Evidence map›Paper›PMID 29021870›Full record

ReviewHereditary cancer in clinical practice2017

The potential role of miRNAs in therapy of breast and ovarian cancers associated with BRCA1 mutation.

Agnieszka Strumidło, Sylwia Skiba, Rodney J Scott, Jan Lubiński

Open access · goldAbstract readReview
In one paragraph

Review in Hereditary cancer in clinical practice, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Recent Advances in miRNA Delivery Systems.Methods and protocols · 2021
    Article
  6. Review
  7. Article
  8. Article
  9. The BRCA1 Methylation and PD-L1 Expression in Sporadic Ovarian Cancer.International journal of gynecological cancer : official journal of the International Gynecological Cancer Society · 2018
    Article
  10. 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

4 authors at 2 institutions in 2 countries.

Agnieszka Strumidło *Pomeranian University of Medicine, Szczecin, Poland.
Sylwia Skiba *Pomeranian University of Medicine, Szczecin, Poland.
Rodney J ScottThe University of Newcastle and Hunter Medical Research Institute, Newcastle, Australia.
Jan LubińskiDepartment of Genetics and Pathology, Pomeranian University of Medicine, Szczecin, Poland.
Pomeranian Medical University · PLHunter Genetics · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Germline variants within BRCA1 or BRCA2 genes account for approximately 25% of familial aggregations of breast-ovarian cancers. Low or no expression of BRCA1 in breast and ovarian cancers is associated with a good clinical response to treatment with platinum therapies and PARP1 inhibitors. Recent studies demonstrated that microRNAs - small non-coding RNAs, involved in the control of gene expression, can decrease BRCA1 expression by targeting the 3'UTR region of the gene. This article reviews reported relationships between various miRNAs, such as miRNA-9, miRNA-146a, miRNA-182 miRNA-218, miRNA-638 and the response to cytostatic drugs, mainly to platins and PARP1 inhbitors, for the treatment of breast and ovarian cancer associated with BRCA1 mutations.

Indexed as

BRCA1Breast cancermicroRNAOvarian cancerTreatment

Identifiers

PMID29021870
PMCPMC5622493
OpenAlexW2757528339

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.