Current promising treatment strategy for glioblastoma multiform: A review

被引:79
作者
Bahadur, Sanjib [1 ]
Sahu, Arvind Kumar [1 ]
Baghel, Pragya [1 ]
Saha, Suman [1 ]
机构
[1] Columbia Inst Pharm, Dept Pharmaceut, Near Vidhan Sabha, Raipur, Chhattisgarh, India
关键词
Glioblastoma; temozolomide; resistance; targeted therapy; TEMOZOLOMIDE PLUS O-6-BENZYLGUANINE; RECURRENT; COMBINATION; THERAPY; TRIAL; CELLS;
D O I
10.4081/oncol.2019.417
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Glioblastoma multiform (GBM) is a heterogeneous group of primary neoplasm resistant to conventional therapies. Due to their infiltrative nature it not fully isolated by aggressive surgery, radiation and chemotherapy showing poor prognosis in glioma patients. Unfortunately, diagnosed patients die Within 1.5-2 year treatment schedule. Currently temozolomide (TMZ) is the first choice for the prognosis of GBM patients. TMZ metabolites methyl triazen imidazol carboxamide form complex With alkyl guanine alkyl transferase (06 MGMT- DNA repair protein) induced DNA damage following resistance properties of TMZ and inhibit the overall survival of the patients. Last few decades different TMZ conjugated strategy is developed to overcome the resistance and enhance the chemotherapy efficacy. The main aim of this review is to introduce the new promising pharmaceutical candidates that significantly influence the therapeutic response of the TMZ in context of targeted therapy of glioblastoma patients. It is hoped that this proposed strategy are highly effective to overcome the current resistance limitations of TMZ in GBM patients and enhance the survival rate of the patients.
引用
收藏
页码:114 / 124
页数:11
相关论文
共 41 条
[1]   Autophagy enhancement contributes to the synergistic effect of vitamin D in temozolomide-based glioblastoma chemotherapy [J].
Bak, Dong-Ho ;
Kang, Seong Hee ;
Choi, Du Ri ;
Gil, Mi Na ;
Yu, Kwang Sik ;
Jeong, Ji Heun ;
Lee, Nam-Seob ;
Lee, Je-Hun ;
Jeong, Young-Gil ;
Kim, Dong Kwan ;
Kim, Do-Kyung ;
Kim, Jwa-Jin ;
Han, Seung-Yun .
EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2016, 11 (06) :2153-2162
[2]   Function of neuronal nitric oxide synthase enzyme in temozolomide-induced damage of astrocytic tumor cells [J].
Borges Resende, Fernando Francisco ;
Titze-de-Almeida, Simoneide Souza ;
Titze-de-Almeida, Ricardo .
ONCOLOGY LETTERS, 2018, 15 (04) :4891-4899
[3]   Nanostructured lipid carriers based temozolomide and gene co-encapsulated nanomedicine for gliomatosis cerebri combination therapy [J].
Chen, Zhihua ;
Lai, Xianliang ;
Song, Shuxin ;
Zhu, Xingen ;
Zhu, Jianming .
DRUG DELIVERY, 2016, 23 (04) :1369-1373
[4]  
Chinot OL, 2014, NEW ENGL J MED, V370, P709, DOI 10.1056/NEJMoa1308345
[5]   Alpha lipoic acid attenuates hypoxia-induced apoptosis, inflammation and mitochondrial oxidative stress via inhibition of TRPA1 channel in human glioblastoma cell line [J].
Deveci, Haci Ahmet ;
Akyuva, Yener ;
Nur, Gokhan ;
Naziroglu, Mustafa .
BIOMEDICINE & PHARMACOTHERAPY, 2019, 111 :292-304
[6]  
Ellis YP, 2015, THESIS
[7]   Combined effects of temozolomide and the ribonucleotide reductase inhibitors didox and trimidox in malignant brain tumor cells [J].
Figul, M ;
Söling, A ;
Dong, HJ ;
Chou, TC ;
Rainov, NG .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2003, 52 (01) :41-46
[8]  
Fujimaki T., 2007, WORLD J SURG ONCOL, V5, P1
[9]  
Gao H., 2013, Scientific reports, V3, P1
[10]   Overcoming Temozolomide Resistance in Glioblastoma via Dual Inhibition of NAD+ Biosynthesis and Base Excision Repair [J].
Goellner, Eva M. ;
Grimme, Bradford ;
Brown, Ashley R. ;
Lin, Ying-Chih ;
Wang, Xiao-Hong ;
Sugrue, Kelsey F. ;
Mitchell, Leah ;
Trivedi, Ram N. ;
Tang, Jiang-Bo ;
Sobol, Robert W. .
CANCER RESEARCH, 2011, 71 (06) :2308-2317