Metformin enhances the radiosensitizing effect of cisplatin in non-small cell lung cancer cell lines with different cisplatin sensitivities.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
04 02 2019
Historique:
received: 08 08 2018
accepted: 18 12 2018
entrez: 6 2 2019
pubmed: 6 2 2019
medline: 20 8 2020
Statut: epublish

Résumé

Cisplatin is an extensively used chemotherapeutic drug for lung cancer, but the development of resistance decreases its effectiveness in the treatments of non-small cell lung cancer (NSCLC). In this study, we examined the effects of metformin, a widely used antidiabetic drug, on cisplatin radiosensitization in NSCLC cell lines. Human NSCLC cell lines, A549 (cisplatin-resistant) and H460 (cisplatin-sensitive), were treated with metformin, cisplatin or a combination of both drugs before ionizing radiation. Cell proliferation, clonogenic assays, western blotting, cisplatin-DNA adduct formation and immunocytochemistry were used to characterize the treatments effects. Metformin increased the radiosensitivity of NSCLC cells. Metformin showed additive and over-additive effects in combination with cisplatin and the radiation response in the clonogenic assay in H460 and A549 cell lines (p = 0.018 for the interaction effect between cisplatin and metformin), respectively. At the molecular level, metformin led to a significant increase in cisplatin-DNA adduct formation compared with cisplatin alone (p < 0.01, ANOVA-F test). This was accompanied by a decreased expression of the excision repair cross-complementation 1 expression (ERCC1), a key enzyme in nucleotide excision repair pathway. Furthermore, compared with each treatment alone metformin in combination with cisplatin yielded the lowest level of radiation-induced Rad51 foci, an essential protein of homologous recombination repair. Ionizing radiation-induced γ-H2AX and 53BP1 foci persisted longer in both cell lines in the presence of metformin. Pharmacological inhibition of AMP-activated protein kinase (AMPK) demonstrated that metformin enhances the radiosensitizing effect of cisplatin through an AMPK-dependent pathway only in H460 but not in A549 cells. Our results suggest that metformin can enhance the effect of combined cisplatin and radiotherapy in NSCLC and can sensitize these cells to radiation that are not sensitized by cisplatin alone.

Identifiants

pubmed: 30718758
doi: 10.1038/s41598-018-38004-5
pii: 10.1038/s41598-018-38004-5
pmc: PMC6361966
doi:

Substances chimiques

Neoplasm Proteins 0
Metformin 9100L32L2N
Cisplatin Q20Q21Q62J

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1282

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Auteurs

Muhammad Assad Riaz (MA)

Department of Radiotherapy, University Hospital Essen, Essen, Germany. assad.muhammad@uni-due.de.

Ali Sak (A)

Department of Radiotherapy, University Hospital Essen, Essen, Germany.

Yasin Bahadir Erol (YB)

Department of Radiotherapy, University Hospital Essen, Essen, Germany.

Michael Groneberg (M)

Department of Radiotherapy, University Hospital Essen, Essen, Germany.

Jürgen Thomale (J)

Institute of Cell Biology, University Hospital Essen, Essen, Germany.

Martin Stuschke (M)

Department of Radiotherapy, University Hospital Essen, Essen, Germany.

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