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Nanomaterial-assisted CRISPR gene-engineering - A hallmark for triple-negative breast cancer therapeutics advancement
Jabeen Farheen1,2, Narayan S Hosmane3, Ruibo Zhao1,2,4
1Institute of Smart Biomedical Materials, School of Materials Science and Engineering, Zhejiang Sci-Tech University, Hangzhou, 310018, PR China.
Abstract:
Triple-negative breast cancer (TNBC) is the most violent class of tumor and accounts for 20-24% of total breast carcinoma, in which frequently rare mutation occurs in high frequency. The poor prognosis, recurrence, and metastasis in the brain, heart, liver and lungs decline the lifespan of patients by about 21 months, emphasizing the need for advanced treatment. Recently, the adaptive immunity mechanism of archaea and bacteria, called clustered regularly interspaced short palindromic repeats (CRISPR) combined with nanotechnology, has been utilized as a potent gene manipulating tool with an extensive clinical application in cancer genomics due to its easeful usage and cost-effectiveness. However, CRISPR/Cas are arguably the efficient technology that can be made efficient via organic material-assisted approaches. Despite the efficacy of the CRISPR/Cas@nano complex, problems regarding successful delivery, biodegradability, and toxicity remain to render its medical implications. Therefore, this review is different in focus from past reviews by (i) detailing all possible genetic mechanisms of TNBC occurrence; (ii) available treatments and gene therapies for TNBC; (iii) overview of the delivery system and utilization of CRISPR-nano complex in TNBC, and (iv) recent advances and related toxicity of CRISPR-nano complex towards clinical trials for TNBC.
Insights
Triple-negative breast cancer (TNBC) requires advanced treatments. This review explores CRISPR-nano complexes for TNBC gene therapy, focusing on delivery, toxicity, and clinical applications.
Area of Science:
- Oncology
- Genomics
- Biotechnology
Background:
- Triple-negative breast cancer (TNBC) is an aggressive malignancy with poor prognosis and high metastatic potential.
- Current treatments are limited, necessitating novel therapeutic strategies.
- CRISPR-Cas gene editing combined with nanotechnology offers a promising avenue for cancer treatment.
Purpose of the Study:
- To detail the genetic mechanisms underlying TNBC development.
- To review current and emerging gene therapies for TNBC.
- To provide an overview of CRISPR-nano complex delivery systems and applications in TNBC.
- To discuss recent advances and toxicity concerns of CRISPR-nano complexes in TNBC clinical trials.
Main Methods:
- Comprehensive literature review of TNBC genetics, current therapies, and CRISPR-nano technology.
- Analysis of gene editing mechanisms and delivery systems for TNBC.
- Evaluation of recent clinical trial data and toxicity profiles of CRISPR-nano complexes.
Main Results:
- TNBC exhibits frequent rare mutations contributing to its aggressive nature.
- CRISPR-nano complexes show potential for targeted gene manipulation in TNBC.
- Challenges in delivery, biodegradability, and toxicity of CRISPR-nano complexes need to be addressed for clinical translation.
Conclusions:
- CRISPR-nano technology holds significant promise for advancing TNBC treatment through precise gene editing.
- Further research is crucial to optimize delivery systems and mitigate toxicity for safe and effective clinical application in TNBC.
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