Combination Therapy of Chloroquine and C2-Ceramide Enhances Cytotoxicity in Lung Cancer H460 and H1299 Cells
Autor: | Shean-Jaw Chiou, Hurng-Wern Huang, Chien-Chih Chiu, Han-Lin Chou, Ruei-Nian Li, Wangta Liu, Yi-Hsiung Lin, Chang-Yi Wu, Chi-Hsien Chou |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Cancer Research Programmed cell death autophagy Autophagosome maturation NSCLC lcsh:RC254-282 Article chloroquine 03 medical and health sciences 0302 clinical medicine medicine Lung cancer Cytotoxicity LAMP2 business.industry Autophagy Cancer medicine.disease lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens respiratory tract diseases C2-ceramide 030104 developmental biology Oncology Apoptosis 030220 oncology & carcinogenesis Cancer research combination treatment business |
Zdroj: | Cancers, Vol 11, Iss 3, p 370 (2019) Cancers Volume 11 Issue 3 |
ISSN: | 2072-6694 |
Popis: | Non-small cell lung cancer (NSCLC) is a type of malignant cancer, and 85% of metastatic NSCLC patients have a poor prognosis. C2-ceramide induces G2/M phase arrest and cytotoxicity in NSCLC cells. In this study, the autophagy-inducing effect of C2-ceramide was demonstrated, and cotreatment with the autophagy inhibitor chloroquine (CQ) was investigated in NSCLC H460 and H1299 cells. The results suggested that C2-ceramide exhibited dose-dependent anticancer effects in H460 and H1299 cells and autophagy induction. Zebrafish-based acridine orange staining confirmed the combined effects in vivo. Importantly, the combination of a sublethal dose of C2-ceramide and CQ resulted in additive cytotoxicity and autophagy in both cell lines. Alterations of related signaling factors, including Src and SIRT1 inhibition and activation of the autophagic regulators LAMP2 and LC3-I/II, contributed to the autophagy-dependent apoptosis. We found that C2-ceramide continuously initiated autophagy however, CQ inhibited autophagosome maturation and degradation during autophagy progression. Accumulated and non-degraded autophagosomes increased NSCLC cell stress, eventually leading to cell death. This study sheds light on improvements to NSCLC chemotherapy to reduce the chemotherapy dose and NSCLC patient burden. |
Databáze: | OpenAIRE |
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