Expression of ATP-binding cassette transporter in human salivary ducts

被引:20
作者
Uematsu, T [1 ]
Yamaoka, M [1 ]
Doto, R [1 ]
Tanaka, H [1 ]
Matsuura, T [1 ]
Furusawa, K [1 ]
机构
[1] Matsumoto Dent Univ, Dept Oral & Maxillofacial Surg, Sch Dent, Nagano 3990781, Japan
关键词
P-glcoprotein; MRP; 1; 2/cMOAT; LRP; salivary gland; normal tissue;
D O I
10.1016/S0003-9969(02)00159-0
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
P-glycoprotein expression has been observed in normal tissues as well as malignant tumours; and thus does not appear to be induced by anticancer drugs. Knowledge of the distribution of ATP-binding cassette (ABC) transporters other than P-glycoprotein in normal salivary tissue is essential for understanding the physiological secretion or excretion of potentially toxic substances. Here the expression of ABC transporters was studied immunohistochemically in normal salivary gland tissue from nine patients. In striated duct cells, staining was strong for P-glycoprotein, multidrug resistance-associated protein (MRP) 1, MRP 2/canalicular multispecific organic anion transporter (cMOAT), and lung resistance-related protein (LRP). The staining intensity of acinar and intercalated duct cells for MRP 1 expression was distinct from that for MRP2/cMOAT, but was similar to that for P-glycoprotein. LRP was observed as particles between the nuclear and luminal membranes in the cytoplasm of intercalated duct cells. The expression of ABC transporters suggests that numerous transporters other than those studied might be isolated from normal salivary tissues. These observations indicate that these ABC transporters may not arise from any previous contact with anticancer drugs but are expressed physiologically. The achieved drug resistance as well as the physiological secretory function of ABC transporters could contribute to the responsiveness to chemotherapy of malignant salivary tumours. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:87 / 90
页数:4
相关论文
共 19 条
  • [1] Interaction of vault particles with estrogen receptor in the MCF-7 breast cancer cell
    Abbondanza, C
    Rossi, V
    Roscigno, A
    Gallo, L
    Belsito, A
    Piluso, G
    Medici, N
    Nigro, V
    Molinari, AM
    Moncharmont, B
    Puca, GA
    [J]. JOURNAL OF CELL BIOLOGY, 1998, 141 (06) : 1301 - 1310
  • [2] SERUM BIOAVAILABILITY AND TISSUE METABOLISM OF TESTOSTERONE AND ESTRADIOL IN RAT SALIVARY-GLAND
    CEFALU, WT
    PARDRIDGE, WM
    CHAUDHURI, G
    JUDD, HL
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1986, 63 (01) : 20 - 28
  • [3] CHUGANI DC, 1993, J CELL SCI, V106, P23
  • [4] EXPRESSION OF A MULTIDRUG-RESISTANCE GENE IN HUMAN-TUMORS AND TISSUES
    FOJO, AT
    UEDA, K
    SLAMON, DJ
    POPLACK, DG
    GOTTESMAN, MM
    PASTAN, I
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (01) : 265 - 269
  • [5] HAIT NW, 1996, DRUG RESISTANCE, P1
  • [6] Characterization of the sea urchin major vault protein: A possible role for vault ribonucleoprotein particles in nucleocytoplasmic transport
    Hamill, DR
    Suprenant, KA
    [J]. DEVELOPMENTAL BIOLOGY, 1997, 190 (01) : 117 - 128
  • [7] Identification of the apical membrane-targeting signal of the multidrug resistance-associated protein 2 (MRP2/cMOAT)
    Harris, MJ
    Kuwano, M
    Webb, M
    Board, PG
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (24) : 20876 - 20881
  • [8] The major vault protein (MVP100) is contained in cholinergic nerve terminals of electric ray electric organ
    Herrmann, C
    Volknandt, W
    Wittich, B
    Kellner, R
    Zimmermann, H
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (23) : 13908 - 13915
  • [9] Keppler D, 1997, BIOL CHEM, V378, P787
  • [10] Structure of the vault, a ubiquitous cellular component
    Kong, LB
    Siva, AC
    Rome, LH
    Stewart, PL
    [J]. STRUCTURE WITH FOLDING & DESIGN, 1999, 7 (04): : 371 - 379