Evidence map›Paper›PMID 30677195›Full record

ArticleCancer science2019

Frizzled 2-induced epithelial-mesenchymal transition correlates with vasculogenic mimicry, stemness, and Hippo signaling in hepatocellular carcinoma.

Huohui Ou, Zhanjun Chen, Leyang Xiang, Yinghao Fang, Yuyan Xu, Qin Liu, Zhigang Hu, Xianghong Li, Yu Huang, Dinghua Yang

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 7% 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

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

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  18. FZD5 prevents epithelial-mesenchymal transition in gastric cancer.Cell communication and signaling : CCS · 2021
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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

10 authors at 1 institution in 1 country.

Huohui OuDepartment of Hepatobiliary Surgery, Nanfang Hospital of Southern Medical University, Guangzhou, China.
Zhanjun ChenDepartment of Hepatobiliary Surgery, Nanfang Hospital of Southern Medical University, Guangzhou, China.
Leyang XiangDepartment of Hepatobiliary Surgery, Nanfang Hospital of Southern Medical University, Guangzhou, China.
Yinghao FangDepartment of Hepatobiliary Surgery, Nanfang Hospital of Southern Medical University, Guangzhou, China.
Yuyan XuDepartment of Hepatobiliary Surgery, Nanfang Hospital of Southern Medical University, Guangzhou, China.
Qin LiuDepartment of Hepatobiliary Surgery, Nanfang Hospital of Southern Medical University, Guangzhou, China.
Zhigang HuDepartment of Hepatobiliary Surgery, Nanfang Hospital of Southern Medical University, Guangzhou, China.
Xianghong LiDepartment of Hepatobiliary Surgery, Nanfang Hospital of Southern Medical University, Guangzhou, China.
Yu HuangDepartment of Laboratory Medicine, Nanfang Hospital of Southern Medical University, Guangzhou, China.
Dinghua YangDepartment of Hepatobiliary Surgery, Nanfang Hospital of Southern Medical University, Guangzhou, China.ORCID https://orcid.org/0000-0002-1442-5240
Nanfang Hospital · CN

Funding

Guangdong Provincial Science and Technology Projects 2017A020215132National Natural Science Foundation of China 81872385
6 · The paper itself

Abstract

Prior observation has indicated that Frizzled 2 (FZD2)-induced epithelial-mesenchymal transition (EMT) could be a key step in metastasis and early recurrence of hepatocellular carcinoma (HCC). However, the mechanism underlying tumor development and progression due to aberrant FZD2 expression is poorly defined. Here, we provide evidence that FZD2 is a driver for EMT, cancer stem cell properties, and vasculogenic mimicry (VM) in HCC. We found that FZD2 was highly expressed in two cohorts of Chinese hepatitis B virus-related HCC patients, and that high FZD2 expression was associated with poor prognosis. Concerning the mechanism, gain- and loss-of-function experiments showed the oncogenic action of FZD2 in HCC cell proliferation, apoptosis, migration, and invasion. Further investigations in vitro and in vivo suggested that FZD2 promotes the EMT process, enhances stem-like properties, and confers VM capacity to HCC cells. Notably, integrative RNA sequencing analysis of FZD2-knockdown cells indicated the enrichment of Hippo signaling pathway. Taken together, our data suggest for the first time that FZD2 could promote clinically relevant EMT, CD44

Indexed as

Signal TransductionAdaptor Proteins, Signal TransducingAdultAgedAnimalsCarcinoma, HepatocellularCell Line, TumorCell MovementCell SurvivalDisease Models, AnimalDisease ProgressionEpithelial-Mesenchymal TransitionFemaleFrizzled ReceptorsGene Expression Regulation, NeoplasticHeterograftsAdaptor Proteins, Signal TransducingFrizzled ReceptorsFZD2 protein, humanPhosphoproteinsProtein Serine-Threonine KinasesTranscription FactorsYAP1 protein, humanYAP-Signaling Proteinscancer stem cellepithelial-mesenchymal transitionFrizzled 2Hippo signaling pathwayvasculogenic mimicry

Identifiers

PMID30677195
PMCPMC6447835
OpenAlexW2912463609

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.