Evidence map›Paper›PMID 19490624›Full record

ArticleMolecular cancer2009

Corticotropin Releasing Factor promotes breast cancer cell motility and invasiveness.

Ariadne Androulidaki, Erini Dermitzaki, Maria Venihaki, Effie Karagianni, Olga Rassouli, Erini Andreakou, Christos Stournaras, Andrew N Margioris, Christos Tsatsanis

Open access · goldAbstract read
In one paragraph

Article in Molecular cancer, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

30 citing papers in PubMed, 54 citations in OpenAlex.

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  12. The expression of corticotropin-releasing hormone family peptides in premalignant and malignant vulvar lesions.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Article
  13. Review
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  15. Article
  16. Effect of chronic stress on tumorigenesis and development.Cellular and molecular life sciences : CMLS · 2022
    Review
  17. Article
  18. Chronic Stress Promotes Cancer Development.Frontiers in oncology · 2020
    Review
  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

9 authors at 1 institution in 1 country.

Ariadne AndroulidakiDepartment of Clinical Chemistry, School of Medicine, University of Crete, Heraklion 71003, Crete, Greece. arandrou@med.uoc.gr
Erini Dermitzaki
Maria Venihaki
Effie Karagianni
Olga Rassouli
Erini Andreakou
Christos Stournaras
Andrew N Margioris
Christos Tsatsanis
University of Crete · GR

Funding

Worldwide Cancer Research 07-0072
6 · The paper itself

Abstract

introductionCancer cells secrete bioactive peptides that act in an autocrine or paracrine fashion affecting tumor growth and metastasis. Corticotropin-releasing factor (CRF), a hypothalamic neuropeptide that controls the response to stress, has been detected in breast cancer tissues and cell lines. CRF can affect breast cancer cells in an autocrine or paracrine manner via its production from innervating sympathetic neurons or immune cells.

methodsIn the present study we report our findings regarding the impact of CRF on breast cancer cell motility and invasiveness. For this purpose we used the MCF7 breast cancer cell line and evaluated the effect of CRF on motility and invasiveness using the wound-healing and boyden-chamber assays. In addition, we measured the effect of CRF on molecules that mediate motility by western blot, immunofluorescence, ELISA and RT-PCR.

resultsOur findings show that: 1. CRF transiently inhibited the apoptosis of MCF7 cells. 2. CRF enhanced MCF7 cell motility in a wound healing assay and their invasiveness through extracellular matrix. 3. CRF increased actin polymerization, phosphorylation of Focal Adhesion Kinase (FAK), providing a potential mechanism for the observed induction of MCF7 motility. 4. CRF induced the expression of Cox-1 but not Cox-2 in MCF7 cells as well as the production of prostaglandins, factors known to promote invasiveness and metastasis.

conclusionOverall, our data suggest that CRF stimulates cell motility and invasiveness of MCF7 cells most probably via induction of FAK phosphorylation and actin filament reorganization and production of prostaglandins via Cox1. Based on these findings we postulate that the stress neuropeptide CRF present in the vicinity of tumors (either produced locally by the tumor cells themselves or by nearby normal cells or secreted from the innervations of surrounding tissues) may play an important role on breast tumor growth and metastatic capacity, providing a potential link between stress and tumor progression.

Indexed as

ActinsAnalysis of VarianceApoptosisBlotting, WesternBreast NeoplasmsCell Line, TumorCell MovementCorticotropin-Releasing HormoneCyclooxygenase 2Enzyme-Linked Immunosorbent AssayFemaleFluorescent Antibody TechniqueFocal Adhesion Kinase 1HumansNeoplasm InvasivenessPhosphorylationActinsCorticotropin-Releasing HormoneCyclooxygenase 2Focal Adhesion Kinase 1ProstaglandinsPTGS2 protein, humanPTK2 protein, human

Identifiers

PMID19490624
PMCPMC2697132
OpenAlexW2138640721

What OpenQuestion holds

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Registered trials

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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.