Evidence map›Paper›PMID 23548611›Full record

ArticleAmerican journal of physiology. Endocrinology and metabolism2013

Sex steroid hormones regulate constitutive expression of Cyp2e1 in female mouse liver.

Maria Konstandi, Jie Cheng, Frank J Gonzalez

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Endocrinology and metabolism, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 45 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. The effects of imidacloprid exposure on the mouse ovary in vivo.Reproductive toxicology (Elmsford, N.Y.) · 2025
    Article
  5. Article
  6. Article
  7. Article
  8. Ovarian antral follicles metabolize imidacloprid in vitro.Toxicological sciences : an official journal of the Society of Toxicology · 2023
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Rhythmic Fluctuations in Levels of Liver Enzymes During Menstrual Cycles of Healthy Women and Effects of Body Weight.Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · 2020
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Cytochrome P450-2E1 is involved in aging-related kidney damage in mice through increased nitroxidative stress.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2017
    Article
  20. 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

3 authors at 2 institutions in 2 countries.

Maria KonstandiDepartment of Pharmacology, School of Medicine, University of Ioannina, GR-45110, Ioannina, Greece. mkonstan@cc.uoi.gr
Jie Cheng
Frank J Gonzalez
National Institutes of Health · USNational Cancer Institute · US

Funding

Xenobiotic receptorsZIABC005562 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GONZALEZ, FRANK J · 2009 to 2025
$26.9M
Intramural NIH HHS
6 · The paper itself

Abstract

CYP2E1 is of paramount toxicological significance because it metabolically activates a large number of low-molecular-weight toxicants and carcinogens. In this context, factors that interfere with Cyp2e1 regulation may critically affect xenobiotic toxicity and carcinogenicity. The aim of this study was to investigate the role of female steroid hormones in the regulation of CYP2E1, as estrogens and progesterone are the bases of contraceptives and hormonal replacement therapy in menopausal women. Interestingly, a fluctuation in the hepatic expression pattern of Cyp2e1 was revealed in the different phases of the estrous cycle of female mice, with higher Cyp2e1 expression at estrus (E) and lower at methestrus (ME), highly correlated with that in plasma gonadal hormone levels. Depletion of sex steroids by ovariectomy repressed Cyp2e1 expression to levels similar to those detected in males and cyclic females at ME. Hormonal supplementation brought Cyp2e1 expression back to levels detected at E. The role of progesterone appeared to be more prominent than that of 17β-estradiol. Progesterone-induced Cyp2e1 upregulation could be attributed to inactivation of the insulin/PI3K/Akt/FOXO1 signaling pathway. Tamoxifen, an anti-estrogen, repressed Cyp2e1 expression potentially via activation of the PI3K/Akt/FOXO1 and GH/STAT5b-linked pathways. The sex steroid hormone-related changes in hepatic Cyp2e1 expression were highly correlated with those observed in Hnf-1α, β-catenin, and Srebp-1c. In conclusion, female steroid hormones are clearly involved in the regulation of CYP2E1, thus affecting the metabolism of a plethora of toxicants and carcinogenic agents, conditions that may trigger several pathologies or exacerbate the outcomes of various pathophysiological states.

Indexed as

AnimalsBlotting, WesternCytochrome P-450 CYP2E1EstradiolEstrogen AntagonistsEstrous CycleFemaleForkhead Box Protein O1Forkhead Transcription FactorsLiverMaleMiceMice, Inbred C57BLMice, TransgenicPhosphatidylinositol 3-KinasesProgesteroneCytochrome P-450 CYP2E1EstradiolEstrogen AntagonistsForkhead Box Protein O1Forkhead Transcription FactorsFoxo1 protein, mousePhosphatidylinositol 3-KinasesProgesteroneProto-Oncogene Proteins c-aktRNASTAT5 Transcription FactorTamoxifen17β-estradiolCyp2e1estrous cyclemiceprogesterone

Identifiers

PMID23548611
PMCPMC3651618
OpenAlexW2099816481

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.