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Gene interfered-ferroptosis therapy for cancers
by
Luo, Tao
, Wang, Jinke
, Gao, Jinliang
in
42/41
/ 42/44
/ 42/89
/ 631/67/1059/153
/ 631/67/1059/602
/ Animals
/ Cancer
/ Cation Transport Proteins - antagonists & inhibitors
/ Cation Transport Proteins - genetics
/ Cation Transport Proteins - metabolism
/ Cell Line, Tumor
/ CRISPR-Associated Proteins - genetics
/ CRISPR-Associated Proteins - metabolism
/ Dependovirus - genetics
/ Dependovirus - metabolism
/ Drug resistance
/ Ferroptosis
/ Ferroptosis - genetics
/ Gene expression
/ Gene Expression Regulation, Neoplastic
/ Genes
/ Growth inhibition
/ Humanities and Social Sciences
/ Humans
/ Interference
/ Iron
/ Iron - metabolism
/ Lipocalin-2 - antagonists & inhibitors
/ Lipocalin-2 - genetics
/ Lipocalin-2 - metabolism
/ Liver - metabolism
/ Liver - pathology
/ Metabolism
/ Mice
/ Mice, Inbred BALB C
/ Mice, Inbred C57BL
/ MicroRNAs - genetics
/ MicroRNAs - metabolism
/ miRNA
/ multidisciplinary
/ Nanoparticles
/ Nanoparticles - administration & dosage
/ Nanoparticles - chemistry
/ Neoplasms - genetics
/ Neoplasms - mortality
/ Neoplasms - pathology
/ Neoplasms - therapy
/ NF-kappa B - genetics
/ NF-kappa B - metabolism
/ NF-κB protein
/ Promoter Regions, Genetic
/ Reactive Oxygen Species - agonists
/ Reactive Oxygen Species - metabolism
/ Ribonucleic acid
/ RNA
/ RNA Interference
/ Science
/ Science (multidisciplinary)
/ Signal Transduction
/ Spleen - metabolism
/ Spleen - pathology
/ Survival Analysis
/ Therapy
/ Tumor Burden
/ Xenograft Model Antitumor Assays
2021
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Gene interfered-ferroptosis therapy for cancers
by
Luo, Tao
, Wang, Jinke
, Gao, Jinliang
in
42/41
/ 42/44
/ 42/89
/ 631/67/1059/153
/ 631/67/1059/602
/ Animals
/ Cancer
/ Cation Transport Proteins - antagonists & inhibitors
/ Cation Transport Proteins - genetics
/ Cation Transport Proteins - metabolism
/ Cell Line, Tumor
/ CRISPR-Associated Proteins - genetics
/ CRISPR-Associated Proteins - metabolism
/ Dependovirus - genetics
/ Dependovirus - metabolism
/ Drug resistance
/ Ferroptosis
/ Ferroptosis - genetics
/ Gene expression
/ Gene Expression Regulation, Neoplastic
/ Genes
/ Growth inhibition
/ Humanities and Social Sciences
/ Humans
/ Interference
/ Iron
/ Iron - metabolism
/ Lipocalin-2 - antagonists & inhibitors
/ Lipocalin-2 - genetics
/ Lipocalin-2 - metabolism
/ Liver - metabolism
/ Liver - pathology
/ Metabolism
/ Mice
/ Mice, Inbred BALB C
/ Mice, Inbred C57BL
/ MicroRNAs - genetics
/ MicroRNAs - metabolism
/ miRNA
/ multidisciplinary
/ Nanoparticles
/ Nanoparticles - administration & dosage
/ Nanoparticles - chemistry
/ Neoplasms - genetics
/ Neoplasms - mortality
/ Neoplasms - pathology
/ Neoplasms - therapy
/ NF-kappa B - genetics
/ NF-kappa B - metabolism
/ NF-κB protein
/ Promoter Regions, Genetic
/ Reactive Oxygen Species - agonists
/ Reactive Oxygen Species - metabolism
/ Ribonucleic acid
/ RNA
/ RNA Interference
/ Science
/ Science (multidisciplinary)
/ Signal Transduction
/ Spleen - metabolism
/ Spleen - pathology
/ Survival Analysis
/ Therapy
/ Tumor Burden
/ Xenograft Model Antitumor Assays
2021
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Gene interfered-ferroptosis therapy for cancers
by
Luo, Tao
, Wang, Jinke
, Gao, Jinliang
in
42/41
/ 42/44
/ 42/89
/ 631/67/1059/153
/ 631/67/1059/602
/ Animals
/ Cancer
