Evidence map›Paper›PMID 21336720›Full record

ArticleJournal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban2011

Antitumor activity of erythromycin on human neuroblastoma cell line (SH-SY5Y).

Jia Yongsheng, Ma Xiaoyun, Wei Xiaoli, Li Xin, Yan Haitao, Liu Xiaoyan, Zheng Jianquan

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban, 2011. 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
0.2field-weighted citation impact, top 45% 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, 8 citations in OpenAlex.

  1. Review
  2. Review
  3. Mitochondrial ribosomes in cancer.Seminars in cancer biology · 2017
    Review
  4. Article
  5. Effect of mouse oocyte vitrification on mitochondrial membrane potential and distribution.Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban · 2014
    Article
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

7 authors at 1 institution in 1 country.

Jia YongshengBeijing Institute of Pharmacology and Toxicology, Beijing, 100850, China.
Ma XiaoyunBeijing Institute of Pharmacology and Toxicology, Beijing, 100850, China.
Wei XiaoliBeijing Institute of Pharmacology and Toxicology, Beijing, 100850, China.
Li XinBeijing Institute of Pharmacology and Toxicology, Beijing, 100850, China.
Yan HaitaoBeijing Institute of Pharmacology and Toxicology, Beijing, 100850, China.
Liu XiaoyanBeijing Institute of Pharmacology and Toxicology, Beijing, 100850, China.
Zheng JianquanBeijing Institute of Pharmacology and Toxicology, Beijing, 100850, China. zhengjq@bmi.ac.cn.
Institute of Pharmacology · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antitumor effects of erythromycin and the related mechanism were investigated in the present study. Neuroblastoma cells (SH-SY5Y) were exposed to erythromycin at different concentrations for different durations. Cell proliferation was measured by cell counting, and cell viability was examined by MTT assay. Cell cycle phase distribution and the cytosolic calcium level were detected by flow cytometry. Mitochondrial membrane potential was measured by the JC-1 probe staining and fluorescent microscopy. The expression of an oncogene (c-Myc) and a tumor suppressor [p21 (WAF1/Cip1)] proteins was analyzed by using Western blotting. Erythromycin could inhibit the proliferation of SH-SY5Y cells in a concentration- and time-dependent manner. The cell cycle was arrested at S phase. Mitochondrial membrane potential collapsed and the cytosolic calcium was overloaded in SH-SY5Y cells when treated with erythromycin. The expression of c-Myc protein was down-regulated, while that of p21 (WAF1/Cip1) protein was up-regulated. It was concluded that erythromycin could restrain the proliferation of SH-SY5Y cells. The antitumor mechanism of erythromycin might involve regulating the expression of c-Myc and p21 (WAF1/Cip1) proteins.

Indexed as

Antineoplastic AgentsCell Line, TumorCell ProliferationCell SurvivalCyclin-Dependent Kinase Inhibitor p21ErythromycinHumansNeuroblastomaProto-Oncogene Proteins c-mycAntineoplastic AgentsCDKN1A protein, humanCyclin-Dependent Kinase Inhibitor p21ErythromycinMYC protein, humanProto-Oncogene Proteins c-myc

Identifiers

PMID21336720
OpenAlexW39300502

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.