Patterns of Gene Expression Profiles Associated with Colorectal Cancer in Colorectal Mucosa by Using Machine Learning Methods

被引:8
作者
Ren, Jing Xin [1 ]
Chen, Lei [2 ]
Guo, Wei [3 ,4 ]
Feng, Kai Yan [5 ]
Cai, Yu-Dong [1 ]
Huang, Tao [6 ,7 ]
机构
[1] Shanghai Univ, Sch Life Sci, Shanghai 200444, Peoples R China
[2] Shanghai Maritime Univ, Coll Informat Engn, Shanghai 201306, Peoples R China
[3] Shanghai Jiao Tong Univ Sch Med SJTUSM, Key Lab Stem Cell Biol, Shanghai 200030, Peoples R China
[4] Chinese Acad Sci, Shanghai Inst Biol Sci SIBS, Shanghai 200030, Peoples R China
[5] Guangdong AIB Polytech Coll, Dept Comp Sci, Guangzhou 510507, Peoples R China
[6] Univ Chinese Acad Sci, Chinese Acad Sci, Shanghai Inst Nutr & Hlth, Biomed Big Data Ctr,CAS Key Lab Computat Biol, Shanghai 200031, Peoples R China
[7] Univ Chinese Acad Sci, Chinese Acad Sci, Shanghai Inst Nutr & Hlth, CAS Key Lab Tissue Microenvironm & Tumor, Shanghai 200031, Peoples R China
基金
国家重点研发计划;
关键词
Colorectal cancer; mucosa; machine learning; biomarker; gene expression; feature selection; ULCERATIVE-COLITIS; TUMOR PROGRESSION; FEATURE-SELECTION; CELL INVASION; IMMUNE-SYSTEM; HOX GENES; COLON; IDENTIFICATION; SOMATOSTATIN; S100A12;
D O I
10.2174/0113862073266300231026103844
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background Colorectal cancer (CRC) has a very high incidence and lethality rate and is one of the most dangerous cancer types. Timely diagnosis can effectively reduce the incidence of colorectal cancer. Changes in para-cancerous tissues may serve as an early signal for tumorigenesis. Comparison of the differences in gene expression between para-cancerous and normal mucosa can help in the diagnosis of CRC and understanding the mechanisms of development.Objectives This study aimed to identify specific genes at the level of gene expression, which are expressed in normal mucosa and may be predictive of CRC risk.Methods A machine learning approach was used to analyze transcriptomic data in 459 samples of normal colonic mucosal tissue from 322 CRC cases and 137 non-CRC, in which each sample contained 28,706 gene expression levels. The genes were ranked using four ranking methods based on importance estimation (LASSO, LightGBM, MCFS, and mRMR) and four classification algorithms (decision tree [DT], K-nearest neighbor [KNN], random forest [RF], and support vector machine [SVM]) were combined with incremental feature selection [IFS] methods to construct a prediction model with excellent performance.Results The top-ranked genes, namely, HOXD12, CDH1, and S100A12, were associated with tumorigenesis based on previous studies.Conclusion This study summarized four sets of quantitative classification rules based on the DT algorithm, providing clues for understanding the microenvironmental changes caused by CRC. According to the rules, the effect of CRC on normal mucosa can be determined.
引用
收藏
页码:2921 / 2934
页数:14
相关论文
共 136 条
  • [1] Molecular evolution of colorectal cancer: from multistep carcinogenesis to the big bang
    Amaro, Adriana
    Chiara, Silvana
    Pfeffer, Ulrich
    [J]. CANCER AND METASTASIS REVIEWS, 2016, 35 (01) : 63 - 74
  • [2] Cloning, overexpression, purification of bacteriocin enterocin-B and structural analysis, interaction determination of enterocin-A, B against pathogenic bacteria and human cancer cells
    Ankaiah, Dasari
    Palanichamy, Esakkiraj
    Antonyraj, Christian Bharathi
    Ayyanna, Repally
    Perumal, Venkatesh
    Ahamed, Syed Ibrahim Basheer
    Arul, Venkatesan
    [J]. INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2018, 116 : 502 - 512
  • [3] CLONING AND CHARACTERIZATION OF THE HUMAN INVASION SUPPRESSOR GENE E-CADHERIN (CDH1)
    BERX, G
    STAES, K
    VANHENGEL, J
    MOLEMANS, F
    BUSSEMAKERS, MJG
    VANBOKHOVEN, A
    VANROY, F
    [J]. GENOMICS, 1995, 26 (02) : 281 - 289
  • [4] Identification of a Developmental Gene Expression Signature, Including HOX Genes, for the Normal Human Colonic Crypt Stem Cell Niche: Overexpression of the Signature Parallels Stem Cell Overpopulation During Colon Tumorigenesis
    Bhatlekar, Seema
    Addya, Sankar
    Salunek, Moreh
    Orr, Christopher R.
    Surrey, Saul
    McKenzie, Steven
    Fields, Jeremy Z.
    Boman, Bruce M.
    [J]. STEM CELLS AND DEVELOPMENT, 2014, 23 (02) : 167 - 179
  • [5] Random forests
    Breiman, L
    [J]. MACHINE LEARNING, 2001, 45 (01) : 5 - 32
  • [6] Years of life lost as a measure of cancer burden on a national level
    Brustugun, O. T.
    Moller, B.
    Helland, A.
    [J]. BRITISH JOURNAL OF CANCER, 2014, 111 (05) : 1014 - 1020
  • [7] Identification of PRTFDC1 silencing and aberrant promoter methylation of GPR150, ITGA8 and HOXD11 in ovarian cancers
    Cai, Li-yi
    Abe, Masanobu
    Izumi, Shun-ichiro
    Imura, Masayoshi
    Yasugi, Toshiharu
    Ushijima, Toshikazu
    [J]. LIFE SCIENCES, 2007, 80 (16) : 1458 - 1465
  • [8] Casnici C, 1997, INT J IMMUNOPHARMACO, V19, P721
  • [9] Chai H, 2009, ANN CLIN LAB SCI, V39, P331
  • [10] The junctional adhesion molecule-C promotes neutrophil transendothelial migration in vitro and in vivo
    Chavakis, T
    Keiper, T
    Matz-Westphal, R
    Hersemeyer, K
    Sachs, UJ
    Nawroth, PP
    Preissner, KT
    Santoso, S
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (53) : 55602 - 55608