Arsenic trioxide in hematological malignancies: The new discovery of an ancient drug

被引:30
作者
Bonati, A.
Rizzoli, V.
Lunghi, P.
机构
[1] Univ Parma, Dept Clin Sci, I-43100 Parma, Italy
[2] Univ Hosp Parma, Unit Hematol & Bone Marrow Transplantat, Parma, Italy
关键词
Arsenic Trioxide; acute promyelocytic leukemia; acute myelogenous leukemia; multiple myeloma; myelodisplastic syndrome; MAP kinase inhibitor; MEK-ERK kinase; p73; pathway; p53; p53AIP1;
D O I
10.2174/138920106779116829
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Currently, Arsenic Trioxide (ATO) is considered the treatment of choice for patients with relapsed acute promyelocytic leukemia (APL). Recently, a durable remission with minimal toxicity by single agent ATO or ATO + ATRA in newly diagnosed APL was reported by different groups. These regimens have minimal toxicity and can be administered on an outpatient basis after remission induction, thus they could become a real, less toxic and more economic option to ATRA + anthracyclines in particular in low risk APL, or in patients that cannot undergo chemotherapy because of age or comorbid conditions and in patients that refuse chemotherapy. Significantly, these therapies are a successful attempt to cure a tumoral disease without chemotherapy. The results of clinical trials of ATO administration as single agent in multiple myeloma (MM) and myelodisplastic syndromes (MDS) were encouraging and showed clinical effects but they were not close to APL success. On the contrary, results of clinical trials to treat non-APL acute myeloid leukemia (AML) were disappointing. We suggest that a combination therapy with drugs targeting specific pro-survival molecules or capable to enhance pro-apoptotic pathways may lead to an improvement of ATO efficacy against hematological malignancies, in particular AML. Our pre-clinical studies showed that ATO is capable to induce cell death in acute leukemia cells but the apoptotic function is limited since it can induce also a mechanism of cell defense by activating pro-survival molecules such as MEK-ERK, Bcl-xL, Bcl-2. By combining ATO with specific MEK inhibitors, we demonstrated that the block of MEK-ERK phosphorylation, the induction of Bad de-phosphorylation, and activation of p53AIP1 apoptotic pathway interrupt the pro-survival mechanisms of ATO and kill the leukemic cells by apoptotic synergism. Our results provide an experimental basis for combined or sequential treatment with MEK inhibitors and ATO in AML. The renaissance of ATO as a drug in moderne medicine may be considered, together with ATRA success, a victory of empirical analysis, that had (and has) great impact on Chinese culture.
引用
收藏
页码:397 / 405
页数:9
相关论文
共 62 条
[1]   Arsenic trioxide in multiple myeloma: Rationale and future directions [J].
Anderson, KC ;
Boise, LH ;
Louie, R ;
Waxman, S .
CANCER JOURNAL, 2002, 8 (01) :12-25
[2]   Oral arsenic trioxide in the treatment of relapsed acute promyelocytic leukemia [J].
Au, WY ;
Kumana, CR ;
Kou, M ;
Mak, R ;
Chan, GCF ;
Lam, CW ;
Kwong, YL .
BLOOD, 2003, 102 (01) :407-408
[3]  
Bahlis NJ, 2002, CLIN CANCER RES, V8, P3658
[4]   Requirement for the PI3K/Akt pathway in MEK1-mediated growth and prevention of apoptosis: identification of an Achilles heel in leukemia [J].
Blalock, WL ;
Navolanic, PM ;
Steelman, LS ;
Shelton, JG ;
Moye, PW ;
Lee, JT ;
Franklin, RA ;
Mirza, A ;
McMahon, M ;
White, MK ;
McCubrey, JA .
LEUKEMIA, 2003, 17 (06) :1058-1067
[5]   Efficacy of melphalan, arsenic trioxide, and ascorbic acid combination therapy (MAC) in relapsed and refractory multiple myeloma [J].
Borad, MJ ;
Swift, R ;
Berenson, JR .
LEUKEMIA, 2005, 19 (01) :154-156
[6]  
Chen GQ, 1997, BLOOD, V89, P3345
[7]   DNA damage-dependent acetylation of p73 dictates the selective activation of apoptotic target genes [J].
Costanzo, A ;
Merlo, P ;
Pediconi, N ;
Fulco, M ;
Sartorelli, V ;
Cole, PA ;
Fontemaggi, G ;
Fanciulli, M ;
Schiltz, L ;
Blandino, G ;
Balsano, C ;
Levrero, M .
MOLECULAR CELL, 2002, 9 (01) :175-186
[8]   Malignant cells can be sensitized to undergo growth inhibition and apoptosis by arsenic trioxide through modulation of the glutathione redox system [J].
Dai, J ;
Weinberg, RS ;
Waxman, S ;
Jing, YK .
BLOOD, 1999, 93 (01) :268-277
[9]   Combined treatment with the checkpoint abrogator UCN-01 and MEK1/2 inhibitors potently induces apoptosis in drug-sensitive and -resistant myeloma cells through an IL-6-independent mechanism [J].
Dai, Y ;
Landowski, TH ;
Rosen, ST ;
Dent, P ;
Grant, S .
BLOOD, 2002, 100 (09) :3333-3343
[10]   Trolox selectively enhances arsenic-mediated oxidative stress and apoptosis in APL and other malignant cell fines [J].
Diaz, Z ;
Colombo, M ;
Mann, KK ;
Su, HX ;
Smith, KN ;
Bohle, DS ;
Schipper, HM ;
Miller, WH .
BLOOD, 2005, 105 (03) :1237-1245