Evidence map›Paper›PMID 32576578›Full record

ReviewCancer genomics & proteomics

Identification of MicroRNAs With

Ulrich H Weidle, Adam Nopora

Open access · diamondAbstract readReview
In one paragraph

Review in Cancer genomics & proteomics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Review
  3. 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

2 authors at 1 institution in 1 country.

Ulrich H WeidleRoche Pharma Research and Early Development, Roche Innovation Center Munich, Penzberg, Germany adam.nopora@roche.com weidle49@t-online.de.
Adam NoporaRoche Pharma Research and Early Development, Roche Innovation Center Munich, Penzberg, Germany adam.nopora@roche.com weidle49@t-online.de.
Roche Pharma AG (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimMultiple myeloma is a B-cell neoplasm, which can spread within the marrow of the bones forming many small tumors. In advanced disease, multiple myeloma can spread to the blood as plasma cell leukemia. In some cases, a localized tumor known as plasmacytoma is found within a single bone. Despite the approval of several agents such as melphalan, corticosteroids, proteasome inhibitors, thalidomide-based immuno-modulatory agents, histone deacetylase inhibitors, a nuclear export inhibitor and monoclonal antibodies daratuzumab and elatuzumab, the disease presently remains uncurable. MATERIALS AND

methodsIn order to define new targets and treatment modalities we searched the literature for microRNAs, which increase or inhibit in vivo efficacy in multiple-myeloma-related xenograft models. RESULTS AND

conclusionWe identified six up-regulated and twelve down-regulated miRs, which deserve further preclinical validation.

Indexed as

Drug Resistance, NeoplasmGene Expression Regulation, NeoplasticAntineoplastic AgentsApoptosisBiomarkers, TumorCell ProliferationHumansMicroRNAsMultiple MyelomaXenograft Model Antitumor AssaysAntineoplastic AgentsBiomarkers, TumorMicroRNAsAntisense-oligonucleotideslocked nucleic acidsmicroRNA deliverymicroRNA mimeticsmultiple myelomareviewtreatment resistance

Identifiers

PMID32576578
PMCPMC7367608
OpenAlexW3037062266

What OpenQuestion holds

Textmetadata
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.