ARE THERE STILL NEW THERAPEUTIC TARGETS IN ARTERIOSCLEROSIS? LXR AND FXR

被引:0
|
作者
Martinez-Gonzalez, J. [1 ]
Badimon, L. [1 ]
机构
[1] Hosp Santa Creu & Sant Pau, CSIC, ICCC, Ctr Invest Cardiovasc, Barcelona, Spain
关键词
Arteriosclerosis; Nuclear receptors; LXR; FXR; Therapeutic targets;
D O I
10.1016/S0214-9168(06)73709-3
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
In the last few years, partly due to the use of modern techniques for differential analysis of gene expression, potential therapeutic targets for arteriosclerosis have been identified. Some of these are transcription factors that regulate metabolic pathways in the liver. Among this type are the nuclear receptors LXR (Liver X receptor) and FXR (Farnesol X receptor), although these nuclear receptors not only act in the liver but are also present in vascular cells and in monocytes/macrophages where they regulate key mechanisms for atherogenesis. These and other nuclear receptors that have recently been identified in the vascular wall constitute a promising field of investigation, as they are involved in many of the processes associated with atherogenesis. Furthermore, because they are activated by ligands, they are ideal targets for its pharmacological modification.
引用
收藏
页码:83 / 92
页数:10
相关论文
共 50 条
  • [1] FXR and PXR: Potential therapeutic targets in cholestasis
    Jonker, Johan W.
    Liddle, Christopher
    Downes, Michael
    JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2012, 130 (3-5): : 147 - 158
  • [2] Liver X Receptors (LXR) as Therapeutic Targets in Dyslipidemia
    Beltowski, Jerzy
    CARDIOVASCULAR THERAPEUTICS, 2008, 26 (04) : 297 - 316
  • [3] Coordinated Actions of FXR and LXR in Metabolism: From Pathogenesis to Pharmacological Targets for Type 2 Diabetes
    Ding, Lin
    Pang, Shuguang
    Sun, Yongmei
    Tian, Yuling
    Yu, Li
    Dang, Ningning
    INTERNATIONAL JOURNAL OF ENDOCRINOLOGY, 2014, 2014
  • [4] TRRAP as a hepatic coactivator of LXR and FXR function
    Unno, A
    Takada, I
    Takezawa, S
    Oishi, H
    Baba, A
    Shimizu, T
    Tokita, A
    Yanagisawa, J
    Kato, S
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 327 (03) : 933 - 938
  • [5] The nuclear receptors FXR and LXRα:: Potential targets for the development of drugs affecting lipid metabolism and neoplastic diseases
    Niesor, EJ
    Flach, J
    Lopes-Antoni, I
    Perez, A
    Bentzen, CL
    CURRENT PHARMACEUTICAL DESIGN, 2001, 7 (04) : 231 - 259
  • [6] LXR and FXR response in human liver cells
    Simunyu, Faith
    Parathath, Saj
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2013, 245
  • [7] Regulation of cell differentiation by FXR and LXR.
    Fujino, T.
    Kato, R.
    Hayakawa, M.
    MOLECULAR BIOLOGY OF THE CELL, 2018, 29 (26)
  • [8] The World of Pseudogenes: New Diagnostic and Therapeutic Targets in Cancers or Still Mystery Molecules?
    Stasiak, Maciej
    Kolenda, Tomasz
    Kozlowska-Maslon, Joanna
    Sobocinska, Joanna
    Poter, Paulina
    Guglas, Kacper
    Paszkowska, Anna
    Blizniak, Renata
    Teresiak, Anna
    Kazimierczak, Urszula
    Lamperska, Katarzyna
    LIFE-BASEL, 2021, 11 (12):
  • [9] MMPs as therapeutic targets - Still a viable option?
    Fingleton, Barbara
    SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2008, 19 (01) : 61 - 68
  • [10] T0901317 is a dual LXR/FXR agonist
    Houck, KA
    Borchert, KM
    Hepler, CD
    Thomas, JS
    Bramlett, KS
    Michael, LF
    Burris, TP
    MOLECULAR GENETICS AND METABOLISM, 2004, 83 (1-2) : 184 - 187