Evidence map›Paper›PMID 25661772›Full record

ReviewMatrix biology : journal of the International Society for Matrix Biology

Matrix metalloproteinases in stem cell regulation and cancer.

Kai Kessenbrock, Chih-Yang Wang, Zena Werb

Open access · hybridAbstract readReview
In one paragraph

Review in Matrix biology : journal of the International Society for Matrix Biology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 108 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
108citing papers in PubMed, 1 pooled it
10.8field-weighted citation impact, top 1% 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

108 citing papers in PubMed, 1 synthesis or guideline pooled it, 209 citations in OpenAlex.

  1. Pooled it
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  13. The regulatory role of m6A in cancer metastasis.Frontiers in cell and developmental biology · 2025
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  19. Appraisal of postbiotics in cancer therapy.Frontiers in pharmacology · 2024
    Review
  20. Article

48 more citing papers are in PubMed but not listed here.

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 at 1 institution in 2 countries.

Kai KessenbrockDepartment of Anatomy and Biomedical Sciences Program, University of California, San Francisco, CA 94143-0452, United States.
Chih-Yang WangDepartment of Anatomy and Biomedical Sciences Program, University of California, San Francisco, CA 94143-0452, United States; Institute of Basic Medical Sciences, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Zena WerbDepartment of Anatomy and Biomedical Sciences Program, University of California, San Francisco, CA 94143-0452, United States. Electronic address: zena.werb@ucsf.edu.
University of California, San Francisco · US

Funding

Role of Metalloproteinases in Mammary Gland RemodelingR01CA057621 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WERB, ZENA · 1993 to 2017
$9.0M
Proteolytic regulation of Wnt signaling in breast cancer stem cellsR00CA181490 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI KESSENBROCK, KAI · 2016 to 2018
$730k
Proteolytic regulation of Wnt signaling in breast cancer stem cellsK99CA181490 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KESSENBROCK, KAI · 2014 to 2015
$268k
NCI NIH HHS K99 CA181490NCI NIH HHS R00 CA181490NCI NIH HHS R01 CA057621NCI NIH HHS R01 CA57621
6 · The paper itself

Abstract

Since Gross and Lapiere firstly discovered matrix metalloproteinases (MMPs) as important collagenolytic enzymes during amphibian tadpole morphogenesis in 1962, this intriguing family of extracellular proteinases has been implicated in various processes of developmental biology. However, the pathogenic roles of MMPs in human diseases such as cancer have also garnered widespread attention. The most straightforward explanation for their role in cancer is that MMPs, through extracellular matrix degradation, pave the way for tumor cell invasion and metastasis. While this notion may be true for many circumstances, we now know that, depending on the context, MMPs may employ additional modes of functionality. Here, we will give an update on the function of MMPs in development and cancer, which may directly regulate signaling pathways that control tissue homeostasis and may even work in a non-proteolytic manner. These novel findings about the functionality of MMPs have important implications for MMP inhibitor design and may allow us to revisit MMPs as drug targets in the context of cancer and other diseases.

Indexed as

Extracellular MatrixHumansMatrix MetalloproteinasesMorphogenesisNeoplasm InvasivenessNeoplasm MetastasisNeoplasmsStem Cell NicheStem CellsMatrix MetalloproteinasesCancerCell differentiationHemopexin domainInvasionStem cell niche

Identifiers

PMID25661772
PMCPMC4498798
OpenAlexW1965815494

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.