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. Author manuscript; available in PMC: 2016 Dec 1.
Published in final edited form as: J Cell Physiol. 2015 Dec;230(12):2936–2950. doi: 10.1002/jcp.25022

Figure 6. DNA damage treatments and serum starvation induce the Nupr1L gene overexpression.

Figure 6

(a) MCF-7 cells were treated with increasing concentrations of Oxaliplatin (10, 20 and 40 μM) for 24 h. Capan-2 (b) and Hela cells (c) were treated with increasing concentrations of Oxaliplatin (10 and 20 μM) for 18 h. MCF-7 (d), Capan-2 (e) and Hela cells (f) were cultured in FBS starvation conditions for 24 h, 60 h and 12 h, respectively. mRNA levels of Nupr1L were analyzed by RT-qPCR. The housekeeping gene Cyclophilin was used as internal control in order to the normalizing of values. Results are expressed as fold change compared with the control ± S.D. Means sharing the same superscript letter are not significantly different from one another (P< 0.05). *P<0.05 and **P<0.01.