Evidence map›Paper›PMID 32594528›Full record

ArticleHepatology (Baltimore, Md.)2021

M2 Macrophage-Derived Exosomes Facilitate HCC Metastasis by Transferring α

Jindao Wu, Wen Gao, Qiyun Tang, Yue Yu, Wei You, Zhengshan Wu, Ye Fan, Long Zhang, Chen Wu, Guoyong Han and 10 more

RetractedOpen access · hybridAbstract readRetracted Publication
In one paragraph

Article in Hepatology (Baltimore, Md.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed
9.8field-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

90 citing papers in PubMed, 178 citations in OpenAlex.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 5 institutions in 2 countries.

Jindao Wu *Hepatobiliary Center, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Wen Gao *Department of Oncology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Qiyun Tang *Department of General Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Yue YuHepatobiliary Center, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Wei YouHepatobiliary Center, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Zhengshan WuHepatobiliary Center, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Ye FanHepatobiliary Center, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Long ZhangHepatobiliary Center, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Chen WuHepatobiliary Center, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Guoyong HanHepatobiliary Center, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Xueliang ZuoHepatobiliary Center, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Yao ZhangHepatobiliary Center, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Zhiqiang ChenHepatobiliary Center, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Wenzhou DingHepatobiliary Center, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Xiangcheng LiHepatobiliary Center, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Fengming LinThe State Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering, Southeast University, Nanjing, China.
Hongbing ShenState Key Laboratory of Reproductive Medicine, Nanjing Medical University, Nanjing, China.
Jinhai TangDepartment of General Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Yaqin ZhangKey Laboratory of Human Functional Genomics of Jiangsu Province, Department of Biochemistry and Molecular Biology, Nanjing Medical University, Nanjing, China.
Xuehao WangHepatobiliary Center, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Chinese Academy of Medical Sciences & Peking Union Medical College · CNChina Pharmaceutical University · CNJiangsu Province Hospital · CNBioElectronics (United States) · USJiangsu Cancer Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsThe development and progression of hepatocellular carcinoma (HCC) is dependent on its local microenvironment. Tumor-associated macrophages (TAMs) are deemed a key factor for the tumor microenvironment and attribute to contribute to tumor aggressiveness. However, the detailed mechanism underlying the pro-metastatic effect of TAMs on HCC remains undefined. APPROACH AND

resultsThe present study proved that TAMs were enriched in HCC. TAMs were characterized by an M2-polarized phenotype and accelerated the migratory potential of HCC cells in vitro and in vivo. Furthermore, we found that M2-derived exosomes induced TAM-mediated pro-migratory activity. With the use of mass spectrometry, we identified that integrin, α

conclusionsCollectively, the exosome-mediated transfer of functional CD11b/CD18 protein from TAMs to tumor cells may have the potency to boost the migratory potential of HCC cells, thus providing insights into the mechanism of tumor metastasis.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsCD11b AntigenCD18 AntigensCell Line, TumorExosomesHumansNeoplasm MetastasisSignal TransductionTumor-Associated MacrophagesTumor MicroenvironmentCD11b AntigenCD18 AntigensITGAM protein, human

Identifiers

PMID32594528
PMCPMC8360085
OpenAlexW3037860162

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.