Evidence map›Paper›PMID 29525942›Full record

ArticleArchives of gynecology and obstetrics2018

The association of CCAT2 rs6983267 SNP with MYC expression and progression of uterine cervical cancer in the Polish population.

Sebastian Łaźniak, Anna Lutkowska, Żaneta Wareńczak-Florczak, Anna Sowińska, Alexander Tsibulski, Andrzej Roszak, Stefan Sajdak, Pawel P Jagodziński

Open access · hybridAbstract read
In one paragraph

Article in Archives of gynecology and obstetrics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
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  3. Article
  4. Article
  5. Article
  6. Single Nucleotide Polymorphisms ofFrontiers in oncology · 2022
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  7. Article
  8. Review
  9. Article
  10. TheInfection and drug resistance · 2021
    Article
  11. Article
  12. 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

8 authors at 1 institution in 1 country.

Sebastian ŁaźniakDepartment of Biochemistry and Molecular Biology, Poznań University of Medical Sciences, 6 Święcickiego St., 60-781, Poznan, Poland.
Anna LutkowskaDepartment of Biochemistry and Molecular Biology, Poznań University of Medical Sciences, 6 Święcickiego St., 60-781, Poznan, Poland.
Żaneta Wareńczak-FlorczakDepartment of Radiotherapy and Gynecological Oncology, Greater Poland Cancer Center, Pozna, Poland.
Anna SowińskaDepartment of Computer Science and Statistics, Poznań University of Medical Sciences, Poznan, Poland.
Alexander TsibulskiDepartment of Biochemistry and Molecular Biology, Poznań University of Medical Sciences, 6 Święcickiego St., 60-781, Poznan, Poland.
Andrzej RoszakDepartment of Radiotherapy and Gynecological Oncology, Greater Poland Cancer Center, Pozna, Poland.
Stefan SajdakClinic of Gynecological Surgery, Poznań University of Medical Sciences, Poznan, Poland.
Pawel P JagodzińskiDepartment of Biochemistry and Molecular Biology, Poznań University of Medical Sciences, 6 Święcickiego St., 60-781, Poznan, Poland. pjagodzi@am.poznan.pl.ORCID 0000-0001-6146-5459
Poznan University of Medical Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePrevious studies have reported a significant contribution of NC_000008.10:g.128413305 G>T (rs6983267) single-nucleotide polymorphism (SNP) in the MYC enhancer region to the susceptibility of various cancers. However, the role of rs6983267 SNP in cervical cancer (CC) development and progression has not been demonstrated to date. Therefore, we evaluated the role of rs6983267 SNP in MYC expression in cervical cancers and non-cancerous cervical tissues. In addition, we assessed the role of this SNP in the development and progression of CC.

methodsUsing high-resolution melting analysis, we evaluated rs6983267 SNP frequency in women diagnosed with cervical squamous cell carcinoma (SCC) (n = 481) and controls (n = 502) in a Polish Caucasian population. Logistic regression analysis was employed to adjust for the effects of age, parity, oral contraceptive use, tobacco smoking, and menopausal status.

resultsDividing patients based on clinical characteristics demonstrated an association of the rs6983267 genotype with tumor stage III and grade of differentiation G2 and G3. The p trend value calculated for the rs6983267 SNP in patients with stage III was 0.0006. We also observed a significant contribution of rs6983267 SNP to tumor grade of differentiation G2 and G3. Additional contributors were oral contraceptive use, smoking, and postmenopausal age. We found statistically significant increase of MYC transcript levels in cervical SCC tissues from carriers of the GG vs. T/T (p < 0.00001), G/T vs. T/T (p = 0.0002), and in the non-cancerous cervical tissues from carriers of the GG vs. T/T (p = 0.00046).

conclusionThe rs6983267 SNP may contribute to the increased MYC expression as well as the spread and rapid growth of cervical SCC as compared to lower grade carcinomas.

Indexed as

Polymorphism, Single NucleotideAdultAgedCarcinoma, Squamous CellCase-Control StudiesDisease ProgressionFemaleGenes, mycGenetic Predisposition to DiseaseHumansMiddle AgedNeoplasm GradingPolandPrevalenceRNA, Long NoncodingUterine Cervical Neoplasmslong non-coding RNA CCAT2, humanRNA, Long NoncodingCervical squamous cell carcinomaMYCPolymorphism

Identifiers

PMID29525942
PMCPMC5897468
OpenAlexW2790468896

What OpenQuestion holds

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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.