Evidence map›Paper›PMID 28301876›Full record

ArticlePloS one2017

Autophagy inhibitor chloroquine increases sensitivity to cisplatin in QBC939 cholangiocarcinoma cells by mitochondrial ROS.

Xianzhi Qu, Jiyao Sheng, Luyan Shen, Jing Su, Yunjie Xu, Qi Xie, Yao Wu, Xuewen Zhang, Liankun Sun

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

60 citing papers in PubMed, 87 citations in OpenAlex.

  1. Article
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  5. dentification and characterization of novelBMJ open diabetes research & care · 2025
    Article
  6. Article
  7. Autophagy in cholangiocarcinoma: a comprehensive review about roles and regulatory mechanisms.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Review
  8. Article
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  10. Review
  11. Article
  12. Review
  13. Article
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  15. Curcumin attenuates hydroxychloroquine-mediated apoptosis and oxidative stress via the inhibition of TRPM2 channel signalling pathways in a retinal pigment epithelium cell line.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2023
    Article
  16. Article
  17. Review
  18. Review
  19. Molecules (Basel, Switzerland) · 2023
    Article
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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 3 institutions in 1 country.

Xianzhi QuDepartment of Hepatobiliary & Pancreat Surgery, The Second Hospital of Jilin University, Jilin University, Changchun, Jilin, China.
Jiyao ShengDepartment of Hepatobiliary & Pancreat Surgery, The Second Hospital of Jilin University, Jilin University, Changchun, Jilin, China.
Luyan ShenDepartment of Pathophysiology, School of Basic Medical Sciences, Jilin University, Changchun, Jilin, China.
Jing SuDepartment of Pathophysiology, School of Basic Medical Sciences, Jilin University, Changchun, Jilin, China.
Yunjie XuDepartment of Pathophysiology, School of Basic Medical Sciences, Jilin University, Changchun, Jilin, China.
Qi XieDepartment of Pathophysiology, School of Basic Medical Sciences, Jilin University, Changchun, Jilin, China.
Yao WuDepartment of Pathophysiology, School of Basic Medical Sciences, Jilin University, Changchun, Jilin, China.
Xuewen ZhangDepartment of Hepatobiliary & Pancreat Surgery, The Second Hospital of Jilin University, Jilin University, Changchun, Jilin, China.
Liankun SunDepartment of Pathophysiology, School of Basic Medical Sciences, Jilin University, Changchun, Jilin, China.
Jilin Medical University · CNJilin University · CNSecond Affiliated Hospital of Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tumor cells have some metabolic characteristics of the original tissues, and the metabolism of the tumor cells is closely related to autophagy. However, the mechanism of autophagy and metabolism in chemotherapeutic drug resistance is still poorly understood. In this study, we investigated the role and mechanism of autophagy and glucose metabolism in chemotherapeutic drug resistance by using cholangiocarcinoma QBC939 cells with primary cisplatin resistance and hepatocellular carcinoma HepG2 cells. We found that QBC939 cells with cisplatin resistance had a higher capacity for glucose uptake, consumption, and lactic acid generation, and higher activity of the pentose phosphate pathway compared with HepG2 cells, and the activity of PPP was further increased after cisplatin treatment in QBC939 cells. It is suggested that there are some differences in the metabolism of glucose in hepatocellular carcinoma and cholangiocarcinoma cells, and the activation of PPP pathway may be related to the drug resistance. Through the detection of autophagy substrates p62 and LC3, found that QBC939 cells have a higher flow of autophagy, autophagy inhibitor chloroquine can significantly increase the sensitivity of cisplatin in cholangiocarcinoma cells compared with hepatocellular carcinoma HepG2 cells. The mechanism may be related to the inhibition of QBC939 cells with higher activity of the PPP, the key enzyme G6PDH, which reduces the antioxidant capacity of cells and increases intracellular ROS, especially mitochondrial ROS. Therefore, we hypothesized that autophagy and the oxidative stress resistance mediated by glucose metabolism may be one of the causes of cisplatin resistance in cholangiocarcinoma cells. It is suggested that according to the metabolism characteristics of tumor cells, inhibition of autophagy lysosome pathway with chloroquine may be a new route for therapeutic agents against cholangiocarcinoma.

Indexed as

Antineoplastic AgentsAntioxidantsAutophagyBile Duct NeoplasmsCell Line, TumorChloroquineCholangiocarcinomaCisplatinDrug Resistance, NeoplasmDrug SynergismHumansMitochondriaReactive Oxygen SpeciesAntineoplastic AgentsAntioxidantsChloroquineCisplatinReactive Oxygen Species

Identifiers

PMID28301876
PMCPMC5354635
OpenAlexW2596985509

What OpenQuestion holds

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Registered trials

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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.