Evidence map›Paper›PMID 29370526›Full record

ArticleACS nano2018

Nanoparticle-Mediated Trapping of Wnt Family Member 5A in Tumor Microenvironments Enhances Immunotherapy for B-Raf Proto-Oncogene Mutant Melanoma.

Qi Liu, Hongda Zhu, Karthik Tiruthani, Limei Shen, Fengqian Chen, Keliang Gao, Xueqiong Zhang, Lin Hou, Degeng Wang, Rihe Liu and 1 more

Open access · greenAbstract read
In one paragraph

Article in ACS nano, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
5.9field-weighted citation impact, top 3% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.

  1. Pooled it
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  5. Recent advances in drug delivery and targeting for the treatment of pancreatic cancer.Journal of controlled release : official journal of the Controlled Release Society · 2024
    Review
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  8. Nanocarrier-Mediated Immunogenic Cell Death for Melanoma Treatment.International journal of nanomedicine · 2023
    Review
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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

11 authors at 2 institutions in 2 countries.

Qi Liu
Hongda ZhuSchool of Food and Biology Engineering, Key Laboratory of Fermentation Engineering, Hubei University of Technology , Wuhan 430068, China.
Karthik Tiruthani
Limei Shen
Fengqian ChenDepartment of Environmental Toxicology, The Institute of Environmental and Human Health (TIEHH) and the Center for Biotechnology & Genomics, Texas Tech University , Lubbock, Texas 79416, United States.
Keliang Gao
Xueqiong Zhang
Lin Hou
Degeng WangDepartment of Environmental Toxicology, The Institute of Environmental and Human Health (TIEHH) and the Center for Biotechnology & Genomics, Texas Tech University , Lubbock, Texas 79416, United States.
Rihe Liu
Texas Tech University · USHubei University of Technology · CN

Funding

Small Animal Imaging CoreU54CA198999 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LI, ZIBO · 2015 to 2019
$11.9M
Novel Single Domain Antibodies with Multivalency and MultispecificityR01CA157738 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LIU, RIHE · 2012 to 2016
$1.5M
To Combine CRISPR/Cas9 Genome Editing, Nanotech and Chemical Genetics toward in vivo Protein Kinase AnalysisR15GM122006 · NIGMS · TEXAS TECH UNIVERSITY · PI WANG, DEGENG · 2017 to 2019
$535k
NCI NIH HHS R01 CA157738NCI NIH HHS U54 CA198999NIGMS NIH HHS R15 GM122006
6 · The paper itself

Abstract

Development of an effective treatment against advanced tumors remains a major challenge for cancer immunotherapy. Approximately 50% of human melanoma is driven by B-Raf proto-oncogene mutation (BRAF mutant). Tumors with such mutation are desmoplastic, highly immunosuppressive, and often resistant to immune checkpoint therapies. We have shown that immunotherapy mediated by low-dose doxorubicin-induced immunogenic cell death was only partially effective for this type of tumor and not effective in long-term inhibition of tumor progression. Wnt family member 5A (Wnt5a), a signaling protein highly produced by BRAF mutant melanoma cells, has been implicated in inducing dendritic cell tolerance and tumor fibrosis, thus hindering effective antigen presentation and T-cell infiltration. We hypothesized that Wnt5a is a key molecule controlling the immunosuppressive tumor microenvironment in metastatic melanoma. Accordingly, we have designed and generated a trimeric trap protein, containing the extracellular domain of Fizzled 7 receptor that binds Wnt5a with a K

Indexed as

AnimalsAntibiotics, AntineoplasticCell LineCell ProliferationCell SurvivalDose-Response Relationship, DrugDoxorubicinDrug Screening Assays, AntitumorFemaleMelanomaMiceMice, Inbred C57BLMutationNanoparticlesProto-Oncogene MasProto-Oncogene Proteins B-rafAntibiotics, AntineoplasticBraf protein, mouseDoxorubicinMAS1 protein, humanProto-Oncogene MasProto-Oncogene Proteins B-rafWnt-5a ProteinWnt5a protein, mouseB-Raf proto-oncogene mutant melanomaimmune trapimmunogenic cell deathnanoparticletumor microenvironmentWnt family member 5A

Identifiers

PMID29370526
PMCPMC5834397
OpenAlexW2784498391

What OpenQuestion holds

Textmetadata
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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.