brain tumor, and glioblastoma accounts for 82% of cases of malignant glioma. Glioblastomas arise from glial precursor cells and are characterized histologically by considerable cellularity, mitotic activity, vascular proliferation, and necrosis. They are highly invasive, infiltrating surrounding brain tissues, yet they are typically confined to the central nervous system and do not metastasize.1 From a molecular standpoint, malignant glioblastomas are heterogeneous tumors, and genome studies have
utility [4] especially because of high rate of tumor recurrence. Alternative platinum-based regimens incorporating OX have demonstrated only marginal benefits in PC and CC patients [5]. Emerging evidence suggests that the poor response to the current treatment modalities in GI cancer is linked to aberrations in multiple signaling pathways together with the presence of a small subpopulation of drug-resistant CSCs/CSLCs that have the propensity to promote tumor recurrence, invasion and metastasis [6]. Although