Evidence map›Paper›PMID 27121053›Full record

ArticleOncotarget2016

Reduced expression of CD109 in tumor-associated endothelial cells promotes tumor progression by paracrine interleukin-8 in hepatocellular carcinoma.

Bo-Gen Ye, Hui-Chuan Sun, Xiao-Dong Zhu, Zong-Tao Chai, Yuan-Yuan Zhang, Jian-Yang Ao, Hao Cai, De-Ning Ma, Cheng-Hao Wang, Cheng-Dong Qin and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 16 citations in OpenAlex.

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  4. TGF-β superfamily co-receptors in cancer.Developmental dynamics : an official publication of the American Association of Anatomists · 2022
    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

12 authors at 5 institutions in 1 country.

Bo-Gen YeLiver Cancer Institute and Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Hui-Chuan SunLiver Cancer Institute and Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Xiao-Dong ZhuLiver Cancer Institute and Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Zong-Tao ChaiGeneral Surgery, Changhai Hospital, Second Military Medical University, Shanghai 200433, China.
Yuan-Yuan ZhangLiver Cancer Institute and Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Jian-Yang AoThe First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, China.
Hao CaiLiver Cancer Institute and Zhongshan Hospital, Fudan University, Shanghai 200032, China.
De-Ning MaLiver Cancer Institute and Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Cheng-Hao WangLiver Cancer Institute and Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Cheng-Dong QinLiver Cancer Institute and Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Dong-Mei GaoLiver Cancer Institute and Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Zhao-You TangLiver Cancer Institute and Zhongshan Hospital, Fudan University, Shanghai 200032, China.
Ministry of Education of the People's Republic of China · CNZhongshan Hospital · CNFudan University · CNChanghai Hospital · CNWenzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor-associated endothelial cells (TEC) directly facilitate tumor progression, but little is known about the mechanisms. We investigated the function of CD109 in TEC and its clinical significance in hepatocellular carcinoma (HCC). The correlation between CD109 expressed on tumor vessels and the prognosis after surgical resection of HCC was studied. The effect of human umbilical vein endothelial cells (HUVEC) with different CD109 expression on hepatoma cell proliferation, migration, and invasion was compared in co-culture assay. Associated key factors were screened by human cytokine antibody array and validated thereafter. HUVEC with different CD109 expression were co-implanted with HCCLM3 or HepG2 cells in nude mice to investigate the effect of CD109 expression on tumor growth and metastasis. Reduced expression of CD109 on tumor vessels was associated with large tumor size, microvascular invasion, and advanced tumor stage. CD109 was an independent risk factor for disease-free survival (P = 0.001) after curative resection of HCC. CD109 knockdown in HUVEC promoted hepatoma cell proliferation, migration, and invasion. Interleukin-8 (IL-8) was a key tumor-promoting factor secreted from CD109 knockdown HUVEC. CD109 knockdown upregulated IL-8 expression through activation of TGF-β/Akt/NF-κB pathway in HUVEC. Co-implantation with CD109 knockdown HUVEC accelerated tumor growth and metastasis in mice models. In conclusion, CD109 expression on tumor vessels is a potential prognostic marker for HCC, and its reduced expression on TEC promoted tumor progression by paracrine IL-8.

Indexed as

AnimalsAntigens, CDBiomarkers, TumorCarcinoma, HepatocellularCell Line, TumorCoculture TechniquesDisease-Free SurvivalDisease ProgressionDown-RegulationEndothelial CellsGPI-Linked ProteinsHeterograftsHumansHuman Umbilical Vein Endothelial CellsInterleukin-8Kaplan-Meier EstimateAntigens, CDBiomarkers, TumorCD109 protein, humanCXCL8 protein, humanGPI-Linked ProteinsInterleukin-8Neoplasm ProteinsCD109hepatocellular carcinomainterleukin-8TGF-βtumor-associated endothelial cells

Identifiers

PMID27121053
PMCPMC5045399
OpenAlexW2340928134

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.