Frequent expression of the multi-drug resistance-associated protein BCRP/MXR/ABCP/ABCG2 in human tumours detected by the BXP-21 monoclonal antibody in paraffin-embedded material

被引:249
作者
Diestra, JE
Scheffer, GL
Català, I
Maleipaad, M
Schellens, JHM
Scheper, RJ
Germà-Lluch, JR
Izquierdo, MA
机构
[1] Catalan Inst Oncol, Dept Med Oncol, Barcelona 08907, Spain
[2] Catalan Inst Oncol, Lab Translat Res, Barcelona 08907, Spain
[3] Free Univ Amsterdam Hosp, Dept Pathol, NL-1081 HV Amsterdam, Netherlands
[4] Ciutat Sanitaria & Univ Bellvitge, Dept Pathol, Barcelona, Spain
[5] Netherlands Canc Inst, Div Expt Therapy, NL-1066 CX Amsterdam, Netherlands
关键词
ABCG2; ATP-binding-cassette transporters; breast cancer resistance protein; drug resistance; multi-drug resistance;
D O I
10.1002/path.1203
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Breast cancer resistance protein (BCPP/MXR/ABCP/ABCG2; hereafter ABCG2) is a member of the ATP-binding-cassette family of transporters that causes multi-drug resistance to various anticancer drugs. The expression of ABCG2 in human tumours and its potential involvement in clinical drug resistance are unknown. Recently, two monoclonal antibodies against human ABCG2 were produced, BXP-34 and BXP-21. This study describes an immunohistochemical method using BXP-21 to study ABCG2 expression in formalin-fixed, paraffin-embedded tissues. No staining was seen using BXP-34 with the same protocols. The expression of ABCG2 was then investigated in a panel of 150 untreated human solid tumours comprising 21 tumour types. Overall, ABCG2 expression was frequent. Specificity of immunohistochemistry was confirmed by the detection of a 72 kD band in western blotting. ABCG2 expression was seen in all tumour types, but it seemed more frequent in adenocarcinomas of the digestive tract, endometrium, and lung, and melanoma. Positive tumours showed membranous and cytoplasmic staining. In certain adenocarcinomas, prominent membranous staining was seen. Endothelial cells frequently displayed moderate to strong staining. ABCG2 is widely present in untreated human solid tumours and may represent a clinically relevant mechanism of drug resistance. Future studies in specific tumour types are needed to ascertain its clinical relevance. BXP-21 and the immunohistochemical protocol described here will be of value in these investigations. Copyright (C) 2002 John Wiley Sons, Ltd.
引用
收藏
页码:213 / 219
页数:7
相关论文
共 25 条
  • [1] Allikmets R, 1998, CANCER RES, V58, P5337
  • [2] Brangi M, 1999, CANCER RES, V59, P5938
  • [3] Reversal of resistance by GF120918 in cell lines expressing the ABC half-transporter, MXR
    de Bruin, M
    Miyake, K
    Litman, T
    Robey, R
    Bates, SE
    [J]. CANCER LETTERS, 1999, 146 (02) : 117 - 126
  • [4] DIESTRA JE, 2001, P AN M AM SOC CLIN, V20, pA73
  • [5] A multidrug resistance transporter from human MCF-7 breast cancer cells
    Doyle, LA
    Yang, WD
    Abruzzo, LV
    Krogmann, T
    Gao, YM
    Rishi, AK
    Ross, DD
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (26) : 15665 - 15670
  • [6] GRANT CE, 1994, CANCER RES, V54, P357
  • [7] IZQUIERDO MA, 1995, JNCI-J NATL CANCER I, V87, P1230
  • [8] Role of breast cancer resistance protein in the bioavailability and fetal penetration of topotecan
    Jonker, JW
    Smit, JW
    Brinkhuis, RF
    Maliepaard, M
    Beijnen, JH
    Schellens, JHM
    Schinkel, AH
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2000, 92 (20): : 1651 - 1656
  • [9] Expression of multidrug resistance-related transporters in human breast carcinoma
    Kanzaki, A
    Toi, M
    Nakayama, K
    Bando, H
    Mutoh, M
    Uchida, T
    Fukumoto, M
    Takebayashi, Y
    [J]. JAPANESE JOURNAL OF CANCER RESEARCH, 2001, 92 (04): : 452 - 458
  • [10] Enhanced transport of anticancer agents and leukotriene C4 by the human canalicular multispecific organic anion transporter (cMOAT/MRP2)
    Kawabe, T
    Chen, ZS
    Wada, M
    Uchiumi, T
    Ono, M
    Akiyama, S
    Kuwano, M
    [J]. FEBS LETTERS, 1999, 456 (02): : 327 - 331