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让我们个体化治疗:CRISPR 工具在操控细胞死亡通路以治疗癌症中的应用。

Let's make it personal: CRISPR tools in manipulating cell death pathways for cancer treatment.

机构信息

Infectious and Tropical Diseases Research Center, Tabriz University of Medical Sciences, Tabriz, 15731, Iran.

出版信息

Cell Biol Toxicol. 2024 Jul 29;40(1):61. doi: 10.1007/s10565-024-09907-z.


DOI:10.1007/s10565-024-09907-z
PMID:39075259
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11286699/
Abstract

Advancements in the CRISPR technology, a game-changer in experimental research, have revolutionized various fields of life sciences and more profoundly, cancer research. Cell death pathways are among the most deregulated in cancer cells and are considered as critical aspects in cancer development. Through decades, our knowledge of the mechanisms orchestrating programmed cellular death has increased substantially, attributed to the revolution of cutting-edge technologies. The heroic appearance of CRISPR systems have expanded the available screening platform and genome engineering toolbox to detect mutations and create precise genome edits. In that context, the precise ability of this system for identification and targeting of mutations in cell death signaling pathways that result in cancer development and therapy resistance is an auspicious choice to transform and accelerate the individualized cancer therapy. The concept of personalized cancer therapy stands on the identification of molecular characterization of the individual tumor and its microenvironment in order to provide a precise treatment with the highest possible outcome and minimum toxicity. This study explored the potential of CRISPR technology in precision cancer treatment by identifying and targeting specific cell death pathways. It showed the promise of CRISPR in finding key components and mutations involved in programmed cell death, making it a potential tool for targeted cancer therapy. However, this study also highlighted the challenges and limitations that need to be addressed in future research to fully realize the potential of CRISPR in cancer treatment.

摘要

CRISPR 技术的进步是实验研究领域的一个重大突破,它彻底改变了生命科学的各个领域,对癌症研究的影响更为深远。细胞死亡途径在癌细胞中是最失调的,被认为是癌症发展的关键方面。几十年来,由于尖端技术的革新,我们对调控程序性细胞死亡的机制的认识有了显著提高。CRISPR 系统的出现极大地扩展了可用的筛选平台和基因组工程工具包,以检测突变并进行精确的基因组编辑。在这种情况下,该系统精确识别和靶向导致癌症发展和治疗耐药性的细胞死亡信号通路中的突变的能力,是改变和加速个体化癌症治疗的一个很好的选择。个体化癌症治疗的概念基于识别个体肿瘤及其微环境的分子特征,以便提供最高可能的疗效和最小毒性的精确治疗。本研究通过识别和靶向特定的细胞死亡途径,探讨了 CRISPR 技术在精准癌症治疗中的潜力。它表明了 CRISPR 在发现涉及程序性细胞死亡的关键成分和突变方面的潜力,使其成为靶向癌症治疗的潜在工具。然而,本研究也强调了未来研究中需要解决的挑战和局限性,以充分发挥 CRISPR 在癌症治疗中的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a39/11286699/9551d0a4aab5/10565_2024_9907_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a39/11286699/711baf4d67fe/10565_2024_9907_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a39/11286699/8a0ac27b96ed/10565_2024_9907_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a39/11286699/db95d33ea6a8/10565_2024_9907_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a39/11286699/2303d685beb5/10565_2024_9907_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a39/11286699/2dccec096b1d/10565_2024_9907_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a39/11286699/38569d017fef/10565_2024_9907_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a39/11286699/9551d0a4aab5/10565_2024_9907_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a39/11286699/711baf4d67fe/10565_2024_9907_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a39/11286699/8a0ac27b96ed/10565_2024_9907_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a39/11286699/db95d33ea6a8/10565_2024_9907_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a39/11286699/2303d685beb5/10565_2024_9907_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a39/11286699/2dccec096b1d/10565_2024_9907_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a39/11286699/38569d017fef/10565_2024_9907_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a39/11286699/9551d0a4aab5/10565_2024_9907_Fig7_HTML.jpg

相似文献

[1]
Let's make it personal: CRISPR tools in manipulating cell death pathways for cancer treatment.

