Evidence map›Paper›PMID 9387040›Full record

ReviewInvestigational new drugs1997

Matrix metalloproteinase inhibitors: present achievements and future prospects.

L J Denis, J Verweij

Abstract readReview
PubMed Publisher
In one paragraph

Review in Investigational new drugs, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. New Derivatives ofInternational journal of molecular sciences · 2023
    Article
  2. Article
  3. Article
  4. Article
  5. POVME: an algorithm for measuring binding-pocket volumes.Journal of molecular graphics & modelling · 2011
    Article
  6. Article
  7. Reduction of experimental laser-induced choroidal neovascularization by orally administered BPHA, a selective metalloproteinase inhibitor.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2003
    Article
  8. Article
  9. Review
  10. Review
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  12. [Anti-angiogenesis: a new approach to tumor therapy?].Medizinische Klinik (Munich, Germany : 1983) · 1999
    Article
  13. Article
  14. Article
  15. Molecular cloning and characterization of prostase, an androgen-regulated serine protease with prostate-restricted expression.Proceedings of the National Academy of Sciences of the United States of America · 1999
    Article
  16. An odyssey from breast to bone: multi-step control of mammary metastases and osteolysis by matrix metalloproteinases.APMIS : acta pathologica, microbiologica, et immunologica Scandinavica · 1999
    Review
  17. Article
  18. Article
  19. 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

2 authors.

L J DenisDepartment of Medical Oncology, Rotterdam Cancer Institute (Daniel den Hoed Kliniek) and University Hospital, The Netherlands.
J Verweij

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Matrix metalloproteinases (MMPs) are a class of structurally related enzymes that function in the degradation of extracellular matrix proteins that constitute the pericellular connective tissue and play an important role in both normal and pathological tissue remodelling. Increased MMP activity is detected in a wide range of cancers and seems correlated to their invasive and metastatic potential. MMPs thus seem an attractive target for both diagnostic and therapeutic purposes. Several synthetic matrix metalloproteinase inhibitors (MMPIs) are currently being developed. Preclinical studies are promising as they suggest inhibition of several steps in the metastatic process. Marimastat is the first MMPI to enter comparative phase III trials after early clinical trials established the safety profile. Clinical trials will need to be specifically designed to optimally evaluate the therapeutic potential of this novel class of cytostatic drugs. Safety studies should consider the markedly different toxicity profile and determine the range of biologically active dosage, while efficacy studies should be performed in selected clinical settings with appropriate end-points. We review the present achievements in preclinical and clinical studies with MMPIs, discuss specific considerations for appropriate study design and reflect on the future prospects of this novel class of agents.

Indexed as

Hydroxamic AcidsAnimalsAntineoplastic AgentsClinical Trials as TopicEnzyme InhibitorsExtracellular MatrixHumansMetalloendopeptidasesNeoplasm MetastasisNeoplasmsPhenylalanineProtease InhibitorsThiophenesAntineoplastic AgentsbatimastatEnzyme InhibitorsHydroxamic AcidsmarimastatMetalloendopeptidasesPhenylalanineProtease InhibitorsThiophenes

Identifiers

What OpenQuestion holds

Textmetadata
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.