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  1. Article ; Online: CRISPR/Cas9: A powerful genome editing technique for the treatment of cancer cells with present challenges and future directions.

    Hazafa, Abu / Mumtaz, Muhammad / Farooq, Muhammad Fras / Bilal, Shahid / Chaudhry, Sundas Nasir / Firdous, Musfira / Naeem, Huma / Ullah, Muhammad Obaid / Yameen, Muhammad / Mukhtiar, Muhammad Shahid / Zafar, Fatima

    Life sciences

    2020  Volume 263, Page(s) 118525

    Abstract: ... proved as a powerful technique in the treatment of cancer cells due to its multifunctional properties ... invasion and inducing the apoptosis during the treatment of malignancies in the near future. The present ... review also discussed the current challenges and barriers, and proposed future recommendations ...

    Abstract Cancer is one of the most leading causes of death and a major public health problem, universally. According to accumulated data, annually, approximately 8.5 million people died because of the lethality of cancer. Recently, a novel RNA domain-containing endonuclease-based genome engineering technology, namely the clustered regularly interspaced short palindromic repeat (CRISPR)-associated protein-9 (Cas9) have been proved as a powerful technique in the treatment of cancer cells due to its multifunctional properties including high specificity, accuracy, time reducing and cost-effective strategies with minimum off-target effects. The present review investigates the overview of recent studies on the newly developed genome-editing strategy, CRISPR/Cas9, as an excellent pre-clinical therapeutic option in the reduction and identification of new tumor target genes in the solid tumors. Based on accumulated data, we revealed that CRISPR/Cas9 significantly inhibited the robust tumor cell growth (breast, lung, liver, colorectal, and prostate) by targeting the oncogenes, tumor-suppressive genes, genes associated to therapies by inhibitors, genes associated to chemotherapies drug resistance, and suggested that CRISPR/Cas9 could be a potential therapeutic target in inhibiting the tumor cell growth by suppressing the cell-proliferation, metastasis, invasion and inducing the apoptosis during the treatment of malignancies in the near future. The present review also discussed the current challenges and barriers, and proposed future recommendations for a better understanding.
    MeSH term(s) CRISPR-Cas Systems ; Gene Editing ; Genetic Therapy ; Genome, Human ; Humans ; Neoplasms/genetics ; Neoplasms/pathology ; Neoplasms/therapy
    Keywords covid19
    Language English
    Publishing date 2020-10-05
    Publishing country Netherlands
    Document type Journal Article ; Review
    ZDB-ID 3378-9
    ISSN 1879-0631 ; 0024-3205
    ISSN (online) 1879-0631
    ISSN 0024-3205
    DOI 10.1016/j.lfs.2020.118525
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: CRISPR/Cas9: A powerful genome editing technique for the treatment of cancer cells with present challenges and future directions

    Hazafa, Abu / Mumtaz, Muhammad / Farooq, Muhammad Fras / Bilal, Shahid / Chaudhry, Sundas Nasir / Firdous, Musfira / Naeem, Huma / Ullah, Muhammad Obaid / Yameen, Muhammad / Mukhtiar, Muhammad Shahid / Zafar, Fatima

    Life sciences. 2020 Dec. 15, v. 263

    2020  

    Abstract: ... proved as a powerful technique in the treatment of cancer cells due to its multifunctional properties ... invasion and inducing the apoptosis during the treatment of malignancies in the near future. The present ... review also discussed the current challenges and barriers, and proposed future recommendations ...

    Abstract Cancer is one of the most leading causes of death and a major public health problem, universally. According to accumulated data, annually, approximately 8.5 million people died because of the lethality of cancer. Recently, a novel RNA domain-containing endonuclease-based genome engineering technology, namely the clustered regularly interspaced short palindromic repeat (CRISPR)-associated protein-9 (Cas9) have been proved as a powerful technique in the treatment of cancer cells due to its multifunctional properties including high specificity, accuracy, time reducing and cost-effective strategies with minimum off-target effects. The present review investigates the overview of recent studies on the newly developed genome-editing strategy, CRISPR/Cas9, as an excellent pre-clinical therapeutic option in the reduction and identification of new tumor target genes in the solid tumors. Based on accumulated data, we revealed that CRISPR/Cas9 significantly inhibited the robust tumor cell growth (breast, lung, liver, colorectal, and prostate) by targeting the oncogenes, tumor-suppressive genes, genes associated to therapies by inhibitors, genes associated to chemotherapies drug resistance, and suggested that CRISPR/Cas9 could be a potential therapeutic target in inhibiting the tumor cell growth by suppressing the cell-proliferation, metastasis, invasion and inducing the apoptosis during the treatment of malignancies in the near future. The present review also discussed the current challenges and barriers, and proposed future recommendations for a better understanding.
    Keywords CRISPR-Cas systems ; RNA ; apoptosis ; breasts ; cell growth ; cell proliferation ; cost effectiveness ; death ; drug resistance ; gene editing ; liver ; lungs ; metastasis ; neoplasm cells ; neoplasms ; oncogenes ; people ; public health ; therapeutics
    Language English
    Dates of publication 2020-1215
    Publishing place Elsevier Inc.
    Document type Article
    Note NAL-light
    ZDB-ID 3378-9
    ISSN 1879-0631 ; 0024-3205
    ISSN (online) 1879-0631
    ISSN 0024-3205
    DOI 10.1016/j.lfs.2020.118525
    Database NAL-Catalogue (AGRICOLA)

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