Evidence map›Paper›PMID 27492253›Full record

ReviewCurrent hematologic malignancy reports2016

Targeting Splicing in the Treatment of Myelodysplastic Syndromes and Other Myeloid Neoplasms.

Charlotte K Brierley, David P Steensma

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current hematologic malignancy reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Molecular Targeted Therapy and Immunotherapy for Myelodysplastic Syndrome.International journal of molecular sciences · 2021
    Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Six Exonic Variants in theFrontiers in genetics · 2020
    Article
  11. Article
  12. Article
  13. Myeloid neoplasms with germline DDX41 mutation.International journal of hematology · 2017
    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 2 institutions in 2 countries.

Charlotte K BrierleyDepartment of Haematology, Oxford University Hospitals NHS Trust, Churchill Hospital, Old Road, Oxford, OX3 7LE, UK.
David P SteensmaAdult Leukemia Program, Division of Hematologic Malignancies, Department of Medical Oncology, Dana-Farber Cancer Institute, D2037, 450 Brookline Ave, Boston, MA, 02215, USA. David_Steensma@DFCI.HARVARD.EDU.
Dana-Farber Cancer Institute · USOxford University Hospitals NHS Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genome sequencing of primary cells from patients with myelodysplastic syndromes (MDS) led to the identification of recurrent heterozygous mutations in gene encoding components of the spliceosome, the cellular machinery which processes pre-messenger RNA (mRNA) to mature mRNA during gene transcription. Splicing mutations are mutually exclusive with one another and collectively represent the most common mutation class in MDS, occurring in approximately 60 % of patients overall and more than 80 % of those with ring sideroblasts. Evidence from animal models suggests that homozygous splicing mutations are lethal, and that in heterozygously mutated models, any further disruption of splicing triggers apoptosis and cell death. MDS cells with spliceosome mutations are thus uniquely vulnerable to therapies targeting splicing, which may be tolerated by healthy cells. The spliceosome is emerging as a novel therapeutic target in MDS and related myeloid neoplasms, with the first clinical trial of a splicing modulator opening in 2016.

Indexed as

RNA SplicingAnimalsEpoxy CompoundsHematologic NeoplasmsHumansIndolesMacrolidesMutationMyelodysplastic SyndromesMyeloproliferative DisordersRibonucleoprotein, U2 Small NuclearRNA Splicing FactorsSpliceosomesE 7107Epoxy CompoundsIndolesMacrolidesRibonucleoprotein, U2 Small NuclearRNA Splicing FactorsE7107Myelodysplastic syndromesSF3B1SplicingTargeted therapy

Identifiers

PMID27492253
OpenAlexW2495059346

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.