Evidence map›Paper›PMID 9010034›Full record

ArticleBritish journal of cancer1997

Type I insulin-like growth factor receptor gene expression in normal human breast tissue treated with oestrogen and progesterone.

R B Clarke, A Howell, E Anderson

Open access · bronzeAbstract read
In one paragraph

Article in British journal of cancer, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
6.6field-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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 93 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. The Role of Metabolic Factors in Renal Cancers.International journal of molecular sciences · 2020
    Review
  4. Review
  5. Assessment of Multifactor Gene-Environment Interactions and Ovarian Cancer Risk: Candidate Genes, Obesity, and Hormone-Related Risk Factors.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2016
    Article
  6. Emerging targeted agents in metastatic breast cancer.Nature reviews. Clinical oncology · 2013
    Review
  7. Article
  8. Article
  9. Article
  10. Regulation of MDMX expression by mitogenic signaling.Molecular and cellular biology · 2008
    Article
  11. Article
  12. Review
  13. Breast cancer prevention trials using retinoids.Journal of mammary gland biology and neoplasia · 2003
    Review
  14. Review
  15. Xenograft models of premalignant breast disease.Journal of mammary gland biology and neoplasia · 2000
    Review
  16. Article
  17. Review
  18. Estrogen responsiveness and control of normal human breast proliferation.Journal of mammary gland biology and neoplasia · 1998
    Review
  19. 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

3 authors at 1 institution in 1 country.

R B ClarkeClinical Research Department, Christie Hospital NHS Trust, Withington, Manchester, UK.
A Howell
E Anderson
The Christie Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The epithelial proliferation of normal human breast tissue xenografts implanted into athymic nude mice is significantly increased from basal levels by oestradiol (E2), but not progesterone (Pg) treatment at serum concentrations similar to those observed in the luteal phase of the human menstrual cycle. Type I IGF receptor (IGFR-I) mRNA and protein have been shown to be up-regulated by E2 in MCF-7 breast cancer cells in vitro in which IGF-I and E2 act synergistically to stimulate proliferation. We have investigated the expression of the IGFR-I mRNA in normal human breast xenografts treated with or without E2 or Pg alone and in combination. Northern analysis of 20 micrograms of RNA extracted from the breast xenograft samples showed no hybridization with 32P-labelled IGFR-I probe, although an 11-kb species of IGFR-I mRNA could be seen when 20 micrograms of RNA extracted from either MCF-7 breast cancer cells or human breast carcinomas was examined in this way. In order to analyse the expression of IGFR-I mRNA in breast xenografts, a quantitative reverse transcription-polymerase chain reaction (RT-PCR) was employed in which RNA loading, reverse transcription and PCR efficiencies were internally controlled. The data indicate that the IGFR-I mRNA is up-regulated by two to threefold compared with untreated levels by 7 and 14 days E2 treatment. In contrast, 7 or 14 days Pg treatment down-regulates the receptor mRNA to approximately half that of untreated levels, whereas combination E2 and Pg treatment produced a twofold increase in IGFR-I mRNA levels compared with untreated tissue. The results are consistent with the suggestion that E2 may act to stimulate proliferation indirectly via a paracrine mechanism involving IGFs in normal as well as malignant human breast epithelial cells.

Indexed as

AnimalsBreastCell DivisionEstradiolFemaleGene Expression Regulation, NeoplasticHumansMiceMice, NudeNeoplasm TransplantationProgesteroneReceptor, IGF Type 1RNA, MessengerRNA, NeoplasmTumor Cells, CulturedEstradiolProgesteroneReceptor, IGF Type 1RNA, MessengerRNA, Neoplasm

Identifiers

PMID9010034
PMCPMC2063278
OpenAlexW2166368284

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.