3 × 10
5 MFC cells were subcutaneously injected into nude mice. Ten days after injection, BMDMs‐exo, M2‐exo, M2‐si‐control‐exo, or M2‐si‐CRNDE‐exo (10 µg) was injected into the center of the homograft tumors of mice (
n = 7 each group), followed by intraperitoneal injection of CDDP (10 mg/kg). Six days after CDDP treatment, all mice were sacrificed and the homograft tumors were collected.
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A
Growth curves of MFC subcutaneous homograft tumors (The homograft tumor sizes were recorded from the day of CDDP treatment). *P < 0.05, **P < 0.01 vs. BMDMs‐exo; #P < 0.05, ##P < 0.01 vs. M2‐si‐control‐exo.
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B, C
The homograft tumors (B) photos and (C) weight of each mouse on day 6 after CDDP injection. **P < 0.01.
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D
LncRNA CRNDE expression in homograft tumors of mice. **P < 0.01.
Data information: Data are expressed as mean ± SD. (A, C and D): one‐way ANOVA.