Evidence map›Paper›PMID 27323779›Full record

ArticleOncotarget2016

Analysis of clock gene-miRNA correlation networks reveals candidate drivers in colorectal cancer.

Gianluigi Mazzoccoli, Tommaso Colangelo, Anna Panza, Rosa Rubino, Cristiana Tiberio, Orazio Palumbo, Massimo Carella, Domenico Trombetta, Annamaria Gentile, Francesca Tavano and 10 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  8. Review
  9. Role of Non-Coding RNAs in Lung Circadian Clock Related Diseases.International journal of molecular sciences · 2020
    Review
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  11. 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

20 authors at 4 institutions in 1 country.

Gianluigi MazzoccoliDivision of Internal Medicine and Chronobiology Unit, IRCCS "Casa Sollievo della Sofferenza", San Giovanni Rotondo (FG), Italy.
Tommaso ColangeloDepartment of Sciences and Technologies, University of Sannio, Benevento, Italy.
Anna PanzaDivision of Gastroenterology and Research Laboratory, IRCCS "Casa Sollievo della Sofferenza", San Giovanni Rotondo (FG), Italy.
Rosa RubinoDivision of Internal Medicine and Chronobiology Unit, IRCCS "Casa Sollievo della Sofferenza", San Giovanni Rotondo (FG), Italy.
Cristiana TiberioDivision of Internal Medicine and Chronobiology Unit, IRCCS "Casa Sollievo della Sofferenza", San Giovanni Rotondo (FG), Italy.
Orazio PalumboMedical Genetics Service, IRCCS "Casa Sollievo della Sofferenza", San Giovanni Rotondo (FG), Italy.
Massimo CarellaMedical Genetics Service, IRCCS "Casa Sollievo della Sofferenza", San Giovanni Rotondo (FG), Italy.
Domenico TrombettaOncology-Research Laboratory, IRCCS "Casa Sollievo della Sofferenza", San Giovanni Rotondo (FG), Italy.
Annamaria GentileDivision of Gastroenterology and Research Laboratory, IRCCS "Casa Sollievo della Sofferenza", San Giovanni Rotondo (FG), Italy.
Francesca TavanoDivision of Gastroenterology and Research Laboratory, IRCCS "Casa Sollievo della Sofferenza", San Giovanni Rotondo (FG), Italy.
Maria Rosa ValvanoDivision of Gastroenterology and Research Laboratory, IRCCS "Casa Sollievo della Sofferenza", San Giovanni Rotondo (FG), Italy.
Clelia Tiziana StorlazziDepartment of Biology, University of Bari, Bari, Italy.
Gemma MacchiaDepartment of Biology, University of Bari, Bari, Italy.
Angelo De CataDivision of Internal Medicine and Chronobiology Unit, IRCCS "Casa Sollievo della Sofferenza", San Giovanni Rotondo (FG), Italy.
Giovanni BiscegliaDepartment of Surgical Sciences, IRCCS "Casa Sollievo della Sofferenza", San Giovanni Rotondo (FG), Italy.
Daniele CapocefaloBioinformatics Unit, IRCCS "Casa Sollievo della Sofferenza", San Giovanni Rotondo (FG), Italy.
Vittorio ColantuoniDepartment of Sciences and Technologies, University of Sannio, Benevento, Italy.
Lina SabatinoDepartment of Sciences and Technologies, University of Sannio, Benevento, Italy.
Ada PiepoliDivision of Epidemiology and Health Statistics, IRCCS "Casa Sollievo della Sofferenza", San Giovanni Rotondo (FG), Italy.
Tommaso MazzaBioinformatics Unit, IRCCS "Casa Sollievo della Sofferenza", San Giovanni Rotondo (FG), Italy.
Istituti di Ricovero e Cura a Carattere Scientifico · ITCasa Sollievo della Sofferenza · ITUniversity of Sannio · ITUniversity of Bari Aldo Moro · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Altered functioning of the biological clock is involved in cancer onset and progression. MicroRNAs (miRNAs) interact with the clock genes modulating the function of genetically encoded molecular clockworks. Collaborative interactions may take place within the coding-noncoding RNA regulatory networks. We aimed to evaluate the cross-talk among miRNAs and clock genes in colorectal cancer (CRC). We performed an integrative analysis of miRNA-miRNA and miRNA-mRNA interactions on high-throughput molecular profiling of matched human CRC tissue and non-tumor mucosa, pinpointing core clock genes and their targeting miRNAs. Data obtained in silico were validated in CRC patients and human colon cancer cell lines. In silico we found severe alterations of clock gene-related coding-noncoding RNA regulatory networks in tumor tissues, which were later corroborated by the analysis of human CRC specimens and experiments performed in vitro. In conclusion, specific miRNAs target and regulate the transcription/translation of clock genes and clock gene-related miRNA-miRNA as well as mRNA-miRNA interactions are altered in colorectal cancer. Exploration of the interplay between specific miRNAs and genes, which are critically involved in the functioning of the biological clock, provides a better understanding of the importance of the miRNA-clock genes axis and its derangement in colorectal cancer.

Indexed as

AgedAged, 80 and overCell Line, TumorCLOCK ProteinsColorectal NeoplasmsFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticGene Regulatory NetworksHumansMaleMicroRNAsMiddle AgedTranscriptomeCLOCK ProteinsMicroRNAscircadianclock genescolorectal cancermiRNA-mRNA

Identifiers

PMID27323779
PMCPMC5216733
OpenAlexW2424342676

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.