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Table 5 Future directions for CRISPR-based cancer therapy

From: Comprehensive review of CRISPR-based gene editing: mechanisms, challenges, and applications in cancer therapy

Research Priorities

Emerging Technologies

Translational Opportunities

Collaborative Efforts

Societal Impact

Ref

Development of more precise and efficient delivery systems

Expansion of genome editing tools beyond gene knockout and correction

Development of biomarkers to predict treatment response

Collaborative development of ethical guidelines for CRISPR-based therapy

Equitable access to CRISPR-based cancer therapy

[268]

Development of gene editing tools to target non-coding regions of the genome

Application of CRISPR screens to identify new therapeutic targets

Use of gene editing to improve immunotherapy response

Collaboration between academic institutions and industry to accelerate drug development

Impacts on healthcare economics and resource allocation

[269]

Exploration of combination therapies that include CRISPR-based interventions

Integration of CRISPR technology with emerging imaging and sensing technologies

Application of CRISPR gene editing to develop personalized cancer vaccines

Collaborative development of CRISPR-based diagnostic tools

Ethical implications of germline editing for cancer prevention and treatment

[271]

Developing new approaches to improve specificity of CRISPR-Cas9 gene editing

Exploring the use of CRISPR gene regulation to modulate gene expression

Testing the efficacy of CRISPR-based cancer therapy in combination with other standard therapies

Development of international regulatory frameworks for gene editing technology

Education and public outreach to promote understanding and acceptance of gene editing technology

[272]

Studying the impact of CRISPR gene editing on tumor microenvironment and the immune system

Developing CRISPR-based tools for non-invasive cancer detection and monitoring

Incorporating CRISPR gene editing into patient stratification and clinical trial design

Collaboration among researchers to advance the understanding of CRISPR mechanisms and their role in cancer biology

Addressing issues of genetic discrimination and privacy concerns related to gene editing technology

[18]

Designing CRISPR gene editing systems for the treatment of rare or difficult-to-treat cancers

Advancing gene editing technology to target complex genetic abnormalities in cancer cells

Establishing international databases to promote sharing of CRISPR-based therapy data and protocols

Development of guidelines and standards for quality control and product safety for CRISPR-based therapies

Ensuring equitable access to CRISPR-based cancer therapy in diverse patient populations

[270]

Developing gene editing strategies to overcome resistance to standard cancer therapies

Integration of CRISPR technology with nanotechnology for enhanced delivery and targeting of cancer cells

Establishing public–private partnerships to accelerate the development of CRISPR-based cancer therapies

Collaboration between clinicians and basic researchers to optimize the design and delivery of CRISPR-based cancer therapies

Evaluation of the long-term safety and efficacy of CRISPR-based cancer therapy

[273, 274]