Evidence map›Paper›PMID 27376254›Full record

ArticleMolecules (Basel, Switzerland)2016

Pingyangmycin and Bleomycin Share the Same Cytotoxicity Pathway.

Yanli He, Ying Lan, Yong Liu, Haibo Yu, Zhangrun Han, Xiulian Li, Lijuan Zhang

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 32% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Bleomycin for orbital and peri-orbital veno-lymphatic malformations - A systematic review.Interventional neuroradiology : journal of peritherapeutic neuroradiology, surgical procedures and related neurosciences · 2021
    Pooled it
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  3. Review
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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

7 authors at 1 institution in 1 country.

Yanli HeSchool of Medicine and Pharmacy, Ocean University of China, 5 Yushan Road, Qingdao 266003, China. heyanli0219@163.com.
Ying LanSchool of Medicine and Pharmacy, Ocean University of China, 5 Yushan Road, Qingdao 266003, China. yinglanone@yeah.net.
Yong LiuSchool of Medicine and Pharmacy, Ocean University of China, 5 Yushan Road, Qingdao 266003, China. liuyong19900820@163.com.
Haibo YuCollege of Animal Science and Technology, Northwest A&F University, Xianyang 712100, China. yuhaiboper@163.com.
Zhangrun HanSchool of Medicine and Pharmacy, Ocean University of China, 5 Yushan Road, Qingdao 266003, China. hzrhan@126.com.
Xiulian LiSchool of Medicine and Pharmacy, Ocean University of China, 5 Yushan Road, Qingdao 266003, China. ouclixiulian@163.com.
Lijuan ZhangSchool of Medicine and Pharmacy, Ocean University of China, 5 Yushan Road, Qingdao 266003, China. lijuanzhang@ouc.edu.cn.
Ocean University of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pingyangmycin is an anticancer drug known as bleomycin A5 (A5), discovered in the Pingyang County of Zhejiang Province of China. Bleomycin (BLM) is a mixture of mainly two compounds (A2 and B2), which is on the World Health Organization's list of essential medicines. Both BLM and A5 are hydrophilic molecules that depend on transporters or endocytosis receptors to get inside of cells. Once inside, the anticancer activities rely on their abilities to produce DNA breaks, thus leading to cell death. Interestingly, the half maximal inhibitory concentration (IC50) of BLMs in different cancer cell lines varies from nM to μM ranges. Different cellular uptake, DNA repair rate, and/or increased drug detoxification might be some of the reasons; however, the molecules and signaling pathways responsible for these processes are largely unknown. In the current study, we purified the A2 and B2 from the BLM and tested the cytotoxicities and the molecular mechanisms of each individual compound or in combination with six different cell lines, including a Chinese hamster ovary (CHO) cell line defective in glycosaminoglycan biosynthesis. Our data suggested that glycosaminoglycans might be involved in the cellular uptake of BLMs. Moreover, both BLM and A5 shared similar signaling pathways and are involved in cell cycle and apoptosis in different cancer cell lines.

Indexed as

AnimalsAntibiotics, AntineoplasticApoptosisApoptosis Regulatory ProteinsBleomycinCell Cycle CheckpointsCell Cycle ProteinsCell Line, TumorCHO CellsChromatography, High Pressure LiquidCricetulusErbB ReceptorsGene ExpressionHumansInhibitory Concentration 50Molecular StructureAntibiotics, AntineoplasticApoptosis Regulatory ProteinsbleomycetinBleomycinCell Cycle ProteinsErbB Receptorsapoptosisbleomycin A2bleomycin A5 or pingyangmycinbleomycin B2cell cyclecytotoxicity

Identifiers

PMID27376254
PMCPMC6274306
OpenAlexW2460204032

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.