4.8 Article

Nanomaterial-assisted CRISPR gene-engineering-A hallmark for triple-negative breast cancer therapeutics advancement

期刊

MATERIALS TODAY BIO
卷 16, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.mtbio.2022.100450

关键词

CRISPR; Cas9; Genetic mechanism; Gene therapy; Nanocarriers; Triple -negative breast cancer

资金

  1. National Natural Science Foundation of China [81950410638]
  2. Zhejiang Natural Science Foundation of China [LQ19E020010]
  3. Zhejiang International Science and Technology Cooperation Project [2021C01180]
  4. Zhejiang Sci-Tech University (ZSTU) , Hangzhou, China through the ZSTU common fund [11113132612110]

向作者/读者索取更多资源

This review provides an overview of the genetic mechanisms, available treatments, and gene therapies for TNBC, as well as the application and recent advances of CRISPR-nano complex in TNBC. However, challenges still remain in delivery, biodegradability, and toxicity of CRISPR-nano complex.
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 clus-tered 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.

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