Aquaporin 9, a promising predictor for the cytocidal effects of arsenic trioxide in acute promyelocytic leukemia cell lines and primary blasts

被引:21
作者
Iriyama, Noriyoshi [1 ]
Yuan, Bo [2 ]
Yoshino, Yuta [2 ]
Hatta, Yoshihiro [1 ]
Horikoshi, Akira [1 ]
Aizawa, Shin [3 ]
Takeuchi, Jin [1 ]
Toyoda, Hiroo [2 ]
机构
[1] Nihon Univ, Sch Med, Itabashi Hosp, Dept Hematol & Rheumatol,Itabashi Ki, Tokyo 1738610, Japan
[2] Tokyo Univ Pharm & Life Sci, Dept Clin Mol Genet, Sch Pharm, Hachioji, Tokyo 1920392, Japan
[3] Nihon Univ, Sch Med, Dept Funct Morphol, Itabashi Hosp,Itabashi Ku, Tokyo 1738610, Japan
关键词
aquaporin; 9; acute promyelocytic leukemia; arsenic trioxide; NB4; HT93A; CHORION TROPHOBLAST CELLS; TRANS-RETINOIC ACID; RESISTANCE-ASSOCIATED PROTEIN-2; NITRIC-OXIDE SYNTHASE; APOPTOSIS INDUCTION; PROGNOSTIC-SIGNIFICANCE; EXPRESSION; SENSITIVITY; AS2O3; ALPHA;
D O I
10.3892/or.2013.2388
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A close correlation between the cytocidal effects of arsenic trioxide (ATO) and aquaporin-9 (AQP9) expression levels has been proposed, yet detailed studies are still needed to confirm this association. Thus, in the present study, the correlation between the expression levels of AQP9 and sensitivity to ATO was investigated using two acute promyelocytic leukemia (APL) cell lines, NB4 and HT93A, as well as primary APL cells from newly diagnosed and relapsed APL patients. A substantially higher sensitivity to ATO-mediated induction of apoptosis was observed in the NB4 cells when compared to that in the HT93A cells. In addition, markedly higher expression levels of AQP9, as assessed using flow cytometry, along with more intracellular arsenic accumulation, were observed in the NB4 cells. More importantly, similar to APL cell lines, the trend of expression levels of AQP9 correlated closely with the differential sensitivity to ATO-mediated induction of apoptosis in primary APL cells. In contrast, no correlation was observed between ATO sensitivity associated with AQP9 expression levels and the expression profiles of cell surface markers as well as chromosomal alterations. These results provide direct evidence that the expression levels of AQP9, rather than other biomarkers such as cell surface markers and chromosomal alterations, correlate closely with the sensitivity to ATO in both APL cell lines and primary blasts. These findings suggest that the AQP9 expression status of APL patients is a predictive marker for the successful outcome of ATO treatment, since AQP9 plays a pivotal role in various arsenite-mediated biological effects on normal and cancer cells. Moreover, flow cytometry may be a new convenient and valuable tool for analyzing the AQP9 status of APL patients compared to current methods such as western blotting.
引用
收藏
页码:2362 / 2368
页数:7
相关论文
共 37 条
[1]  
Andus T, REG IMMUNOL, V5, P11
[2]   Drug uptake and pharmacological modulation of drug sensitivity in leukemia by AQP9 [J].
Bhattacharjee, H ;
Carbrey, J ;
Rosen, BP ;
Mukhopadhyay, R .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 322 (03) :836-841
[3]   Presenting white blood cell count and kinetics of molecular remission predict prognosis in acute promyelocytic leukemia treated with all-trans retinoic acid:: Result of the randomized MRC trial [J].
Burnett, AK ;
Grimwade, D ;
Solomon, E ;
Wheatley, K ;
Goldstone, AH .
BLOOD, 1999, 93 (12) :4131-4143
[4]   Arsenic trioxide-induced apoptosis and differentiation are associated respectively with mitochondrial transmembrane potential collapse and retinoic acid signaling pathways in acute promyelocytic leukemia [J].
Cai, X ;
Shen, YL ;
Zhu, Q ;
Jia, PM ;
Yu, Y ;
Zhou, L ;
Huang, Y ;
Zhang, JW ;
Xiong, SM ;
Chen, SJ ;
Wang, ZY ;
Chen, Z ;
Chen, GQ .
LEUKEMIA, 2000, 14 (02) :262-270
[5]  
Chen GQ, 1997, BLOOD, V89, P3345
[6]  
Chen GQ, 1996, BLOOD, V88, P1052
[7]   Drug approval summaries: Arsenic trioxide, tamoxifen citrate, anastrazole, paclitaxel, bexarotene [J].
Cohen, MH ;
Hirschfeld, S ;
Honig, SF ;
Ibrahim, A ;
Johnson, JR ;
O'Leary, JJ ;
White, RM ;
Williams, GA ;
Pazdur, R .
ONCOLOGIST, 2001, 6 (01) :4-11
[8]   THE T(15-17) TRANSLOCATION OF ACUTE PROMYELOCYTIC LEUKEMIA FUSES THE RETINOIC ACID RECEPTOR-ALPHA GENE TO A NOVEL TRANSCRIBED LOCUS [J].
DETHE, H ;
CHOMIENNE, C ;
LANOTTE, M ;
DEGOS, L ;
DEJEAN, A .
NATURE, 1990, 347 (6293) :558-561
[9]  
Di Bona E, 2002, HAEMATOLOGICA, V87, P250
[10]   Arsenical-based cancer drugs [J].
Dilda, Pierre J. ;
Hogg, Philip J. .
CANCER TREATMENT REVIEWS, 2007, 33 (06) :542-564