Cited by 118Protease and Inhibitor MechanismsTGF-β signaling in diseasesMechanisms of cancer metastasis

RECKing MMP function: implications for cancer development

Rhee, J·2002·Trends in Cell Biology

Abstract

Cancer is a multistage process requiring progressive genetic and epigenetic changes in neoplastic and responding stromal cells. Many alterations that occur during the process of malignant progression are regulated by the matrix metalloproteinase (MMP) family of extracellular proteases and their endogenous inhibitors. Recent work has identified a new cell-surface inhibitor of MMPs - RECK. RECK regulates MMP-induced pericellular signaling cascades during embryogenesis and tumorigenesis. Homozygous loss of RECK results in embryonic lethality and attenuated tumor development in adults - thus providing further support for an efficacious role for protease inhibitors as anticancer therapeutics.

Integrity signals

Registry

Crossref · 10.1016/s0962-8924(02)02280-8

Cites

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Cited by

Sorted by citations

Authors
Rhee, J.
Affiliations
University of California, San Francisco (US)
Corresponding author
Rhee, J
Venue
Trends in Cell Biology
Publisher
Elsevier BV
Published
2002-05-01
Volume
12
Issue
5
Pages
209-211
ISSN
0962-8924 (ISSN-L)
OpenAlex
W2068498906
Cited by
118
References
0
Citations by year
2026: 1 · 2025: 2 · 2024: 3 · 2023: 1 · 2022: 1 · 2021: 7 · 2020: 1 · 2019: 1 · 2018: 2 · 2017: 4 · 2016: 2 · 2015: 8 · 2014: 9 · 2013: 6 · 2012: 7
FWCI
3.03
Type
journal article
Language
en
Open access
closed
Locations
  • Trends in Cell Biology (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • V Foundation for Cancer Research
  • Edward Mallinckrodt, Jr. Foundation
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Protease and Inhibitor Mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › TGF-β signaling in diseases
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mechanisms of cancer metastasis
Keywords
RECK, matrix metalloproteinases, matrix metalloproteinase inhibitors, extracellular protease, tumor stroma, malignant progression, tumor microenvironment, protease inhibitors, anticancer agents, embryonic lethality
MeSH terms
Animals, Catalysis, Humans, Membrane Glycoproteins, Models, Biological, Neoplasms, Signal Transduction, Gene Expression Regulation, Enzymologic, Matrix Metalloproteinase 2, Matrix Metalloproteinase 9, Matrix Metalloproteinases, GPI-Linked Proteins

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review