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We are analyzing https://link.springer.com/article/10.1186/s11658-022-00348-2.

Title:
CRISPR/Cas9 gene editing: a new approach for overcoming drug resistance in cancer | Cellular & Molecular Biology Letters
Description:
The CRISPR/Cas9 system is an RNA-based adaptive immune system in bacteria and archaea. Various studies have shown that it is possible to target a wide range of human genes and treat some human diseases, including cancers, by the CRISPR/Cas9 system. In fact, CRISPR/Cas9 gene editing is one of the most efficient genome manipulation techniques. Studies have shown that CRISPR/Cas9 technology, in addition to having the potential to be used as a new therapeutic approach in the treatment of cancers, can also be used to enhance the effectiveness of existing treatments. Undoubtedly, the issue of drug resistance is one of the main obstacles in the treatment of cancers. Cancer cells resist anticancer drugs by a variety of mechanisms, such as enhancing anticancer drugs efflux, enhancing DNA repair, enhancing stemness, and attenuating apoptosis. Mutations in some proteins of different cellular signaling pathways are associated with these events and drug resistance. Recent studies have shown that the CRISPR/Cas9 technique can be used to target important genes involved in these mechanisms, thereby increasing the effectiveness of anticancer drugs. In this review article, studies related to the applications of this technique in overcoming drug resistance in cancer cells will be reviewed. In addition, we will give a brief overview of the limitations of the CRISP/Cas9 gene-editing technique.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Science
  • Health & Fitness
  • Education

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

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Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {💸}

We're unsure how the site profits.

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Keywords {🔍}

cancer, pubmed, resistance, cells, drug, article, google, scholar, cas, crisprcas, study, central, cell, showed, gene, technology, cancers, involved, treatment, results, dna, studies, targeting, expression, system, genes, repair, signaling, drugs, role, technique, important, wang, editing, zhang, chemotherapy, breast, target, effects, mechanisms, sensitivity, inhibition, shown, enhance, doxorubicin, genomewide, liu, overcoming, overcome, lung,

Topics {✒️}

gag//gtaa ac → gag//gtaa gt genome-wide crispr/cas9 screens genome-wide crispr/cas9 screen crispr/cas9-mediated genome engineering crispr/cas9-based genome editing crispr/cas9 gene-editing technology crispr/cas9-mediated gene knockout crispr/cas9 genome-wide loss crispr/cas9 gene-editing technique crisp/cas9 gene-editing technique cas9 generates double-strand break crispr/cas9 genome editing akt-yb1-mdr1 signaling pathway crispr/cas9 gene editing wnt/b-catenin signaling pathway crispr-cas9 knockout screening genome-wide crispr libraries crispr/cas9-mediated knockout p-glycoprotein-mediated multidrug resistance p-gp-overexpressing mcf-7 cells article vaghari-tabari etoposide-resistant leukemia cells mammalian n6-methyladenosine sites kras/braf-mutated colorectal cancers writing—original draft preparation triple-negative breast cancer crispr/cas9-mediated mutagenesis dna-targeting anti-cancer therapies drug-resistant cell lines crispr-cas9-mediated silencing article download pdf muscle-invasive bladder cancer pi3k-akt-mtor pathway pi3k/akt/mtor pathway small-cell lung cancer crispr/cas9-mediated inhibition cutaneous t-cell lymphoma crispr/cas9 technique enhances cas9-mediated gene disruption multidrug-resistant cancer cells genome editing techniques target single-strand break drug-resistant cancer cell create single-strand breaks cisplatin-mediated cell death suppressing mdr1/p-gp expression drug-resistant colorectal cancer central nervous system platelet-derived growth factor crispr/cas9 system delivery

Questions {❓}

  • Limitation of CRISPR/Cas9 gene editing: is there a long way to the clinic?
  • The role of DNA damage response in chemo- and radio-resistance of cancer cells: can DDR inhibitors sole the problem?
  • Tyrosine kinase inhibitors in chronic myeloid leukaemia: which, when, for whom?

