Evidence map›Paper›PMID 29300334›Full record

ReviewInternational journal of molecular sciences2018

Understanding the Progression of Bone Metastases to Identify Novel Therapeutic Targets.

Annie Schmid-Alliana, Heidy Schmid-Antomarchi, Rasha Al-Sahlanee, Patricia Lagadec, Jean-Claude Scimeca, Elise Verron

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.5field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
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  11. A new therapeutic approach for bone metastasis in colorectal cancer: intratumoral melittin.The journal of venomous animals and toxins including tropical diseases · 2022
    Article
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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

6 authors at 4 institutions in 2 countries.

Annie Schmid-AllianaCentre National de la Recherche Scientifique (CNRS), Université Côte d'Azur, Inserm, iBV, 06108 Nice, France. Annie.SCHMID-ALLIANA@unice.fr.
Heidy Schmid-AntomarchiCentre National de la Recherche Scientifique (CNRS), Université Côte d'Azur, Inserm, iBV, 06108 Nice, France. Heidy.SCHMID-ANTOMARCHI@unice.fr.
Rasha Al-SahlaneeCentre National de la Recherche Scientifique (CNRS), Université Côte d'Azur, Inserm, iBV, 06108 Nice, France. rasha.al-sahlanee@unice.fr.
Patricia LagadecCentre National de la Recherche Scientifique (CNRS), Université Côte d'Azur, Inserm, iBV, 06108 Nice, France. Patricia.Lagadec@unice.fr.
Jean-Claude ScimecaCentre National de la Recherche Scientifique (CNRS), Université Côte d'Azur, Inserm, iBV, 06108 Nice, France.
Elise VerronRegenerative Medicine and Skeleton. RMeS-Lab, INSERM UMR 1229, University of Nantes, 44000 Nantes, France. elise.verron@univ-nantes.fr.
Université Côte d'Azur · FRCentre National de la Recherche Scientifique · FRInserm · FRUniversity of Baghdad · IQ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone is one of the most preferential target site for cancer metastases, particularly for prostate, breast, kidney, lung and thyroid primary tumours. Indeed, numerous chemical signals and growth factors produced by the bone microenvironment constitute factors promoting cancer cell invasion and aggression. After reviewing the different theories proposed to provide mechanism for metastatic progression, we report on the gene expression profile of bone-seeking cancer cells. We also discuss the cross-talk between the bone microenvironment and invading cells, which impacts on the tumour actions on surrounding bone tissue. Lastly, we detail therapies for bone metastases. Due to poor prognosis for patients, the strategies mainly aim at reducing the impact of skeletal-related events on patients' quality of life. However, recent advances have led to a better understanding of molecular mechanisms underlying bone metastases progression, and therefore of novel therapeutic targets.

Indexed as

Disease ProgressionAntineoplastic AgentsBone NeoplasmsHumansModels, BiologicalNeoplasm MetastasisTumor MicroenvironmentAntineoplastic Agentsbone metastasesbone microenvironmentbone tropismmolecular mechanismstherapeutic strategies

Identifiers

PMID29300334
PMCPMC5796097
OpenAlexW2782475392

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.