Research Paper Volume 13, Issue 1 pp 163—180

Identification of a novel and potent small molecule inhibitor of SRPK1: mechanism of dual inhibition of SRPK1 for the inhibition of cancer progression

Relative expression of apoptotic factors determined by quantitative real time PCR (qRT-PCR) analysis of (A) Tumour necrosis factor-α (TNF-α), (B) Tumour suppressor (P53), (C) Apoptosis regulator (BAX), (D) Apoptotic protease activating factor 1 (APAF 1), (E) Cytochrome-c and (F) Caspase 3 genes in Jurkat cells treated with 10μm Compound C02 for 24 h. mRNA levels of apoptotic factors were determined relative to the endogenous control Actin, according to the formula 2 to the power of delta cycle threshold (2DCt), where DCt¼Ct, reference gene – Ct, test gene. Differences between experimental groups were tested for significance using nonparametric Mann–Whitney test (GraphPad Prism version 5, San Diego, CA), for both mRNA, protein expressions and other analysis. Levels of significance are indicated by p

Figure 4. Relative expression of apoptotic factors determined by quantitative real time PCR (qRT-PCR) analysis of (A) Tumour necrosis factor-α (TNF-α), (B) Tumour suppressor (P53), (C) Apoptosis regulator (BAX), (D) Apoptotic protease activating factor 1 (APAF 1), (E) Cytochrome-c and (F) Caspase 3 genes in Jurkat cells treated with 10μm Compound C02 for 24 h. mRNA levels of apoptotic factors were determined relative to the endogenous control Actin, according to the formula 2 to the power of delta cycle threshold (2DCt), where DCt¼Ct, reference gene – Ct, test gene. Differences between experimental groups were tested for significance using nonparametric Mann–Whitney test (GraphPad Prism version 5, San Diego, CA), for both mRNA, protein expressions and other analysis. Levels of significance are indicated by p< 0.05.