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Table 3 The application of CRISPR/Cas9 in Rhabdomyosarcoma research

From: Applications of CRISPR/Cas9 in the research of malignant musculoskeletal tumors

Target Genes

Cell lines

CRISPR/Cas9 Applications

Effects

References

Pax3,Foxo1

Foxo1-inv+/+ myoblasts (mice)/primary myoblasts

induce chromosomal translocation

Pax3-Foxo1 chromosomal translocation ARSM model, no function research

[82]

DMD

CCL-136 RD

knock out

Produce DMD deletion - immortalized muscle cell line

[83, 84]

DYSF

TE671

knock out

Myogenin↓,TSP-1 expression↑,membrane Repair ability ↓,

[85]

Dozens genes

JR1,RD

knock out

Validates oncogenes and tumors suppressors defined by iExCN tool

[79]

HDAC1–10 genes (class I and II HDAC genes)

381 T, RD,SMS-CTR, Rh3,Rh5,Rh30

knock out

cell growth↓,

myogenic differentiation↑,

xenografts tumor proliferation↓,differentiation↑,

[86]

PAX3-FOXO1

Dbt-MYCN / indP3F parental cellsa, recurrent tumour-derived cells.

knock out

Fail to form tumor in Dbt-MYCN/indP3F parental cells, form tumor in recurrent tumour-derived cells

[80]

NRAS,HRAS

381 T,SMS-CTR ERMS cells

knock out

Cell viability↓,

apoptosis↑,

G1 phase arrest,

expression of key cell-cycle and DNA replication genes↓,

median survival of mice↑,xenografts tumor growth↓,

myogenic differentiation↑,

tumor regression

Perk expression↓

[87]

  1. Notes
  2. a:Dbt-MYCN/indP3F cells: immortalized human myoblasts containing constitutive MYCN and inducible PAX3–FOXO1; ↑:Up-regulation: ↓:Down-regulation