Evidence map›Paper›PMID 34023505›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2021

A novel CXCR4 antagonist counteracts paradoxical generation of cisplatin-induced pro-metastatic niches in lung cancer.

Giulia Bertolini, Valeria Cancila, Massimo Milione, Giuseppe Lo Russo, Orazio Fortunato, Nadia Zaffaroni, Monica Tortoreto, Giovanni Centonze, Claudia Chiodoni, Federica Facchinetti and 12 more

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06536179 (New Preclinical and Clinical Approaches to Mesothelioma, an Archetypal Inflammatory Tumor), which is not on this map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 20% 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.

NCT06536179 recruitingnot on this mapstarted 2024, after this paper: background citation

New Preclinical and Clinical Approaches to Mesothelioma, an Archetypal Inflammatory Tumor

TypeobservationalSponsorMarco Emilio BianchiRan2024 to 2027Enrolled70ConditionsMesothelioma
3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Mechanical stress during confined migration causes aberrant mitoses and c-MYC amplification.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  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

22 authors at 3 institutions in 1 country.

Giulia BertoliniTumor Genomics Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy. Electronic address: giulia.bertolini@istitutotumori.mi.it.
Valeria CancilaTumor Immunology Unit, University of Palermo, Palermo, Italy.
Massimo Milione1st Pathology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Giuseppe Lo RussoThoracic Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Orazio FortunatoTumor Genomics Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Nadia ZaffaroniMolecular Pharmacology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Monica TortoretoMolecular Pharmacology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Giovanni CentonzeTumor Genomics Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Claudia ChiodoniMolecular Immunology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Federica FacchinettiTumor Genomics Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Giuliana PollaciTumor Genomics Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Giulia TaièTumor Genomics Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Francesca GiovinazzoTumor Genomics Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Massimo MoroTumor Genomics Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Chiara CamisaschiBiomarkers Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Alessandro De TomaThoracic Oncology Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Crescenzo D'AlterioFunctional Genomics, Istituto Nazionale per lo Studio e la Cura dei Tumori-IRCCS-Fondazione "G. Pascale," Naples, Italy.
Ugo PastorinoThoracic Surgery Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Claudio TripodoTumor Immunology Unit, University of Palermo, Palermo, Italy.
Stefania ScalaFunctional Genomics, Istituto Nazionale per lo Studio e la Cura dei Tumori-IRCCS-Fondazione "G. Pascale," Naples, Italy. Electronic address: s.scala@istitutotumori.na.it.
Gabriella SozziTumor Genomics Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Luca RozTumor Genomics Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Fondazione IRCCS Istituto Nazionale dei Tumori · ITIstituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITUniversity of Palermo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Platinum-based chemotherapy remains widely used in advanced non-small cell lung cancer (NSCLC) despite experimental evidence of its potential to induce long-term detrimental effects, including the promotion of pro-metastatic microenvironments. In this study, we investigated the interconnected pathways underlying the promotion of cisplatin-induced metastases. In tumor-free mice, cisplatin treatment resulted in an expansion in the bone marrow of CCR2

Indexed as

A549 CellsAC133 AntigenAnimalsCarcinoma, Non-Small-Cell LungCell Line, TumorChemokine CXCL12CisplatinDrug InteractionsHumansLung NeoplasmsMaleMiceMonocytesNeoplasm MetastasisNeoplastic Stem CellsPeptidesAC133 AntigenChemokine CXCL12CisplatinCXCL12 protein, humanCXCR4 protein, humanPeptidesPROM1 protein, humanReceptors, CXCR4chemotherapycombination therapyinflammatory monocyteslung cancer stem cellsmetastasispeptide anti-CXCR4SDF-1/CXCR4 axis

Identifiers

PMID34023505
PMCPMC8530918
OpenAlexW3165014438

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.