Evidence map›Paper›PMID 26297052›Full record

ArticleMolecular oncology2016

Determination of cell uptake pathways for tumor inhibitor lysyl oxidase propeptide.

Gokhan Baris Ozdener, Manish V Bais, Philip C Trackman

Abstract read
In one paragraph

Article in Molecular oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–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

22 citing papers in PubMed.

  1. Role of Caveolae and Caveolin in Vascular Physiology and Pathology.Journal of the American Heart Association · 2026
    Review
  2. Rab27b Promotes Lysosomal Function and Alpha-Synuclein Clearance in Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Development of an AAV-Based MicroRNA Gene Therapy to Treat Machado-Joseph Disease.Molecular therapy. Methods & clinical development · 2019
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Functional importance of lysyl oxidase family propeptide regions.Journal of cell communication and signaling · 2018
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Lysyl Oxidase and the Tumor Microenvironment.International journal of molecular sciences · 2016
    Review
  19. Review
  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

3 authors.

Gokhan Baris OzdenerBoston University, Department of Molecular and Cell Biology, Boston, MA 02118, United States.
Manish V BaisBoston University, Department of Molecular and Cell Biology, Boston, MA 02118, United States.
Philip C TrackmanBoston University, Department of Molecular and Cell Biology, Boston, MA 02118, United States. Electronic address: trackman@bu.edu.

Funding

Cellular or Extracellular Targeting of Lysyl Oxidase Propeptide for Oral CancerR21DE023973 · NIDCR · BOSTON UNIVERSITY MEDICAL CAMPUS · PI TRACKMAN, PHILIP C · 2014 to 2015
$450k
NIDCR NIH HHS R21 DE023973NIDCR NIH HHS R21DE023973
6 · The paper itself

Abstract

The lysyl oxidase propeptide (LOX-PP) is derived from pro-lysyl oxidase (Pro-LOX) by extracellular biosynthetic proteolysis. LOX-PP inhibits breast and prostate cancer xenograft tumor growth and has tumor suppressor activity. Although, several intracellular targets and molecular mechanisms of action of LOX-PP have been identified, LOX-PP uptake pathways have not been reported. Here we demonstrate that the major uptake pathway for recombinant LOX-PP (rLOX-PP) is PI3K-dependent macropinocytosis in PWR-1E, PC3, SCC9, MDA-MB-231 cell lines. A secondary pathway appears to be dynamin- and caveola dependent. The ionic properties of highly basic rLOX-PP provide buffering capacity at both high and low pHs. We suggest that the buffering capacity of rLOX-PP, which serves to limit endosomal acidification, sustains PI3K-dependent macropinocytosis in endosomes which in turn is likely to facilitate LOX-PP endosomal escape into the cytoplasm and its observed interactions with cytoplasmic targets and nuclear uptake.

Indexed as

Cell Line, TumorDynaminsEndocytosisHumansPeptidesProtein-Lysine 6-OxidaseDynaminsPeptidesProtein-Lysine 6-OxidaseEndocytosisLysyl oxidaseMacropinocytosisPropeptideTumor suppressor

Identifiers

PMID26297052
PMCPMC4549800

What OpenQuestion holds

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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.