Evidence map›Paper›PMID 28558682›Full record

ArticleBMC urology2017

Anti-proliferative potential of Glucosamine in renal cancer cells via inducing cell cycle arrest at G0/G1 phase.

Long-Sheng Wang, Shao-Jun Chen, Jun-Feng Zhang, Meng-Nan Liu, Jun-Hua Zheng, Xu-Dong Yao

Open access · goldAbstract read
In one paragraph

Article in BMC urology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 30% 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

14 citing papers in PubMed, 23 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

6 authors at 1 institution in 1 country.

Long-Sheng WangDepartment of Urology, Shanghai Tenth People's Hospital, Tongji University, School of Medicine, Shanghai, 200072, China.
Shao-Jun ChenDepartment of Urology, Shanghai Tenth People's Hospital, Tongji University, School of Medicine, Shanghai, 200072, China.
Jun-Feng ZhangDepartment of Urology, Shanghai Tenth People's Hospital, Tongji University, School of Medicine, Shanghai, 200072, China.
Meng-Nan LiuDepartment of Urology, Shanghai Tenth People's Hospital, Tongji University, School of Medicine, Shanghai, 200072, China.
Jun-Hua ZhengDepartment of Urology, Shanghai Tenth People's Hospital, Tongji University, School of Medicine, Shanghai, 200072, China. zhengjunhua2016@163.com.
Xu-Dong YaoDepartment of Urology, Shanghai Tenth People's Hospital, Tongji University, School of Medicine, Shanghai, 200072, China. yaoxudong1967@163.com.
Tongji University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRenal cell carcinoma (RCC) is one of the most common types of cancer in urological system worldwide. Recently, the anticancer role of Glucosamine has been studied in many types of cancer. The aim of this study was to investigate the effects of Glucosamine on RCC.

methodsThe effects of Glucosamine on RCC cell proliferation and apoptosis were investigated by MTT assay and Annexin V-FITC Apoptosis assay, respectively in vitro. Cell cycle was detected by flow cytometry after treatment with Glucosamine. Protein levels of several cell cycle associated markers were examined by Western Blot.

resultsOur data showed that Glucosamine significantly inhibited the proliferation of renal cancer 786-O and Caki-1 cells in a dose-dependent manner. Besides, Glucosamine treatment resulted in cell cycle arrest at G0/G1 phase in both cell lines. Meanwhile, the expression of several regulators that contribute to G1/S phased transition, such as Cyclin D1, CDK4 and CDK6, were significantly down-regulated with the up-regulation of cell cycle inhibitors, p21 and p53, after treatment with glucosamine. However, the apoptosis rate of RCC cells was down-regulated when treatment with Glucosamine at 1 mM and 5 mM, while up-regulated at 10 mM.

conclusionsOur findings indicated that Glucosamine inhibited the proliferation of RCC cells by promoting cell cycle arrest at G0/G1 phase, but not promoting apoptosis. The present results suggested that Glucosamine might be a potential therapeutic agent in RCC treatment in the future.

Indexed as

ApoptosisCarcinoma, Renal CellCell Cycle CheckpointsCell ProliferationG1 PhaseGlucosamineHumansKidney NeoplasmsTumor Cells, CulturedGlucosamineCell cycleGlucosamineProliferationRenal cell carcinoma

Identifiers

PMID28558682
PMCPMC5450348
OpenAlexW2619817304

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LicenceCC BY
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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.