Evidence map›Paper›PMID 33802237›Full record

Trial reportInternational journal of molecular sciences2021

Role of Genetic Variation in Cytochromes P450 in Breast Cancer Prognosis and Therapy Response.

Viktor Hlaváč, Radka Václavíková, Veronika Brynychová, Pavel Ostašov, Renata Koževnikovová, Katerina Kopečková, David Vrána, Jiří Gatěk, Pavel Souček

Abstract readClinical Trial
In one paragraph

Trial report in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Human Orphan Cytochromes P450: An Update.Current drug metabolism · 2022
    Article
  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

9 authors.

Viktor HlaváčToxicogenomics Unit, National Institute of Public Health, 100 00 Prague, Czech Republic.ORCID 0000-0003-0695-0552
Radka VáclavíkováToxicogenomics Unit, National Institute of Public Health, 100 00 Prague, Czech Republic.
Veronika BrynychováToxicogenomics Unit, National Institute of Public Health, 100 00 Prague, Czech Republic.
Pavel OstašovBiomedical Center, Faculty of Medicine in Pilsen, Charles University, 301 00 Pilsen, Czech Republic.ORCID 0000-0001-7168-6431
Renata KoževnikovováDepartment of Oncosurgery, MEDICON, 140 00 Prague, Czech Republic.
Katerina KopečkováDepartment of Oncology, Second Faculty of Medicine, Charles University and Motol University Hospital, 150 00 Prague, Czech Republic.
David VránaComprehensive Cancer Center Novy Jicin, Hospital Novy Jicin, 741 01 Novy Jicin, Czech Republic.ORCID 0000-0002-7419-822X
Jiří GatěkDepartment of Surgery, EUC Hospital Zlin and Tomas Bata University in Zlin, 763 02 Zlin, Czech Republic.
Pavel SoučekToxicogenomics Unit, National Institute of Public Health, 100 00 Prague, Czech Republic.ORCID 0000-0002-4294-6799

Funding

Charles University Research Fund Progress Q39Czech Medical Council NV19-08-00113Czech Ministry of Education, Youth and Sports INTER-EXCELLENCE LTA-USA no. 19032
6 · The paper itself

Abstract

Breast cancer is the most frequent cancer in the female population worldwide. The role of germline genetic variability in cytochromes P450 (CYP) in breast cancer prognosis and individualized therapy awaits detailed elucidation. In the present study, we used the next-generation sequencing to assess associations of germline variants in the coding and regulatory sequences of all human CYP genes with response of the patients to the neoadjuvant cytotoxic chemotherapy and disease-free survival (n = 105). A total of 22 prioritized variants associating with a response or survival in the above evaluation phase were then analyzed by allelic discrimination in the large confirmation set (n = 802). Associations of variants in

Indexed as

Breast NeoplasmsCytochrome P-450 Enzyme SystemGenetic VariationNeoadjuvant TherapyNeoplasm ProteinsDisease-Free SurvivalFemaleHumansMiddle AgedSurvival RateCytochrome P-450 Enzyme SystemNeoplasm Proteinsbreast cancercytochrome P450next-generation sequencingprognosisresponsesurvivaltherapy

Identifiers

PMID33802237
PMCPMC8001203

What OpenQuestion holds

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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.