Discovery and Development of Topoisomerase Inhibitors as Anticancer Agents

被引:29
作者
Kathiravan, Muthu K. [1 ]
Kale, Anuj N. [2 ]
Nilewar, Shrikant [2 ]
机构
[1] SRM Univ, SRM Coll Pharm, Dept Pharmaceut Chem, Kancheepuram Dt 603203, Tamil Nadu, India
[2] Sinhgad Coll Pharm, Dept Pharmaceut Chem, Pune 411041, MS, India
关键词
Anticancer; topoisomerase types and inhibitors; structure activity relationship; topoisomerase inhibitors; MEDIATED DNA CLEAVAGE; ETOPOSIDE-INDUCED APOPTOSIS; PLANT ANTITUMOR AGENTS; ACUTE MYELOID-LEUKEMIA; CANCER-CELL-LINES; II INHIBITORS; BETA-LAPACHONE; IN-VITRO; CAMPTOTHECIN ANALOGS; POLYAMINE TRANSPORT;
D O I
10.2174/1389557516666160822110819
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
As one of the leading causes of deaths worldwide, cancer is posing threat despite efforts being taken to develop effective anticancer drugs. There is an increase in number of chemotherapy treatments due to growing number of manifestations causing increasing toxicities of cytotoxic agents. Almost all the anticancer agents available till date have one or the other side effects. Topoisomerases are the attractive targets to develop effective anticancer agents. There has been development of many topoisomerase inhibitors till date and has shown good anticancer activity but their side effects outnumber their anticancer potential. Hence, there is an urgent need to develop effective therapeutic agents with fewer side effects. This review deals with design and development aspect of topoisomerase inhibitors as exciting novel anticancer agents. The emphasis has been laid in particular on the new potential heterocyles as TOP inhibitors in the field of medicinal chemistry. The review discusses about the topoisomerase poisons, TOP1 suppressors, TOP inhibitors and Dual TOP 1/2 inhibitors.
引用
收藏
页码:1219 / 1229
页数:11
相关论文
共 120 条
[1]  
Adams Val R., 2000, Pharmacotherapy, V20, p96S, DOI 10.1592/phco.20.10.96S.35230
[2]  
[Anonymous], 2000, IARC MON EV CARC RIS, V76, P175
[3]   Rational design and synthesis of topoisomerase I and II inhibitors based on oleanolic acid moiety for new anti-cancer drugs [J].
Ashour, Ahmed ;
El-Sharkawy, Saleh ;
Amer, Mohamed ;
Bar, Fatma Abdel ;
Katakura, Yoshinori ;
Miyamoto, Tomofumi ;
Toyota, Nozomi ;
Tran Hai Bang ;
Kondo, Ryuichiro ;
Shimizu, Kuniyoshi .
BIOORGANIC & MEDICINAL CHEMISTRY, 2014, 22 (01) :211-220
[4]  
BACHUR NR, 1992, MOL PHARMACOL, V41, P993
[5]   INCREASED TENIPOSIDE CLEARANCE WITH CONCOMITANT ANTICONVULSANT THERAPY [J].
BAKER, DK ;
RELLING, MV ;
PUI, CH ;
CHRISTENSEN, ML ;
EVANS, WE ;
RODMAN, JH .
JOURNAL OF CLINICAL ONCOLOGY, 1992, 10 (02) :311-315
[6]   EFFECTS OF ANALOGS OF THE DNA MINOR GROOVE BINDER HOECHST-33258 ON TOPOISOMERASE-II AND TOPOISOMERASE-I MEDIATED ACTIVITIES [J].
BEERMAN, TA ;
MCHUGH, MM ;
SIGMUND, R ;
LOWN, JW ;
RAO, KE ;
BATHINI, Y .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1131 (01) :53-61
[7]   NATURALLY-OCCURRING INHIBITORS OF TOPOISOMERASE-I MEDIATED DNA RELAXATION [J].
BERRY, DE ;
MACKENZIE, L ;
SHULTIS, EA ;
CHAN, JA ;
HECHT, SM .
JOURNAL OF ORGANIC CHEMISTRY, 1992, 57 (02) :420-422
[8]   Topoisomerase II is required for mitoxantrone to signal nuclear factor κB activation in HL60 cells [J].
Boland, MP ;
Fitzgerald, KA ;
O'Neill, LAJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (33) :25231-25238
[9]  
BOOTHMAN DA, 1989, CANCER RES, V49, P605
[10]   EXPERIMENTAL ANTITUMOR PROPERTIES OF 3 CONGENERS OF ACRIDYLMETHANESULFONANILIDE (AMSA) SERIES [J].
CAIN, BF ;
ATWELL, GJ .
EUROPEAN JOURNAL OF CANCER, 1974, 10 (08) :539-549