Sulfonamides and Sulfonylated Derivatives as Anticancer Agents

被引:292
作者
Casini, Angela [1 ]
Scozzafava, Andrea [1 ]
Mastrolorenzo, Antonio [2 ]
Supuran, Claudiu T. [1 ]
机构
[1] Univ Florence, Dipartimento Chim, Lab Chim Inorgan & Bioinorgan, I-50121 Florence, Italy
[2] Univ Florence, Centro MTS, Dipartimento Sci Dermatol, I-50121 Florence, Italy
关键词
D O I
10.2174/1568009023334060
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The sulfonamides constitute an important class of drugs, with several types of pharmacological agents possessing antibacterial, anti-carbonic anhydrase, diuretic, hypoglycemic and antithyroid activity among others. A host of structurally novel sulfonamide derivatives have recently been reported to show substantial antitumor activity in vitro and/or in vivo. Although they have a common chemical motif of aromatic/heterocyclic sulfonamide, there are a variety of mechanisms of their antitumor action, such as carbonic anhydrase inhibition, cell cycle arrest in the G1 phase, disruption of microtubule assembly, functional suppression of the transcriptional activator NF-Y, and angiogenesis (matrix metalloproteinase, MMP) inhibition among others. Some of these compounds selected via elaborate preclinical screenings or obtained based on computer-aided drug design, are currently being evaluated in clinical trials. This review summarizes recent classes of sulfonamides and related sulfonyl derivatives disclosed ultimately as effective tumor cell growth inhibitors, or for the treatment of different types of cancer.
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收藏
页码:55 / 75
页数:21
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共 84 条
  • [31] Development of potent non-estrogenic estrone sulfatase inhibitors
    Li, PK
    Chu, GH
    Guo, JP
    Peters, A
    Selcer, KW
    [J]. STEROIDS, 1998, 63 (7-8) : 425 - 432
  • [32] Blockage of drug resistance in vitro by disulfiram, a drug used to treat alcoholism
    Loo, TW
    Clarke, DM
    [J]. JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2000, 92 (11): : 898 - 902
  • [33] Discovery of CGS 27023A, a non-peptidic, potent, and orally active stromelysin inhibitor that blocks cartilage degradation in rabbits
    MacPherson, LJ
    Bayburt, EK
    Capparelli, MP
    Carroll, BJ
    Goldstein, R
    Justice, MR
    Zhu, LJ
    Hu, SI
    Melton, RA
    Fryer, L
    Goldberg, RL
    Doughty, JR
    Spirito, S
    Blancuzzi, V
    Wilson, D
    OByrne, EM
    Ganu, V
    Parker, DT
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1997, 40 (16) : 2525 - 2532
  • [34] RELATIONS BETWEEN STRUCTURE AND BIOLOGICAL-ACTIVITY OF SULFONAMIDES
    MAREN, TH
    [J]. ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, 1976, 16 : 309 - 327
  • [35] Novel antineoplastic agents with efficacy against multidrug resistant tumor cells
    Medina, JC
    Shan, B
    Beckmann, H
    Farrell, RP
    Clark, DL
    Learned, RM
    Roche, D
    Li, A
    Baichwal, V
    Case, C
    Baeuerle, PA
    Rosen, T
    Jaen, JC
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1998, 8 (19) : 2653 - 2656
  • [36] Novel halogenated sulfonamides inhibit the growth of multidrug resistant MCF-7/ADR cancer cells
    Medina, JC
    Roche, D
    Shan, B
    Learned, RM
    Frankmoelle, WP
    Clark, DL
    Rosen, T
    Jaen, JC
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1999, 9 (13) : 1843 - 1846
  • [37] Phase II trial of chloroquinoxaline sulfonamide (CQS) in patients with stage III and IV non-small-cell lung cancer
    Miller, VA
    Rigas, JR
    Tong, WP
    Reid, JR
    Pisters, KMW
    Grant, SC
    Heelan, RT
    Kris, MG
    [J]. CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1997, 40 (05) : 415 - 418
  • [38] SULFONYLUREAS - A NEW CLASS OF CANCER CHEMOTHERAPEUTIC-AGENTS
    MOHAMADI, F
    SPEES, MM
    GRINDEY, GB
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1992, 35 (16) : 3012 - 3016
  • [39] Isolation and characterization of CA XIV, a novel membrane-bound carbonic anhydrase from mouse kidney
    Mori, K
    Ogawa, Y
    Ebihara, K
    Tamura, N
    Tashiro, K
    Kuwahara, T
    Mukoyama, M
    Sugawara, A
    Ozaki, S
    Tanaka, I
    Nakao, K
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (22) : 15701 - 15705
  • [40] A circulating form of NADH oxidase activity responsive to the antitumor sulfonylurea N-4-(methylphenylsulfonyl)-N'-(4-chlorophenyl)urea (LY181984) specific to sera from cancer patients
    Morre, DJ
    Reust, T
    [J]. JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 1997, 29 (03) : 281 - 289