DNA minor groove binders: Back in the groove

被引:92
作者
Cai, Xuemei [2 ]
Gray, Phillip J., Jr. [1 ]
Von Hoff, Daniel D. [3 ]
机构
[1] Johns Hopkins Univ, Sch Med, Baltimore, MD 21231 USA
[2] Harvard Univ, Sch Med, Boston, MA 02215 USA
[3] Translat Genom Res Inst, Phoenix, AZ 85004 USA
关键词
Minor groove; Trabectidin; Irofulven; Brostallicin; Alkylators; ADVANCED SOLID TUMORS; SOFT-TISSUE SARCOMA; PHASE-I; ANTITUMOR-ACTIVITY; ALKYLATING AGENT; CANCER-CELLS; BROSTALLICIN PNU-166196; ANTINEOPLASTIC ACTIVITY; SEQUENCE SPECIFICITY; INTRAVENOUS-INFUSION;
D O I
10.1016/j.ctrv.2009.02.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
With recent approval of the minor groove binding agent trabectidin in Europe for the treatment of patients with soft tissue sarcomas, there has been renewed interest in minor groove binders. Though previously considered to be without clinical value due to their initial significant toxicities, new minor groove binders are emerging which are challenging that perception. Toxicities in the most recently completed and ongoing trials have been easily manageable. These agents have demonstrable anti-tumor activity against a wide variety of tumor types including leukemias, sarcomas, melanomas, breast and ovarian cancers. Applying these agents according to a particular tumor's context of vulnerability might reveal previously unconsidered applications for this diverse class of agents. This review provides a look at how minor groove binding agents have progressed from the lab through the clinic with particular emphasis on identifying the contexts of vulnerabilities of patient tumors which increase the effectiveness of these drugs. (C) 2009 Elsevier Ltd. All rights reserved
引用
收藏
页码:437 / 450
页数:14
相关论文
共 98 条
[71]  
Reddy BSP, 2001, CURR MED CHEM, V8, P475
[72]  
Rossi R, 1996, ANTICANCER RES, V16, P3779
[73]  
Sabatino MA, 2003, CLIN CANCER RES, V9, P5402
[74]   ADDITIONAL ANTITUMOR ECTEINASCIDINS FROM A CARIBBEAN TUNICATE - CRYSTAL-STRUCTURES AND ACTIVITIES INVIVO [J].
SAKAI, R ;
RINEHART, KL ;
GUAN, Y ;
WANG, AHJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (23) :11456-11460
[75]   A phase I study of bizelesin, a highly potent and selective DNA-interactive agent, in patients with advanced solid malignancies [J].
Schwartz, GH ;
Patnaik, A ;
Hammond, LA ;
Rizzo, J ;
Berg, K ;
Von Hoff, DD ;
Rowinsky, EK .
ANNALS OF ONCOLOGY, 2003, 14 (05) :775-782
[76]   PHASE-I STUDY OF THE NOVEL DISTAMYCIN DERIVATIVE TALLIMUSTINE (FCE-24517) [J].
SESSA, C ;
PAGANI, O ;
ZURLO, MG ;
DEJONG, J ;
HOFMANN, C ;
LASSUS, M ;
MARRARI, P ;
BENEDETTI, MS ;
CAVALLI, E .
ANNALS OF ONCOLOGY, 1994, 5 (10) :901-907
[77]   PHASE-I STUDY OF ADOZELESIN (U-73,975) IN PATIENTS WITH SOLID TUMORS [J].
SHAMDAS, GJ ;
ALBERTS, DS ;
MODIANO, M ;
WIGGINS, C ;
POWER, J ;
KASUNIC, DA ;
ELFRING, GL ;
EARHART, RH .
ANTI-CANCER DRUGS, 1994, 5 (01) :10-14
[78]   A phase II pilot study of KW-2189 in patients with advanced renal cell carcinoma [J].
Small, EJ ;
Figlin, R ;
Petrylak, D ;
Vaughn, DJ ;
Sartor, O ;
Horak, I ;
Pincus, R ;
Kremer, A ;
Bowden, C .
INVESTIGATIONAL NEW DRUGS, 2000, 18 (02) :193-197
[79]   SYNERGISTIC AND ADDITIVE COMBINATIONS OF SEVERAL ANTITUMOR DRUGS AND OTHER AGENTS WITH THE POTENT ALKYLATING AGENT ADOZELESIN [J].
SMITH, KS ;
FOLZ, BA ;
ADAMS, EG ;
BHUYAN, BK .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1995, 35 (06) :471-482
[80]   ANTITUMOR-ACTIVITY OF FCE-26644 A NEW GROWTH-FACTOR COMPLEXING MOLECULE [J].
SOLA, F ;
FARAO, M ;
PESENTI, E ;
MARSIGLIO, A ;
MONGELLI, N ;
GRANDI, M .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1995, 36 (03) :217-222