Evidence map›Paper›PMID 34676052›Full record

ArticleOncotarget2021

TP53 mutations determined by targeted NGS in breast cancer: a case-control study.

Angeliki Andrikopoulou, Evangelos Terpos, Spyridoula Chatzinikolaou, Kleoniki Apostolidou, Ioannis Ntanasis-Stathopoulos, Maria Gavriatopoulou, Meletios-Athanasios Dimopoulos, Flora Zagouri

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 7% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. The Genomic and Biologic Landscapes of Breast Cancer and Racial Differences.International journal of molecular sciences · 2024
    Review
  5. Article
  6. Implementing precision oncology for sarcoma patients: the CCCJournal of cancer research and clinical oncology · 2023
    Article
  7. Article
  8. Article
  9. 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

8 authors at 1 institution in 1 country.

Angeliki AndrikopoulouDepartment of Clinical Therapeutics, Alexandra Hospital Medical School, Athens 11528, Greece.
Evangelos TerposDepartment of Clinical Therapeutics, Alexandra Hospital Medical School, Athens 11528, Greece.
Spyridoula ChatzinikolaouDepartment of Clinical Therapeutics, Alexandra Hospital Medical School, Athens 11528, Greece.
Kleoniki ApostolidouDepartment of Clinical Therapeutics, Alexandra Hospital Medical School, Athens 11528, Greece.
Ioannis Ntanasis-StathopoulosDepartment of Clinical Therapeutics, Alexandra Hospital Medical School, Athens 11528, Greece.
Maria GavriatopoulouDepartment of Clinical Therapeutics, Alexandra Hospital Medical School, Athens 11528, Greece.
Meletios-Athanasios DimopoulosDepartment of Clinical Therapeutics, Alexandra Hospital Medical School, Athens 11528, Greece.
Flora ZagouriDepartment of Clinical Therapeutics, Alexandra Hospital Medical School, Athens 11528, Greece.
Alexandra Hospital · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTumor protein 53 (TP53) gene mutations are identified in up to 37% of breast tumors especially in HER-2 positive and basal-like subtype. Previous studies have indicated TP53 mutations as a prognostic biomarker in breast cancer. However, most of these studies performed immunohistochemistry (IHC) for the detection of TP53 mutations.

aimThe purpose of our study is to evaluate the role of TP53 somatic mutations detected via next-generation sequencing (NGS) as a potential prognostic marker in patients with breast cancer. MATERIALS AND

methods82 female patients with Stage I-III breast cancer underwent NGS in paraffin blocks and blood samples during the period 25/09/2019 through 25/05/2021. 23 cases of somatic TP53 mutations and 23 cases of healthy controls were matched on age at diagnosis, menopausal status, histological subtype, histological grade, ki67 expression and disease stage.

resultsMean age at diagnosis was 52.35 (SD; 11.47) years. The somatic TP53 mutation

conclusionsOur case-control study suggests that TP53 somatic mutations detected by next-generation sequencing (NGS) are associated with an adverse prognosis in breast cancer.

Indexed as

biomarkerbreast cancernext-generation sequencingprognosisTP53 mutations

Identifiers

PMID34676052
PMCPMC8522843
OpenAlexW3199936041

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.