Related Experiment Video
Updated: Apr 18, 2026

06:30
Author Spotlight: Purifying High-Quality Tubulin to Study Protein Dynamics and Therapeutic Applications
Published on: October 11, 2024
2.4K
Tubulins - the target for anticancer therapy
N G Vindya, Nishant Sharma, Mukesh Yadav
1School of Advanced Sciences, VIT University, Vellore, 632014, India. ethukr@gmail.com.
Current Topics in Medicinal Chemistry
|January 13, 2015
Summary
Tubulin inhibitors are crucial anticancer agents targeting cancer chemotherapy. This review highlights recent advances and trends in developing novel tubulin-targeting drugs for cancer treatment.
Area of Science:
- Biochemistry
- Pharmacology
- Oncology
Background:
- Tubulin is a key target in drug discovery due to its role in cell division.
- Naturally occurring agents targeting tubulin are vital in cancer chemotherapy.
- Tubulin inhibitors are classified based on their binding sites and mechanisms of action.
Purpose of the Study:
- To review recent advancements in tubulin-interfering agents.
- To outline current trends in the development of tubulin inhibitors for cancer therapy.
Main Methods:
- Literature review of scientific publications.
- Analysis of tubulin inhibitor classification and mechanisms.
- Synthesis of recent research findings on tubulin-targeting agents.
Main Results:
- Tubulin inhibitors represent a significant class of anticancer agents.
- Classification includes colchicine site binders, vinca-alkaloid related drugs, and Taxol site binders.
- Ongoing research focuses on novel tubulin inhibitors with improved efficacy.
Conclusions:
- Tubulin remains a promising target for anticancer drug development.
- Continued research into tubulin inhibitors is essential for advancing cancer chemotherapy.
- Understanding tubulin-drug interactions guides the design of new therapeutic strategies.
More Related Videos
Related Concept Videos
Drugs that Stabilize Microtubules
2.9K
Microtubules are dynamic structures that undergo cycles of catastrophe and rescue. The microtubules play a central role in cell division by forming the spindle apparatus for segregating the chromosomes. This makes them ideal targets for regulating dividing cells in tumors and malignant cancer cells. Microtubule stabilizing drugs help stabilize the microtubule formation and promote its polymerization. Paclitaxel was the first microtubule stabilizing agent used as anticancer drug in chemotherapy...
2.9K
Targeted Cancer Therapies
9.2K
The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against...
There are several types of targeted therapies against...
9.2K
Targeted Cancer Therapies
1.8K
1.8K
Drugs that Destabilize Microtubules
4.4K
Microtubules are dynamic structures and can be regulated by microtubule targeting agents (MTAs). Microtubule destabilizing drugs are a class of MTAs that destabilize and prevent microtubules' polymerization. Both natural and synthetic chemicals can be found under this class of drugs. Vincristine and vinblastine, two vinca alkaloids, and colchicine were among the first to be discovered. These drugs can affect cells in various ways, either by inducing a change in cell morphology, preventing...
4.4K
Destabilization of Microtubules
3.9K
The destabilization of microtubules can occur during different stages of the microtubule lifecycle, such as nucleation or elongation. It can take place at either end of the microtubule or in the microtubule lattices as a whole. The lifespan of individual microtubules within a cell varies according to the cell type and stage of the cell cycle. During interphase, the lifespan of the microtubule is about 30 minutes, while during cell division, it is about 15 minutes. In axonal microtubules of...
3.9K
Inhibition of Cdk Activity
6.3K
The orderly progression of the cell cycle depends on the activation of Cdk protein by binding to its cyclin partner. However, the cell cycle must be restricted when undergoing abnormal changes. Most cancers correlate to the deregulated cell cycle, and since Cdks are a central component of the cell cycle, Cdk inhibitors are extensively studied to develop anticancer agents. For instance, cyclin D associates with several Cdks, such as Cdk 4/6, to form an active complex. The cyclin D-Cdk4/6 complex...
6.3K

