Evidence map›Paper›PMID 19524120›Full record

ArticleMolecular and cellular endocrinology2009

Complex prolactin crosstalk in breast cancer: new therapeutic implications.

Kristopher C Carver, Lisa M Arendt, Linda A Schuler

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular endocrinology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.7field-weighted citation impact, top 6% 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. Trial
  2. Article
  3. Article
  4. Article
  5. Review
  6. Prolactin: The Third Hormone in Breast Cancer.Frontiers in endocrinology · 2022
    Review
  7. Article
  8. Article
  9. Observational
  10. 17Journal of the Endocrine Society · 2018
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. The prolactin receptor: Diverse and emerging roles in pathophysiology.Journal of clinical & translational endocrinology · 2015
    Review
  17. Phosphorylation of tyrosine 285 of PAK1 facilitates βPIX/GIT1 binding and adhesion turnover.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2015
    Article
  18. Article
  19. 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 1 institution in 1 country.

Kristopher C CarverCellular and Molecular Biology Program, University of Wisconsin-Madison, Madison, WI 53706, USA.
Lisa M Arendt
Linda A Schuler
University of Wisconsin–Madison · US

Funding

BIOTECHNOLOGY TRAINING PROGRAMT32GM008349 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI FOX, BRIAN G · 1989 to 2019
$22.5M
MAMMARY PROLACTIN PRODUCTION AND BREAST CANCERR01CA078312 · NCI · UNIVERSITY OF WISCONSIN MADISON · PI SCHULER, LINDA A. · 1999 to 2005
$1.3M
Endocytosis and trafficking of PRL receptor isoformsR01DK062783 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI SCHULER, LINDA A. · 2003 to 2006
$891k
Interactions of PRL, Estrogen, and TFFa in Mammary CancerK01RR021858 · NCRR · UNIVERSITY OF WISCONSIN-MADISON · PI ARENDT, LISA M · 2006 to 2010
$564k
NCI NIH HHS R01 CA078312NCI NIH HHS R01 CA78312NCRR NIH HHS K01 RR021858NCRR NIH HHS K01 RR21858NIDDK NIH HHS DK62783NIDDK NIH HHS R01 DK062783NIGMS NIH HHS T32 GM008349NIGMS NIH HHS T32 GM08349
6 · The paper itself

Abstract

The contributions of prolactin (PRL) to breast cancer are becoming increasingly recognized. To better understand the role for PRL in this disease, its interactions with other oncogenic growth factors and hormones must be characterized. Here, we review our current understanding of PRL crosstalk with other mammary oncogenic factors, including estrogen, epidermal growth factor (EGF) family members, and insulin-like growth factor-I (IGF-I). The ability of PRL to potentiate the actions of these targets of highly successful endocrine and molecular therapies suggests that PRL and/or its receptor (PRLR) may be an attractive therapeutic target(s). We discuss the potential benefit of PRL/PRLR-targeted therapy in combination with established therapies and implications for de novo and acquired resistance to treatment.

Indexed as

Breast NeoplasmsFemaleHumansProlactinSignal TransductionProlactin

Identifiers

PMID19524120
PMCPMC3190192
OpenAlexW2087187453

What OpenQuestion holds

Textmetadata
LicenceTDM
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.