Evidence map›Paper›PMID 9144901›Full record

ReviewWorld journal of urology1997

Molecular and immunopathology studies of oncogenes and tumor-suppressor genes in bladder cancer.

C Cordon-Cardo, J Sheinfeld

Abstract readReview
PubMed Publisher
In one paragraph

Review in World journal of urology, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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.

C Cordon-CardoDepartment of Pathology, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
J Sheinfeld
Memorial Sloan Kettering Cancer Center · US

Funding

MARKERS OF EXFOLIATED BENIGN AND MALIGNANT BLADDER CELLSR01CA047538 · NCI · MEMORIAL HOSPITAL FOR CANCER &ALLIED DI · PI CORDON-CARDO, CARLOS · 1988 to 1991
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BLADDER CANCER CHEMOPREVENTION (4HPR)--MOLECULAR STUDIESR01CA058514 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SHEINFELD, JOEL · 1993 to 1997
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MOLECULAR &IMMUNOPHENOTYPIC ANALYSIS OF BLADDER TUMORSU01CA047538 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI CORDON-CARDO, CARLOS · 1992 to 1999
–
NCI NIH HHS CA-47538NCI NIH HHS CA-58514
6 · The paper itself

Abstract

Target genes implicated in cellular transformation and tumor progression have been divided into two categories: proto-oncogenes (that when activated become dominant events characterized by gain of function) and tumor-suppressor genes (recessive events characterized by the loss of function). Alterations in proto-oncogenes and tumor-suppressor genes seem equally prevalent among human cancers. Multiple mutations appear to be required to conform the malignant phenotype. It is therefore conceivable that cancer be viewed fundamentally as a genetic disease entailing inherited (also called germ-line) and/or acquired (also termed somatic) mutations of genes in these two categories. Molecular studies of bladder neoplasms have identified a series of nonrandom genetic alterations affecting a particular set of oncogenes and tumor-suppressor genes. Because the modality of therapy for patients with bladder neoplasms primarily depends on morphological evaluation and clinical staging, the diagnosis carries significant consequences. However, it is well known that morphologically similar tumors presenting in any assigned stage may behave in radically different fashions, which seriously hampers the physician's ability accurately to predict clinical behavior in a given case. Recent studies have shown that inactivation of certain tumor-suppressor genes, such as RB and TP53, occur in bladder tumors that have a more aggressive clinical outcome and poor prognosis. In the present paper we review the molecular abnormalities associated with these dominant and recessive genes in bladder cancer and discuss the potential clinical use of their detection. The implementation of objective predictive assays to identify these alterations in clinical material will enhance our ability to assess tumor biological activities and to design effective treatment regimens. The need now is to translate this newly developed scientific knowledge into diagnostic and therapeutic strategies, which in turn will enhance the quality of life and prolong the survival of patients with bladder cancer.

Indexed as

Genes, Tumor SuppressorOncogenesCytogeneticsHumansImmunologic TechniquesMolecular BiologyPathologyUrinary Bladder Neoplasms

Identifiers

PMID9144901
OpenAlexW2036779033

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.