Evidence map›Paper›PMID 36755063›Full record

ArticleBritish journal of cancer2023

Tumour-derived small extracellular vesicles contribute to the tumour progression through reshaping the systemic immune macroenvironment.

Zhimin Du, Hui Zhang, Yueyuan Feng, Dewen Zhan, Shuya Li, Chenggong Tu, Jinbao Liu, Jinheng Wang

Open access · greenAbstract read
In one paragraph

Article in British journal of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Extracellular vesicles in spine tumors: biological roles, immune modulation, and therapeutic implications.European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society · 2026
    Review
  6. Article
  7. Review
  8. Article
  9. 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

8 authors at 2 institutions in 1 country.

Zhimin Du *Affiliated Cancer Hospital & Institute of Guangzhou Medical University, 510095, Guangzhou, China.
Hui Zhang *Affiliated Cancer Hospital & Institute of Guangzhou Medical University, 510095, Guangzhou, China.
Yueyuan FengAffiliated Cancer Hospital & Institute of Guangzhou Medical University, 510095, Guangzhou, China.
Dewen ZhanAffiliated Cancer Hospital & Institute of Guangzhou Medical University, 510095, Guangzhou, China.
Shuya LiAffiliated Cancer Hospital & Institute of Guangzhou Medical University, 510095, Guangzhou, China.
Chenggong TuAffiliated Cancer Hospital & Institute of Guangzhou Medical University, 510095, Guangzhou, China.
Jinbao LiuAffiliated Cancer Hospital & Institute of Guangzhou Medical University, 510095, Guangzhou, China. jliu@gzhmu.edu.cn.ORCID 0000-0003-2220-2407
Jinheng WangAffiliated Cancer Hospital & Institute of Guangzhou Medical University, 510095, Guangzhou, China. wangjh89@gzhmu.edu.cn.ORCID 0000-0002-2650-3816
State Key Laboratory of Respiratory Disease · CNGuangzhou Medical University Cancer Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTumour-derived small extracellular vesicles (sEVs) play a crucial role in cancer immunomodulation. In addition to tumour immune microenvironment, the peripheral immune system also contributes significantly to cancer progression and is essential for anticancer immunity. However, a comprehensive definition of which and how peripheral immune lineages are regulated by tumour-derived sEVs during cancer development remains incomplete.

methodsIn this study, we used mass cytometry with extensive antibody panels to comprehensively construct the systemic immune landscape in response to tumour development and tumour-derived sEVs.

resultsSystemic immunity was dramatically altered by tumour growth and tumour-derived sEVs. Tumour-derived sEVs significantly and extensively affected immune cell population composition as well as intracellular pathways, resulting in an immunosuppressive peripheral and tumour immune microenvironment, characterised by increased myeloid-derived suppressor cells and decreased Ly6C

conclusionsThese results highlight that tumour-derived sEVs function as a bridge between peripheral immunity regulation and the tumour microenvironment, and contribute to cancer progression through altering the composition and function of the global immune macroenvironment.

Indexed as

Extracellular VesiclesCD8-Positive T-LymphocytesCell DifferentiationHumansImmunomodulationImmunosuppressive AgentsImmunosuppressive Agents

Identifiers

PMID36755063
PMCPMC10050072
OpenAlexW4319590477

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.