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Testing Targeted Therapies in Cancer using Structural DNA Alteration Analysis and Patient-Derived Xenografts
Published on: July 25, 2020
Unlocking the Therapeutic Potential of DNA-PKcs in Cancer: Comprehensive Insights into Mechanisms and Clinical
Tong Zheng1,2,3, Chao Sun1,3, Cijun Yun1,2,3
1Institute of Modern Physics, Chinese Academy of Sciences, Lanzhou 730000, China.
Abstract:
Cancer remains one of the most pressing global health challenges, with current therapies often hindered by limited efficacy and the emergence of resistance. The DNA-dependent protein kinase catalytic subunit (DNA-PKcs), a key regulator of DNA repair and cell cycle progression, plays a critical role in maintaining genomic stability, and growing evidence indicates its dysregulation in various cancers, with overexpression frequently associated with aggressive tumor phenotypes. To evaluate DNA-PKcs as a therapeutic target, we systematically analyzed literature from PubMed and Web of Science (2000-2024) using keywords including DNA-PKcs, targeted therapy, DNA repair, and tumor resistance following PRISMA guidelines, with 185 of 1250 initial records meeting inclusion criteria after screening. The review explores the multifaceted roles of DNA-PKcs in tumor biology and resistance mechanisms, evaluates the current landscape of DNA-PKcs inhibitors, including their clinical progress and combination strategies with radiotherapy and chemotherapy, and discusses key determinants of therapeutic efficacy, such as tumor type and mutation status. Additionally, it uniquely integrates emerging insights into the roles of DNA-PKcs in immunomodulation and metabolism, critically assesses next-generation inhibitors, and proposes strategies to address remaining challenges. Through this comprehensive analysis, we highlight the therapeutic potential of DNA-PKcs inhibition as a novel strategy to circumvent treatment resistance, providing innovative insights for optimizing cancer management, especially for aggressive tumor subtypes, thereby advancing drug discovery efforts and paving the way for more effective therapeutic interventions in clinical practice.
Insights
Targeting DNA-dependent protein kinase catalytic subunit (DNA-PKcs) shows promise for overcoming cancer treatment resistance. Inhibiting DNA-PKcs offers a novel strategy for managing aggressive tumors and advancing drug discovery.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Cancer therapies face challenges with efficacy and resistance.
- DNA-dependent protein kinase catalytic subunit (DNA-PKcs) is crucial for DNA repair and genomic stability.
- DNA-PKcs dysregulation and overexpression are linked to aggressive cancers.
Purpose of the Study:
- To evaluate DNA-PKcs as a therapeutic target for cancer.
- To review DNA-PKcs roles in tumor biology and resistance mechanisms.
- To assess current and next-generation DNA-PKcs inhibitors and combination strategies.
Main Methods:
- Systematic literature review of PubMed and Web of Science (2000-2024).
- Keywords: DNA-PKcs, targeted therapy, DNA repair, tumor resistance.
- PRISMA guidelines followed for screening 1250 records, with 185 included.
Main Results:
- DNA-PKcs plays multifaceted roles in tumor progression and resistance.
- Current DNA-PKcs inhibitors show clinical progress, with combination strategies showing potential.
- Emerging roles in immunomodulation and metabolism are highlighted.
Conclusions:
- DNA-PKcs inhibition is a promising strategy to overcome cancer treatment resistance.
- Optimizing therapeutic efficacy requires considering tumor type and mutation status.
- Further research into next-generation inhibitors and combination therapies is warranted for aggressive tumors.
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