RNA is highly labile, and will quickly degrade if you do not protect it. This will lead to false negative results. If you are referring to an experiment already conducted I would say No. If you are referring to an upcommng experiment you need to chemically stabilize the RNA as this will (hopefully) maintain the gene expression profile.
I traditionally, snap freeze cells in liquid nitrogen before freezing at -80, followed by a kit RNA extraction.
Thanks Nicklas for your anwer. As the LDH measurement is already performed I will try classical extraction followed by QC with bioanalyser nano chips the RIN number will be a decisive information