Differential gene expression profiles of normal human parotid and submandibular glands

被引:16
作者
Sun, Q-F [1 ,2 ]
Sun, Q-H [3 ]
Du, J. [1 ,2 ]
Wang, S. [1 ,2 ]
机构
[1] Capital Med Univ, Sch Stomatol, Salivary Gland Dis Ctr, Beijing 100050, Peoples R China
[2] Capital Med Univ, Sch Stomatol, Mol Lab Gene Therapy, Beijing 100050, Peoples R China
[3] Beijing Inst Radiat Med, Dept Immunol, Beijing, Peoples R China
关键词
salivary glands; microarray; tumor-associated genes; mucin-associated genes;
D O I
10.1111/j.1601-0825.2007.01408.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
BACKGROUND: Parotid and submandibular glands have different properties including characteristics of the secreted saliva and tumor incidences. The differences in properties of parotid and submandibular glands are not clear from a genetic viewpoint. OBJECTIVE: To study differential gene expression profiles between normal human parotid and submandibular glands. MATERIALS AND METHODS: Three pairs of normal parotid and submandibular glands were obtained. RNA was extracted from these samples. After reverse transcription, the cDNA was in vitro-transcribed to produce biotin-labeled cRNA. The purified biotin-labeled cRNA samples were hybridized to microarray chips. RESULTS: Among the 54 675 tested transcripts, 47 transcripts were upregulated at least twofold in the parotid gland compared with the submandibular gland, including tumor-associated genes (pleiotrophin, WNT5A, ABCC1) and transport-associated genes (SLCO1A2, SLC13A5, KCNJ15). Ninety-eight transcripts were upregulated at least twofold in the submandibular gland compared with the parotid gland, including the chloride channel CFTR and mucin-associated genes that belong to the starch and sucrose metabolism pathway (GalNAc-T4, GalNAc-T7 and GalNAc-T13). Quantitative real-time reverse transcriptase-polymerase chain reaction (RT-PCR) analysis of nine differentially expressed genes confirmed the microarray results. CONCLUSION: This study revealed the different gene expression profiles of normal human parotid and submandibular glands, providing a genetic basis for their differing properties.
引用
收藏
页码:500 / 509
页数:10
相关论文
共 30 条
  • [1] FatiGO:: a web tool for finding significant associations of Gene Ontology terms with groups of genes
    Al-Shahrour, F
    Díaz-Uriarte, R
    Dopazo, J
    [J]. BIOINFORMATICS, 2004, 20 (04) : 578 - 580
  • [2] Expression of membrane-bound mucins (MUC1 and MUC4) and secreted mucins (MUC2, MUC5AC, MUCH, MUC6 and MUC7) in mucoepidermoid carcinomas of salivary glands
    Alos, L
    Lujan, B
    Castillo, M
    Nadal, A
    Carreras, M
    Caballero, M
    de Bolos, C
    Cardesa, A
    [J]. AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2005, 29 (06) : 806 - 813
  • [3] EVALUATION OF STIMULATED PAROTID-SALIVA FLOW-RATE IN DIFFERENT AGE-GROUPS
    BAUM, BJ
    [J]. JOURNAL OF DENTAL RESEARCH, 1981, 60 (07) : 1292 - 1296
  • [4] Wnt-5a gene expression in malignant human neuroblasts
    Blanc, E
    Goldschneider, D
    Douc-Rasy, S
    Bénard, J
    Raguénez, G
    [J]. CANCER LETTERS, 2005, 228 (1-2) : 117 - 123
  • [5] BOBEK LA, 1993, J BIOL CHEM, V268, P20563
  • [6] PLEIOTROPHIN TRANSFORMS NIH 3T3 CELLS AND INDUCES TUMORS IN NUDE-MICE
    CHAUHAN, AK
    LI, YS
    DEUEL, TF
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (02) : 679 - 682
  • [7] OVEREXPRESSION OF A TRANSPORTER GENE IN A MULTIDRUG-RESISTANT HUMAN LUNG-CANCER CELL-LINE
    COLE, SPC
    BHARDWAJ, G
    GERLACH, JH
    MACKIE, JE
    GRANT, CE
    ALMQUIST, KC
    STEWART, AJ
    KURZ, EU
    DUNCAN, AMV
    DEELEY, RG
    [J]. SCIENCE, 1992, 258 (5088) : 1650 - 1654
  • [8] Mutations in components of the Wnt signaling pathway in adenoid cystic carcinoma
    Daa, T
    Kashima, K
    Kaku, N
    Suzuki, M
    Yokoyama, S
    [J]. MODERN PATHOLOGY, 2004, 17 (12) : 1475 - 1482
  • [9] DAVID: Database for annotation, visualization, and integrated discovery
    Dennis, G
    Sherman, BT
    Hosack, DA
    Yang, J
    Gao, W
    Lane, HC
    Lempicki, RA
    [J]. GENOME BIOLOGY, 2003, 4 (09)
  • [10] A new inward rectifier potassium channel gene (KCNJ15) localized on chromosome 21 in the Down syndrome chromosome region 1 (DCR1)
    Gosset, P
    Ghezala, GA
    Korn, B
    Yaspo, ML
    Poutska, A
    Lehrach, H
    Sinet, PM
    Creau, N
    [J]. GENOMICS, 1997, 44 (02) : 237 - 241