KRN5500: a novel therapeutic agent with in vitro activity against human B-cell chronic lymphocytic leukemia cells mediates cytotoxicity via the intrinsic pathway of apoptosis

被引:16
作者
Byrd, JC
Lucas, DM
Mone, AP
Kitner, JB
Drabick, JJ
Grever, MR
机构
[1] Ohio State Univ, Div Hematol Oncol, Dept Med, Columbus, OH 43210 USA
[2] Walter Reed Army Med Ctr, Div Hematol Oncol, Dept Med, Washington, DC 20307 USA
关键词
D O I
10.1182/blood-2002-08-2623
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Therapy of B-cell chronic lymphocytic leukemia (CLL) is currently palliative, emphasizing the need for identification of new therapies for this disease. KRN5500 is a novel agent that has a unique sensitivity pattern in the National Cancer Institute cell line screening panel, suggesting a unique mechanism of action. To assess its in vitro activity in CLL, we exposed peripheral mononuclear cells from CLL patients (n = 11) to varying concentrations of this agent. Viability of the CLL cells was reduced by 50% (LC50) at 4 hours, 24 hours, and 4 days at KRN5500 concentrations of 2.50 muM, 0.276 muM, and 0.139 muM, respectively. KRN5500 induced cellular injury via caspase-dependent apoptosis involving the intrinsic mitochondrial (caspase-9) initiating caspase and caspase-3 effector caspase; however, expression of the antiapoptotic mitochondrial membrane protein BcI-2 was unaffected. These data demonstrate KRN5500 has significant in vitro activity against human CLL cells, thus providing support for introduction of this agent into clinical trials for patients with CLL. (C) 2003 by The American Society of Hematology.
引用
收藏
页码:4547 / 4550
页数:4
相关论文
共 19 条
[1]  
Burger AM, 1997, CLIN CANCER RES, V3, P455
[2]   Flavopiridol induces apoptosis in chronic lymphocytic leukemia cells via activation of caspase-3 without evidence of bcl-2 modulation or dependence on functional p53 [J].
Byrd, JC ;
Shinn, C ;
Waselenko, JK ;
Fuchs, EJ ;
Lehman, TA ;
Nguyen, PL ;
Flinn, IW ;
Diehl, LF ;
Sausville, E ;
Grever, MR .
BLOOD, 1998, 92 (10) :3804-3816
[3]   Rituximab using a thrice weekly dosing schedule in B-Cell chronic lymphocytic leukemia and small lymphocytic lymphoma demonstrates clinical activity and acceptable toxicity [J].
Byrd, JC ;
Murphy, T ;
Howard, RS ;
Lucas, MS ;
Goodrich, A ;
Park, K ;
Pearson, M ;
Waselenko, JK ;
Ling, G ;
Grever, MR ;
Grillo-Lopez, AJ ;
Rosenberg, J ;
Kunkel, L ;
Flinn, IW .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (08) :2153-2164
[4]  
Byrd JC, 2000, SEMIN ONCOL, V27, P587
[5]   National Cancer Institute-sponsored Working Group guidelines for chronic lymphocytic leukemia: Revised guidelines for diagnosis and treatment [J].
Cheson, BD ;
Bennett, JM ;
Grever, M ;
Kay, N ;
Keating, MJ ;
OBrien, S ;
Rai, KR .
BLOOD, 1996, 87 (12) :4990-4997
[6]  
CLARK JW, 1998, P AN M AM SOC CLIN, V17, pA231
[7]   Cancer statistics, 2002 [J].
Jemal, A ;
Thomas, A ;
Murray, T ;
Thun, M .
CA-A CANCER JOURNAL FOR CLINICIANS, 2002, 52 (01) :23-47
[8]   Inhibitory effect of a spicamycin derivative, KRN5500, on the growth of hepatic metastasis of human colon cancer-producing tissue polypeptide antigen [J].
Kamishohara, M ;
Kawai, H ;
Sakai, T ;
Uchida, T ;
Tsuruo, T ;
Otake, N .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1996, 38 (06) :495-498
[9]   STRUCTURE-ANTITUMOR ACTIVITY RELATIONSHIP OF SEMISYNTHETIC SPICAMYCIN ANALOGS [J].
KAMISHOHARA, M ;
KAWAI, H ;
ODAGAWA, A ;
ISOE, T ;
MOCHIZUKI, J ;
UCHIDA, T ;
HAYAKAWA, Y ;
SETO, H ;
TSURUO, T ;
OTAKE, N .
JOURNAL OF ANTIBIOTICS, 1993, 46 (09) :1439-1446
[10]   ANTITUMOR-ACTIVITY OF SPM-VIII, A DERIVATIVE OF THE NUCLEOSIDE ANTIBIOTIC SPICAMYCIN, AGAINST HUMAN TUMOR XENOGRAFTS [J].
KAMISHOHARA, M ;
KAWAI, H ;
ODAGAWA, A ;
ISOE, T ;
MOCHIZUKI, JI ;
UCHIDA, T ;
HAYAKAWA, Y ;
SETO, H ;
TSURUO, T ;
OTAKE, N .
JOURNAL OF ANTIBIOTICS, 1994, 47 (11) :1305-1311