Schema {🗺️}

WebPage:
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         headline:CRISPR/Cas9 gene editing: a new approach for overcoming drug resistance in cancer
         description:The CRISPR/Cas9 system is an RNA-based adaptive immune system in bacteria and archaea. Various studies have shown that it is possible to target a wide range of human genes and treat some human diseases, including cancers, by the CRISPR/Cas9 system. In fact, CRISPR/Cas9 gene editing is one of the most efficient genome manipulation techniques. Studies have shown that CRISPR/Cas9 technology, in addition to having the potential to be used as a new therapeutic approach in the treatment of cancers, can also be used to enhance the effectiveness of existing treatments. Undoubtedly, the issue of drug resistance is one of the main obstacles in the treatment of cancers. Cancer cells resist anticancer drugs by a variety of mechanisms, such as enhancing anticancer drugs efflux, enhancing DNA repair, enhancing stemness, and attenuating apoptosis. Mutations in some proteins of different cellular signaling pathways are associated with these events and drug resistance. Recent studies have shown that the CRISPR/Cas9 technique can be used to target important genes involved in these mechanisms, thereby increasing the effectiveness of anticancer drugs. In this review article, studies related to the applications of this technique in overcoming drug resistance in cancer cells will be reviewed. In addition, we will give a brief overview of the limitations of the CRISP/Cas9 gene-editing technique.
         datePublished:2022-06-17T00:00:00Z
         dateModified:2022-06-17T00:00:00Z
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            Gene editing
            Chemoresistance
            Malignancy
            Cancer treatment
            Cell Biology
            Biochemistry
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      headline:CRISPR/Cas9 gene editing: a new approach for overcoming drug resistance in cancer
      description:The CRISPR/Cas9 system is an RNA-based adaptive immune system in bacteria and archaea. Various studies have shown that it is possible to target a wide range of human genes and treat some human diseases, including cancers, by the CRISPR/Cas9 system. In fact, CRISPR/Cas9 gene editing is one of the most efficient genome manipulation techniques. Studies have shown that CRISPR/Cas9 technology, in addition to having the potential to be used as a new therapeutic approach in the treatment of cancers, can also be used to enhance the effectiveness of existing treatments. Undoubtedly, the issue of drug resistance is one of the main obstacles in the treatment of cancers. Cancer cells resist anticancer drugs by a variety of mechanisms, such as enhancing anticancer drugs efflux, enhancing DNA repair, enhancing stemness, and attenuating apoptosis. Mutations in some proteins of different cellular signaling pathways are associated with these events and drug resistance. Recent studies have shown that the CRISPR/Cas9 technique can be used to target important genes involved in these mechanisms, thereby increasing the effectiveness of anticancer drugs. In this review article, studies related to the applications of this technique in overcoming drug resistance in cancer cells will be reviewed. In addition, we will give a brief overview of the limitations of the CRISP/Cas9 gene-editing technique.
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      dateModified:2022-06-17T00:00:00Z
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         CRISPR/Cas9
         Gene editing
         Chemoresistance
         Malignancy
         Cancer treatment
         Cell Biology
         Biochemistry
         general
         Biological and Medical Physics
         Biophysics
         Biotechnology
         Molecular Medicine
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      name:Faezeh Malakoti
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            name:Tabriz University of Medical Sciences
            address:
               name:Department of Clinical Biochemistry and Laboratory Medicine, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
               type:PostalAddress
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      name:Forough Alemi
      affiliation:
            name:Tabriz University of Medical Sciences
            address:
               name:Department of Clinical Biochemistry and Laboratory Medicine, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
               type:PostalAddress
            type:Organization
      name:Durdi Qujeq
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            address:
               name:Cellular and Molecular Biology Research Center (CMBRC), Health Research Institute, Babol University of Medical Sciences, Babol, Iran
               type:PostalAddress
            type:Organization
            name:Babol University of Medical Sciences
            address:
               name:Department of Clinical Biochemistry, Babol University of Medical Sciences, Babol, Iran
               type:PostalAddress
            type:Organization
      name:Zatollah Asemi
      affiliation:
            name:Kashan University of Medical Sciences
            address:
               name:Research Center for Biochemistry and Nutrition in Metabolic Diseases, Kashan University of Medical Sciences, Kashan, Iran
               type:PostalAddress
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      email:[email protected]
      name:Bahman Yousefi
      affiliation:
            name:Tabriz University of Medical Sciences
            address:
               name:Department of Clinical Biochemistry and Laboratory Medicine, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
               type:PostalAddress
            type:Organization
            name:Tabriz University of Medical Sciences
            address:
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               type:PostalAddress
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      email:[email protected]
PostalAddress:
      name:Department of Clinical Biochemistry and Laboratory Medicine, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
      name:Department of Clinical Biochemistry and Laboratory Medicine, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
      name:Department of Clinical Biochemistry and Laboratory Medicine, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
      name:Department of Clinical Biochemistry and Laboratory Medicine, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
      name:Department of Clinical Biochemistry and Laboratory Medicine, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
      name:Cellular and Molecular Biology Research Center (CMBRC), Health Research Institute, Babol University of Medical Sciences, Babol, Iran
      name:Department of Clinical Biochemistry, Babol University of Medical Sciences, Babol, Iran
      name:Research Center for Biochemistry and Nutrition in Metabolic Diseases, Kashan University of Medical Sciences, Kashan, Iran
      name:Department of Clinical Biochemistry and Laboratory Medicine, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
      name:Molecular Medicine Research Center, Tabriz University of Medical Sciences, Tabriz, Iran

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