Evidence map›Paper›PMID 33608672›Full record

ArticleActa pharmacologica Sinica2021

Autophagy inhibitors increase the susceptibility of KRAS-mutant human colorectal cancer cells to a combined treatment of 2-deoxy-D-glucose and lovastatin.

Xiao-Ming Huang, Jia-Jun Huang, Jing-Jing Du, Na Zhang, Ze Long, You Yang, Fang-Fang Zhong, Bo-Wen Zheng, Yun-Fu Shen, Zhe Huang and 5 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

18 citing papers in PubMed, 28 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 1 institution in 1 country.

Xiao-Ming HuangState Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Macau, China.
Jia-Jun HuangState Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Macau, China.
Jing-Jing DuState Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Macau, China.
Na ZhangState Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Macau, China.
Ze LongState Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Macau, China.
You YangState Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Macau, China.
Fang-Fang ZhongState Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Macau, China.
Bo-Wen ZhengState Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Macau, China.
Yun-Fu ShenState Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Macau, China.
Zhe HuangState Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Macau, China.
Xiang QinState Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Macau, China.
Jun-He ChenState Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Macau, China.
Qian-Yu LinState Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Macau, China.
Wan-Jun LinState Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Macau, China.
Wen-Zhe MaState Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Macau, China. wzma@must.edu.mo.
Macau University of Science and Technology · MO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RAS-driven colorectal cancer relies on glucose metabolism to support uncontrolled growth. However, monotherapy with glycolysis inhibitors like 2-deoxy-D-glucose causes limited effectiveness. Recent studies suggest that anti-tumor effects of glycolysis inhibition could be improved by combination treatment with inhibitors of oxidative phosphorylation. In this study we investigated the effect of a combination of 2-deoxy-D-glucose with lovastatin (a known inhibitor of mevalonate pathway and oxidative phosphorylation) on growth of KRAS-mutant human colorectal cancer cell lines HCT116 and LoVo. A combination of lovastatin (>3.75 μM) and 2-deoxy-D-glucose (>1.25 mM) synergistically reduced cell viability, arrested cells in the G

Indexed as

AnimalsAntimetabolitesAutophagyCell SurvivalChloroquineColorectal NeoplasmsDeoxyglucoseDose-Response Relationship, DrugDrug Therapy, CombinationFemaleHCT116 CellsHEK293 CellsHumansHydroxymethylglutaryl-CoA Reductase InhibitorsLovastatinMiceAntimetabolitesChloroquineDeoxyglucoseHydroxymethylglutaryl-CoA Reductase InhibitorsKRAS protein, humanLovastatinProto-Oncogene Proteins p21(ras)2DGautophagychloroquineglycolysishuman colorectal cancershydroxychloroquinelovastatinOXPHOS

Identifiers

PMID33608672
PMCPMC8564510
OpenAlexW3133159261

What OpenQuestion holds

Textmetadata
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.