Evidence map›Paper›PMID 26606055›Full record

ArticlePloS one2015

Functional Cross-Talking between Differentially Expressed and Alternatively Spliced Genes in Human Liver Cancer Cells Treated with Berberine.

Zhen Sheng, Yi Sun, Ruixin Zhu, Na Jiao, Kailin Tang, Zhiwei Cao, Chao Ma

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 20% 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, 11 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

7 authors at 1 institution in 1 country.

Zhen ShengSchool of Life Science and Technology, Tongji University, Shanghai, People's Republic of China.
Yi SunSchool of Life Science and Technology, Tongji University, Shanghai, People's Republic of China.
Ruixin ZhuSchool of Life Science and Technology, Tongji University, Shanghai, People's Republic of China.
Na JiaoSchool of Life Science and Technology, Tongji University, Shanghai, People's Republic of China.
Kailin TangSchool of Life Science and Technology, Tongji University, Shanghai, People's Republic of China.
Zhiwei CaoSchool of Life Science and Technology, Tongji University, Shanghai, People's Republic of China.
Chao MaSchool of Life Science and Technology, Tongji University, Shanghai, People's Republic of China.
Tongji University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Berberine has been identified with anti-proliferative effects on various cancer cells. Many researchers have been trying to elucidate the anti-cancer mechanisms of berberine based on differentially expressed genes. However, differentially alternative splicing genes induced by berberine might also contribute to its pharmacological actions and have not been reported yet. Moreover, the potential functional cross-talking between the two sets of genes deserves further exploration. In this study, RNA-seq technology was used to detect the differentially expressed genes and differentially alternative spliced genes in BEL-7402 cancer cells induced by berberine. Functional enrichment analysis indicated that these genes were mainly enriched in the p53 and cell cycle signalling pathway. In addition, it was statistically proven that the two sets of genes were locally co-enriched along chromosomes, closely connected to each other based on protein-protein interaction and functionally similar on Gene Ontology tree. These results suggested that the two sets of genes regulated by berberine might be functionally cross-talked and jointly contribute to its cell cycle arresting effect. It has provided new clues for further researches on the pharmacological mechanisms of berberine as well as the other botanical drugs.

Indexed as

Alternative SplicingEpistasis, GeneticAntineoplastic AgentsBerberineCarcinoma, HepatocellularCell Line, TumorCluster AnalysisComputational BiologyGene Expression ProfilingGene Expression Regulation, NeoplasticHigh-Throughput Nucleotide SequencingHumansLiver NeoplasmsMolecular Sequence AnnotationProtein Interaction MappingProtein Interaction MapsAntineoplastic AgentsBerberine

Identifiers

PMID26606055
PMCPMC4659683
OpenAlexW2178475696

What OpenQuestion holds

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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.