Cell Biol Toxicol. 2024-7-29

[2]
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[3]
CRISPR-Cas13 System as a Promising and Versatile Tool for Cancer Diagnosis, Therapy, and Research.

ACS Synth Biol. 2021-6-18

[4]
Harnessing the evolving CRISPR/Cas9 for precision oncology.

J Transl Med. 2024-8-8

[5]
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J Transl Med. 2024-5-30

[6]
Targeting miRNA by CRISPR/Cas in cancer: advantages and challenges.

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[7]
Revolutionizing personalized cancer treatment: the synergy of next-generation sequencing and CRISPR/Cas9.

Per Med. 2024

[8]
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Indian J Med Microbiol. 2025

[9]
Recent advances in CRISPR technologies for genome editing.

Arch Pharm Res. 2021-6

[10]
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Front Immunol. 2024

引用本文的文献

[1]
Ferroptosis and non-coding RNAs in breast cancer: insights into CAF and TAM interactions.

Discov Oncol. 2025-8-31

[2]
Targeting Metastasis: Exploring the Impact of Microbial Infections on Cancer Progression Through Innovative Biological Models.

Curr Microbiol. 2025-6-7

[3]
The CRISPR-Cas revolution in head and neck cancer: a new era of targeted therapy.

Funct Integr Genomics. 2025-5-30

[4]
Interferon and immunity: the role of microRNA in viral evasion strategies.

Front Immunol. 2025-5-9

[5]
To be or not to be: navigating the influence of MicroRNAs on cervical cancer cell death.

Cancer Cell Int. 2025-4-18

[6]
Battlegrounds of treatment resistance: decoding the tumor microenvironment.

Naunyn Schmiedebergs Arch Pharmacol. 2025-3-25

[7]
Circular RNAs: driving forces behind chemoresistance and immune evasion in bladder cancer.

Naunyn Schmiedebergs Arch Pharmacol. 2025-3-25

[8]
JAK/STAT signaling as a key regulator of ferroptosis: mechanisms and therapeutic potentials in cancer and diseases.

Cancer Cell Int. 2025-3-7

[9]
Bile's Hidden Weapon: Modulating the Microbiome and Tumor Microenvironment.

Curr Microbiol. 2024-11-30

本文引用的文献

[1]
CRISPR screens reveal convergent targeting strategies against evolutionarily distinct chemoresistance in cancer.

Nat Commun. 2024-6-29

[2]
Resistance to death pathway induction as a potential targeted therapy in CRISPR/Cas-9 knock-out colorectal cancer cell lines.

Prz Gastroenterol. 2024

[3]
TRPML1 triggers ferroptosis defense and is a potential therapeutic target in AKT-hyperactivated cancer.

Sci Transl Med. 2024-6-26

[4]
CRISPR activation screens identify the SWI/SNF ATPases as suppressors of ferroptosis.

Cell Rep. 2024-6-25

[5]
CRISPR/Cas9 screen reveals that targeting TRIM34 enhances ferroptosis sensitivity and augments immunotherapy efficacy in hepatocellular carcinoma.

Cancer Lett. 2024-7-1

[6]
Overexpression of Klotho gene using CRISPR/Cas9 induces apoptosis and inhibits cell motility in the human colorectal cancer cells.

Biotechnol J. 2024-2

[7]
In vivo CRISPR knockout screen identifies p47 as a suppressor of HER2+ breast cancer metastasis by regulating NEMO trafficking and autophagy flux.

Cell Rep. 2024-2-27

[8]
Significance of TRAIL/Apo-2 ligand and its death receptors in apoptosis and necroptosis signalling: Implications for cancer-targeted therapeutics.

Biochem Pharmacol. 2024-3

[9]
Oncoviruses: Induction of cancer development and metastasis by increasing anoikis resistance.

Heliyon. 2023-11-27

[10]
A CRISPR-Cas9 library screening identifies CARM1 as a critical inhibitor of ferroptosis in hepatocellular carcinoma cells.

Mol Ther Nucleic Acids. 2023-10-20

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