Identification of genes associated with SiHa cell sensitivity to paclitaxel by CRISPR-Cas9 knockout screening

被引:0
作者
Wei, Wei [1 ]
He, Yue [1 ]
Wu, Yu-Mei [1 ]
机构
[1] Capital Med Univ, Beijing Obstet & Gynecol Hosp, Dept Gynecol Oncol, 17 Qihelou St, Beijing 100006, Peoples R China
来源
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL PATHOLOGY | 2018年 / 11卷 / 04期
关键词
Paclitaxel sensitivity; cervical cancer; CRISPR-Cas9; technology; TAXOL-INDUCED APOPTOSIS; BREAST-CANCER; PI3K/AKT/MTOR PATHWAY; MULTIDRUG-RESISTANCE; PROTEIN PHOSPHATASE; SIGNALING PATHWAYS; CARCINOMA CELLS; NVP-BEZ235; MAPK; AKT;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Although chemotherapy has significantly improved the prognosis of patients with cervical cancer, many patients exhibit selective responses to chemotherapy. This study aimed to identify genes associated with the sensitivity of cervical cancer cells to paclitaxel. SiHa cells were transfected with lentiCRISPR (genome-scale CRISPR knockout library v. 2) and then treated with paclitaxel or vehicle for 14 days. Subsequently, we screened for candidate genes whose loss resulted in sensitivity to paclitaxel. We obtained 374 candidates, some of which were consistent with those reported in previous studies, including ABCC9, IL37, EIF3C, AKT1S1, and several members of the PPP gene family (PPP1R7, PPP2R5B, PPP1R7, and PPP1R11). Importantly, our findings highlighted the newly identified genes that could provide novel insights into the mechanisms of paclitaxel sensitivity in cervical cancer. Cas9 technology provides a reliable method for the exploration of more effective combination chemotherapies for patients at the gene level.
引用
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页码:1972 / 1978
页数:7
相关论文
共 39 条
  • [11] Protein phosphatase 2A: a highly regulated family of serine/threonine phosphatases implicated in cell growth and signalling
    Janssens, V
    Goris, J
    [J]. BIOCHEMICAL JOURNAL, 2001, 353 : 417 - 439
  • [12] Apoptosis: A link between cancer genetics and chemotherapy
    Johnstone, RW
    Ruefli, AA
    Lowe, SW
    [J]. CELL, 2002, 108 (02) : 153 - 164
  • [13] SURFACE GLYCOPROTEIN MODULATING DRUG PERMEABILITY IN CHINESE-HAMSTER OVARY CELL MUTANTS
    JULIANO, RL
    LING, V
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1976, 455 (01) : 152 - 162
  • [14] KEGG for integration and interpretation of large-scale molecular data sets
    Kanehisa, Minoru
    Goto, Susumu
    Sato, Yoko
    Furumichi, Miho
    Tanabe, Mao
    [J]. NUCLEIC ACIDS RESEARCH, 2012, 40 (D1) : D109 - D114
  • [15] Pathological roles of MAPK signaling pathways in human diseases
    Kim, Eun Kyung
    Choi, Eui-Ju
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2010, 1802 (04): : 396 - 405
  • [16] IL-37 induces autophagy in hepatocellular carcinoma cells by inhibiting the PI3K/AKT/mTOR pathway
    Li, Ting-Ting
    Zhu, Di
    Mou, Tong
    Guo, Zhen
    Pu, Jun-Liang
    Chen, Qing-Song
    Wei, Xu-Fu
    Wu, Zhong-Jun
    [J]. MOLECULAR IMMUNOLOGY, 2017, 87 : 132 - 140
  • [17] Reversal of Taxol resistance in hepatoma by cyclosporin A: involvement of the PI-3 kinase-AKT I pathway
    Lin, HL
    Lui, WY
    Liu, TY
    Chi, CW
    [J]. BRITISH JOURNAL OF CANCER, 2003, 88 (06) : 973 - 980
  • [18] Activities of multiple cancer-related pathways are associated with BRAF mutation and predict the resistance to BRAF/MEK inhibitors in melanoma cells
    Liu, Dingxie
    Liu, Xuan
    Xing, Mingzhao
    [J]. CELL CYCLE, 2014, 13 (02) : 208 - 219
  • [19] Liu Liying, 2016, Zhong Nan Da Xue Xue Bao Yi Xue Ban, V41, P1016
  • [20] RNA-Guided Human Genome Engineering via Cas9
    Mali, Prashant
    Yang, Luhan
    Esvelt, Kevin M.
    Aach, John
    Guell, Marc
    DiCarlo, James E.
    Norville, Julie E.
    Church, George M.
    [J]. SCIENCE, 2013, 339 (6121) : 823 - 826