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. 2016 Mar 14;7(22):33461–33471. doi: 10.18632/oncotarget.8075

Table 2. Representative factors that can be manipulated by different types of CRISPR genome editing technologies for brain tumor modeling.

Factors Role in tumorigenesis Proposed CRISPR methods Previous methods Ref
p53 (a) (b) tumor suppression CRISPR KO CRISPR KO [43, 44]
Nf1 (a) tumor suppression CRISPR KO CRISPR KO [44]
Pten (a) (b) tumor suppression CRISPR KO CRISPR KO [43, 44]
Ptch1 (c) tumor suppression CRISPR KO CRISPR KO [44]
Bmi1 (a) (d) tumor facilitation CRISPR KI Bmi1 shRNA [83, 84]
Met (e) tumor facilitation CRISPR KI CRISPR KO [85]
Notch1(a) tumor facilitation CRISPR KI Notch1 siRNA [86]
CDK6(a) tumor facilitation CRISPR KI CDK6 shRNA [87]
miR-10b(a) tumor facilitation CRISPRa miR-10b mimics [88]
TERT(e) tumor facilitation CRISPRa CRISPRa [90]
LSD1(f) tumor facilitation CRISPRa CRISPRa [90]
miR-218(a) tumor suppression CRISPRi anti- miR-218 [28]
miR-128(a) tumor suppression CRISPRi anti-miR-128 [91]

Abbreviations: CRISPR KO: CRISPR knock out; CRISPR KI: CRISPR knock in; CRISPRa: CRISPR activation; CRISPRi: CRISPR interference.

Note: (a) glioma; (b) liver; (c) medulloblastoma; (d) breast cancer with brain metastases; (e) HEK293 cell line; (f) embryonic stem cell