Evidence map›Paper›PMID 31820782›Full record

ArticleThe Journal of cell biology2020

SNX27-retromer assembly recycles MT1-MMP to invadopodia and promotes breast cancer metastasis.

Priyanka Sharma, Sameena Parveen, Lekha V Shah, Madhumita Mukherjee, Yannis Kalaidzidis, Anthony J Kozielski, Roberto Rosato, Jenny C Chang, Sunando Datta

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

28 citing papers in PubMed, 53 citations in OpenAlex.

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  11. Cytoplasmic Tail of MT1-MMP: A Hub of MT1-MMP Regulation and Function.International journal of molecular sciences · 2023
    Review
  12. Review
  13. Article
  14. Article
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  16. Article
  17. Tex264 Binding to SNX27 Regulates ItgBioMed research international · 2022
    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

9 authors at 3 institutions in 4 countries.

Priyanka SharmaDepartment of Biological Sciences, Indian Institute of Science Education and Research, Bhopal, Bhopal, India.
Sameena ParveenDepartment of Biological Sciences, Indian Institute of Science Education and Research, Bhopal, Bhopal, India.
Lekha V ShahDepartment of Biological Sciences, Indian Institute of Science Education and Research, Bhopal, Bhopal, India.
Madhumita MukherjeeDepartment of Chemistry, Indian Institute of Science Education and Research, Bhopal, Bhopal, India.
Yannis KalaidzidisMax Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany.
Anthony J KozielskiHouston Methodist Research Institute, Houston, TX.
Roberto RosatoHouston Methodist Research Institute, Houston, TX.
Jenny C ChangHouston Methodist Research Institute, Houston, TX.
Sunando DattaDepartment of Biological Sciences, Indian Institute of Science Education and Research, Bhopal, Bhopal, India.
Indian Institute of Science Education and Research, Bhopal · INHouston Methodist · USLomonosov Moscow State University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A variety of metastatic cancer cells use actin-rich membrane protrusions, known as invadopodia, for efficient ECM degradation, which involves trafficking of proteases from intracellular compartments to these structures. Here, we demonstrate that in the metastatic breast cancer cell line MDA-MB-231, retromer regulates the matrix invasion activity by recycling matrix metalloprotease, MT1-MMP. We further found that MT2-MMP, another abundantly expressed metalloprotease, is also invadopodia associated. MT1- and MT2-MMP showed a high degree of colocalization but were located on the distinct endosomal domains. Retromer and its associated sorting nexin, SNX27, phenocopied each other in matrix degradation via selectively recycling MT1-MMP but not MT2-MMP. ITC-based studies revealed that both SNX27 and retromer could directly interact with MT1-MMP. Analysis from a publicly available database showed SNX27 to be overexpressed or frequently altered in the patients having invasive breast cancer. In xenograft-based studies, SNX27-depleted cell lines showed prolonged survival of SCID mice, suggesting a possible implication for overexpression of the sorting nexin in tumor samples.

Indexed as

AnimalsApoptosisBiomarkers, TumorBreast NeoplasmsCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansLung NeoplasmsMatrix Metalloproteinase 14Matrix Metalloproteinase 15MiceMice, SCIDNeoplasm InvasivenessPodosomesBiomarkers, TumorMatrix Metalloproteinase 14Matrix Metalloproteinase 15MMP14 protein, humanMMP15 protein, humanSNX27 protein, humanSorting Nexins

Identifiers

PMID31820782
PMCPMC7039210
OpenAlexW2995298326

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.