Evidence map›Paper›PMID 1972691›Full record

ArticleHuman genetics1990

Loss of heterozygosity of the L-myc oncogene in human breast tumors.

I Bieche, M H Champeme, G Merlo, C J Larsen, R Callahan, R Lidereau

Abstract read
PubMed Publisher
In one paragraph

Article in Human genetics, 1990. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

7 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
  2. Genetic analysis of breast cancer progression.Journal of mammary gland biology and neoplasia · 1996
    Review
  3. Review
  4. Review
  5. Tumor suppressor genes and their roles in breast cancer.Breast cancer research and treatment · 1994
    Review
  6. Article
  7. 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

6 authors at 2 institutions in 1 country.

I BiecheCentre René Huguenin, St. Cloud, France.
M H Champeme
G Merlo
C J Larsen
R Callahan
R Lidereau
Hôpital René Huguenin · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies suggest that loss of heterozygosity may play an important role in various human neoplasia. Cytogenetic abnormalities detected in primary breast tumors led us to examine breast tumor DNAs for deletions. In the present study, we demonstrate, using restriction fragment length polymorphism (RFLP) analysis at the L-myc proto-oncogene (chromosome 1p32), a frequent loss of heterozygosity in primary breast tumor DNAs (55 out of 152 informative tumor DNAs). Most of these deletions appear to be limited to chromosome 1p. No correlation was observed between this genetic alteration and several parameters of each patient's history or characteristics of the tumor. However, a significantly (P = 0.011) shorter survival period after relapse was observed for patients with loss of heterozygosity at L-myc in primary tumor DNAs compared with patients with tumor DNAs lacking this alteration.

Indexed as

HeterozygoteBlotting, SouthernBreast NeoplasmsChromosome DeletionChromosomes, Human, Pair 1DNA, NeoplasmFemaleHumansOncogenesPolymorphism, Restriction Fragment LengthProto-Oncogene MasProto-Oncogene ProteinsProto-Oncogene Proteins c-mycRegression AnalysisDNA, NeoplasmMAS1 protein, humanProto-Oncogene MasProto-Oncogene ProteinsProto-Oncogene Proteins c-myc

Identifiers

PMID1972691
OpenAlexW2014316726

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.