Well, a bit more information would be helpful. What sizes products do you expect for your GAPDH and ACTIN primer sets? Which ladder did you use (and what size is the smallest band?)
My impression is that these gels are showing primer dimers, do you have a negative control for comparison? The gel on the bottom right has some larger smears that look a bit suspect (possible gDNA carryover).
Do your primers also work for gDNA (and if so what size bands do you expect)? You'll want to check that everything is working well so if you can you gDNA as a positive control for the primers and cycle conditions that would be helpful. It won't help tell if the cDNA is good but it will be a start on checking the experimental setup in general.
Can you obtain a bit of cDNA that you know is good and use that as a positive control?