TY - JOUR
T1 - Chemoresistance and chemotherapy targeting stem-like cells in malignant glioma
AU - Sørensen, Mia Dahl
AU - Fosmark, Sigurd
AU - Hellwege, Sofie
AU - Beier, Dagmar
AU - Kristensen, Bjarne Winther
AU - Beier, Christoph Patrick
PY - 2015
Y1 - 2015
N2 - Glioblastoma remains a tumor with a dismal prognosis because of failure of current treatment. Glioblastoma cells with stem cell (GSC) properties survive chemotherapy and give rise to tumor recurrences that invariably result in the death of the patients. Here we summarize the current knowledge on chemoresistance of malignant glioma with a strong focus on GSC. Chemoresistant GSC are the most likely cause of tumor recurrence, but it remains controversial if GSC and under which conditions GSC are more chemoresistant than non-GSC within the tumor. Regardless of this uncertainty, the chemoresistance varies and it is mainly mediated by intrinsic factors. O6-methyl-guanidine methyltransferase (MGMT) remains the most potent mediator of chemoresistance, but disturbed mismatch repair system and multidrug resistance proteins contribute substantially. However, the intrinsic resistance by MGMT expression is regulated by extrinsic factors like hypoxia increasing MGMT expression and thereby resistance to alkylating chemotherapy. The search of new biomarkers helping to predict the tumor response to chemotherapy is ongoing and will complement the already known markers like MGMT.
AB - Glioblastoma remains a tumor with a dismal prognosis because of failure of current treatment. Glioblastoma cells with stem cell (GSC) properties survive chemotherapy and give rise to tumor recurrences that invariably result in the death of the patients. Here we summarize the current knowledge on chemoresistance of malignant glioma with a strong focus on GSC. Chemoresistant GSC are the most likely cause of tumor recurrence, but it remains controversial if GSC and under which conditions GSC are more chemoresistant than non-GSC within the tumor. Regardless of this uncertainty, the chemoresistance varies and it is mainly mediated by intrinsic factors. O6-methyl-guanidine methyltransferase (MGMT) remains the most potent mediator of chemoresistance, but disturbed mismatch repair system and multidrug resistance proteins contribute substantially. However, the intrinsic resistance by MGMT expression is regulated by extrinsic factors like hypoxia increasing MGMT expression and thereby resistance to alkylating chemotherapy. The search of new biomarkers helping to predict the tumor response to chemotherapy is ongoing and will complement the already known markers like MGMT.
KW - Animals
KW - Antineoplastic Agents, Alkylating/therapeutic use
KW - Brain Neoplasms/drug therapy
KW - DNA Mismatch Repair/genetics
KW - DNA Modification Methylases/physiology
KW - DNA Repair Enzymes/physiology
KW - Dacarbazine/analogs & derivatives
KW - Drug Resistance, Neoplasm/genetics
KW - Glioma/drug therapy
KW - Humans
KW - Neoplastic Stem Cells/drug effects
KW - Temozolomide
KW - Tumor Suppressor Proteins/physiology
U2 - 10.1007/978-3-319-16537-0_7
DO - 10.1007/978-3-319-16537-0_7
M3 - Review
C2 - 25895710
SN - 0065-2598
VL - 853
SP - 111
EP - 138
JO - Advances in Experimental Medicine and Biology
JF - Advances in Experimental Medicine and Biology
ER -