Evidence map›Paper›PMID 35943683›Full record

ArticleInvestigational new drugs2022

Ketamine promotes breast tumor growth in a mouse breast tumor model involving with high expression of miR-27b-3p and EGFR.

Li-Kuei Chen, Chien-Hung Shih, Shiou-Sheng Chen, Zi-Xuan Huang, Yu-Jung Chang, Linyi Chen, Tsung-Hsien Chuang, Kuen-Bao Chen

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Article in Investigational new drugs, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

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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

8 authors at 5 institutions in 1 country.

Li-Kuei ChenCollege of Medicine, China Medical University, Taichung, Taiwan.
Chien-Hung ShihInstitute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan.
Shiou-Sheng ChenDivision of Urology, Taipei City Hospital, Zhong Xiao Branch, Taipei, Taiwan.
Zi-Xuan HuangInstitute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan.
Yu-Jung ChangInstitute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan.
Linyi ChenInstitute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan.
Tsung-Hsien ChuangImmunology Research Center, National Health Research Institutes, Miaoli, Taiwan.
Kuen-Bao ChenCollege of Medicine, China Medical University, Taichung, Taiwan. kuenbaochen876@foxmailvip.cn.
National Tsing Hua University · TWChina Medical University · TWChina Medical University Hospital · TWNational Health Research Institutes · TWTaipei City Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-medical use of ketamine as an adulterant to ecstasy is more prevalent than amphetamine in Taiwan. Ketamine's effect on immunosuppression might play some functional role in tumor growth, while it is still controversial whether ketamine abuse could increase tumor growth or not. This study aimed to investigate the influence of ketamine addiction in breast tumors and related gene expressions. The effect of ketamine treatment on proliferation, colony formation, migration, and invasion of triple-negative breast cancer cell line EO771 was examined. In addition, a ketamine addiction mice model was established by intraperitoneal injection (IP) of ketamine in mice and used to investigate the effects of ketamine addiction on tumor growth and the possible mechanisms. In the in vitro studies, ketamine treatment at different concentrations did not affect EO771 cell proliferation and colony formation. But ketamine did enhance migration and invasion of EO771 cells. The in vivo experiments showed significantly increased breast tumor volume and weight in ketamine-addicted mice than in normal saline groups. miR-27b-3p level, human epidermal growth factor receptor 2 (HER2), and epidermal growth factor receptor (EGFR) significantly increased in tumors of ketamine addiction mice compared to control mice. In vivo evidence showed that Ketamine might increase tumor growth on the tumor microenvironment, and miR-27b-3p, HER2, and EGFR might play a role in the process.

Indexed as

Breast NeoplasmsKetamineMicroRNAsAnimalsCell Line, TumorCell ProliferationErbB ReceptorsFemaleGene Expression Regulation, NeoplasticHumansMiceTumor MicroenvironmentEGFR protein, humanErbB ReceptorsKetamineMicroRNAsBreast cancer biomarkerEpidermal growth factor receptorKetaminemiR-27b-3p

Identifiers

PMID35943683
OpenAlexW4294009692

What OpenQuestion holds

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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.