Evidence map›Paper›PMID 12537941›Full record

ReviewCurrent urology reports2003

Antisense oligonucleotide therapy for urologic tumors.

Ingo Kausch, Andreas Böhle

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current urology reports, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

1 citing paper in PubMed, 8 citations in OpenAlex.

  1. 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 at 1 institution in 1 country.

Ingo KauschDepartment of Urology, Medical University of Lübeck, Ratzeburger Allee 160, Germany.
Andreas Böhle
University of Lübeck · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Modulation of gene expression using antisense oligonucleotides has advanced from the laboratory to the clinic. Numerous companies can, at least partially, attribute their success to the development of antisense techniques, and one antisense drug is currently on the market. Antisense compounds have been used in clinical trials that included patients with urologic tumors, mostly directed at proliferation- or apoptosis-related targets. Furthermore, therapeutic inhibition of many new identified genes is being investigated in preclinical tests. This review provides a contemporary overview of current preclinical and clinical antisense oligonucleotide concepts for the treatment of urologic tumors.

Indexed as

AnimalsGene Expression Regulation, NeoplasticGenes, mycGenes, rasHumansKi-67 AntigenOligonucleotides, AntisenseProtein KinasesProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins c-rafTransforming Growth Factor betaUrologic NeoplasmsKi-67 AntigenOligonucleotides, AntisenseProtein KinasesProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins c-rafTransforming Growth Factor beta

Identifiers

PMID12537941
OpenAlexW2036335910

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.