and NF-κB pathways. Quinacrine, an antimalarial drug, and other derivatives of 9 aminoacridine have been shown to simultaneously repress NF-κB and activate p53 in renal cell carcinoma [192]. Other molecules with similar potential include nutlins [193, 194], cisplatin [195, 196], leptomycin B [197, 198], adenosine-2,3-dialdehyde [199], the NSAID JTE-522 [200], and the cyclin-dependent kinase inhibitors R-roscovitine [201, 202]; and flavopiridol [203, 204].