Evidence map›Paper›PMID 21845130›Full record

ArticleOchsner journal1999

Tobacco smoke: chemical carcinogenesis and genetic lesions.

J L Cook

Open access · greenAbstract read
In one paragraph

Article in Ochsner journal, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 96% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

1 author at 1 institution in 1 country.

J L CookCo-Director Molecular Genetics, Division of Research, Alton Ochsner Medical Foundation.
Ochsner Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer is the primary cause of cancer-related death in the United States and smoking is the major contributing factor. An amazing array of carcinogenic and precarcinogenic agents has been identified in cigarette smoke. This review addresses the mechanisms by which some of the predominant lung carcinogens mutagenize DNA and explores some of the pivotal genes that are both susceptible to mutagenesis and contribute to the process of tumorigenesis and carcinogenesis. In addition, genes, gene products, and genetic polymorphisms, which curtail the processes leading to carcinogenesis, are discussed. The availability of clinically serviceable methods for analysis of genetic changes that can contribute to lung cancer is imperative to the development of timely, accurate, and cost-effective diagnostic and prognostic tests.A more thorough understanding of the step-wise conversion of precarcinogens to carcinogens, binding of carcinogens to DNA, mutation of DNA, DNA repair, and cellular destruction of carcinogens should contribute to the design of drugs that can modify these processes. In addition, introduction of genes (such as the p53 tumor supressor gene) into susceptible lung cells may impede carcinogenesis. Early stage clinical trials for the treatment of lung cancer using this and other genes are presently underway.

Identifiers

PMID21845130
PMCPMC3145448
OpenAlexW1655744316

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.