/ Cation Transport Proteins - antagonists & inhibitors
/ Cation Transport Proteins - genetics
/ Cation Transport Proteins - metabolism
/ Cell Line, Tumor
/ CRISPR-Associated Proteins - genetics
/ CRISPR-Associated Proteins - metabolism
/ Dependovirus - genetics
/ Dependovirus - metabolism
/ Drug resistance
/ Ferroptosis
/ Ferroptosis - genetics
/ Gene expression
/ Gene Expression Regulation, Neoplastic
/ Genes
/ Growth inhibition
/ Humanities and Social Sciences
/ Humans
/ Interference
/ Iron
/ Iron - metabolism
/ Lipocalin-2 - antagonists & inhibitors
/ Lipocalin-2 - genetics
/ Lipocalin-2 - metabolism
/ Liver - metabolism
/ Liver - pathology
/ Metabolism
/ Mice
/ Mice, Inbred BALB C
/ Mice, Inbred C57BL
/ MicroRNAs - genetics
/ MicroRNAs - metabolism
/ miRNA
/ multidisciplinary
/ Nanoparticles
/ Nanoparticles - administration & dosage
/ Nanoparticles - chemistry
/ Neoplasms - genetics
/ Neoplasms - mortality
/ Neoplasms - pathology
/ Neoplasms - therapy
/ NF-kappa B - genetics
/ NF-kappa B - metabolism
/ NF-κB protein
/ Promoter Regions, Genetic
/ Reactive Oxygen Species - agonists
/ Reactive Oxygen Species - metabolism
/ Ribonucleic acid
/ RNA
/ RNA Interference
/ Science
/ Science (multidisciplinary)
/ Signal Transduction
/ Spleen - metabolism
/ Spleen - pathology
/ Survival Analysis
/ Therapy
/ Tumor Burden
/ Xenograft Model Antitumor Assays
2021
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Journal Article
Gene interfered-ferroptosis therapy for cancers
2021
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Overview
Although some effective therapies have been available for cancer, it still poses a great threat to human health and life due to its drug resistance and low response in patients. Here, we develop a ferroptosis-based therapy by combining iron nanoparticles and cancer-specific gene interference. The expression of two iron metabolic genes (
FPN
and
LCN2
) was selectively knocked down in cancer cells by Cas13a or microRNA controlled by a NF-κB-specific promoter. Cells were simultaneously treated by iron nanoparticles. As a result, a significant ferroptosis was induced in a wide variety of cancer cells. However, the same treatment had little effect on normal cells. By transferring genes with adeno-associated virus and iron nanoparticles, the significant tumor growth inhibition and durable cure were obtained in mice with the therapy. In this work, we thus show a cancer therapy based on gene interference-enhanced ferroptosis.
Improved therapeutic strategies are needed as drug resistance limits the therapeutic efficacy of several clinically approved cancer therapeutics. Here, the authors report a ferroptosis-based therapy using a combination of iron nanoparticles with gene interference to knockdown iron metabolic genes, FPN and LCN2.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
/ 42/44
/ 42/89
/ Animals
/ Cancer
/ Cation Transport Proteins - antagonists & inhibitors
/ Cation Transport Proteins - genetics
/ Cation Transport Proteins - metabolism
/ CRISPR-Associated Proteins - genetics
/ CRISPR-Associated Proteins - metabolism
/ Gene Expression Regulation, Neoplastic
/ Genes
/ Humanities and Social Sciences
/ Humans
/ Iron
/ Lipocalin-2 - antagonists & inhibitors
/ Mice
/ miRNA
/ Nanoparticles - administration & dosage
/ Reactive Oxygen Species - agonists
/ Reactive Oxygen Species - metabolism
/ RNA
/ Science
/ Therapy
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