Evidence map›Paper›PMID 27467932›Full record

ArticleOncoimmunology2016

Leukocytes recruited by tumor-derived HMGB1 sustain peritoneal carcinomatosis.

Lucia Cottone, Annalisa Capobianco, Chiara Gualteroni, Antonella Monno, Isabella Raccagni, Silvia Valtorta, Tamara Canu, Tiziano Di Tomaso, Angelo Lombardo, Antonio Esposito and 6 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 18% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. HMGB1 released by mesothelial cells drives the development of asbestos-induced mesothelioma.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  3. Integration of Genomic Biology Into Therapeutic Strategies of Gastric Cancer Peritoneal Metastasis.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2022
    Review
  4. Review
  5. Early Adaptation of Colorectal Cancer Cells to the Peritoneal Cavity Is Associated with Activation of "Stemness" Programs and Local Inflammation.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Observational
  6. Article
  7. Review
  8. Review
  9. Article
  10. GlutathioneFrontiers in immunology · 2018
    Article
  11. Review
  12. Review
  13. Article
  14. Review
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

16 authors at 4 institutions in 1 country.

Lucia CottoneDivision of Immunology, Transplantation & Infectious Diseases, San Raffaele Scientific Institute, Milano, Italy; Vita-Salute San Raffaele University, School of Medicine, Milano, Italy.
Annalisa CapobiancoDivision of Immunology, Transplantation & Infectious Diseases, San Raffaele Scientific Institute , Milano, Italy.
Chiara GualteroniDivision of Immunology, Transplantation & Infectious Diseases, San Raffaele Scientific Institute , Milano, Italy.
Antonella MonnoDivision of Immunology, Transplantation & Infectious Diseases, San Raffaele Scientific Institute , Milano, Italy.
Isabella RaccagniExperimental Imaging Center, IRCCS San Raffaele Scientific Institute, Milano, Italy; Medicine and Surgery Department, University of Milano Bicocca, Milano, Italy.
Silvia ValtortaExperimental Imaging Center, IRCCS San Raffaele Scientific Institute, Milano, Italy; IBFM, CNR, Milano, Italy.
Tamara CanuDepartment of Radiology and Preclinical Imaging Facility of the Experimental Imaging Center, San Raffaele Scientific Institute , Milano, Italy.
Tiziano Di TomasoSan Raffaele Telethon Institute for Gene Therapy (SR-Tiget), Division of Regenerative Medicine, Stem Cells and Gene Therapy, San Raffaele Scientific Institute , Milano, Italy.
Angelo LombardoVita-Salute San Raffaele University, School of Medicine, Milano, Italy; San Raffaele Telethon Institute for Gene Therapy (SR-Tiget), Division of Regenerative Medicine, Stem Cells and Gene Therapy, San Raffaele Scientific Institute, Milano, Italy.
Antonio EspositoVita-Salute San Raffaele University, School of Medicine, Milano, Italy; Department of Radiology and Preclinical Imaging Facility of the Experimental Imaging Center, San Raffaele Scientific Institute, Milano, Italy.
Rosa Maria MorescoExperimental Imaging Center, IRCCS San Raffaele Scientific Institute, Milano, Italy; Medicine and Surgery Department, University of Milano Bicocca, Milano, Italy.
Alessandro Del MaschioVita-Salute San Raffaele University, School of Medicine, Milano, Italy; Department of Radiology and Preclinical Imaging Facility of the Experimental Imaging Center, San Raffaele Scientific Institute, Milano, Italy.
Luigi NaldiniVita-Salute San Raffaele University, School of Medicine, Milano, Italy; San Raffaele Telethon Institute for Gene Therapy (SR-Tiget), Division of Regenerative Medicine, Stem Cells and Gene Therapy, San Raffaele Scientific Institute, Milano, Italy.
Patrizia Rovere-QueriniDivision of Immunology, Transplantation & Infectious Diseases, San Raffaele Scientific Institute, Milano, Italy; Vita-Salute San Raffaele University, School of Medicine, Milano, Italy.
Marco E BianchiVita-Salute San Raffaele University, School of Medicine, Milano, Italy; Division of Genetics & Cell Biology, San Raffaele Scientific Institute, Milano, Italy.
Angelo A ManfrediDivision of Immunology, Transplantation & Infectious Diseases, San Raffaele Scientific Institute, Milano, Italy; Vita-Salute San Raffaele University, School of Medicine, Milano, Italy.
Vita-Salute San Raffaele University · ITIstituto di Ricovero e Cura a Carattere Scientifico San RaffaeleThe San Raffaele Telethon Institute for Gene Therapy · ITUniversity of Milano-Bicocca · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The factors that determine whether disseminated transformed cells in vivo yield neoplastic lesions have only been partially identified. We established an ad hoc model of peritoneal carcinomatosis by injecting colon carcinoma cells in mice. Tumor cells recruit inflammatory leukocytes, mostly macrophages, and generate neoplastic peritoneal lesions. Phagocyte depletion via clodronate treatment reduces neoplastic growth. Colon carcinoma cells release a prototypic damage-associated molecular pattern (DAMP)/alarmin, High Mobility Group Box1 (HMGB1), which attracts leukocytes. Exogenous HMGB1 accelerates leukocyte recruitment, macrophage infiltration, tumor growth and vascularization. Lentiviral-based HMGB1 knockdown or pharmacological interference with its extracellular impair macrophage recruitment and tumor growth. Our findings provide a preclinical proof of principle that strategies based on preventing HMGB1-driven recruitment of leukocytes could be used for treating peritoneal carcinomatosis.

Indexed as

AlarminBoxAdamage-associated molecular patternDAMPGFPgreen fluorescent proteinHigh Mobility Box 1HMGB1leukocytesmacrophagesMC-38murine colon adenocarcinoma cell lineperitoneal carcinomatosisshort hairpin RNAShRNAvascularization

Identifiers

PMID27467932
PMCPMC4910728
OpenAlexW2413918016

What OpenQuestion holds

Textmetadata
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.