Evidence map›Paper›PMID 32019064›Full record

ReviewCancers2020

The Non-Coding RNA Landscape of Plasma Cell Dyscrasias.

Eugenio Morelli, Annamaria Gullà, Roberta Rocca, Cinzia Federico, Lavinia Raimondi, Stefano Malvestiti, Valter Agosti, Marco Rossi, Giosuè Costa, Gianluca Giavaresi and 9 more

Abstract readReview
In one paragraph

Review in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–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

25 citing papers in PubMed.

  1. Review
  2. Article
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  5. Review
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  7. Review
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  11. Review
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  14. Review
  15. Article
  16. Article
  17. Myeloma Bone Disease: A Comprehensive Review.International journal of molecular sciences · 2021
    Review
  18. Review
  19. Article
  20. 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

19 authors.

Eugenio MorelliDana Farber Cancer Institute, Harvard Medical School, Boston, MA 02215, USA.
Annamaria GullàDana Farber Cancer Institute, Harvard Medical School, Boston, MA 02215, USA.
Roberta RoccaDepartment of Experimental and Clinical Medicine, Magna Graecia University of Catanzaro, 88100 Catanzaro, Italy.
Cinzia FedericoDepartment of Radiation Oncology, Cancer Biology Division, Washington University in St. Louis School of Medicine, St. Louis, MO 63108, USA.
Lavinia RaimondiIRCCS Istituto Ortopedico Rizzoli, 40136 Bologna, Italy.
Stefano MalvestitiDana Farber Cancer Institute, Harvard Medical School, Boston, MA 02215, USA.
Valter AgostiDepartment of Experimental and Clinical Medicine, Magna Graecia University of Catanzaro, 88100 Catanzaro, Italy.
Marco RossiDepartment of Experimental and Clinical Medicine, Magna Graecia University of Catanzaro, 88100 Catanzaro, Italy.
Giosuè CostaDepartment of Health Science, Magna Graecia University of Catanzaro, 88100 Catanzaro, Italy.
Gianluca GiavaresiIRCCS Istituto Ortopedico Rizzoli, 40136 Bologna, Italy.
Kareem A AzabDepartment of Radiation Oncology, Cancer Biology Division, Washington University in St. Louis School of Medicine, St. Louis, MO 63108, USA.
Antonia CagnettaIRCCS, Ospedale Policlinico San Martino, 16100 Genoa, Italy.
Michele CeaIRCCS, Ospedale Policlinico San Martino, 16100 Genoa, Italy.
Pierosandro TagliaferriDepartment of Experimental and Clinical Medicine, Magna Graecia University of Catanzaro, 88100 Catanzaro, Italy.
Antonino NeriDepartment of Oncology and Hemato-oncology, University of Milan and Hematology, Fondazione Cà Granda IRCCS Policlinico, 20122 Milan, Italy.
Nikhil C MunshiDana Farber Cancer Institute, Harvard Medical School, Boston, MA 02215, USA.
Giuseppe VigliettoDepartment of Experimental and Clinical Medicine, Magna Graecia University of Catanzaro, 88100 Catanzaro, Italy.
Pierfrancesco TassoneDepartment of Experimental and Clinical Medicine, Magna Graecia University of Catanzaro, 88100 Catanzaro, Italy.
Nicola AmodioDepartment of Experimental and Clinical Medicine, Magna Graecia University of Catanzaro, 88100 Catanzaro, Italy.

Funding

Associazione Italiana per la Ricerca sul Cancro 9980Associazione Italiana per la Ricerca sul Cancro IG21588
6 · The paper itself

Abstract

Despite substantial advancements have been done in the understanding of the pathogenesis of plasma cell (PC) disorders, these malignancies remain hard-to-treat. The discovery and subsequent characterization of non-coding transcripts, which include several members with diverse length and mode of action, has unraveled novel mechanisms of gene expression regulation often malfunctioning in cancer. Increasing evidence indicates that such non-coding molecules also feature in the pathobiology of PC dyscrasias, where they are endowed with strong therapeutic and/or prognostic potential. In this review, we aim to summarize the most relevant findings on the biological and clinical features of the non-coding RNA landscape of malignant PCs, with major focus on multiple myeloma. The most relevant classes of non-coding RNAs will be examined, along with the mechanisms accounting for their dysregulation and the recent strategies used for their targeting in PC dyscrasias. It is hoped these insights may lead to clinical applications of non-coding RNA molecules as biomarkers or therapeutic targets/agents in the near future.

Indexed as

lncRNAmiRNAmultiple myelomanon-coding RNAplasma cell dyscrasia

Identifiers

PMID32019064
PMCPMC7072200

What OpenQuestion holds

Textmetadata
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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.