Evidence map›Paper›PMID 30248044›Full record

ArticleCancer biomarkers : section A of Disease markers2018

Upregulated FFAR4 correlates with the epithelial-mesenchymal transition and an unfavorable prognosis in human cholangiocarcinoma.

Fu-Tao Meng, Mei Huang, Feng Shao, Qiang Huang

Abstract read
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Article in Cancer biomarkers : section A of Disease markers, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 27% of its field
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Clinicopathologic and genomic characteristics of mucinous gastric adenocarcinoma.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2022
    Article
  6. Observational
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4 · The record

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5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Fu-Tao MengDepartment of General Surgery, Affiliated Anhui Provincial Hospital, Hefei, Anhui, China.
Mei HuangDepartment of General Surgery, Affiliated Anhui Provincial Hospital, Hefei, Anhui, China.
Feng ShaoDepartment of General Surgery, Affiliated Anhui Provincial Hospital, Hefei, Anhui, China.
Qiang HuangDepartment of General Surgery, Affiliated Anhui Provincial Hospital, Hefei, Anhui, China.
Anhui Provincial Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFree fatty acid receptor 4 (FFAR4) is associated with the epithelial mesenchymal transition (EMT) and is involved in the progression of several types of cancer. However, the role of FFAR4 in cholangiocarcinoma (CCA) remains unclear.

objectiveThe present study evaluated the diagnosis and prognosis of CCA using FFAR4 as a biomarker.

methodsImmunohistochemistry was employed to detect expression of FFAR4 in 98 samples of CCA tissues and adjacent tissues. In addition, expression of E-cadherin, vimentin, Snail-1, CK7 and CK19 in the 98 samples of CCA tissues was detected, and relationships with FFAR4 were analyzed. Correlation between FFAR4 and clinical pathological factors and prognosis was also analyzed.

resultsFFAR4 was highly expressed in 72.4% (71/98) of CCA tissues and 29.6% (29/98) of adjacent tissues, with a statistically significant difference between the two tissue types (P< 0.05). A negative correlation between high expression FFAR4 and E-cadherin expression in CCA tissues was also observed (r=-0.445, P< 0.001), and high expression of FFAR4 was positively correlated with vimentin (r= 0.354, P< 0.001), Snail-1(r= 0.496, P< 0.001), CK7(r= 0.494, P< 0.001) and CK19 (r= 0.532, P< 0.001). Moreover, the degree of FFAR4 expression was associated with aggressive clinicopathological characteristics, such as histological grade, perineural invasion (PNI), lymph node metastasis (LNM), advanced TNM stage and preoperative serum CA19-9 level (P< 0.05). In terms of prognosis, CCA patients with high FFAR4 expression showed shorter disease-free survival (DFS) (P< 0.05) and overall survival (OS) (P< 0.05) than did patients with low FFAR4 expression.

conclusionsFFAR4 overexpression may mediate the process of CCA EMT. In addition, FFAR4 is promising as a new diagnostic molecule and therapeutic target for CCA.

Indexed as

PrognosisAdultAgedAntigens, Tumor-Associated, CarbohydrateBiomarkers, TumorCell Line, TumorCell MovementCholangiocarcinomaDisease-Free SurvivalDisease ProgressionEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHumansLymphatic MetastasisMaleAntigens, Tumor-Associated, CarbohydrateBiomarkers, Tumorcarbohydrate antigen 199, humanFFAR4 protein, humanReceptors, G-Protein-Coupledcytokeratin19cytokeratin7E-cadherinFFAR4ImmunohistochemistryprognosisSnail-1vimentin

Identifiers

PMID30248044
PMCPMC13078563
OpenAlexW2890066358

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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.