Evidence map›Paper›PMID 7678720›Full record

ArticleThe American journal of pathology1993

Interphase cytogenetics in paraffin sections of lung tumors by non-isotopic in situ hybridization. Mapping genotype/phenotype heterogeneity.

S Y Kim, J S Lee, J Y Ro, M L Gay, W K Hong, W N Hittelman

Open access · greenAbstract read
In one paragraph

Article in The American journal of pathology, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
7.6field-weighted citation impact, top 2% 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

16 citing papers in PubMed, 80 citations in OpenAlex.

  1. The use of genetic markers to identify lung cancer in fine needle aspiration samples.Clinical cancer research : an official journal of the American Association for Cancer Research · 2008
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  9. Confirmation of the copy number of chromosome 1 in interphase nuclei from paraffin sections of breast tumours by fluorescence in situ hybridization.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 1995
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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

6 authors at 1 institution in 1 country.

S Y KimDepartment of Medical Oncology, University of Texas M. D. Anderson Cancer Center, Houston 77030.
J S Lee
J Y Ro
M L Gay
W K Hong
W N Hittelman
The University of Texas MD Anderson Cancer Center · US

Funding

TRANSLATIONAL STUDY OF RETINOID REVERSAL OR ORAL CARCINOGENESISP01CA052051 · NCI · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI SPITZ, MARGARET R · 1991 to 2002
$4.2M
TUMOR CYTOGENETICS BY PREMATURE CHROMOSOME CONDENSATIONR01CA045746 · NCI · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI HITTELMAN, WALTER N. · 1987 to 1989
–
CHEMOPREVENTION IN HUMAN BRONCHIAL METAPLASIA/DYSPLASIAU01CA048369 · NCI · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI HONG, WAUN KI · 1988 to 1991
–
NCI NIH HHS CA45746NCI NIH HHS CA48369NCI NIH HHS CA52051
6 · The paper itself

Abstract

To better understand the relationship between specific chromosome changes found in human lung tumors and their phenotypic consequences at the tissue level, an in situ hybridization procedure was optimized for use on formalin-fixed paraffin-embedded tissue sections of human lung tumors. Pretreatment heating of sections, pepsin concentration, duration of pepsin treatment, hybridization conditions, and posthybridization washing conditions were varied to determine optimum conditions. The deparaffinized sections were stained with centromeric probes for chromosomes 7 and 17, and a chromosome index for each tumor was derived by dividing the mean number of chromosome signals found on the tumor cells by the mean number of chromosome signals on normal cells (lymphocytes and fibroblasts) in the same section. This chromosome index was then compared with the DNA index determined in an adjacent section by Feulgen staining followed by image analysis quantitation. The chromosome index correlated well with the DNA index, but in some cases, chromosome 7, or 17 in other cases, was either over- or under-represented compared with the corresponding DNA index. In addition, chromosome and DNA alterations were shown to be differentially expressed within the same tissue section, correlating with a change in tumor differentiation status. These results suggest that in situ hybridization will prove to be an important tool for determining the underlying genetic basis for tissue phenotype heterogeneity by allowing genetic determinations to be made on paraffin-embedded tissue sections where tumor histological architecture is preserved.

Indexed as

Chromosome MappingGenotypeIn Situ HybridizationInterphasePhenotypeCarcinoma, Non-Small-Cell LungChromosomes, HumanDNA ProbesHumansLung NeoplasmsMicrotomyParaffin EmbeddingProtein DenaturationStaining and LabelingDNA Probes

Identifiers

PMID7678720
PMCPMC1886817
OpenAlexW2231620971

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.