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Targeted Cancer Therapies02:57

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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.
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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...
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Combining two or more treatment methods increases the life span of cancer patients while reducing damage to vital organs or tissue from the overuse of a single treatment. Combination therapy also targets different cancer-inducing pathways, thus reducing the chances of developing resistance to treatment.
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Related Experiment Video

Updated: Apr 25, 2026

A Method for Screening and Validation of Resistant Mutations Against Kinase Inhibitors
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Kinase Inhibitors: A Promising Approach for Targeted Cancer Therapy.

Vishakha Sharma1, Ankush Kumar2, Rajesh Gour3

  • 1Department of Pharmaceutical Chemistry, Indo-Soviet Friendship College of Pharmacy (ISFCP), Moga, Punjab, India.

Chemistry & Biodiversity
|April 24, 2026
PubMed
Summary

This review evaluates novel kinase inhibitors targeting receptor tyrosine kinases (RTKs) and Snf1/AMPK pathways for cancer treatment. It highlights recent advancements and future directions for developing more effective anticancer drugs.

Keywords:
acetyl coenzyme Acancerkinase inhibitorsmutationsresistancesignaling pathways

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Area of Science:

  • Oncology
  • Molecular Biology
  • Drug Discovery

Background:

  • Cancer is a leading cause of non-infectious disease fatalities globally, with increasing incidence projected.
  • Current cancer therapies face challenges including drug resistance, limited selectivity, and adverse side effects.
  • Kinase inhibitors offer targeted therapy by modulating dysregulated signaling pathways crucial for cancer progression.

Purpose of the Study:

  • To systematically review and evaluate recently synthesized kinase inhibitors (2020-2025).
  • To focus on inhibitors targeting receptor tyrosine kinases (RTKs) and sucrose non-fermenting-1/AMP-activated protein kinase (Snf1/AMPK) pathways.
  • To summarize structural activity relationships and identify future research avenues for anticancer kinase inhibitor development.

Main Methods:

  • Literature review of scientific publications and databases.
  • Systematic evaluation of kinase inhibitors targeting specific pathways like EGFR, VEGFR, MELK, and acetyl-CoA related pathways.
  • Analysis of structural activity relationships for recently developed molecules.

Main Results:

  • Identification of promising kinase inhibitors with potential for targeted cancer therapy.
  • Summary of novel molecules developed between 2020-2025 targeting key cancer-related pathways.
  • Elucidation of structure-activity relationships guiding future drug design.

Conclusions:

  • Recent advancements in kinase inhibitor development show promise for overcoming limitations of current cancer therapies.
  • Targeting RTKs and Snf1/AMPK pathways represents a key strategy in developing novel anticancer agents.
  • Further research into structural activity relationships is crucial for optimizing kinase inhibitors for clinical application.