Evidence map›Paper›PMID 24978137›Full record

ArticleOncotarget2014

Tumor-derived exosomes promote tumor progression and T-cell dysfunction through the regulation of enriched exosomal microRNAs in human nasopharyngeal carcinoma.

Shu-Biao Ye, Ze-Lei Li, Dong-Hua Luo, Bi-Jun Huang, Yu-Suan Chen, Xiao-Shi Zhang, Jun Cui, Yi-Xin Zeng, Jiang Li

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 212 papers.

0numbers the graph read from it
0cells of the map it votes in
212citing papers in PubMed
11.5field-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

212 citing papers in PubMed, 335 citations in OpenAlex.

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152 more citing papers are in PubMed but not listed here.

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 1 country.

Shu-Biao YeState Key Laboratory of Oncology in South China, Sun Yat-Sen University Cancer Center, Guangzhou, China. Collaborative Innovation Center of Cancer Medicine, Sun Yat-Sen University Cancer Center, Guangzhou, China. Department of Biotherapy, Sun Yat-Sen University Cancer Center, Guangzhou, China.
Ze-Lei LiState Key Laboratory of Oncology in South China, Sun Yat-Sen University Cancer Center, Guangzhou, China. Collaborative Innovation Center of Cancer Medicine, Sun Yat-Sen University Cancer Center, Guangzhou, China. Department of Biotherapy, Sun Yat-Sen University Cancer Center, Guangzhou, China.
Dong-Hua LuoState Key Laboratory of Oncology in South China, Sun Yat-Sen University Cancer Center, Guangzhou, China. Collaborative Innovation Center of Cancer Medicine, Sun Yat-Sen University Cancer Center, Guangzhou, China. Department of Nasopharyngeal Carcinoma, Sun Yat-Sen University Cancer Center, Guangzhou, China.
Bi-Jun HuangState Key Laboratory of Oncology in South China, Sun Yat-Sen University Cancer Center, Guangzhou, China. Collaborative Innovation Center of Cancer Medicine, Sun Yat-Sen University Cancer Center, Guangzhou, China.
Yu-Suan ChenState Key Laboratory of Oncology in South China, Sun Yat-Sen University Cancer Center, Guangzhou, China. Collaborative Innovation Center of Cancer Medicine, Sun Yat-Sen University Cancer Center, Guangzhou, China. Department of Radiotherapy, Sun Yat-Sen University Cancer Center, Guangzhou, China.
Xiao-Shi ZhangState Key Laboratory of Oncology in South China, Sun Yat-Sen University Cancer Center, Guangzhou, China. Collaborative Innovation Center of Cancer Medicine, Sun Yat-Sen University Cancer Center, Guangzhou, China. Department of Biotherapy, Sun Yat-Sen University Cancer Center, Guangzhou, China.
Jun CuiKey Laboratory of Gene Engineering of the Ministry of Education, State Key Laboratory of Biocontrol, College of Life Sciences, Sun Yat-sen University, Guangzhou, China.
Yi-Xin ZengState Key Laboratory of Oncology in South China, Sun Yat-Sen University Cancer Center, Guangzhou, China. Collaborative Innovation Center of Cancer Medicine, Sun Yat-Sen University Cancer Center, Guangzhou, China.
Jiang LiState Key Laboratory of Oncology in South China, Sun Yat-Sen University Cancer Center, Guangzhou, China. Collaborative Innovation Center of Cancer Medicine, Sun Yat-Sen University Cancer Center, Guangzhou, China. Department of Biotherapy, Sun Yat-Sen University Cancer Center, Guangzhou, China.
Sun Yat-sen University · CNSun Yat-sen University Cancer Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor-derived exosomes contain biologically active proteins and messenger and microRNAs (miRNAs). These particles serve as vehicles of intercellular communication and are emerging mediators of tumorigenesis and immune escape. Here, we isolated 30-100 nm exosomes from the serum of patients with nasopharyngeal carcinoma (NPC) or the supernatant of TW03 cells. Increased circulating exosome concentrations were correlated with advanced lymphoid node stage and poor prognosis in NPC patients (P< 0.05). TW03-derived exosomes impaired T-cell function by inhibiting T-cell proliferation and Th1 and Th17 differentiation and promoting Treg induction by NPC cells in vitro. These results are associated with decreases in ERK, STAT1, and STAT3 phosphorylation and increases in STAT5 phosphorylation in exosome-stimulated T-cells. TW03-derived exosomes increased the proinflammatory cytokines IL-1β, IL-6, and IL-10 but decreased IFNγ, IL-2, and IL-17 release from CD4+ or CD8+ T-cells. Furthermore, five commonly over-expressed miRNAs were identified in the exosomes from patient sera or NPC cells: hsa-miR-24-3p, hsa-miR-891a, hsa-miR-106a-5p, hsa-miR-20a-5p, and hsa-miR-1908. These over-expressed miRNA clusters down-regulated the MARK1 signaling pathway to alter cell proliferation and differentiation. Overall, these observations reveal the clinical relevance and prognostic value of tumor-derived exosomes and identify a unique intercellular mechanism mediated by tumor-derived exosomes to modulate T-cell function in NPC.

Indexed as

CarcinomaCell DifferentiationCell ProliferationDisease-Free SurvivalDisease ProgressionExosomesHumansMicroRNAsNasopharyngeal CarcinomaNasopharyngeal NeoplasmsPhosphorylationSignal TransductionT-LymphocytesMicroRNAs

Identifiers

PMID24978137
PMCPMC4170615
OpenAlexW1578530056

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.