Statistical analysis of differential gene expression profile for colon cancer

被引:0
作者
Lodhi, Sharad S. [1 ,5 ]
Farmer, Rohit [2 ]
Singh, Atul Kumar [3 ]
Wadhwa, Meenu [4 ]
Jaiswal, Yogesh K. [5 ]
Wadhwa, Gulshan [1 ]
机构
[1] Minist Sci & Technol, Dept Biotechnol, New Delhi 110003, India
[2] Sam Higginbottom Ist Agr Technol & Sci, Jacob Sch Biotechnol & Bioengn, Dept Computat Biol & Bioinformat, Allahabad 211007, Uttar Pradesh, India
[3] Indian Inst Technol, Dept Text Technol, New Delhi 110016, India
[4] Kendriya Vidyalaya, New Delhi 110095, India
[5] Jiwaji Univ, Sch Studies Biochem, Gwalior 474011, India
来源
INDIAN JOURNAL OF BIOTECHNOLOGY | 2012年 / 11卷 / 04期
关键词
Colorectal cancer; DNA micro array; EST; Naive Bayes Classifier Algorithm; Pearson's correlation distance; BONE MORPHOGENETIC PROTEIN; HUMAN COLORECTAL-CANCER; MICROSATELLITE INSTABILITY; CENTROMERE PROTEIN; GLYCOPROTEIN MAG; PROXIMAL COLON; CENP-B; TISSUE; VASOPRESSIN; MICROARRAYS;
D O I
暂无
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
To analyze differentially expressed genes in colon cancer, we compared expression profiles of colorectal cancer cells from normal colonic cells using data of DNA microarray consisting of 6584 human genes. Each probe set on the array consisted of EST (expressed sequence tag) sequence of 20 feature pairs of 25 bp sequence. The data set comprised of 61 samples, divided into two groups of 40 samples for tumor cells (Group 1) and 21 samples for normal cells (Group 2). In order to do background adjustments for the negative expression values, the data was transformed into log base 2 and estimation of missing values was performed by K-nearest neighbor method, followed by normalization using 'minimum mean ratio' among arrays. The basic statistics used for the significance analysis was J5 test, which was computed for each probe and for each contrast with a threshold value of 4.0 and mean as the measure of central tendency. The differentially expressed genes were expressed at high frequency in tumour samples. The Naive. Bayes Classifier Algorithm was used to test defined classification of samples of genes. Correlation distance was measured with the help of Pearson's correlation distance. On the basis of J5 test scores, top 5 upregulated genes, viz., vasopressin-neurophysin 2-copeptin preproprotein, cytochrome, P450 2A7 isoform, major centromere autoantigen B, myelin associated glycoprotein and bone morphogenetic protein 1 isoform 3 precursor, were selected for further analysis. The above said genes have not yet been reported to be differentially overexpressed in colon cancer cells, while their overexpression was reported in other cancers, such as, lung and breast cancer, etc. These genes can be used for prediction and analyses of the gene products, which will help in designing new diagnostic and treatment strategies for the colon cancer.
引用
收藏
页码:396 / 403
页数:8
相关论文
共 31 条
  • [1] Broad patterns of gene expression revealed by clustering analysis of tumor and normal colon tissues probed by oligonucleotide arrays
    Alon, U
    Barkai, N
    Notterman, DA
    Gish, K
    Ybarra, S
    Mack, D
    Levine, AJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (12) : 6745 - 6750
  • [2] AUGENLICHT LH, 1987, CANCER RES, V47, P6017
  • [3] PATTERNS OF GENE-EXPRESSION THAT CHARACTERIZE THE COLONIC MUCOSA IN PATIENTS AT GENETIC RISK FOR COLONIC-CANCER
    AUGENLICHT, LH
    TAYLOR, J
    ANDERSON, L
    LIPKIN, M
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (08) : 3286 - 3289
  • [4] CENP-B specific anti-centromere autoantibodies heralding small-cell lung cancer - A case study and review of the literature
    Briasoulis, Evangelos
    Kamposioras, Konstantinos
    Tzovaras, Vasilis
    Pafitanis, George
    Kostoula, Angeliki
    Mavridis, Anestis
    Pavlidis, Nicholas
    [J]. LUNG CANCER, 2008, 60 (02) : 302 - 306
  • [5] Loss of imprinting in normal tissue of colorectal cancer patients with microsatellite instability
    Cui, HM
    Horon, IL
    Ohlsson, R
    Hamilton, SR
    Feinberg, AP
    [J]. NATURE MEDICINE, 1998, 4 (11) : 1276 - 1280
  • [6] Metastatic transcriptional pattern revealed by gene expression profiling in primary colorectal carcinoma
    D'Arrigo, A
    Belluco, C
    Ambrosi, A
    Digito, M
    Esposito, G
    Bertola, A
    Fabris, M
    Nofrate, V
    Mammano, E
    Leon, A
    Nitti, D
    Lise, M
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2005, 115 (02) : 256 - 262
  • [7] DELATTRE O, 1989, LANCET, V2, P353
  • [8] A GENETIC MODEL FOR COLORECTAL TUMORIGENESIS
    FEARON, ER
    VOGELSTEIN, B
    [J]. CELL, 1990, 61 (05) : 759 - 767
  • [9] Dukes B colorectal cancer - Distinct genetic categories and clinical outcome based on proximal or distal tumor location
    Gervaz, P
    Bouzourene, H
    Cerottini, JP
    Chaubert, P
    Benhattar, J
    Secic, M
    Wexner, S
    Givel, JC
    Belin, B
    [J]. DISEASES OF THE COLON & RECTUM, 2001, 44 (03) : 364 - 372
  • [10] Colorectal Cancer-Specific Cytochrome P450 2W1: Intracellular Localization, Glycosylation, and Catalytic Activity
    Gomez, Alvin
    Nekvindova, Jana
    Travica, Sandra
    Lee, Mi-Young
    Johansson, Inger
    Edler, David
    Mkrtchian, Souren
    Ingelman-Sundberg, Magnus
    [J]. MOLECULAR PHARMACOLOGY, 2010, 78 (06) : 1004 - 1011