Evidence map›Paper›PMID 8291601›Full record

ArticleThe American journal of pathology1994

Deletion mapping of chromosome 8p in colorectal carcinoma and dysplasia arising in ulcerative colitis, prostatic carcinoma, and malignant fibrous histiocytomas.

M Chang, K Tsuchiya, R H Batchelor, P S Rabinovitch, B G Kulander, R C Haggitt, G C Burmer

Open access · greenAbstract read
In one paragraph

Article in The American journal of pathology, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
8.7field-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

10 citing papers in PubMed, 67 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Leukotriene B4 plays a critical role in the progression of collagen-induced arthritis.Proceedings of the National Academy of Sciences of the United States of America · 1995
    Article
  8. Prostate cancer progression. Implications of histopathology.The American journal of pathology · 1994
    Review
  9. Article
  10. 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

7 authors at 1 institution in 1 country.

M ChangDepartment of Pathology, University of Washington School of Medicine, Seattle.
K Tsuchiya
R H Batchelor
P S Rabinovitch
B G Kulander
R C Haggitt
G C Burmer
University of Washington · US

Funding

STRUCTURE AND FUNCTION OF HUMAN GASTROINTESTINAL MUCOSAP01DK032971 · NIDDK · UNIVERSITY OF WASHINGTON · PI RUBIN, CYRUS E · 1986 to 1993
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CLONING OF THE WERNER'S SYNDROME DEFECTR29AG007359 · NIA · UNIVERSITY OF WASHINGTON · PI BURMER, GLENNA C · 1988 to 1992
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NIA NIH HHS AG07359NIDDK NIH HHS NIDDK PO1 DK32971
6 · The paper itself

Abstract

Short tandem repeat polymorphism markers on the short arm of chromosome 8 were used to search for loss of heterozygosity (LOH) in colorectal carcinoma and dysplasia complicating ulcerative colitis, in prostatic carcinoma, and in malignant fibrous histiocytoma (MFH). Fifty percent of prostatic carcinomas (13/26), 44% of carcinomas or dysplasias arising in ulcerative colitis (7/16), and 30% (4/12) of MFH cases showed LOH for markers on 8p. Detailed mapping demonstrated variability in the size of the chromosomal region showing LOH; however, the data suggest a common 30-centimorgan region of LOH on chromosome 8p between the LPL locus and pter in colorectal and prostatic cancers. In addition, LOH was observed on 8p in both high-grade and low-grade dysplasia in ulcerative colitis, indicating that LOH on 8p may occur at an early stage of neoplastic development in this disorder. In contrast, MFH cases exhibited LOH for marker D8S87, which has been identified as being near the putative Werner's syndrome locus. These results suggest that a tumor suppressor gene, located on the distal portion of chromosome 8p, exists in common for prostatic and colorectal carcinomas, and a second tumor suppressor gene may exist linked to the Werner's syndrome locus.

Indexed as

Chromosome DeletionChromosomes, Human, Pair 8Chromosome MappingColitis, UlcerativeColorectal NeoplasmsGenetic MarkersHeterozygoteHistiocytoma, Benign FibrousHumansMalePolymorphism, GeneticProstatic NeoplasmsRepetitive Sequences, Nucleic AcidGenetic Markers

Identifiers

PMID8291601
PMCPMC1887129
OpenAlexW272049967

What OpenQuestion holds

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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.