Evidence map›Paper›PMID 26918036›Full record

ArticleJournal of Cancer2016

Delivery System of CpG Oligodeoxynucleotides through Eliciting an Effective T cell Immune Response against Melanoma in Mice.

Wei Sun, Mingli Fang, Yajing Chen, Zhaogang Yang, Yue Xiao, Min Wan, Hua Wang, Yongli Yu, Liying Wang

Open access · goldAbstract read
In one paragraph

Article in Journal of Cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Preclinical study of TLR stimulation combined PD-1 antibody enhance the therapeutic effect of microwave ablation on NSCLC.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
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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

9 authors at 2 institutions in 2 countries.

Wei Sun1. Department of Molecular Biology, College of Basic Medical Sciences, Jilin University, Changchun 130021, China.
Mingli Fang1. Department of Molecular Biology, College of Basic Medical Sciences, Jilin University, Changchun 130021, China.
Yajing Chen1. Department of Molecular Biology, College of Basic Medical Sciences, Jilin University, Changchun 130021, China.
Zhaogang Yang3. NSF Nanoscale Science and Engineering Center (NSEC), The Ohio State University, Columbus, OH 43212, USA.
Yue Xiao1. Department of Molecular Biology, College of Basic Medical Sciences, Jilin University, Changchun 130021, China.
Min Wan1. Department of Molecular Biology, College of Basic Medical Sciences, Jilin University, Changchun 130021, China.
Hua Wang1. Department of Molecular Biology, College of Basic Medical Sciences, Jilin University, Changchun 130021, China.
Yongli Yu2. Department of Immunology, College of Basic Medical Sciences, Jilin University, Changchun 130021, China.
Liying Wang1. Department of Molecular Biology, College of Basic Medical Sciences, Jilin University, Changchun 130021, China.
Jilin University · CNThe Ohio State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeIn order to improve the immunogenicity of whole tumor cell lysate for tumor vaccine, we have designed a series of CpG ODNs to study their transport and to evaluate their anti-tumor activity in B16 melanoma mouse models.

methodsIn this study, we investigated whether C-class CpG ODN (CpG ODN-685) could facilitate tumor cell lysate to induce vigorous anti-tumor activity against tumors in mice both prophylactically and therapeutically.

resultsIt was found that the combination of tumor cell lysate and CpG ODN-685 could inhibit the growth of B16 melanoma and prolong the survival of tumor-bearing mice. Moreover CpG ODN-685 with the addition of tumor cell lysate can also cause the generation of tumor specific immune memory by inducing specific cytotoxic T lymphocytes and helper T lymphocytes in mice.

conclusionThe results suggest that CpG ODN-685 could be developed as an efficient adjuvant for tumor vaccines against melanoma.

Indexed as

CpG ODNmelanomaT lymphocytestumor cell lysate

Identifiers

PMID26918036
PMCPMC4747877
OpenAlexW2417560063

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.