Evidence map›Paper›PMID 10665475›Full record

ReviewInvestigational new drugs1999

Tyrosine kinase inhibitors in preclinical development.

M L Levitt, P P Koty

Abstract readReview
PubMed Publisher
In one paragraph

Review in Investigational new drugs, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

6 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
  2. Development and Evaluation ofScientific reports · 2017
    Article
  3. Article
  4. Synthesis and anti-breast cancer activities of substituted quinolines.Bioorganic & medicinal chemistry letters · 2008
    Article
  5. Article
  6. Review
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 at 2 institutions in 2 countries.

M L LevittChaim Sheba Medical Center, Tel Hashomer, Israel.
P P Koty
Tel Aviv University · ILUniversity of Pittsburgh · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to the limited efficacy of cytotoxic chemotherapy in the treatment of advanced malignancy and its excessive toxicity precluding its use in chemoprevention, new therapeutic and preventive strategies have been sought. One of the most interesting of these new approaches is the manipulation of signal transduction pathways. Among the approaches being considered to eventuate such a strategy is the inhibition of autophosphorylation, a critical first step in the signal transduction pathways of many cell surface receptor tyrosine kinases, as well as of non-receptor tyrosine kinases. This article is intended to review those tyrosine kinase inhibitors that are currently in preclinical development, for which there are data to support consideration for their use in chemoprevention or cancer treatment. We will focus upon those agents that have received attention in the past several years.

Indexed as

Angiogenesis InhibitorsAnimalsAntineoplastic AgentsEnzyme InhibitorsErbB ReceptorsHumansProtein-Tyrosine KinasesQuinolinesQuinonesAngiogenesis InhibitorsAntineoplastic AgentsEnzyme InhibitorsErbB ReceptorsProtein-Tyrosine KinasesQuinolinesQuinones

Identifiers

PMID10665475
OpenAlexW56039399

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.