Evidence map›Paper›PMID 30144133›Full record

Trial reportHematological oncology2018

Circulating exosomal long noncoding RNA PRINS-First findings in monoclonal gammopathies.

Lenka Sedlarikova, Bozena Bollova, Lenka Radova, Lucie Brozova, Jiri Jarkovsky, Martina Almasi, Miroslav Penka, Petr Kuglík, Viera Sandecká, Martin Stork and 2 more

Abstract readClinical Trial
In one paragraph

Trial report in Hematological oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing 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

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

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Long non‑coding RNAs in multiple myeloma (Review).International journal of oncology · 2023
    Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Review
  19. Review
  20. Review
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

12 authors.

Lenka SedlarikovaBabak Myeloma Group, Department of Pathological Physiology, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Bozena BollovaBabak Myeloma Group, Department of Pathological Physiology, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Lenka RadovaCentral European Institute of Technology, Masaryk University, Brno, Czech Republic.
Lucie BrozovaInstitute of Biostatistics and Analyses, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Jiri JarkovskyInstitute of Biostatistics and Analyses, Faculty of Medicine, Masaryk University, Brno, Czech Republic.
Martina AlmasiDepartment of Clinical Hematology, University Hospital Brno, Brno, Czech Republic.
Miroslav PenkaDepartment of Clinical Hematology, University Hospital Brno, Brno, Czech Republic.
Petr KuglíkDepartment of Experimental Biology, Faculty of Science, Masaryk University, Brno, Czech Republic.
Viera SandeckáDepartment of Internal Medicine, Hematology and Oncology, University Hospital Brno, Brno, Czech Republic.
Martin StorkDepartment of Internal Medicine, Hematology and Oncology, University Hospital Brno, Brno, Czech Republic.
Ludek PourDepartment of Internal Medicine, Hematology and Oncology, University Hospital Brno, Brno, Czech Republic.
Sabina SevcikovaBabak Myeloma Group, Department of Pathological Physiology, Faculty of Medicine, Masaryk University, Brno, Czech Republic.ORCID http://orcid.org/0000-0002-7194-6771

Funding

Czech Ministry of Health AZV 15-29508A
6 · The paper itself

Abstract

Multiple myeloma is the second most common hematological malignancy characterized by focal lesions of malignant plasma cells in the bone marrow. These lesions contain subclones that directly influence survival of patients. Bone marrow biopsies are single-site biopsies and thus cannot contain all information about the tumor. In contrast, liquid biopsies analyze circulating cells and molecules that are secreted from all sites of the tumor. Long noncoding RNA molecules are one class of these molecules. We performed a two-phase biomarker study investigating lncRNA expression profiles in exosomes of peripheral blood serum of newly diagnosed multiple myeloma (MM) patients, monoclonal gammopathy of undetermined significance (MGUS) patients in comparison with healthy donors (HD). Surprisingly, this analysis revealed dysregulation of only one exosomal lncRNA PRINS in MM vs HD. Overall, MM and MGUS patients were distinguished from HD with sensitivity of 84.9% and specificity of 83.3%. Our study suggests a possible diagnostic role for exosomal lncRNA PRINS in monoclonal gammopathies patients.

Indexed as

Multiple MyelomaAdultAgedAged, 80 and overDisease-Free SurvivalExosomesFemaleHumansMaleMiddle AgedRNA, Long NoncodingRNA, NeoplasmSurvival RateRNA, Long NoncodingRNA, Neoplasmbiomarkerlong noncoding RNAmonoclonal gammopathy of undetermined significancemultiple myelomaqPCR

Identifiers

PMID30144133
PMCPMC6585732

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.