Figure 2
(A) HeLa cells were transfected with HOTAIR siRNA or scramble for 24 h, the mRNA levels of HOTAIR were measured by qRT-PCR. (B) HeLa cells were transfected with HOTAIR siRNA or scramble for 24, 48, 72, and 96 h, the cell viability was assayed by CCK-8 kit. (C) The cell apoptosis was analyzed by Annexin V flow cytometry. (D) Apoptotic cell quantitation for three independent experiments. (E) Protein levels of Ki67 and PCNA were assayed by Western blot. (F) Protein levels of cleaved caspase-3 and cleaved caspase-9 were assayed by Western blot. All the experiments were repeated at least three times and the representative data were shown. GAPDH was used as loading control; *P<0.05, **P<0.01 compared with scramble.
HOTAIR knockdown increases apoptosis in cervical cancer cells

(A) HeLa cells were transfected with HOTAIR siRNA or scramble for 24 h, the mRNA levels of HOTAIR were measured by qRT-PCR. (B) HeLa cells were transfected with HOTAIR siRNA or scramble for 24, 48, 72, and 96 h, the cell viability was assayed by CCK-8 kit. (C) The cell apoptosis was analyzed by Annexin V flow cytometry. (D) Apoptotic cell quantitation for three independent experiments. (E) Protein levels of Ki67 and PCNA were assayed by Western blot. (F) Protein levels of cleaved caspase-3 and cleaved caspase-9 were assayed by Western blot. All the experiments were repeated at least three times and the representative data were shown. GAPDH was used as loading control; *P<0.05, **P<0.01 compared with scramble.

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