Evidence map›Paper›PMID 21901170›Full record

ArticleGenes & cancer2011

Ranpirnase Interferes with NF-κB Pathway and MMP9 Activity, Inhibiting Malignant Mesothelioma Cell Invasiveness and Xenograft Growth.

Masaki Nasu, Michele Carbone, Giovanni Gaudino, Bevan H Ly, Pietro Bertino, David Shimizu, Paul Morris, Harvey I Pass, Haining Yang

Open access · bronzeAbstract read
In one paragraph

Article in Genes & cancer, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. BAP1 is a novel regulator of HIF-1α.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  4. Article
  5. Medical and Surgical Care of Patients With Mesothelioma and Their Relatives Carrying Germline BAP1 Mutations.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2022
    Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Development of dual reporter imaging system forClinical and experimental vaccine research · 2018
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. CSPG4 as a target of antibody-based immunotherapy for malignant mesothelioma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2012
    Article
  20. 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

9 authors at 4 institutions in 1 country.

Masaki NasuUniversity of Hawai'i Cancer Center, University of Hawai'i at Manoa, Honolulu, HI, USA.
Michele Carbone
Giovanni Gaudino
Bevan H Ly
Pietro Bertino
David Shimizu
Paul Morris
Harvey I Pass
Haining Yang
University of Hawaiʻi at Mānoa · USColumbia University Irving Medical Center · USQueen's Medical Center · USUniversity of Hawaii System · US

Funding

PATHOLOGY, VIROLOGY, AND ANIMAL COREP01CA114047 · NCI · UNIVERSITY OF HAWAII AT MANOA · PI TESTA, JOSEPH R. · 2006 to 2010
$8.0M
SV40 sequences in human tumors: analysis &biologic*R01CA092657 · NCI · UNIVERSITY OF HAWAII AT MANOA · PI CARBONE, MICHELE · 2002 to 2006
$1.7M
Role of Cell Mediators in Asbestos-SV40 CarcinogenesisR01CA106567 · NCI · UNIVERSITY OF HAWAII AT MANOA · PI CARBONE, MICHELE · 2005 to 2009
$1.3M
NCI NIH HHS P01 CA114047NCI NIH HHS R01 CA092657NCI NIH HHS R01 CA106567
6 · The paper itself

Abstract

The ribonuclease ranpirnase (Onconase) has been used empirically to treat malignant mesothelioma (MM) patients, and some of them had prolonged survivals. The aim of this study was to investigate the mechanisms of the therapeutic function of ranpirnase in MM cells. The effects of ranpirnase were studied in vivo and in vitro on 2 MM cell lines (epithelioid REN and sarcomatoid PPM-Mill). We found that ranpirnase was able to inhibit NF-κB nuclear translocation, evaluated by cell fractionation and immunoblotting as well as by immunofluorescence. Also, MMP9 secretion by MM cells was decreased by ranpirnase treatment, as assessed by the reduction of metalloproteinase activity, evaluated by zymography on culture-conditioned media. Ranpirnase induced apoptosis of MM cells in vitro and in vivo, causing a powerful inhibition of MM tumor growth in SCID xenografts, determined by In Vivo Imaging System (IVIS) of tumor cells engineered by lentiviral transduction of the luciferase gene. Finally, mice treated with ranpirnase showed a significantly prolonged survival. Our data provide a mechanistic rationale to explain the beneficial antitumor activity observed in some patients treated with ranpirnase and demonstrate that ranpirnase interferes with the NF-κB pathway, thus influencing MM tumor cell invasiveness and survival. It is hoped that this information will also facilitate the identification of those patients who are more likely to benefit from this drug and will also open a new frontier for the use of this drug in tumor types other than MM.

Indexed as

mesotheliomaMMP9NF-κBranpirnaseTNF-α

Identifiers

PMID21901170
PMCPMC3161417
OpenAlexW2106996100

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.