Evidence map›Paper›PMID 23478628›Full record

ArticleEpigenetics2013

Novel tumor suppressor candidates on chromosome 3 revealed by NotI-microarrays in cervical cancer.

Vera N Senchenko, Natalia P Kisseljova, Tatyana A Ivanova, Alexey A Dmitriev, George S Krasnov, Anna V Kudryavtseva, Grigory V Panasenko, Evgeny B Tsitrin, Michael I Lerman, Fyodor L Kisseljov and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Epigenetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

42 citing papers in PubMed, 70 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

12 authors at 8 institutions in 6 countries.

Vera N SenchenkoEngelhardt Institute of Molecular Biology; Russian Academy of Sciences; Moscow, Russia.
Natalia P KisseljovaN.N. Blokhin Russian Cancer Research Center; Russian Academy of Medical Sciences; Moscow, Russia.
Tatyana A IvanovaN.N. Blokhin Russian Cancer Research Center; Russian Academy of Medical Sciences; Moscow, Russia; Karolinska Institute; Department of Microbiology, Tumour and Cell Biology; Stockholm, Sweden.
Alexey A DmitrievEngelhardt Institute of Molecular Biology; Russian Academy of Sciences; Moscow, Russia.
George S KrasnovEngelhardt Institute of Molecular Biology; Russian Academy of Sciences; Moscow, Russia; I.I.Mechnikov Scientific Research Institute of Vaccines and Sera; Russian Academy of Medical Sciences; Moscow, Russia.
Anna V KudryavtsevaEngelhardt Institute of Molecular Biology; Russian Academy of Sciences; Moscow, Russia.
Grigory V PanasenkoInstitute of Molecular Biology and Genetics; Ukrainian Academy of Sciences; Kiev, Ukraine.
Evgeny B TsitrinKoltzov Institute of Developmental Biology; Russian Academy of Sciences; Moscow, Russia.
Michael I LermanAffina Biotechnologies; Stamford, CT USA.
Fyodor L KisseljovN.N. Blokhin Russian Cancer Research Center; Russian Academy of Medical Sciences; Moscow, Russia.
Vladimir I KashubaInstitute of Molecular Biology and Genetics; Ukrainian Academy of Sciences; Kiev, Ukraine.
Eugene R ZabarovskyKarolinska Institute; Department of Microbiology, Tumour and Cell Biology; Stockholm, Sweden.
Russian Academy of Sciences · RUInstituto de Biomedicina y Genética Molecular de Valladolid · ESRussian Cancer Research Center NN Blokhin · RUAcademy of Medical Sciences · GBEngelhardt Institute of Molecular Biology · RUKarolinska Institutet · SEKoltzov Institute of Developmental Biology · RUStamford Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic and epigenetic alterations in cervical carcinomas were investigated using NotI-microarrays containing 180 cloned sequences flanking all NotI-sites associated with genes on chromosome 3. In total, 48 paired normal/tumor DNA samples, specifically enriched in NotI-sites, were hybridized to NotI-microarrays. Thirty genes, including tumor suppressors or candidates (for example, VHL, RBSP3/CTDSPL, ITGA9, LRRC3B, ALDH1L1, EPHB1) and genes previously unknown as cancer-associated (ABHD5, C3orf77, PRL32, LOC285375, FGD5 and others), showed methylation/deletion in 21-44% of tumors. The genes were more frequently altered in squamous cell carcinomas (SCC) than in adenocarcinomas (ADC, p<0.01). A set of seven potential markers (LRRN1, PRICKLE2, VHL, BHLHE40, RBSP3, CGGBP1 and SOX14) is promising for discrimination of ADC and SCC. Alterations of more than 20 genes simultaneously were revealed in 23% of SCC. Bisulfite sequencing analysis confirmed methylation as a frequent event in SCC. High down-regulation frequency was shown for RBSP3, ITGA9, VILL, APRG1/C3orf35 and RASSF1 (isoform A) genes (3p21.3 locus) in SCC. Both frequency and extent of RASSF1A and RBSP3 mRNA level decrease were more pronounced in tumors with lymph node metastases compared with non-metastatic ones (p ≤ 0.05). We confirmed by bisulfite sequencing that RASSF1 promoter methylation was a rare event in SCC and, for the first time, demonstrated RASSF1A down-regulation at both the mRNA and protein levels without promoter methylation in tumors of this histological type. Thus, our data revealed novel tumor suppressor candidates located on chromosome 3 and a frequent loss of epigenetic stability of 3p21.3 locus in combination with down-regulation of genes in cervical cancer.

Indexed as

Genes, Tumor SuppressorAdenocarcinomaBase SequenceBiomarkers, TumorCarcinoma, Squamous CellChromosomes, Human, Pair 3Deoxyribonucleases, Type II Site-SpecificDNA MethylationDown-RegulationEpigenesis, GeneticFemaleGene Expression ProfilingHumansMutation RateOligonucleotide Array Sequence AnalysisSequence DeletionBiomarkers, TumorDeoxyribonucleases, Type II Site-SpecificGCGGCCGC-specific type II deoxyribonucleasesRASSF1 protein, humanTumor Suppressor Proteinscervical cancerchromosome 3deletionsDNA methylationexpressionNotI-microarraystumor-suppressors genes

Identifiers

PMID23478628
PMCPMC3674050
OpenAlexW2044169243

What OpenQuestion holds

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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.