Early investigational tubulin inhibitors as novel cancer therapeutics

被引:31
|
作者
Nepali, Kunal [1 ]
Ojha, Ritu [1 ]
Lee, Hsueh-Yun [1 ]
Liou, Jing-Ping [1 ]
机构
[1] Taipei Med Univ, Sch Pharm, Coll Pharm, Taipei, Taiwan
关键词
Tubulin inhibitors; microtubules; progression free survival; objective response; overall survival; efficacy; solid tumors; colchicine; taxanes; VASCULAR-DISRUPTING AGENT; PHASE-I TRIAL; DOCOSAHEXAENOIC ACID-PACLITAXEL; METASTATIC BREAST-CANCER; EVERY; WEEKS; ANTITUMOR-ACTIVITY; OMBRABULIN AVE8062; POLYMERIZATION INHIBITOR; TUMOR VASCULATURE; COMBRETASTATIN-A4; PHOSPHATE;
D O I
10.1080/13543784.2016.1189901
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Microtubules represent one of the most logical and strategic molecular targets amongst the current targets for chemotherapy, alongside DNA. In the past decade, tubulin inhibitors as cancer therapeutics have been an area of focus due to the improved understanding and biological relevance of microtubules in cellular functions. Fueled by the objective of developing novel chemotherapeutics and with the aim of establishing the benefits of tubulin inhibition, several clinical trials have been conducted with others ongoing.Area covered: At present, the antitubulin development pipeline contains an armful of agents under clinical investigation. This review focuses on novel tubulin inhibitors as cancer therapeutics. The article covers the agents which have completed the phase II studies along with the agents demonstrating promising results in phase I studies.Expert opinion: Countless clinical trials evaluating the efficacy, safety and pharmacokinetics of novel tubulin inhibitors highlights the scientific efforts being paid to establish their candidature as cancer therapeutics. Colchicine binding site inhibitors as vascular disrupting agents (VDAs) and new taxanes appear to be the most likely agents for future clinical interest. Numerous agents have demonstrated clinical benefits in terms of efficacy and survival in phase I and II studies. However conclusive benefits can only be ascertained on the basis of phase III studies.
引用
收藏
页码:917 / 936
页数:20
相关论文
共 50 条
  • [41] Thoughts on investigational hedgehog pathway inhibitors for the treatment of cancer
    Jaeger, Tarkan
    Ocker, Matthias
    Kiesslich, Tobias
    Neureiter, Elen
    Neureiter, Daniel
    EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2017, 26 (02) : 133 - 136
  • [42] Current and Investigational Therapeutics for Fabry Disease
    Felis, Andrew
    Whitlow, Michael
    Kraus, Abigayle
    Warnock, David G.
    Wallace, Eric
    KIDNEY INTERNATIONAL REPORTS, 2020, 5 (04): : 407 - 413
  • [43] Modulation of angiogenesis with siRNA inhibitors for novel therapeutics
    Lu, PY
    Xie, FY
    Woodle, MC
    TRENDS IN MOLECULAR MEDICINE, 2005, 11 (03) : 104 - 113
  • [44] Histone deacetylase inhibitors as novel anticancer therapeutics
    Walkinshaw, D. R.
    Yang, X. J.
    CURRENT ONCOLOGY, 2008, 15 (05) : 237 - 243
  • [45] Immune checkpoint inhibitors for the treatment of myeloma: novel investigational options
    Le Calvez, Baptiste
    Moreau, Philippe
    Touzeau, Cyrille
    EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2021, 30 (09) : 965 - 973
  • [46] Novel inhibitors of STAT signaling: Potential selective anti-cancer therapeutics.
    Glenn, MP
    Kim, JS
    Turkson, J
    Sebti, SM
    Jove, R
    Hamilton, A
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2003, 226 : U48 - U48
  • [47] PNAs as novel cancer therapeutics
    Luca Mologni
    Carlo Gambacorti-Passerini
    Letters in Peptide Science, 2003, 10 : 297 - 308
  • [48] Novel therapeutics for lung cancer
    Bunn, Paul A., Jr.
    Herbst, Roy S.
    Johnson, David H.
    JOURNAL OF THORACIC ONCOLOGY, 2006, 1 (07) : 736 - 736
  • [49] PNAs as novel cancer therapeutics
    Mologni, L
    Gambacorti-Passerini, C
    LETTERS IN PEPTIDE SCIENCE, 2003, 10 (3-4): : 297 - 308
  • [50] Novel therapeutics in colorectal cancer
    McWilliams, RR
    Erlichman, C
    DISEASES OF THE COLON & RECTUM, 2005, 48 (08) : 1632 - 1650