 6050–6062. doi: 10.1111/j.1742-4658.2009.07329.x
    MENON R and OMENN G S. Proteomic characterization of novel alternative splice variant proteins in human epidermal growth factor receptor 2/neu-induced breast cancers[J]. Cancer Research, 2010, 70(9): 3440–3449. doi: 10.1158/0008-5472.CAN-09-2631
    DAVID C J and MANLEY J L. Alternative pre-mRNA splicing regulation in cancer: Pathways and programs unhinged[J]. Genes & Development, 2010, 24(21): 2343–2364. doi: 10.1101/gad.1973010
    BLACK D L. Mechanisms of alternative pre-messenger RNA splicing[J]. Annual Review of Biochemistry, 2003, 72: 291–336. doi: 10.1146/annurev.biochem.72.121801.161720
    ALMENDRO V, MARUSYK A, and POLYAK K. Cellular heterogeneity and molecular evolution in cancer[J]. Annual Review of Pathology: Mechanisms of Disease, 2013, 8: 277–302. doi: 10.1146/annurev-pathol-020712-163923
    PAL S, BI Yingtao, MACYSZYN L, et al. Isoform-level gene signature improves prognostic stratification and accurately classifies glioblastoma subtypes[J]. Nucleic Acids Research, 2014, 42(8): e64. doi: 10.1093/nar/gku121
    PEROU C M, SØRLIE T, EISEN M B, et al. Molecular portraits of human breast tumours[J]. Nature, 2000, 406(6797): 747–752. doi: 10.1038/35021093
    ZHAO Wei, HOADLEY K A, PARKER J S, et al. Identification of mRNA isoform switching in breast cancer[J]. BMC Genomics, 2016, 17: 181. doi: 10.1186/s12864-016-2521-9
    SØRLIE T, TIBSHIRANI R, PARKER J, et al. Repeated observation of breast tumor subtypes in independent gene expression data sets[J]. Proceedings of the National Academy of Sciences of the United States of America, 2003, 100(14): 8418–8423. doi: 10.1073/pnas.0932692100
    STRICKER T P, BROWN C D, BANDLAMUDI C, et al. Robust stratification of breast cancer subtypes using differential patterns of transcript isoform expression[J]. PLoS Genetics, 2017, 13(3): e1006589. doi: 10.1371/journal.pgen.1006589
    曾勇, 舒欢, 胡江平, 等. 基于BP神经网络的自适应伪最近邻分类[J]. 电子与信息学报, 2016, 38(11): 2774–2779. doi: 10.11999/JEIT160133

    ZENG Yong, SHU Huan, HU Jiangping, et al. Adaptive pseudo nearest neighbor classification based on BP neural network[J]. Journal of Electronics &Information Technology, 2016, 38(11): 2774–2779. doi: 10.11999/JEIT160133
    AKRAM M, IQBAL M, DANIYAL M, et al. Awareness and current knowledge of breast cancer[J]. Biological Research, 2017, 50: 33. doi: 10.1186/s40659-017-0140-9
    刘文斌, 陈杰, 方刚, 等. 基于药物互作网络的协同与拮抗预测研究[J]. 电子与信息学报, 2020, 42(6): 1428–1435. doi: 10.11999/JEIT190867

    LIU Wenbin, CHEN Jie, FANG Gang, et al. Prediction of drug synergy and antagonism based on drug-drug interaction network[J]. Journal of Electronics &Information Technology, 2020, 42(6): 1428–1435. doi: 10.11999/JEIT190867
    CALIFANO A and ALVAREZ M J. The recurrent architecture of tumour initiation, progression and drug sensitivity[J]. Nature Reviews Cancer, 2017, 17(2): 116–130. doi: 10.1038/nrc.2016.124
    KIMURA S. AT-9283, a small-molecule multi-targeted kinase inhibitor for the potential treatment of cancer[J]. Current Opinion in Investigational Drugs, 2010, 11(12): 1442–1449.
    ZHOU Donghu, JIANG Ying, and HE Fuchu. Alternative splicing in lifeomics era[J]. Scientia Sinica Vitae, 2015, 45(12): 1177–1184. doi: 10.1360/N052015-00135
  • 加载中

Catalog

    通讯作者: 陈斌, bchen63@163.com
    • 1. 

      沈阳化工大学材料科学与工程学院 沈阳 110142

    1. 本站搜索
    2. 百度学术搜索
    3. 万方数据库搜索
    4. CNKI搜索

    Figures(5)  / Tables(3)

    Article Metrics

    Article views (1701) PDF downloads(71) Cited by()
    Proportional views
    Related

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return