Nasal mucosal gene expression in patients with allergic rhinitis with and without nasal polyps

被引:59
作者
Fritz, SB
Terrell, JE
Conner, ER
Kukowska-Latallo, JF
Baker, JR
机构
[1] Univ Michigan, Sch Med, Ctr Biol Nanotechnol, Div Clin Immunol & Allergy,Med Ctr, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Med Ctr, Dept Otolaryngol, Ann Arbor, MI 48103 USA
关键词
nasal polyps; allergic rhinitis; gene expression; gene-chip array; quantitative PCR;
D O I
10.1016/j.jaci.2003.09.042
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Nasal polyps are a common problem that is difficult to diagnose and treat, in part because the cause of nasal polyposis is unknown. Although information on the pathogenesis of polyposis is lacking, there are reports suggesting that a genetic predisposition underlies this disorder. Objective: We sought to better understand the basis of nasal polyposis associated with allergic rhinitis. We hypothesize that the expression of unique genes is associated with the nasal polyposis phenotype. Methods: We examined 12,000 human genes transcribed in the nasal mucosa of patients with allergic rhinitis with and without nasal polyps. Biopsy specimens of the mucosa of patients with and without polyps were obtained after the patients refrained from the use of topical or systemic steroid therapy for 2 weeks. Results: Thirty-four genes were differentially expressed between the patient groups, including those for inflammatory molecules and putative growth factors. The greatest differential expression identified by the array analysis was for a group of genes associated with neoplasia, including mammaglobin, a gene transcribed 12-fold higher in patients with polyps compared with control patients with rhinitis alone. Quantitative RT-PCR confirmed this differential expression and documented that the number of mammaglobin mRNA copies is actually 64-fold greater in tissues of patients with polyps versus control patients. The specificity of mammaglobin protein expression was evaluated by means of immunohistochemistry, which showed specific staining in nasal polyp mucosal goblet cells only in patients with polyps. Conclusion: These data suggest that nasal polyposis involves deregulated cell growth, using gene activation in some ways similar to a neoplasm. In addition, mammaglobin, a gene of unknown function associated with breast neoplasia, might be related to polyp growth.
引用
收藏
页码:1057 / 1063
页数:7
相关论文
共 35 条
[1]   Overexpression of allograft inflammatory factor-1 promotes proliferation of vascular smooth muscle cells by cell cycle deregulation [J].
Autieri, MV ;
Carbone, CM .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2001, 21 (09) :1421-1426
[2]   Mast cell tryptase stimulates the synthesis of type I collagen in human lung fibroblasts [J].
Cairns, JA ;
Walls, AF .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (06) :1313-1321
[3]  
Carter D, 2003, CLIN CANCER RES, V9, P749
[4]   ALLELE SHARING ON CHROMOSOME-11Q13 IN SIBS WITH ASTHMA AND ATOPY [J].
COLLEE, JM ;
TENKATE, LP ;
DEVRIES, HG ;
KLIPHUIS, JW ;
BOUMAN, K ;
SCHEFFER, H ;
GERRITSEN, J .
LANCET, 1993, 342 (8876) :936-936
[5]  
Diamandis EP, 2002, CLIN CHEM, V48, P1198
[6]   Allelic association of gene markers on chromosomes 5q and 11q with atopy and bronchial hyperresponsiveness [J].
Doull, IJM ;
Lawrence, S ;
Watson, M ;
Begishvili, T ;
Beasley, RW ;
Lampe, F ;
Holgate, ST ;
Morton, NE .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 153 (04) :1280-1284
[7]   CLINICAL PROFILE AND RECURRENCE OF NASAL POLYPS [J].
DRAKELEE, AB ;
LOWE, D ;
SWANSTON, A ;
GRACE, A .
JOURNAL OF LARYNGOLOGY AND OTOLOGY, 1984, 98 (08) :783-793
[8]   Mammaglobin, a breast-specific gene, and its utility as a marker for breast cancer [J].
Fleming, TP ;
Watson, MA .
UTEROGLOBIN/CLARA CELL PROTEIN FAMILY, 2000, 923 :78-89
[9]   PURIFICATION AND DISTRIBUTION OF A MAJOR PROTEIN IN RAT PROSTATE THAT BINDS ESTRAMUSTINE, A NITROGEN-MUSTARD DERIVATIVE OF ESTRADIOL-17-BETA [J].
FORSGREN, B ;
BJORK, P ;
CARLSTROM, K ;
GUSTAFSSON, JA ;
POUSETTE, A ;
HOGBERG, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (07) :3149-3153
[10]   Hereditary factor for nasal polyps [J].
Greisner, WA ;
Settipane, GA .
ALLERGY AND ASTHMA PROCEEDINGS, 1996, 17 (05) :283-286