Evidence map›Paper›PMID 28105922›Full record

ArticleBMC genomics2016

Differential expression of alternatively spliced transcripts related to energy metabolism in colorectal cancer.

Anastasiya Vladimirovna Snezhkina, George Sergeevich Krasnov, Andrew Rostislavovich Zaretsky, Alex Zhavoronkov, Kirill Mikhailovich Nyushko, Alexey Alexandrovich Moskalev, Irina Yurievna Karpova, Anastasiya Isaevna Afremova, Anastasiya Valerievna Lipatova, Dmitriy Vladimitovich Kochetkov and 11 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 54 citations in OpenAlex.

  1. Pooled it
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  12. Prognostic Value of Enolase Gene Family in Colon Cancer.Medical science monitor : international medical journal of experimental and clinical research · 2020
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  19. Mutational load in carotid body tumor.BMC medical genomics · 2019
    Article
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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

21 authors at 6 institutions in 2 countries.

Anastasiya Vladimirovna SnezhkinaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.
George Sergeevich KrasnovEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.
Andrew Rostislavovich ZaretskyShemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow, Russia.
Alex ZhavoronkovInsilico Medicine, Inc., Emerging Technology Centers, Johns Hopkins University Eastern Campus, Baltimore, Maryland, USA.
Kirill Mikhailovich NyushkoNational Medical Research Radiological Center, Ministry of Health of the Russian Federation, Moscow, Russia.
Alexey Alexandrovich MoskalevEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.
Irina Yurievna KarpovaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.
Anastasiya Isaevna AfremovaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.
Anastasiya Valerievna LipatovaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.
Dmitriy Vladimitovich KochetkovEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.
Maria Sergeena FedorovaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.
Nadezhda Nikolaevna VolchenkoNational Medical Research Radiological Center, Ministry of Health of the Russian Federation, Moscow, Russia.
Asiya Fayazovna SadritdinovaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.
Nataliya Vladimirovna MelnikovaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.
Dmitry Vladimirovich SidorovNational Medical Research Radiological Center, Ministry of Health of the Russian Federation, Moscow, Russia.
Anatoly Yurievich PopovState Hospital №57, Moscow, Russia.
Dmitry Valerievich KalininA.V. Vishnevsky Institute of Surgery, Moscow, Russia.
Andrey Dmitrievich KaprinNational Medical Research Radiological Center, Ministry of Health of the Russian Federation, Moscow, Russia.
Boris Yakovlevich AlekseevNational Medical Research Radiological Center, Ministry of Health of the Russian Federation, Moscow, Russia.
Alexey Alexandrovich DmitrievEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia.
Anna Viktorovna KudryavtsevaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow, Russia. rhizamoeba@mail.ru.
Engelhardt Institute of Molecular Biology · RUMinistry of Health of the Russian Federation · RUInstitute of Bioorganic Chemistry · RUInstitute of Surgery named after A. V. Vishnevskogo · RUJohns Hopkins University · USMoscow City Hospital No 29 · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundColorectal cancer (CRC) is one of the most common malignant tumors worldwide. CRC molecular pathogenesis is heterogeneous and may be followed by mutations in oncogenes and tumor suppressor genes, chromosomal and microsatellite instability, alternative splicing alterations, hypermethylation of CpG islands, oxidative stress, impairment of different signaling pathways and energy metabolism. In the present work, we have studied the alterations of alternative splicing patterns of genes related to energy metabolism in CRC.

resultsUsing CrossHub software, we analyzed The Cancer Genome Atlas (TCGA) RNA-Seq datasets derived from colon tumor and matched normal tissues. The expression of 1014 alternative mRNA isoforms involved in cell energy metabolism was examined. We found 7 genes with differentially expressed alternative transcripts whereas overall expression of these genes was not significantly altered in CRC. A set of 8 differentially expressed transcripts of interest has been validated by qPCR. These eight isoforms encoded by OGDH, COL6A3, ICAM1, PHPT1, PPP2R5D, SLC29A1, and TRIB3 genes were up-regulated in colorectal tumors, and this is in concordance with the bioinformatics data. The alternative transcript NM_057167 of COL6A3 was also strongly up-regulated in breast, lung, prostate, and kidney tumors. Alternative transcript of SLC29A1 (NM_001078177) was up-regulated only in CRC samples, but not in the other tested tumor types.

conclusionsWe identified tumor-specific expression of alternative spliced transcripts of seven genes involved in energy metabolism in CRC. Our results bring new knowledge on alternative splicing in colorectal cancer and suggest a set of mRNA isoforms that could be used for cancer diagnosis and development of treatment methods.

Indexed as

Alternative SplicingGene Expression Regulation, NeoplasticAdultAgedBiomarkersColorectal NeoplasmsComputational BiologyEnergy MetabolismFemaleGene Expression ProfilingHumansMaleMiddle AgedNeoplasm StagingOrgan SpecificityRNA IsoformsBiomarkersRNA IsoformsAdenocarcinomaAlternative splicingColorectal cancerEnergy metabolismTumor-specific alternative mRNA transcripts

Identifiers

PMID28105922
PMCPMC5249009
OpenAlexW2566999926

What OpenQuestion holds

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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.