Evidence map›Paper›PMID 12473178›Full record

ReviewMolecular cancer2002

The roles of sex steroid receptor coregulators in cancer.

Xiuhua Gao, Brian W Loggie, Zafar Nawaz

Open access · goldAbstract readReview
In one paragraph

Review in Molecular cancer, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

25 citing papers in PubMed, 80 citations in OpenAlex.

  1. Trial
  2. Influence of biological sex in inflammatory bowel diseases.Nature reviews. Gastroenterology & hepatology · 2025
    Review
  3. Histone acetylation modulators in breast cancer.Breast cancer research : BCR · 2025
    Review
  4. Review
  5. Editorial: The Role of Steroid Hormones and Growth Factors in Cancer.Frontiers in cell and developmental biology · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Neuroprotective actions of brain aromatase.Frontiers in neuroendocrinology · 2009
    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.

Xiuhua GaoCUMC-Cancer Center, Creighton University, 2500 California Plaza, Omaha, NE 68178, USA. xiuhuagao@hotmail.com
Brian W Loggie
Zafar Nawaz
Creighton University · US

Funding

NUCLEAR HORMONE ACTION--ROLE OF UBIQUITIN PATHWAYSR01DK056833 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI NAWAZ, ZAFAR · 2000 to 2003
$883k
Role of E6-AP in the Development of Prostate CancerR01DK060907 · NIDDK · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI NAWAZ, ZAFAR · 2001 to 2004
$876k
NIDDK NIH HHS DK56833NIDDK NIH HHS DK60907NIDDK NIH HHS R01 DK056833NIDDK NIH HHS R01 DK060907
6 · The paper itself

Abstract

Sex steroid hormones, estrogen, progesterone and androgen, play pivotal roles in sex differentiation and development, and in reproductive functions and sexual behavior. Studies have shown that sex steroid hormones are the key regulators in the development and progression of endocrine-related cancers, especially the cancers of the reproductive tissues. The actions of estrogen, progesterone and androgen are mediated through their cognate intracellular receptor proteins, the estrogen receptors (ER), the progesterone receptors (PR) and the androgen receptor (AR), respectively. These receptors are members of the nuclear receptor (NR) superfamily, which function as transcription factors that regulate their target gene expression. Proper functioning of these steroid receptors maintains the normal responsiveness of the target tissues to the stimulations of the steroid hormones. This permits the normal development and function of reproductive tissues. It can be inferred that factors influencing the expression or function of steroid receptors will interfere with the normal development and function of the target tissues, and may induce pathological conditions, including cancers. In addition to the direct contact with the basal transcription machinery, nuclear receptors enhance or suppress transcription by recruiting an array of coactivators and corepressors, collectively named coregulators. Therefore, the mutation or aberrant expression of sex steroid receptor coregulators will affect the normal function of the sex steroid receptors and hence may participate in the development and progression of the cancers.

Indexed as

AndrogensAnimalsEstrogensFemaleHormonesHumansMaleNeoplasmsProgesteroneReceptors, AndrogenReceptors, EstrogenReceptors, ProgesteroneReceptors, SteroidRNA, Long NoncodingRNA, UntranslatedTranscription FactorsAndrogensEstrogensHormonesProgesteroneReceptors, AndrogenReceptors, EstrogenReceptors, ProgesteroneReceptors, SteroidRNA, Long NoncodingRNA, Untranslatedsteroid receptor RNA activatorTranscription Factors

Identifiers

PMID12473178
PMCPMC149410
OpenAlexW2169383696

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.