Identification of A Gene Set Associated with Colorectal Cancer in Microarray Data Using The Entropy Method

被引:6
作者
Bahreini, Fatemeh [1 ]
Soltanian, Ali Reza [2 ,3 ]
机构
[1] Hamadan Univ Med Sci, Sch Med, Dept Mol Med & Genet, Hamadan, Iran
[2] Hamadan Univ Med Sci, Sch Publ Hlth, Modeling Noncommunicable Dis Res Ctr, Hamadan, Iran
[3] Hamadan Univ Med Sci, Sch Publ Hlth, Dept Biostat & Epidemiol, POB 6517838736, Hamadan, Iran
关键词
Cancer; Colorectal; Microarray; Statistical Model; FOCAL ADHESION KINASE; COLON-CANCER; EXPRESSION; CELLS; ADENOCARCINOMA; PLASMINOGEN; PROFILES; DISEASE; GROWTH;
D O I
10.22074/cellj.2019.5688
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objective: We sought to apply Shannon's entropy to determine colorectal cancer genes in a microarray dataset. Materials and Methods: In the retrospective study, 36 samples were analysed, 18 colorectal carcinoma and 18 paired normal tissue samples. After identification of the gene fold-changes, we used the entropy theory to identify an effective gene set. These genes were subsequently categorised into homogenous clusters. Results: We assessed 36 tissue samples. The entropy theory was used to select a set of 29 genes from 3128 genes that had fold-changes greater than one, which provided the most information on colorectal cancer. This study shows that all genes fall into a cluster, except for the R08183 gene. Conclusion: This study has identified several genes associated with colon cancer using the entropy method, which were not detected by custom methods. Therefore, we suggest that the entropy theory should be used to identify genes associated with cancers in a microarray dataset.
引用
收藏
页码:569 / 575
页数:7
相关论文
共 32 条
  • [1] Colorectal cancer prevention in Europe: Burden of disease and status of screening programs
    Altobelli, E.
    Lattanzi, A.
    Paduano, R.
    Varassi, G.
    di Orio, F.
    [J]. PREVENTIVE MEDICINE, 2014, 62 : 132 - 141
  • [2] Identification of MST1/STK4 and SULF1 Proteins as Autoantibody Targets for the Diagnosis of Colorectal Cancer by Using Phage Microarrays
    Babel, Ingrid
    Barderas, Rodrigo
    Diaz-Uriarte, Ramon
    Moreno, Victor
    Suarez, Adolfo
    Jesus Fernandez-Acenero, Maria
    Salazar, Ramon
    Capella, Gabriel
    Ignacio Casal, J.
    [J]. MOLECULAR & CELLULAR PROTEOMICS, 2011, 10 (03)
  • [3] Bahreini F, 2017, CANC GENETICS PSYCHO, P1127
  • [4] Recruitment of a basal polyadenylation factor by the upstream sequence element of the human lamin B2 polyadenylation signal
    Brackenridge, S
    Proudfoot, NJ
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (08) : 2660 - 2669
  • [5] Functional classification analysis of somatically mutated genes in human breast and colorectal cancers
    Chittenden, Thomas W.
    Howe, Eleanor A.
    Culhane, Aedin C.
    Sultana, Razvan
    Taylor, Jennifer M.
    Holmes, Chris
    Quackenbush, John
    [J]. GENOMICS, 2008, 91 (06) : 508 - 511
  • [6] DEBRUIN PAF, 1988, CANCER RES, V48, P4520
  • [7] From Plasminogen to Plasmin: Role of Plasminogen Receptors in Human Cancer
    Didiasova, Miroslava
    Wujak, Lukasz
    Wygrecka, Malgorzata
    Zakrzewicz, Dariusz
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2014, 15 (11) : 21229 - 21252
  • [8] Cancer incidence and mortality worldwide: Sources, methods and major patterns in GLOBOCAN 2012
    Ferlay, Jacques
    Soerjomataram, Isabelle
    Dikshit, Rajesh
    Eser, Sultan
    Mathers, Colin
    Rebelo, Marise
    Parkin, Donald Maxwell
    Forman, David
    Bray, Freddie
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2015, 136 (05) : E359 - E386
  • [9] Golubovskaya VM, 2009, HISTOL HISTOPATHOL, V24, P503, DOI 10.14670/HH-24.503
  • [10] The CXCL7/CXCR1/2 Axis Is a Key Driver in the Growth of Clear Cell Renal Cell Carcinoma
    Grepin, Renaud
    Guyot, Melanie
    Giuliano, Sandy
    Boncompagni, Marina
    Ambrosetti, Damien
    Chamorey, Emmanuel
    Scoazec, Jean-Yves
    Negrier, Sylvie
    Simonnet, Helene
    Pages, Gilles
    [J]. CANCER RESEARCH, 2014, 74 (03) : 873 - 883