Recent advances of CRISPR-based genome editing for enhancing staple crops DOI Creative Commons
Feng Chen, Chen D. Lu, Yan Zhao

и другие.

Frontiers in Plant Science, Год журнала: 2024, Номер 15

Опубликована: Сен. 23, 2024

An increasing population, climate change, and diminishing natural resources present severe threats to global food security, with traditional breeding genetic engineering methods often falling short in addressing these rapidly evolving challenges. CRISPR/Cas systems have emerged as revolutionary tools for precise modifications crops, offering significant advancements resilience, yield, nutritional value, particularly staple crops like rice maize. This review highlights the transformative potential of technology, emphasizing recent innovations such prime base editing, development novel CRISPR-associated proteins, which significantly improved specificity, efficiency, scope genome editing agriculture. These enable targeted that enhance tolerance abiotic stresses well biotic stresses. Additionally, plays a crucial role improving crop yield quality by enhancing photosynthetic nutrient uptake, resistance lodging, while also taste, texture, shelf life, content through biofortification. Despite challenges off-target effects, need more efficient delivery methods, ethical regulatory concerns, underscores importance security sustainability It calls continued research integration CRISPR other emerging technologies nanotechnology, synthetic biology, machine learning fully realize its developing resilient, productive, sustainable agricultural systems.

Язык: Английский

Exploring treatment options in cancer: Tumor treatment strategies DOI Creative Commons
Beilei Liu, Hongyu Zhou, Licheng Tan

и другие.

Signal Transduction and Targeted Therapy, Год журнала: 2024, Номер 9(1)

Опубликована: Июль 17, 2024

Traditional therapeutic approaches such as chemotherapy and radiation therapy have burdened cancer patients with onerous physical psychological challenges. Encouragingly, the landscape of tumor treatment has undergone a comprehensive remarkable transformation. Emerging fervently pursued modalities are small molecule targeted agents, antibody-drug conjugates (ADCs), cell-based therapies, gene therapy. These cutting-edge not only afford personalized precise targeting, but also provide enhanced comfort potential to impede disease progression. Nonetheless, it is acknowledged that these strategies still harbour untapped for further advancement. Gaining understanding merits limitations holds promise offering novel perspectives clinical practice foundational research endeavours. In this review, we discussed different modalities, including drugs, peptide antibody cell therapy, It will detailed explanation each method, addressing their status development, challenges, solutions. The aim assist clinicians researchers in gaining deeper diverse options, enabling them carry out effective advance more efficiently.

Язык: Английский

Процитировано

219

Lipid Nanoparticle (LNP) Enables mRNA Delivery for Cancer Therapy DOI
Yan Zong, Yi Lin, Tuo Wei

и другие.

Advanced Materials, Год журнала: 2023, Номер 35(51)

Опубликована: Май 17, 2023

Abstract Messenger RNA (mRNA) has received great attention in the prevention and treatment of various diseases due to success coronavirus disease 2019 (COVID‐19) mRNA vaccines (Comirnaty Spikevax). To meet therapeutic purpose, it is required that must enter target cells express sufficient proteins. Therefore, development effective delivery systems necessary crucial. Lipid nanoparticle (LNP) represents a remarkable vehicle indeed accelerated applications humans, as several mRNA‐based therapies have already been approved or are clinical trials. In this review, focus on mRNA‐LNP‐mediated anticancer therapy. It summarizes main strategies mRNA‐LNP formulations, discusses representative approaches cancer, points out current challenges possible future directions research field. hoped these delivered messages can help further improve application technology cancer

Язык: Английский

Процитировано

195

Past, present, and future of CRISPR genome editing technologies DOI Creative Commons

Martin Pacesa,

Oana Pelea, Martin Jínek

и другие.

Cell, Год журнала: 2024, Номер 187(5), С. 1076 - 1100

Опубликована: Фев. 1, 2024

Genome editing has been a transformative force in the life sciences and human medicine, offering unprecedented opportunities to dissect complex biological processes treat underlying causes of many genetic diseases. CRISPR-based technologies, with their remarkable efficiency easy programmability, stand at forefront this revolution. In Review, we discuss current state CRISPR gene technologies both research therapy, highlighting limitations that constrain them technological innovations have developed recent years address them. Additionally, examine summarize landscape applications context health therapeutics. Finally, outline potential future developments could shape coming years.

