Therapeutic potential of patupilone in epithelial ovarian cancer and future directions

被引:3
作者
Rogalska, Aneta [1 ]
Marczak, Agnieszka [1 ]
机构
[1] Univ Lodz, Fac Biol & Environm Protect, Inst Biophys, Dept Med Biophys, Pomorska14-143 St, Lodz, Poland
关键词
Combined therapy; Epothilone; Ovarian cancer; Taxane; Therapeutic strategies; EPOTHILONE-B; GENE-EXPRESSION; CELL-DEATH; IN-VITRO; BETA-TUBULIN; APOPTOSIS; PACLITAXEL; AGENTS; PATHWAY; DRUG;
D O I
10.1016/j.lfs.2018.04.058
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Ovarian cancer is the most lethal gynecologic malignancy worldwide with extremely poor patient prognosis. Elucidation of the detailed mechanisms of action of drugs targeting this cancer type is necessary to optimize treatment efficacy. Epothilones, a new class of microtubule-stabilizing anticancer drugs, show strong cytotoxic properties in vitro and in vivo and are additionally effective in taxane-resistant cells. In this report, we focus on inhibitors of microtubule depolymerization, taxanes, and the novel antimicrotubule agents, epothilones. Current knowledge regarding the effects of epothilone B on ovarian tumor cell metabolism is reviewed, along with recent advances in therapeutic strategies, such as novel agents and biologic drug combinations containing epothilone that target aberrant pathways in ovarian cancer.
引用
收藏
页码:38 / 44
页数:7
相关论文
共 66 条
[1]   Proteomics of Cancer Cell Lines Resistant to MicrotubuleStabilizing Agents [J].
Albrethsen, Jakob ;
Angeletti, Ruth H. ;
Horwitz, Susan Band ;
Yang, Chia-Ping Huang .
MOLECULAR CANCER THERAPEUTICS, 2014, 13 (01) :260-269
[2]   Inhibition of cellular efflux pumps involved in multi xenobiotic resistance (MXR) in echinoid larvae as a possible mode of action for increased ecotoxicological risk of mixtures [J].
Anselmo, Henrique M. R. ;
van den Berg, Johannes H. J. ;
Rietjens, Ivonne M. C. M. ;
Murk, AlberTinka J. .
ECOTOXICOLOGY, 2012, 21 (08) :2276-2287
[3]   Hydrogen peroxide induces apoptosis of chondrocytes; involvement of calcium ion and extracellular signal-regulated protein kinase [J].
Asada, S ;
Fukuda, K ;
Nishisaka, F ;
Matsukawa, M ;
Hamanisi, C .
INFLAMMATION RESEARCH, 2001, 50 (01) :19-23
[4]   Combinatorial strategies for the induction of immunogenic cell death [J].
Bezu, Lucillia ;
Gomes-de-Silva, Ligia C. ;
Dewitte, Heleen ;
Breckpot, Karine ;
Fucikova, Jitka ;
Spisek, Radek ;
Galluzzi, Lorenzo ;
Kepp, Oliver ;
Kroemer, Guido .
FRONTIERS IN IMMUNOLOGY, 2015, 6
[5]   Macrophage recognition of externalized phosphatidylserine and phagocytosis of apoptotic Jurkat cells - existence of a threshold [J].
Borisenko, GG ;
Matsura, T ;
Liu, SX ;
Tyurin, VA ;
Jiang, JF ;
Serinkan, FB ;
Kagan, VE .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2003, 413 (01) :41-52
[6]  
Bukowska Barbara, 2016, Asian Pac J Cancer Prev, V17, P1299
[7]   Patupilone in cancer treatment [J].
Bystricky, Branislav ;
Chau, Ian .
EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2011, 20 (01) :107-117
[8]   Stabilized Polymer Micelles for the Development of IT-147, an Epothilone D Drug-Loaded Formulation [J].
Carie, Adam ;
Sullivan, Bradford ;
Ellis, Tyler ;
Semple, J. Edward ;
Buley, Taylor ;
Costich, Tara Lee ;
Crouse, Richard ;
Bakewell, Suzanne ;
Sill, Kevin .
JOURNAL OF DRUG DELIVERY, 2016, 2016
[9]   PARP-1 cleavage fragments: signatures of cell-death proteases in neurodegeneration [J].
Chaitanya, Ganta Vijay ;
Steven, Alexander J. ;
Babu, Phanithi Prakash .
CELL COMMUNICATION AND SIGNALING, 2010, 8
[10]  
Chen JG, 2003, CANCER RES, V63, P7891