Evidence map›Paper›PMID 26471394›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2015

CpG expedites regression of local and systemic tumors when combined with activatable nanodelivery.

Azadeh Kheirolomoom, Elizabeth S Ingham, Lisa M Mahakian, Sarah M Tam, Matthew T Silvestrini, Spencer K Tumbale, Josquin Foiret, Neil E Hubbard, Alexander D Borowsky, William J Murphy and 1 more

Abstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 23% 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, 27 citations in OpenAlex.

  1. Article
  2. Barriers to immune cell infiltration in tumors.Journal for immunotherapy of cancer · 2023
    Review
  3. Article
  4. Review
  5. Review
  6. Development of thermosensitive resiquimod-loaded liposomes for enhanced cancer immunotherapy.Journal of controlled release : official journal of the Controlled Release Society · 2021
    Article
  7. Ultrasound-mediated delivery of miRNA-122 and anti-miRNA-21 therapeutically immunomodulates murine hepatocellular carcinoma in vivo.Journal of controlled release : official journal of the Controlled Release Society · 2020
    Article
  8. Combining activatable nanodelivery with immunotherapy in a murine breast cancer model.Journal of controlled release : official journal of the Controlled Release Society · 2019
    Article
  9. Review
  10. Article
  11. Review
  12. Intracellular trafficking of a pH-responsive drug metal complex.Journal of controlled release : official journal of the Controlled Release Society · 2016
    Article
  13. Article
  14. Metallic Nanoparticles for Cancer Immunotherapy.Materials today (Kidlington, England)
    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

11 authors at 3 institutions in 1 country.

Azadeh KheirolomoomUniversity of California, Davis, Department of Biomedical Engineering, 451 East Health Sciences Drive, Davis, CA 95616, USA.
Elizabeth S InghamUniversity of California, Davis, Department of Biomedical Engineering, 451 East Health Sciences Drive, Davis, CA 95616, USA.
Lisa M MahakianUniversity of California, Davis, Department of Biomedical Engineering, 451 East Health Sciences Drive, Davis, CA 95616, USA.
Sarah M TamUniversity of California, Davis, Department of Biomedical Engineering, 451 East Health Sciences Drive, Davis, CA 95616, USA.
Matthew T SilvestriniUniversity of California, Davis, Department of Biomedical Engineering, 451 East Health Sciences Drive, Davis, CA 95616, USA.
Spencer K TumbaleUniversity of California, Davis, Department of Biomedical Engineering, 451 East Health Sciences Drive, Davis, CA 95616, USA.
Josquin FoiretUniversity of California, Davis, Department of Biomedical Engineering, 451 East Health Sciences Drive, Davis, CA 95616, USA.
Neil E HubbardUniversity of California, Davis, Center for Comparative Medicine, Davis, CA 95616, USA.
Alexander D BorowskyUniversity of California, Davis, Center for Comparative Medicine, Davis, CA 95616, USA.
William J MurphyUniversity of California, Davis, Department of Dermatology, 2921 Stockton Blvd., Institute for Regenerative Cures, Suite 1630, Sacramento, CA 95817, USA.
Katherine W FerraraUniversity of California, Davis, Department of Biomedical Engineering, 451 East Health Sciences Drive, Davis, CA 95616, USA. Electronic address: kwferrara@ucdavis.edu.
West Health · USUniversity of California, Davis · USCalifornia Institute for Regenerative Medicine · US

Funding

Ultrasound Imaging and Local Drug Delivery in TumorsR01CA103828 · NCI · UNIVERSITY OF CALIFORNIA DAVIS · PI FERRARA, KATHERINE W · 2004 to 2013
$10.4M
Ultrasound imaging and enhanced therapeutic responseR01CA134659 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI FERRARA, KATHERINE W · 2009 to 2017
$4.4M
Optimized ultrasound-enhanced immunotherapyR01CA199658 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI FERRARA, KATHERINE W · 2015 to 2019
$2.5M
NCI NIH HHS NIHR01CA103828NCI NIH HHS NIHR01CA134659NCI NIH HHS NIHR01CA199658NCI NIH HHS R01 CA103828NCI NIH HHS R01 CA134659NCI NIH HHS R01 CA199658
6 · The paper itself

Abstract

Ultrasonic activation of nanoparticles provides the opportunity to deliver a large fraction of the injected dose to insonified tumors and produce a complete local response. Here, we evaluate whether the local and systemic response to chemotherapy can be enhanced by combining such a therapy with locally-administered CpG as an immune adjuvant. In order to create stable, activatable particles, a complex between copper and doxorubicin (CuDox) was created within temperature-sensitive liposomes. Whereas insonation of the CuDox liposomes alone has been shown to produce a complete response in murine breast cancer after 8 treatments of 6 mg/kg delivered over 4 weeks, combining this treatment with CpG resolved local cancers within 3 treatments delivered over 7 days. Further, contralateral tumors regressed as a result of the combined treatment, and survival was extended in systemic disease. In both the treated and contralateral tumor site, the combined treatment increased leukocytes and CD4+ and CD8+ T-effector cells and reduced myeloid-derived suppressor cells (MDSCs). Taken together, the results suggest that this combinatorial treatment significantly enhances the systemic efficacy of locally-activated nanotherapy.

Indexed as

NanoparticlesAdjuvants, ImmunologicAnimalsAntibiotics, AntineoplasticBreast NeoplasmsCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCombined Modality TherapyDNADoxorubicinDrug CompoundingFemaleImmunotherapyLiposomesLymphocytes, Tumor-InfiltratingMacrophagesAdjuvants, ImmunologicAntibiotics, AntineoplasticCpG phosphorothioate ODN 1826-SDNADoxorubicindoxorubicin-copper(II) complexLiposomesOrganometallic CompoundsCpGDoxorubicinImmunotherapyTemperature-sensitive liposomeUltrasound

Identifiers

PMID26471394
PMCPMC4688109
OpenAlexW2174545311

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.