Язык: Английский

Процитировано

152

Assessing and advancing the safety of CRISPR-Cas tools: from DNA to RNA editing DOI Creative Commons
Jianli Tao, Daniel E. Bauer, Roberto Chiarle

и другие.

Nature Communications, Год журнала: 2023, Номер 14(1)

Опубликована: Янв. 13, 2023

CRISPR-Cas gene editing has revolutionized experimental molecular biology over the past decade and holds great promise for treatment of human genetic diseases. Here we review development CRISPR-Cas9/Cas12/Cas13 nucleases, DNA base editors, prime RNA focusing on assessment improvement their precision safety, pushing limit specificity efficiency. We summarize capabilities limitations each CRISPR tool from to editing, highlight opportunities future improvements applications in basic research, as well therapeutic clinical considerations use patients.

Язык: Английский

Процитировано

111

A comprehensive overview of cotton genomics, biotechnology and molecular biological studies DOI

Xingpeng Wen,

Zhiwen Chen, Zuoren Yang

и другие.

Science China Life Sciences, Год журнала: 2023, Номер 66(10), С. 2214 - 2256

Опубликована: Март 6, 2023

Язык: Английский

Процитировано

86

CRISPR technologies for genome, epigenome and transcriptome editing DOI
Lukas Villiger,

Julia Joung,

Luke W. Koblan

и другие.

Nature Reviews Molecular Cell Biology, Год журнала: 2024, Номер 25(6), С. 464 - 487

Опубликована: Фев. 2, 2024

Язык: Английский

Процитировано

77

Ex vivo prime editing of patient haematopoietic stem cells rescues sickle-cell disease phenotypes after engraftment in mice DOI Creative Commons
Kelcee A. Everette, Gregory A. Newby, Rachel M. Levine

и другие.

Nature Biomedical Engineering, Год журнала: 2023, Номер 7(5), С. 616 - 628

Опубликована: Апрель 17, 2023

Sickle-cell disease (SCD) is caused by an A·T-to-T·A transversion mutation in the β-globin gene (HBB). Here we show that prime editing can correct SCD allele (HBB

Язык: Английский

Процитировано

76

Clinical delivery of circular RNA: Lessons learned from RNA drug development DOI
Tiana L. Young, Kevin Chang Wang, Andrew Varley

и другие.

Advanced Drug Delivery Reviews, Год журнала: 2023, Номер 197, С. 114826 - 114826

Опубликована: Апрель 23, 2023

Язык: Английский

Процитировано

72

Improving prime editing with an endogenous small RNA-binding protein DOI Creative Commons
Jun Yan, Paul Oyler, Purnima Ravisankar

и другие.

Nature, Год журнала: 2024, Номер 628(8008), С. 639 - 647

Опубликована: Апрель 3, 2024

Abstract Prime editing enables the precise modification of genomes through reverse transcription template sequences appended to 3′ ends CRISPR–Cas guide RNAs 1 . To identify cellular determinants prime editing, we developed scalable reporters and performed genome-scale CRISPR-interference screens. From these screens, a single factor emerged as strongest mediator editing: small RNA-binding exonuclease protection La. Further investigation revealed that La promotes across approaches (PE2, PE3, PE4 PE5), edit types (substitutions, insertions deletions), endogenous loci cell but has no consistent effect on genome-editing rely standard, unextended RNAs. Previous work shown binds polyuridine tracts at RNA polymerase III transcripts 2 We found functionally interacts with polyuridylated (pegRNAs). Guided by results, editor protein (PE7) fused RNA-binding, N-terminal domain This improved expressed pegRNAs engineered (epegRNAs), well synthetic optimized for binding. Together, our results provide key insights into how components interact environment suggest general strategies stabilizing exogenous therein.

Язык: Английский

Процитировано

71

Deafness: from genetic architecture to gene therapy DOI
Christine Petit, Crystel Bonnet, Saaïd Safieddine

и другие.

Nature Reviews Genetics, Год журнала: 2023, Номер 24(10), С. 665 - 686

Опубликована: Май 12, 2023

Язык: Английский

Процитировано

67