Evidence map›Paper›PMID 18511743›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2008

Progesterone stimulates the proliferation of female and male cholangiocytes via autocrine/paracrine mechanisms.

Shannon Glaser, Sharon DeMorrow, Heather Francis, Yoshiyuki Ueno, Eugenio Gaudio, Shelley Vaculin, Julie Venter, Antonio Franchitto, Paolo Onori, Bradley Vaculin and 7 more

RetractedOpen access · greenAbstract readRetracted Publication
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

29 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Estrogens in polycystic liver disease: A target for future therapies?Liver international : official journal of the International Association for the Study of the Liver · 2021
    Review
  5. Cholangiocyte pathobiology.Nature reviews. Gastroenterology & hepatology · 2019
    Review
  6. Article
  7. Cellular crosstalk during cholestatic liver injury.Liver research (Beijing, China) · 2017
    Article
  8. Review
  9. Effect of genotype on the severity and volume progression of polycystic liver disease in autosomal dominant polycystic kidney disease.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2016
    Article
  10. Article
  11. Women and primary biliary cirrhosis.Clinical reviews in allergy & immunology · 2015
    Review
  12. Article
  13. Dynamic expression of desmin, α-SMA and TGF-β1 during hepatic fibrogenesis induced by selective bile duct ligation in young rats.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2014
    Article
  14. Review
  15. Chronic nicotine exposure stimulates biliary growth and fibrosis in normal rats.Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver · 2013
    Article
  16. Role of follicle-stimulating hormone on biliary cyst growth in autosomal dominant polycystic kidney disease.Liver international : official journal of the International Association for the Study of the Liver · 2013
    Article
  17. Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 7 institutions in 3 countries.

Shannon GlaserDepartment of Medicine, Scott & White Hospital and Texas A&M University System Health Science Center, College of Medicine, Temple, Texas 76504, USA. sglaser@tamu.edu
Sharon DeMorrow
Heather Francis
Yoshiyuki Ueno
Eugenio Gaudio
Shelley Vaculin
Julie Venter
Antonio Franchitto
Paolo Onori
Bradley Vaculin
Marco Marzioni
Candace Wise
Metaneeya Pilanthananond
Jennifer Savage
Lisa Pierce
Romina Mancinelli
Gianfranco Alpini
Sapienza University of Rome · ITTexas A&M University System · USCentral Texas Veterans Health Care System · USMarche Polytechnic University · ITTexas A&M Health Science Center · USTohoku University · JPUniversity of L'Aquila · IT

Funding

Endocannabinoid Regulation of Cholangiocarcinoma Cell GrowthK01DK078532 · NIDDK · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI DEMORROW, SHARON · 2007 to 2011
$697k
NIDDK NIH HHS K01 DK-078532
6 · The paper itself

Abstract

During cholestatic liver diseases, cholangiocytes express neuroendocrine phenotypes and respond to a number of hormones and neuropeptides by paracrine and autocrine mechanisms. We examined whether the neuroendocrine hormone progesterone is produced by and targeted to cholangiocytes, thereby regulating biliary proliferation during cholestasis. Nuclear (PR-A and PR-B) and membrane (PRGMC1, PRGMC2, and mPRalpha) progesterone receptor expression was evaluated in liver sections and cholangiocytes from normal and bile duct ligation (BDL) rats, and NRC cells (normal rat cholangiocyte line). In vivo, normal rats were chronically treated with progesterone for 1 wk, or immediately after BDL, rats were treated with a neutralizing progesterone antibody for 1 wk. Cholangiocyte growth was measured by evaluating the number of bile ducts in liver sections. The expression of the progesterone synthesis pathway was evaluated in liver sections, cholangiocytes and NRC. Progesterone secretion was evaluated in supernatants from normal and BDL cholangiocytes and NRC. In vitro, NRC were stimulated with progesterone and cholangiocyte supernatants in the presence or absence of antiprogesterone antibody. Aminoglutethimide was used to block progesterone synthesis. Cholangiocytes and NRC express the PR-B nuclear receptor and PRGMC1, PRGMC2, and mPRalpha. In vivo, progesterone increased the number of bile ducts of normal rats, whereas antiprogesterone antibody inhibited cholangiocyte growth stimulated by BDL. Normal and BDL cholangiocytes expressed the biosynthetic pathway for and secrete progesterone. In vitro, 1) progesterone increased NRC proliferation; 2) cholangiocyte supernatants increased NRC proliferation, which was partially inhibited by preincubation with antiprogesterone; and 3) inhibition of progesterone steroidogenesis prevented NRC proliferation. In conclusion, progesterone may be an important autocrine/paracrine regulator of cholangiocyte proliferation.

Indexed as

3-Hydroxysteroid DehydrogenasesAnimalsAutocrine CommunicationBile DuctsCell ProliferationCytochrome P-450 Enzyme SystemFemaleGene Expression RegulationMaleParacrine CommunicationPhosphoproteinsProgesteroneRatsRats, Inbred F344Receptors, ProgesteroneSex Characteristics3-Hydroxysteroid DehydrogenasesCytochrome P-450 Enzyme SystemPhosphoproteinsProgesteroneReceptors, ProgesteroneSteroidogenic Acute Regulatory Protein

Identifiers

PMID18511743
PMCPMC2494724
OpenAlexW2164080063

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.