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Published on: April 11, 2016
CRISPR/Cas9 and next generation sequencing in the personalized treatment of Cancer
Sushmaa Chandralekha Selvakumar1, K Auxzilia Preethi1, Kehinde Ross2
1Centre for Cellular and Molecular Research, Saveetha Dental College and Hospitals, Saveetha Institute of Medical and Technical Sciences (SIMATS), Saveetha University, Chennai, Tamil Nadu, 600077, India.
Background:
Cancer is caused by a combination of genetic and epigenetic abnormalities. Current cancer therapies are limited due to the complexity of their mechanism, underlining the need for alternative therapeutic approaches. Interestingly, combining the Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR/Cas9) system with next-generation sequencing (NGS) has the potential to speed up the identification, validation, and targeting of high-value targets.
Main Text:
Personalized or precision medicine combines genetic information with phenotypic and environmental characteristics to produce healthcare tailored to the individual and eliminates the constraints of "one-size-fits-all" therapy. Precision medicine is now possible thanks to cancer genome sequencing. Having advantages over limited sample requirements and the recent development of biomarkers have made the use of NGS a major leap in personalized medicine. Tumor and cell-free DNA profiling using NGS, proteome and RNA analyses, and a better understanding of immunological systems, are all helping to improve cancer treatment choices. Finally, direct targeting of tumor genes in cancer cells with CRISPR/Cas9 may be achievable, allowing for eliminating genetic changes that lead to tumor growth and metastatic capability.
Conclusion:
With NGS and CRISPR/Cas9, the goal is no longer to match the treatment for the diagnosed tumor but rather to build a treatment method that fits the tumor exactly. Hence, in this review, we have discussed the potential role of CRISPR/Cas9 and NGS in advancing personalized medicine.
Insights
Next-generation sequencing (NGS) and Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR/Cas9) advance personalized cancer medicine by enabling precise tumor targeting and tailored treatments, moving beyond one-size-fits-all approaches.
Area of Science:
- Oncology
- Genomics
- Biotechnology
Background:
- Cancer arises from genetic and epigenetic changes, necessitating novel therapeutic strategies.
- Current cancer therapies face limitations due to complex mechanisms, highlighting the need for alternative approaches.
- The Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR/Cas9) system and next-generation sequencing (NGS) offer potential for rapid target identification and validation.
Purpose of the Study:
- To review the synergistic potential of CRISPR/Cas9 and NGS in advancing personalized cancer medicine.
- To explore how these technologies facilitate tailored treatment strategies for individual tumors.
- To discuss the transition from generalized treatment matching to precise, tumor-specific therapeutic design.
Main Methods:
- Integration of CRISPR/Cas9 gene-editing technology with NGS for comprehensive cancer genome analysis.
- Utilizing NGS for tumor and cell-free DNA profiling, proteome, and RNA analysis.
- Leveraging CRISPR/Cas9 for direct targeting of oncogenic drivers within cancer cells.
Main Results:
- NGS has revolutionized personalized medicine through its ability to analyze genetic information with minimal sample requirements.
- CRISPR/Cas9 enables the direct targeting and potential elimination of genetic alterations driving tumor growth and metastasis.
- Combined application accelerates the identification, validation, and targeting of high-value therapeutic targets in cancer.
Conclusions:
- The combination of NGS and CRISPR/Cas9 represents a significant advancement in personalized cancer therapy.
- These technologies facilitate the development of bespoke treatment regimens precisely matched to individual tumor profiles.
- The future of cancer treatment lies in precisely tailored therapies enabled by genomic insights and gene-editing capabilities.
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