Caffeine Sensitizes U87-MG Human Glioblastoma Cells to Temozolomide through Mitotic Catastrophe by Impeding G2 Arrest

• Published in: BioMed research international Vol. 2018; no. 2018; pp. 1 - 10
• Main Authors: Cheng, Stephen Yin, Kiang, Karrie Mei Yee, Zhang, Pingde, Li, Ning, Leung, Gilberto K. K.
• Format: Journal Article
• Language: English
• Published: Cairo, Egypt Hindawi Publishing Corporation 01.01.2018; Hindawi; Hindawi Limited
• Subjects: Anticancer properties; Antineoplastic Agents, Alkylating - pharmacology; Apoptosis; Biology; Brain cancer; Brain research; Caffeine; Caffeine - pharmacology; Camptothecin; Cancer therapies; Cell cycle; Cell death; Cell Line, Tumor; Central Nervous System Stimulants - pharmacology; Chemoresistance; Chemotherapy; Cisplatin; Combined treatment; Cyclin-dependent kinase inhibitor p21; Cytotoxicity; Dacarbazine; Deoxyribonucleic acid; DNA; DNA damage; G2 phase; G2 Phase Cell Cycle Checkpoints - drug effects; Gene expression; Glioblastoma; Glioblastoma - pathology; Glioblastoma cells; Glioblastoma multiforme; Humans; Leukemia; Medical research; Mitosis; Neoplasm Recurrence, Local; p53 Protein; Phosphorylation; Senescence; Signal transduction; Temozolomide; Temozolomide - pharmacology; Tumors; United States > US
• ISSN: 2314-6133; 2314-6141
• DOI: 10.1155/2018/5364973

Temozolomide (TMZ) is the first-line chemotherapeutic agent in the treatment of glioblastoma multiforme (GBM). Despite its cytotoxic effect, TMZ also induces cell cycle arrest that may lead to the development of chemoresistance and eventual tumor recurrence. Caffeine, a widely consumed neurostimulant, shows anticancer activities and is reported to work synergistically with cisplatin and camptothecin. The present study aimed to investigate the effects and the mechanisms of action of caffeine used in combination with TMZ in U87-MG GBM cells. As anticipated, TMZ caused DNA damage mediated by the ATM/p53/p21 signaling pathway and induced significant G2 delay. Concurrent treatment with caffeine repressed proliferation and lowered clonogenic capacity on MTT and colony formation assays, respectively. Mechanistic study showed that coadministration of caffeine and TMZ suppressed the phosphorylation of ATM and p53 and downregulated p21 expression, thus releasing DNA-damaged cells from G2 arrest into premature mitosis. Cell cycle analysis demonstrated that the proportion of cells arrested in G2 phase decreased when caffeine was administered together with TMZ; at the same time, the amount of cells with micronucleation and multipolar spindle poles increased, indicative of enhanced mitotic cell death. Pretreatment of cells with caffeine further enhanced mitotic catastrophe development in combined treatment and sensitized cells to apoptosis when followed by TMZ alone. In conclusion, our study demonstrated that caffeine enhanced the efficacy of TMZ through mitotic cell death by impeding ATM/p53/p21-mediated G2 arrest.