Evidence map›Paper›PMID 28769537›Full record

ReviewMediators of inflammation2017

Osteopontin at the Crossroads of Inflammation and Tumor Progression.

Luigi Mario Castello, Davide Raineri, Livia Salmi, Nausicaa Clemente, Rosanna Vaschetto, Marco Quaglia, Massimiliano Garzaro, Sergio Gentilli, Paolo Navalesi, Vincenzo Cantaluppi and 3 more

Open access · goldAbstract readReview
In one paragraph

Review in Mediators of inflammation, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed
16.3field-weighted citation impact, top 1% 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

101 citing papers in PubMed, 173 citations in OpenAlex.

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  20. The Role of Osteopontin in Respiratory Health and Disease.Journal of personalized medicine · 2023
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41 more citing papers are in PubMed but not listed here.

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

13 authors at 2 institutions in 1 country.

Luigi Mario CastelloDepartment of Translational Medicine, University of Eastern Piedmont, Novara, Italy.
Davide RaineriDepartment of Health Sciences and Interdisciplinary Research Center of Autoimmune Diseases (IRCAD), University of Eastern Piedmont, Novara, Italy.
Livia SalmiDepartment of Translational Medicine, University of Eastern Piedmont, Novara, Italy.
Nausicaa ClementeDepartment of Health Sciences and Interdisciplinary Research Center of Autoimmune Diseases (IRCAD), University of Eastern Piedmont, Novara, Italy.ORCID 0000-0002-9860-0148
Rosanna VaschettoSCDU Anestesia e Rianimazione, Azienda Ospedaliero-Universitaria Maggiore della Carità, Novara, Italy.
Marco QuagliaDepartment of Translational Medicine, Nephrology and Kidney Transplant Unit, University of Eastern Piedmont, Novara, Italy.
Massimiliano GarzaroDepartment of Health Sciences, University of Eastern Piedmont, Novara, Italy.
Sergio GentilliDepartment of Surgery, University of Eastern Piedmont, Novara, Italy.
Paolo NavalesiAnestesia e Rianimazione, Università "Magna Graecia" di Catanzaro, Catanzaro, Italy.
Vincenzo CantaluppiDepartment of Translational Medicine, Nephrology and Kidney Transplant Unit, University of Eastern Piedmont, Novara, Italy.
Umberto DianzaniDepartment of Health Sciences and Interdisciplinary Research Center of Autoimmune Diseases (IRCAD), University of Eastern Piedmont, Novara, Italy.ORCID 0000-0001-6723-3931
Anna AspesiDepartment of Health Sciences, University of Eastern Piedmont, Novara, Italy.ORCID 0000-0003-4944-0990
Annalisa ChiocchettiDepartment of Health Sciences and Interdisciplinary Research Center of Autoimmune Diseases (IRCAD), University of Eastern Piedmont, Novara, Italy.ORCID 0000-0002-4349-1087
Università degli Studi del Piemonte Orientale “Amedeo Avogadro” · ITMagna Graecia University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Complex interactions between tumor and host cells regulate systemic tumor dissemination, a process that begins early at the primary tumor site and goes on until tumor cells detach themselves from the tumor mass and start migrating into the blood or lymphatic vessels. Metastatic cells colonize the target organs and are capable of surviving and growing at distant sites. In this context, osteopontin (OPN) appears to be a key determinant of the crosstalk between cancer cells and the host microenvironment, which in turn modulates immune evasion. OPN is overexpressed in several human carcinomas and has been implicated in inflammation, tumor progression, and metastasis. Thus, it represents one of the most attracting targets for cancer therapy. Within the tumor mass, OPN is secreted in various forms either by the tumor itself or by stroma cells, and it can exert either pro- or antitumorigenic effects according to the cell type and tumor microenvironment. Thus, targeting OPN for therapeutic purposes needs to take into account the heterogeneous functions of the multiple OPN forms with regard to cancer formation and progression. In this review, we will describe the role of systemic, tumor-derived, and stroma-derived OPN, highlighting its pivotal role at the crossroads of inflammation and tumor progression.

Indexed as

AnimalsDisease ProgressionHumansInflammationNeoplasm MetastasisOsteopontinOsteopontin

Identifiers

PMID28769537
PMCPMC5523273
OpenAlexW2733318469

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.