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Recent Progress on Tubulin Inhibitors with Dual Targeting Capabilities for Cancer Therapy
- Source :
- Journal of Medicinal Chemistry. 64:7963-7990
- Publication Year :
- 2021
- Publisher :
- American Chemical Society (ACS), 2021.
-
Abstract
- Microtubules play a crucial role in multiple cellular functions including mitosis, cell signaling, and organelle trafficking, which makes the microtubule an important target for cancer therapy. Despite the great successes of microtubule-targeting agents in the clinic, the development of drug resistance and dose-limiting toxicity restrict their clinical efficacy. In recent years, multitarget therapy has been considered an effective strategy to achieve higher therapeutic efficacy, in particular dual-target drugs. In terms of the synergetic effect of tubulin and other antitumor agents such as receptor tyrosine kinases inhibitors, histone deacetylases inhibitors, DNA-damaging agents, and topoisomerase inhibitors in combination therapy, designing dual-target tubulin inhibitors is regarded as a promising approach to overcome these limitations and improve therapeutic efficacy. In this Perspective, we discussed rational target combinations, design strategies, structure-activity relationships, and future directions of dual-target tubulin inhibitors.
- Subjects :
- Cell signaling
Combination therapy
medicine.drug_class
Antineoplastic Agents
Apoptosis
01 natural sciences
Receptor tyrosine kinase
Mice
Structure-Activity Relationship
03 medical and health sciences
Microtubule
Cell Line, Tumor
Drug Discovery
medicine
Animals
Humans
Enzyme Inhibitors
Mitosis
030304 developmental biology
0303 health sciences
Molecular Structure
biology
Chemistry
Cell Cycle Checkpoints
Tubulin Modulators
0104 chemical sciences
010404 medicinal & biomolecular chemistry
Histone
Tubulin
Drug Design
Cancer research
biology.protein
Molecular Medicine
Drug Screening Assays, Antitumor
Topoisomerase inhibitor
Subjects
Details
- ISSN :
- 15204804 and 00222623
- Volume :
- 64
- Database :
- OpenAIRE
- Journal :
- Journal of Medicinal Chemistry
- Accession number :
- edsair.doi.dedup.....0141af8a1d10526e59b4dd824ea54902