Evidence map›Paper›PMID 30669581›Full record

ArticleCancers2019

PKA at a Cross-Road of Signaling Pathways Involved in the Regulation of Glioblastoma Migration and Invasion by the Neuropeptides VIP and PACAP.

Souheyla Bensalma, Soumaya Turpault, Annie-Claire Balandre, Madryssa De Boisvilliers, Afsaneh Gaillard, Corinne Chadéneau, Jean-Marc Muller

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

15 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. AKT kinases as therapeutic targets.Journal of experimental & clinical cancer research : CR · 2024
    Review
  5. Glioma and Peptidergic Systems: Oncogenic and Anticancer Peptides.International journal of molecular sciences · 2024
    Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Targeting Akt in cancer for precision therapy.Journal of hematology & oncology · 2021
    Review
  12. Article
  13. Review
  14. Article
  15. 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

7 authors at 3 institutions in 1 country.

Souheyla BensalmaTeam Récepteurs, Régulations, Cellules Tumorales (2RCT), EA3842 CAPTuR, Pôle Biologie-Santé, Université de Poitiers, F-86022 Poitiers, France. souheyla.bensalma@gmail.com.
Soumaya TurpaultTeam Récepteurs, Régulations, Cellules Tumorales (2RCT), EA3842 CAPTuR, Pôle Biologie-Santé, Université de Poitiers, F-86022 Poitiers, France. soumaya.turpault@gmail.com.
Annie-Claire BalandreSTIM Laboratory, CNRS ERL 7003-EA7349, Pôle Biologie-Santé, Université de Poitiers, F-86022 Poitiers, France. annie-claire.balandre@univ-poitiers.fr.
Madryssa De BoisvilliersTeam Récepteurs, Régulations, Cellules Tumorales (2RCT), EA3842 CAPTuR, Pôle Biologie-Santé, Université de Poitiers, F-86022 Poitiers, France. m.de.boisvilliers@outlook.fr.
Afsaneh GaillardLaboratoire de Neurosciences Expérimentales et Cliniques (LNEC)⁻INSERM UMR-S1084, Pôle Biologie-Santé, Université de Poitiers, F-86022 Poitiers, France. afsaneh.gaillard@univ-poitiers.fr.
Corinne ChadéneauTeam Récepteurs, Régulations, Cellules Tumorales (2RCT), EA3842 CAPTuR, Pôle Biologie-Santé, Université de Poitiers, F-86022 Poitiers, France. corinne.chadeneau@univ-poitiers.fr.
Jean-Marc MullerTeam Récepteurs, Régulations, Cellules Tumorales (2RCT), EA3842 CAPTuR, Pôle Biologie-Santé, Université de Poitiers, F-86022 Poitiers, France. jean.marc.muller@univ-poitiers.fr.ORCID 0000-0001-6009-7471
Université de Poitiers · FRCentre National de la Recherche Scientifique · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GBM) remains an incurable disease, mainly due to the high migration and invasion potency of GBM cells inside the brain. PI3K/Akt, Sonic Hedgehog (SHH), and PKA pathways play major regulatory roles in the progression of GBM. The vasoactive intestinal peptide (VIP) family of neuropeptides and their receptors, referred in this article as the "VIP-receptor system", has been reported to regulate proliferation, differentiation, and migration in a number of tumor cell types and more particularly in GBM cells. These neuropeptides are potent activators of the cAMP/PKA pathway. The present study aimed to investigate the cross-talks between the above cited signaling cascades. Regulation by VIP-related neuropeptides of GBM migration and invasion was evaluated ex vivo in rat brain slices explanted in culture. Effects of different combinations of VIP-related neuropeptides and of pharmacological and siRNA inhibitors of PKA, Akt, and of the SHH/GLI1 pathways were tested on GBM migration rat C6 and human U87 GBM cell lines using the wound-healing technique. Quantification of nuclear GLI1, phospho-Akt, and phospho-PTEN was assessed by western-immunoblotting. The VIP-receptor system agonists VIP and PACAP-38 significantly reduced C6 cells invasion in the rat brain parenchyma ex vivo, and C6 and U87 migration in vitro. A VIP-receptor system antagonist, VIP

Indexed as

Aktglioblastomaprotein kinase APTENSonic HedgehogVIP-receptor system

Identifiers

PMID30669581
PMCPMC6356933
OpenAlexW2908857200

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.