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The most common genetic alterations in GBM involve the inactivation of tumor suppressor genes, such as p53, PTEN, and retinoblastoma (RB1), leading to uncontrolled cell proliferation, escape from apoptosis, and genomic instability [14, 16]

In this review, we summarize current knowledge concerning transport of Cd and its complexes (mainly Cd bound to glutathione) by the ABC transporters ABCB1 (P-glycoprotein, MDR1), ABCB6, ABCC1 (multidrug resistance related protein 1, MRP1), ABCC7 (cystic fibrosis transmembrane regulator, CFTR), and ABCG2 (breast cancer related protein, BCRP)