Evidence map›Paper›PMID 31986121›Full record

ArticleAging2020

Autocrine CXCL8-dependent invasiveness triggers modulation of actin cytoskeletal network and cell dynamics.

Andrea Antonosante, Laura Brandolini, Michele d'Angelo, Elisabetta Benedetti, Vanessa Castelli, Mattia Del Maestro, Sabino Luzzi, Antonio Giordano, Annamaria Cimini, Marcello Allegretti

Open access · greenAbstract read
In one paragraph

Article in Aging, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Targeting the medulloblastoma: a molecular-based approach.Acta bio-medica : Atenei Parmensis · 2020
    Review
  11. Article
  12. Trauma Coagulopathy and Its Outcomes.Medicina (Kaunas, Lithuania) · 2020
    Observational
  13. 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

10 authors at 4 institutions in 2 countries.

Andrea AntonosanteDepartment of Life, Health and Environmental Sciences, University of L'Aquila, L'Aquila, Italy.
Laura BrandoliniDompé Farmaceutici SpA, L'Aquila, Italy.
Michele d'AngeloDepartment of Life, Health and Environmental Sciences, University of L'Aquila, L'Aquila, Italy.
Elisabetta BenedettiDepartment of Life, Health and Environmental Sciences, University of L'Aquila, L'Aquila, Italy.
Vanessa CastelliDepartment of Life, Health and Environmental Sciences, University of L'Aquila, L'Aquila, Italy.
Mattia Del MaestroSan Matteo Hospital, University of Pavia, Pavia, Italy.
Sabino LuzziSan Matteo Hospital, University of Pavia, Pavia, Italy.
Antonio GiordanoDepartment of Medical Biotechnologies, University of Siena, Siena, Italy.
Annamaria CiminiDepartment of Life, Health and Environmental Sciences, University of L'Aquila, L'Aquila, Italy.
Marcello AllegrettiDompé Farmaceutici SpA, L'Aquila, Italy.
University of L'Aquila · ITDompé (Italy) · ITUniversity of Pavia · ITUniversity of Siena · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GB) is the most representative form of primary malignant brain tumour. Several studies indicated a pleiotropic role of CXCL8 in cancer due to its ability to modulate the tumour microenvironment, growth and aggressiveness of tumour cell. Previous studies indicated that CXCL8 by its receptors (CXCR1 and CXCR2) induced activation of the PI3K/p-Akt pathway, a crucial event in the regulation of cytoskeleton rearrangement and cell mobilization. Human GB primary cell culture and U-87MG cell line were used to study the effects of CXCR1 and CXCR2 blockage, by a dual allosteric antagonist, on cell migration and cytoskeletal dynamics. The data obtained point towards a specific effect of autocrine CXCL8 signalling on GB cell invasiveness by the activation of pathways involved in cell migration and cytoskeletal dynamics, such as PI3K/p-Akt/p-FAK, p-cortactin, RhoA, Cdc42, Acetylated α-tubulin and MMP2. All the data obtained support the concept that autocrine CXCL8 signalling plays a key role in the activation of an aggressive phenotype in primary glioblastoma cells and U-87MG cell line. These results provide new insights about the potential of a pharmacological approach targeting CXCR1/CXCR2 pathways to decrease migration and invasion of GB cells in the brain parenchyma, one of the principal mechanisms of recurrence.

Indexed as

Cell MovementActinsCell Line, TumorCytoskeletonHumansImmunophenotypingInterleukin-8MicrotubulesPhenylacetatesPhosphorylationProtein BindingProtein TransportReceptors, Interleukin-8AReceptors, Interleukin-8BSignal TransductionThiazolesActinsCXCL8 protein, humanDF2755AInterleukin-8PhenylacetatesReceptors, Interleukin-8AReceptors, Interleukin-8BThiazolescell migrationchemokineCXCL8cytoskeletonglioblastoma

Identifiers

PMID31986121
PMCPMC7053615
OpenAlexW3003401061

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.