Evidence map›Paper›PMID 19022890›Full record

ArticleEndocrinology2009

Insensitivity of human prolactin receptors to nonhuman prolactins: relevance for experimental modeling of prolactin receptor-expressing human cells.

Fransiscus E Utama, Thai H Tran, Amy Ryder, Matthew J LeBaron, Albert F Parlow, Hallgeir Rui

Open access · greenAbstract read
In one paragraph

Article in Endocrinology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

23 citing papers in PubMed, 49 citations in OpenAlex.

  1. Current Insights in Prolactin Signaling and Ovulatory Function.International journal of molecular sciences · 2024
    Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Prolactin: The Third Hormone in Breast Cancer.Frontiers in endocrinology · 2022
    Review
  7. Article
  8. Article
  9. Animal Models to Study Cancer and Its Microenvironment.Advances in experimental medicine and biology · 2020
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. The role of prolactin receptor in GH signaling in breast cancer cells.Molecular endocrinology (Baltimore, Md.) · 2013
    Article
  18. Article
  19. A pathway map of prolactin signaling.Journal of cell communication and signaling · 2012
    Article
  20. Lactogens and estrogens in breast cancer chemoresistance.Expert review of endocrinology & metabolism · 2011
    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 3 institutions in 1 country.

Fransiscus E UtamaDepartment of Cancer Biology, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA. hallgeir.rui@jefferson.edu
Thai H Tran
Amy Ryder
Matthew J LeBaron
Albert F Parlow
Hallgeir Rui
Thomas Jefferson University · USSidney Kimmel Cancer Center · USHarbor–UCLA Medical Center · US

Funding

X-Ray Crystallography and Macromolecular CharacterizationP30CA056036 · NCI · THOMAS JEFFERSON UNIVERSITY · PI DANIEL P SILVER · 1995 to 2026
$94.8M
TRAINING PROGRAMS IN MOLECULAR GENETICS OF CANCERT32CA009678 · NCI · THOMAS JEFFERSON UNIVERSITY · PI BUCHBERG, ARTHUR M. · 1992 to 2008
$2.3M
Experimental Modeling of Human Breast Cancer in MiceR01CA118740 · NCI · THOMAS JEFFERSON UNIVERSITY · PI RUI, HALLGEIR · 2008 to 2012
$1.8M
Stat5 as a gatekeeper in human breast cancer metastasisR01CA101841 · NCI · THOMAS JEFFERSON UNIVERSITY · PI RUI, HALLGEIR · 2004 to 2008
$1.2M
PROLACTIN INDUCED PHOSPHOPROTEIN SIGNAL TRANSDUCTIONR01DK052013 · NIDDK · HENRY M. JACKSON FDN FOR THE ADV MIL/MED · PI RUI, HALLGEIR · 1997 to 2004
$872k
NCI NIH HHS 1P30CA56036NCI NIH HHS BC051251NCI NIH HHS P30 CA056036NCI NIH HHS R01 CA101841NCI NIH HHS R01-CA101841NCI NIH HHS R01 CA118740NCI NIH HHS R01-CA118740NCI NIH HHS T32 CA009678NCI NIH HHS T32-CA09678NIDDK NIH HHS R01 DK052013NIDDK NIH HHS R01-DK52013
6 · The paper itself

Abstract

Prolactin (PRL) receptors are expressed in a broad range of human cell types and in a majority of human breast and prostate cancers. Experimentally, normal and malignant human cells are typically cultured in vitro in media containing bovine PRL (bPRL) from fetal bovine serum or as xenotransplants in vivo in the presence of murine PRL (mPRL). The biological efficacy of bPRL toward hPRL receptors (hPRLR) is controversial, and hPRLR are insensitive to mPRL, but the mechanism is not known. To clarify limitations of current in vitro and in vivo experimental model systems for studies of hPRLR-expressing cells, we tested human and relevant subprimate prolactins in multiple hPRLR bioassays. bPRL and ovine PRL were 10-fold less potent hPRLR agonists than hPRL, although maximal responses at high ligand concentrations (efficacies) equaled that of hPRL. mPRL and rat PRL had greater than 50-fold lower potencies toward hPRLR than hPRL and had 50% reduced efficacies. In fact, mPRL and rat PRL were less effective hPRLR agonists than murine GH. Unexpectedly, mPRL was an effective competitive inhibitor of hPRL binding to hPRLR with an inhibitory constant of 1.3 nm and showed partial antagonist activity, suggesting reduced site-2 binding. Collectively, low bioactivities of bPRL and mPRL toward hPRLR suggest that existing laboratory cancer cell lines grown in 10% bovine serum-supplemented media or in mice are selected for growth under lactogen-depleted conditions. The biology and drug responsiveness of existing human cell lines may therefore not be representative of clinical cancers that are sensitive to circulating PRL.

Indexed as

AnimalsCell Line, TumorHorsesHumansImmunoblottingMiceProlactinProtein BindingRatsReceptors, ProlactinSTAT5 Transcription FactorProlactinReceptors, ProlactinSTAT5 Transcription Factor

Identifiers

PMID19022890
PMCPMC2659276
OpenAlexW2023309088

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.