Evidence map›Paper›PMID 27105519›Full record

ArticleOncotarget2016

High efficacy of tumor-targeting Salmonella typhimurium A1-R on a doxorubicin- and dactolisib-resistant follicular dendritic-cell sarcoma in a patient-derived orthotopic xenograft PDOX nude mouse model.

Tasuku Kiyuna, Takashi Murakami, Yasunori Tome, Kei Kawaguchi, Kentaro Igarashi, Yong Zhang, Ming Zhao, Yunfeng Li, Michael Bouvet, Fuminori Kanaya and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
26.9field-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

55 citing papers in PubMed, 96 citations in OpenAlex.

  1. Review
  2. Review
  3. Acta biochimica et biophysica Sinica · 2023
    Review
  4. Recombinant AttenuatedCancers · 2022
    Review
  5. Integration ofCancers · 2021
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Tumor-targetingHeliyon · 2018
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
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  19. 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

14 authors at 4 institutions in 2 countries.

Tasuku KiyunaAntiCancer Inc., San Diego, CA, USA.
Takashi MurakamiAntiCancer Inc., San Diego, CA, USA.
Yasunori TomeDepartment of Orthopedic Surgery, Graduate School of Medicine, University of the Ryukyus, Okinawa, Japan.
Kei KawaguchiAntiCancer Inc., San Diego, CA, USA.
Kentaro IgarashiAntiCancer Inc., San Diego, CA, USA.
Yong ZhangAntiCancer Inc., San Diego, CA, USA.
Ming ZhaoAntiCancer Inc., San Diego, CA, USA.
Yunfeng LiDepartment of Pathology, University of California, Los Angeles, CA, USA.
Michael BouvetDepartment of Surgery, University of California, San Diego, CA, USA.
Fuminori KanayaDepartment of Orthopedic Surgery, Graduate School of Medicine, University of the Ryukyus, Okinawa, Japan.
Arun SinghDivision of Hematology-Oncology, University of California, Los Angeles, CA, USA.
Sarah DryDepartment of Pathology, University of California, Los Angeles, CA, USA.
Fritz C EilberDivision of Surgical Oncology, University of California, Los Angeles, CA, USA.
Robert M HoffmanAntiCancer Inc., San Diego, CA, USA.
AntiCancer (United States) · USUniversity of California, Los Angeles · USUniversity of California, San Diego · USUniversity of the Ryukyus · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Follicular dendritic-cell sarcoma (FDCS) is a rare and recalcitrant disease. In the present study, a patient-derived orthotopic xenograft (PDOX) mouse model of FDCS was established in the biceps muscle of nude mice. The FDCS PDOX was resistant to both doxorubicin (DOX) and NVP-BEZ235, dactolisib (BEZ) an experimental agent which is a dual pan-phosphoinositide 3-kinase-mammalian target of rapamycin inhibitor. However, in contrast to DOX and BEZ, the FDCS PDOX was sensitive to the tumor-targeting bacterial strain, Salmonella typhimurium A1-R (S. typhimurium A1-R). The combination of S. typhimurium A1-R and either DOX or BEZ did not increase the antitumor efficacy of S. typhimurium A1-R, indicating that DOX and BEZ were not active in this PDOX model. The efficacy of S. typhimurium A1-R in this recalcitrant FDCS gives strong impetus to move bacterial therapy to clinical trials for this disease. The findings of the present study are of particular importance since it demonstrates that S. typhimurium A1-R is effective in a PDOX model of FDCS established from a patient who failed DOX therapy.

Indexed as

AnimalsAntibiotics, AntineoplasticCell Line, TumorDendritic Cell Sarcoma, FollicularDoxorubicinDrug Resistance, NeoplasmFemaleHumansImidazolesMiceMice, NudeQuinolinesSalmonella InfectionsSalmonella typhimuriumXenograft Model Antitumor AssaysAntibiotics, AntineoplasticdactolisibDoxorubicinImidazolesQuinolinesGFPSalmonella typhimurium A1-Rsarcomasoft-tissuetumor-targeting

Identifiers

PMID27105519
PMCPMC5078074
OpenAlexW2342246138

What OpenQuestion holds

Textmetadata
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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.