Evidence map›Paper›PMID 29845349›Full record

ReviewClinical & experimental metastasis2018

Alternative splicing and cancer metastasis: prognostic and therapeutic applications.

Diego M Marzese, Ayla O Manughian-Peter, Javier I J Orozco, Dave S B Hoon

Abstract readReview
PubMed Publisher
In one paragraph

Review in Clinical & experimental metastasis, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

24 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Spatial Isoforms Reveal the Mechanisms of Metastasis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Identification of prognostic alternative splicing signature in gastric cancer.Archives of public health = Archives belges de sante publique · 2022
    Article
  9. Impacts and mechanisms of alternative mRNA splicing in cancer metabolism, immune response, and therapeutics.Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. The Long Noncoding RNAMolecular cancer research : MCR · 2020
    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

4 authors at 1 institution in 1 country.

Diego M MarzeseDepartment of Translational Molecular Medicine, John Wayne Cancer Institute, Santa Monica, CA, USA.ORCID 0000-0002-3258-8852
Ayla O Manughian-PeterDepartment of Translational Molecular Medicine, John Wayne Cancer Institute, Santa Monica, CA, USA.ORCID 0000-0001-7387-6722
Javier I J OrozcoDepartment of Translational Molecular Medicine, John Wayne Cancer Institute, Santa Monica, CA, USA.ORCID 0000-0003-2585-358X
Dave S B HoonDepartment of Translational Molecular Medicine, John Wayne Cancer Institute, Santa Monica, CA, USA. hoond@jwci.org.ORCID 0000-0003-1915-3683
Saint John's Health Center · US

Funding

Identification of Melanoma Brain Metastasis Tumor BiomarkersR01CA167967 · NCI · SAINT JOHN'S CANCER INSTITUTE · PI HOON, DAVE S B · 2013 to 2017
$1.9M
NCI NIH HHS R01 CA167967
6 · The paper itself

Abstract

Metastatic cells exhibit an extraordinary phenotypic plasticity, not only in adapting to unfamiliar microenvironments but also in surviving aggressive treatments and immune responses. A major source of phenotypic variability is alternative splicing (AS) of the pre-messenger RNA. This process is catalyzed by one of the most complex pieces of cellular molecular regulatory events, the spliceosome, which is composed of ribonucleoproteins and polypeptides termed spliceosome factors. With strong evidence indicating that AS affects nearly all genes encoded by the human genome, aberrant AS programs have a significant impact on cancer cell development and progression. In this review, we present insights about the genomic and epigenomic factors affecting AS, summarize the most recent findings linking aberrant AS to metastatic progression, and highlight potential prognostic and therapeutic applications.

Indexed as

PrognosisAlternative SplicingDisease ProgressionHumansMutationNeoplasm MetastasisNeoplasmsRNA, MessengerSpliceosomesRNA, MessengerAlternative splicingCancer metastasisEpigeneticsPrognosticTherapeutics

Identifiers

PMID29845349
OpenAlexW2807284775

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.