Evidence map›Paper›PMID 29409452›Full record

ArticleBMC cancer2018

Whole blood microRNAs as potential biomarkers in post-operative early breast cancer patients.

Marianna Alunni-Fabbroni, Leonie Majunke, Elisabeth K Trapp, Marie Tzschaschel, Sven Mahner, Peter A Fasching, Tanja Fehm, Andreas Schneeweiss, Thomas Beck, Ralf Lorenz and 4 more

Abstract read
In one paragraph

Article in BMC cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. G2/M Checkpoint Modulation: Insights from miRNA Profiles in FAM and Breast Cancer.Asian Pacific journal of cancer prevention : APJCP · 2024
    Article
  5. Circulating tumor cellsTranslational breast cancer research : a journal focusing on translational research in breast cancer · 2024
    Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Role of miRNA-19a in Cancer Diagnosis and Poor Prognosis.International journal of molecular sciences · 2021
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Observational
  16. 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

14 authors.

Marianna Alunni-FabbroniDepartment of Gynecology and Obstetrics, University Hospital, LMU Munich, Munich, Germany. Marianna.Alunni@med.uni-muenchen.de.ORCID 0000-0002-9710-1662
Leonie MajunkeDepartment of Gynecology and Obstetrics, University Hospital, LMU Munich, Munich, Germany.
Elisabeth K TrappDepartment of Gynecology and Obstetrics, University Hospital, LMU Munich, Munich, Germany.
Marie TzschaschelDepartment of Gynecology and Obstetrics, University Hospital, LMU Munich, Munich, Germany.
Sven MahnerDepartment of Gynecology and Obstetrics, University Hospital, LMU Munich, Munich, Germany.
Peter A FaschingDepartment of Gynecology and Obstetrics, Erlangen University Hospital, Erlangen, Germany.
Tanja FehmDepartment of Gynecology and Obstetrics, Medical Faculty and University Hospital, Heinrich-Heine University, Düsseldorf, Germany.
Andreas SchneeweissDepartment of Gynecology and Obstetrics, Heidelberg University Hospital, Heidelberg, Germany.
Thomas BeckRoMed Klinikum Rosenheim, Rosenheim, Germany.
Ralf LorenzGemeinschaftspraxis Lorenz / Hecker / Wesche, Braunschweig, Germany.
Thomas W P FriedlDepartment of Gynecology and Obstetrics, Ulm University Hospital, Ulm, Germany.
Wolfgang JanniDepartment of Gynecology and Obstetrics, Ulm University Hospital, Ulm, Germany.
Brigitte RackDepartment of Gynecology and Obstetrics, University Hospital, LMU Munich, Munich, Germany.
SUCCESS Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundmicroRNAs (miRNAs) are considered promising cancer biomarkers, showing high reliability, sensitivity and stability. Our study aimed to identify associations between whole blood miRNA profiles, presence of circulating tumor cells (CTCs) and clinical outcome in post-operative early breast cancer patients (EBC) to assess the utility of miRNAs as prognostic markers in this setting.

methodA total of 48 post-operative patients, recruited in frame of the SUCCESS A trial, were included in this retrospective study and tested with a panel of 8 miRNAs (miR-10b, -19a, - 21, - 22, -20a, - 127, - 155, -200b). Additional 17 female healthy donors with no previous history of cancer were included in the study as negative controls. Blood samples were collected at different time points (pre-adjuvant therapy, post-adjuvant therapy, 2 years follow up), total RNA was extracted and the relative concentration of each miRNA was measured by quantitative PCR and compared in patients stratified on blood collection time or CTC detection. Furthermore, we compared miRNA profiles of patients, for each time point separately, and healthy donors. CTCs were visualized and quantified with immunocytochemistry analysis. Data were analyzed using non-parametric statistical tests.

resultsIn our experimental system, miR-19a, miR-22 and miR-127 showed the most promising results, differentiating patients at different time points and from healthy controls, while miR-20a, miR-21 and miR-200b did not show any difference among the different groups. miR-10b and miR-155 were never detectable in our experimental system. With respect to patients' clinical characteristics, we found a significant correlation between miR-200b and lymph node status and between miR-20a and tumor type. Furthermore, miR-127 correlated with the presence of CTCs. Finally, we found a borderline significance between Progression Free Survival and miR-19a levels.

conclusionsThis pilot study suggests that profiling whole blood miRNAs could help to better stratify post-operative EBC patients without any sign of metastasis to prevent later relapse or metastatic events.

Indexed as

Gene Expression Regulation, NeoplasticAdultAgedBiomarkers, TumorBreast NeoplasmsDisease-Free SurvivalFemaleGene Expression ProfilingHumansMicroRNAsMiddle AgedNeoplastic Cells, CirculatingPilot ProjectsPostoperative PeriodRetrospective StudiesBiomarkers, TumorMicroRNAsCirculating tumor cellEarly breast cancerImmune systemmicroRNATumor marker

Identifiers

PMID29409452
PMCPMC5802058

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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.