Evidence map›Paper›PMID 31204277›Full record

ArticleEBioMedicine2019

A role for kinesin-1 subunits KIF5B/KLC1 in regulating epithelial mesenchymal plasticity in breast tumorigenesis.

Alaa Moamer, Ibrahim Y Hachim, Najat Binothman, Ni Wang, Jean-Jacques Lebrun, Suhad Ali

Abstract read
In one paragraph

Article in EBioMedicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
–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

23 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. The proteomic landscape shows oncologic relevance in cystitis glandularis.Journal of pathology and translational medicine · 2023
    Article
  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

6 authors.

Alaa MoamerDepartment of Medicine, Cancer Research Program, Centre for Translational Biology, McGill University Health Centre, McGill University, Canada. Electronic address: alaa.moamer@mail.mcgill.ca.
Ibrahim Y HachimDepartment of Medicine, Cancer Research Program, Centre for Translational Biology, McGill University Health Centre, McGill University, Canada. Electronic address: ibrahim.hachim@mail.mcgill.ca.
Najat BinothmanDepartment of Medicine, Cancer Research Program, Centre for Translational Biology, McGill University Health Centre, McGill University, Canada. Electronic address: najat.binothman@mail.mcgill.ca.
Ni WangDepartment of Medicine, Cancer Research Program, Centre for Translational Biology, McGill University Health Centre, McGill University, Canada. Electronic address: ni.wang79@gmail.com.
Jean-Jacques LebrunDepartment of Medicine, Cancer Research Program, Centre for Translational Biology, McGill University Health Centre, McGill University, Canada. Electronic address: jj.lebrun@mcgill.ca.
Suhad AliDepartment of Medicine, Cancer Research Program, Centre for Translational Biology, McGill University Health Centre, McGill University, Canada. Electronic address: suhad.ali@mcgill.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEpithelial mesenchymal plasticity (EMP) is deemed vital in breast cancer progression, metastasis, stemness and resistance to therapy. Therefore, characterizing molecular mechanisms contributing to EMP are in need enabling the development of more advanced therapeutics against breast cancer. While kinesin superfamily proteins (KIFs) are well known for their role in intracellular cargo movement, our knowledge of their function in breast tumorigenesis is still limited.

methodsVarious breast cancer cell lines representing different molecular subtypes were used to determine the role of kinesine-1 subunits KIF5B/KLC1 in regulation of EMP.

findingsIn breast cancer, we show that kinesin family member 5B (KIF5B) and its partner protein kinesin light chain 1 (KLC1), subunits of kinesin-1, to play differential roles in regulating EMP and tumorigenesis. Indeed, we found KIF5B to be expressed in triple negative (TN)-basal-like/claudin low breast cancer subtype and to be an inducer of epithelial-mesenchymal transition (EMT), stemness, invasiveness, tumor formation and metastatic colonization. Whereas, we found KLC1 to be expressed in epithelial/luminal breast cancer subtypes and to be a suppressor of EMT, invasion, metastasis and stem cell markers expression as well as to be an inducer of epithelial/luminal phenotype. Interestingly, in TN-basal-like/claudin low cells we found a novel nuclear accumulation of KIF5B and its interaction with the EMT transcriptional regulator Snail1 independent of KLC1. In addition, TGF-β mediated pro-invasive activity was found to be dependent on KIF5B expression. In contrast, the epithelial differentiation factor and EMT suppressor prolactin (PRL) was found to repress KIF5B gene expression and KIF5B-Snail1 nuclear accumulation, but enhanced KLC1 gene expression and KIF5B-KLC1 interaction.

interpretationTogether, these results highlight a new paradigm for kinesin-1 function in breast tumorigenesis by regulating EMP programing and aggressiveness. FUND: This work was supported by the Canadian Institutes of Health Research (operating grants #233437 and 233438) granted to Suhad Ali.

Indexed as

AnimalsBreast NeoplasmsCarcinogenesisCell Line, TumorCell ProliferationEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHeterograftsHumansKinesinsMiceMicrotubule-Associated ProteinsProlactinTransforming Growth Factor betaKIF5B protein, humanKinesinsKLC1 protein, humanKns2 protein, mouseMicrotubule-Associated ProteinsProlactinTransforming Growth Factor betaCancer stem cellsDifferentiationEMTEpithelial mesenchymal plasticityInvasionKIF5BKLC1ProlactinTGFβXenograft

Identifiers

PMID31204277
PMCPMC6642081

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.