Breast Cancer Resistance Protein and P-Glycoprotein in Brain Cancer: Two Gatekeepers Team Up

被引:207
作者
Agarwal, Sagar [2 ,3 ]
Hartz, Anika M. S. [1 ,3 ]
Elmquist, William F. [2 ,3 ]
Bauer, Bjoern [1 ,3 ]
机构
[1] Univ Minnesota, Coll Pharm, Dept Pharmaceut Sci, Duluth, MN 55812 USA
[2] Univ Minnesota, Coll Pharm, Dept Pharmaceut, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Brain Barriers Res Ctr, Minneapolis, MN USA
基金
美国国家卫生研究院;
关键词
BCRP; P-gp; brain cancer; glioblastoma; multidrug resistance; blood-brain barrier; regulation; inhibition; REVERSES MULTIDRUG-RESISTANCE; NERVOUS-SYSTEM PENETRATION; BINDING CASSETTE TRANSPORTERS; SIDE POPULATION PHENOTYPE; SUBFAMILY-B MEMBER-1; IN-VIVO REVERSAL; BLOOD-BRAIN; ABC TRANSPORTERS; FUNCTIONAL EXPRESSION; MEMBRANE TRANSPORTER;
D O I
10.2174/138161211797440186
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Brain cancer is a devastating disease. Despite extensive research, treatment of brain tumors has been largely ineffective and the diagnosis of brain cancer remains uniformly fatal. Failure of brain cancer treatment may be in part due to limitations in drug delivery, influenced by the ABC drug efflux transporters P-gp and BCRP at the blood-brain and blood-tumor barriers, in brain tumor cells, as well as in brain tumor stem-like cells. P-gp and BCRP limit various anti-cancer drugs from entering the brain and tumor tissues, thus rendering chemotherapy ineffective. To overcome this obstacle, two strategies - targeting transporter regulation and direct transporter inhibition - have been proposed. In this review, we focus on these strategies. We first introduce the latest findings on signaling pathways that could potentially be targeted to down-regulate P-gp and BCRP expression and/or transport activity. We then highlight in detail the new paradigm of P-gp and BCRP working as a "cooperative team of gatekeepers" at the blood-brain barrier, discuss its ramifications for brain cancer therapy, and summarize the latest findings on dual P-gp/BCRP inhibitors. Finally, we provide a brief summary with conclusions and outline the perspectives for future research endeavors in this field.
引用
收藏
页码:2793 / 2802
页数:10
相关论文
共 114 条
  • [1] Agarwal S, 2010, J PHARM EXP THER
  • [2] Delivery of molecularly targeted therapy to malignant glioma, a disease of the whole brain
    Agarwal, Sagar
    Sane, Ramola
    Oberoi, Rajneet
    Ohlfest, John R.
    Elmquist, William F.
    [J]. EXPERT REVIEWS IN MOLECULAR MEDICINE, 2011, 13 : e17
  • [3] Distribution of Gefitinib to the Brain Is Limited by P-glycoprotein (ABCB1) and Breast Cancer Resistance Protein (ABCG2)-Mediated Active Efflux
    Agarwal, Sagar
    Sane, Ramola
    Gallardo, Jose L.
    Ohlfest, John R.
    Elmquist, William F.
    [J]. JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2010, 334 (01) : 147 - 155
  • [4] Allen JD, 2002, MOL CANCER THER, V1, P417
  • [5] Allen JD, 1999, CANCER RES, V59, P4237
  • [6] [Anonymous], 2010, CBTRUS STAT REP PRIM
  • [7] [Anonymous], 2010, CANCER
  • [8] Inhibitors of multidrug resistance to antitumor agents (MDR)
    Avendaño, C
    Menéndez, JC
    [J]. CURRENT MEDICINAL CHEMISTRY, 2002, 9 (02) : 159 - 193
  • [9] ABC transporters and the blood-brain barrier
    Begley, DJ
    [J]. CURRENT PHARMACEUTICAL DESIGN, 2004, 10 (12) : 1295 - 1312
  • [10] Influence of breast cancer resistance protein (Abcg2) and p-glycoprotein (Abcb1a) on the transport of imatinib mesylate (Gleevec®) across the mouse blood-brain barrier
    Bihorel, Sebastien
    Camenisch, Gian
    Lemaire, Michel
    Scherrmann, Jean-Michel
    [J]. JOURNAL OF NEUROCHEMISTRY, 2007, 102 (06) : 1749 - 1757