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. 2018 Jun 18;16(3):3260–3266. doi: 10.3892/ol.2018.8985

Figure 3.

Figure 3.

OVCAR3 and OVCAR8 cell apoptosis detection by fluorescence-activated cell sorting and cell cycle analysis by flow cytometry. (A) Cell apoptosis was analyzed using Annexin V FITC and (B) quantified. The apoptosis rate in the rhAMH treated group (48 h) was significantly increased compared with the control group (OVCAR3, P=0.035; OVCAR8, P=0.020). The apoptosis rate increased at 72 h but was not significantly different compared with the 48 h group (OVCAR3, P=0.145; OVCAR8, P=0.296). (C) Quantified flow cytometry revealed the number of cells at the G1 phase. The percentage of cells at G1 phase in the rhAMH treated group (48 h) increased, but was not significantly different when compared with the control group (OVCAR3, P=0.070; OVCAR8, P=0.051). A significant difference was identified at 72 h compared with the control group (OVCAR3, P=0.016; OVCAR8, P=0.019). (D) Flow cytometry results. *P<0.01 vs. the control. RhAMH, recombinant human anti-Müllerian hormone; FITC, fluorescein isothiocyanate.