Epigenetic therapy in urologic cancers: an update on clinical trials

被引:27
作者
Faleiro, Ines [1 ,2 ,3 ]
Leao, Ricardo [4 ,5 ]
Binnie, Alexandra [1 ,2 ,3 ]
de Mello, Ramon Andrade [1 ,2 ,3 ]
Maia, Ana-Teresa [1 ,2 ,3 ]
Castelo-Branco, Pedro [1 ,2 ,3 ]
机构
[1] Univ Algarve, Dept Biomed Sci & Med, Regenerat Med Program, Faro, Portugal
[2] Univ Algarve, Ctr Biomed Res, Faro, Portugal
[3] Algarve Biomed Ctr, Campus Gambelas,Edificio 2, Faro, Portugal
[4] Univ Toronto, Princess Margaret Canc Ctr, Dept Surg, Div Urol, Toronto, ON, Canada
[5] Univ Coimbra, Coimbra Univ Hosp, Fac Med, Ctr EPE,Renal Transplantat & Urol Serv, Coimbra, Portugal
关键词
epigenetic therapy; urologic cancers; clinical trials; HISTONE DEACETYLASE INHIBITOR; RANDOMIZED PHASE-II; RENAL-CELL CARCINOMA; PROSTATE-CANCER; BLADDER-CANCER; ANTISENSE OLIGONUCLEOTIDE; PROMOTER METHYLATION; MOLECULAR-MECHANISMS; DEMETHYLATING AGENT; ANDROGEN RECEPTOR;
D O I
10.18632/oncotarget.14226
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epigenetic dysregulation is one of many factors that contribute to cancer development and progression. Numerous epigenetic alterations have been identified in urologic cancers including histone modifications, DNA methylation changes, and microRNA expression. Since these changes are reversible, efforts are being made to develop epigenetic drugs that restore the normal epigenetic patterns of cells, and many clinical trials are already underway to test their clinical potential. In this review we analyze multiple clinical trials (n=51) that test the efficacy of these drugs in patients with urologic cancers. The most frequently used epigenetic drugs were histone deacetylase inhibitors followed by antisense oligonucleotides, DNA methyltransferase inhibitors and histone demethylase inhibitors, the last of which are only being tested in prostate cancer. In more than 50% of the clinical trials considered, epigenetic drugs were used as part of combination therapy, which achieved the best results. The epigenetic regulation of some cancers is still matter of research but will undoubtedly open a window to new therapeutic approaches in the era of personalized medicine. The future of therapy for urological malignancies is likely to include multidrug regimens in which epigenetic modifying drugs will play an important role.
引用
收藏
页码:12484 / 12500
页数:17
相关论文
共 113 条
  • [1] MG98, a Second-Generation DNMT1 Inhibitor, in the Treatment of Advanced Renal Cell Carcinoma
    Amato, Robert J.
    Stephenson, Joe
    Hotte, Sebastien
    Nemunaitis, John
    Belanger, Karl
    Reid, Gregory
    Martell, Robert E.
    [J]. CANCER INVESTIGATION, 2012, 30 (05) : 415 - 421
  • [2] [Anonymous], N ENGL J MED
  • [3] [Anonymous], 2014, MANAGEMENT CASTRATIO
  • [4] [Anonymous], 2014, ANN ONCOL
  • [5] [Anonymous], CANCER
  • [6] [Anonymous], EPIGENOMICS
  • [7] [Anonymous], EUR J CANC S
  • [8] Regulation of chromatin by histone modifications
    Bannister, Andrew J.
    Kouzarides, Tony
    [J]. CELL RESEARCH, 2011, 21 (03) : 381 - 395
  • [9] Signaling pathways in renal cell carcinoma
    Banumathy, Gowrishankar
    Cairns, Paul
    [J]. CANCER BIOLOGY & THERAPY, 2010, 10 (07) : 658 - 664
  • [10] DNA methylation and gene silencing in cancer
    Baylin S.B.
    [J]. Nature Clinical Practice Oncology, 2005, 2 (Suppl 1): : S4 - S11