Evidence map›Paper›PMID 30884764›Full record

ArticleCancers2019

Combination Therapy of Chloroquine and C₂-Ceramide Enhances Cytotoxicity in Lung Cancer H460 and H1299 Cells.

Han-Lin Chou, Yi-Hsiung Lin, Wangta Liu, Chang-Yi Wu, Ruei-Nian Li, Hurng-Wern Huang, Chi-Hsien Chou, Shean-Jaw Chiou, Chien-Chih Chiu

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 32 citations in OpenAlex.

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  12. The Phenoxyphenol Compound diTFPP Mediates Exogenous CAntioxidants (Basel, Switzerland) · 2021
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  19. CInternational journal of molecular sciences · 2019
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Han-Lin ChouDepartment of Biotechnology, Kaohsiung Medical University, Kaohsiung 807, Taiwan. d992050005@gmail.com.
Yi-Hsiung LinDepartment of Biotechnology, Kaohsiung Medical University, Kaohsiung 807, Taiwan. caminolin@gmail.com.
Wangta LiuDepartment of Biotechnology, Kaohsiung Medical University, Kaohsiung 807, Taiwan. liuwangta@kmu.edu.tw.
Chang-Yi WuDepartment of Biotechnology, Kaohsiung Medical University, Kaohsiung 807, Taiwan. cywu@mail.nsysu.edu.tw.
Ruei-Nian LiDepartment of Biomedical Science and Environment Biology, Kaohsiung Medical University, Kaohsiung 807, Taiwan. runili@kmu.edu.tw.
Hurng-Wern HuangInstitute of Biomedical Science, National Sun Yat-Sen University, Kaohsiung 804, Taiwan. sting@mail.nsysu.edu.tw.
Chi-Hsien ChouCenter for Research Resources and Development, Kaohsiung Medical University, Kaohsiung 807, Taiwan. chishien@kmu.edu.tw.
Shean-Jaw ChiouDepartment of Biochemistry, College of Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan. sheanjaw@kmu.edu.tw.
Chien-Chih ChiuDepartment of Biotechnology, Kaohsiung Medical University, Kaohsiung 807, Taiwan. cchiu@kmu.edu.tw.ORCID 0000-0001-7307-2468
Kaohsiung Medical University · TWNational Sun Yat-sen University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

autophagyC2-ceramidechloroquinecombination treatmentNSCLC

Identifiers

PMID30884764
PMCPMC6468447
OpenAlexW2921140369

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.