Evidence map›Paper›PMID 28257090›Full record

ReviewInternational journal of molecular sciences2017

From General Aberrant Alternative Splicing in Cancers and Its Therapeutic Application to the Discovery of an Oncogenic DMTF1 Isoform.

Na Tian, Jialiang Li, Jinming Shi, Guangchao Sui

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

15 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Functional analysis of theAnimal biotechnology · 2024
    Article
  4. Article
  5. Characterization of the Testis-specificJournal of the Endocrine Society · 2021
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. 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

4 authors at 2 institutions in 2 countries.

Na TianCollege of Life Science, Northeast Forestry University, Harbin 150040, China. tianna@nefu.edu.cn.
Jialiang LiCollege of Life Science, Northeast Forestry University, Harbin 150040, China. lijialiang@nefu.edu.cn.
Jinming ShiCollege of Life Science, Northeast Forestry University, Harbin 150040, China. jmshi@nefu.edu.cn.
Guangchao SuiCollege of Life Science, Northeast Forestry University, Harbin 150040, China. gcsui@nefu.edu.cn.
Northeast Forestry University · CNWake Forest University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alternative pre-mRNA splicing is a crucial process that allows the generation of diversified RNA and protein products from a multi-exon gene. In tumor cells, this mechanism can facilitate cancer development and progression through both creating oncogenic isoforms and reducing the expression of normal or controllable protein species. We recently demonstrated that an alternative cyclin D-binding myb-like transcription factor 1 (DMTF1) pre-mRNA splicing isoform, DMTF1β, is increasingly expressed in breast cancer and promotes mammary tumorigenesis in a transgenic mouse model. Aberrant pre-mRNA splicing is a typical event occurring for many cancer-related functional proteins. In this review, we introduce general aberrant pre-mRNA splicing in cancers and discuss its therapeutic application using our recent discovery of the oncogenic DMTF1 isoform as an example. We also summarize new insights in designing novel targeting strategies of cancer therapies based on the understanding of deregulated pre-mRNA splicing mechanisms.

Indexed as

Alternative SplicingAnimalsAntineoplastic AgentsBreast NeoplasmsFemaleGene Expression Regulation, NeoplasticHumansMiceMolecular Targeted TherapyNeoplasmsProtein IsoformsTranscription FactorsAntineoplastic AgentsDMTF1 protein, humanProtein IsoformsTranscription Factorsalternative splicingcancer therapyDMTF1tumorigenesis

Identifiers

PMID28257090
PMCPMC5372486
OpenAlexW2592618488

What Socratic 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 Socratic graph.