Arsenical-based cancer drugs

被引:330
作者
Dilda, Pierre J. [1 ]
Hogg, Philip J. [1 ]
机构
[1] Univ New S Wales, Prince Wales Hosp, Canc Res Ctr, Dept Haematol, Sydney, NSW 2052, Australia
关键词
arsenic-based cancer drugs; arsenic trioxide; organic arsenicals; clinical trials;
D O I
10.1016/j.ctrv.2007.05.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Arsenic is a semi-metal or metalloid with two bioiogically important oxidation states, As(III) and As(V). As(III), in particular, reacts with closely spaced protein thiols, forming stable cyclic dithioarsinite complexes in which both sulfur atoms are bound to arsenic. It is this reaction that is mostly responsible for arsenics cytotoxicity. Arsenic compounds have been used as medicinal. agents for many centuries for the treatment of diseases such as psoriasis, syphilis, and rheumatosis. From the 1700's until. the introduction of and use of modern chemotherapy and radiation therapy in the mid 1900's, arsenic was a mainstay in the treatment of leukemia. Concerns about the toxicity of arsenical. compounds led eventually to their abandonment for the treatment of cancer. The discovery in the 1980's that arsenic trioxide induces complete remission in a high percentage of patients with acute promyelocytic leukemia has awakened interest in this metalloid for the treatment of human disease. In particular, a new class or organoarsenicals are being trialed for the treatment of hematological. malignancies and solid tumors. In this review, we discuss the arsenical-based compounds used in the past and present for the treatment of various forms of cancer. Mechanisms of action and selectivity and acute and chronic toxicities are discussed along with the prospects of this class of molecule. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:542 / 564
页数:23
相关论文
共 237 条
[1]   Efficacy and safety results with the combination therapy of arsenic trioxide, dexamethasone, and ascorbic acid in multiple myeloma patients - A phase 2 trial [J].
Abou-Jawde, RM ;
Reed, J ;
Kelly, M ;
Walker, E ;
Andresen, S ;
Baz, R ;
Karam, MA ;
Hussein, M .
MEDICAL ONCOLOGY, 2006, 23 (02) :263-272
[2]  
Ahn WS, 2004, ONCOL REP, V12, P573
[3]   Arsenic trioxide induces apoptosis in neuroblastoma cell lines through the activation of caspase 3 in vitro [J].
Akao, Y ;
Nakagawa, Y ;
Akiyama, K .
FEBS LETTERS, 1999, 455 (1-2) :59-62
[4]  
Aklilu M., 2004, 2004 ASCO ANN M P
[5]  
[Anonymous], 1878, AM J MED SCI
[6]   Activation of Nrf2 and accumulation of ubiquitinated A170 by arsenic in osteoblasts [J].
Aono, J ;
Yanagawa, T ;
Itoh, K ;
Li, BJ ;
Yoshida, H ;
Kumagai, Y ;
Yamamoto, M ;
Ishii, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 305 (02) :271-277
[7]   Combination therapy with arsenic trioxide, all-trans retinoic acid, and gemtuzumab ozogamicin in recurrent acute promyelocytic leukemia [J].
Aribi, Ahmed ;
Kantarjian, Hagop M. ;
Estey, Elihu H. ;
Koller, Charles A. ;
Thomas, Deborah A. ;
Kornblau, Steven M. ;
Faderl, Stefan H. ;
Laddie, Nakia M. ;
Garcia-Manero, Guillermo ;
Cortes, Jorge E. .
CANCER, 2007, 109 (07) :1355-1359
[8]  
Aronson S M, 1994, R I Med, V77, P233
[9]   Arsenic trioxide exposure to ovarian carcinoma cells leads to decreased level of topoisomerase II and cytotoxicity [J].
Askar, N. ;
Cirpan, T. ;
Toprak, E. ;
Karabulut, B. ;
Selvi, N. ;
Terek, M. C. ;
Uslu, R. ;
Sanli, U. A. ;
Goker, E. .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2006, 16 (04) :1552-1556
[10]   Arsenic trioxide and ascorbic acid: synergy with potential implications for the treatment of acute myeloid leukaemia? [J].
Bachleitner-Hofmann, T ;
Gisslinger, B ;
Grumbeck, E ;
Gisslinger, H .
BRITISH JOURNAL OF HAEMATOLOGY, 2001, 112 (03) :783-786