Evidence map›Paper›PMID 31584009›Full record

ArticleAging2019

The prognostic value of major facilitator superfamily domain-containing protein 2A in patients with hepatocellular carcinoma.

Shan Xing, Jun Kan, Aishan Su, Qiao-Dan Liu, Kailin Wang, Xiuyu Cai, Jun Dong

Open access · greenAbstract read
In one paragraph

Article in Aging, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
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  8. Wnt/β-catenin-driven EMT regulation in human cancers.Cellular and molecular life sciences : CMLS · 2024
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  13. The Role of Mfsd2a in Nervous System Diseases.Frontiers in neuroscience · 2021
    Review
  14. Article
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

7 authors at 6 institutions in 1 country.

Shan XingDepartment of Laboratory, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou 510060, P. R. China.
Jun KanDepartment of Oncology, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou 510006, China.
Aishan SuDepartment of GCP Center, Nanfang Hospital of Southern Medical University, Guangzhou 510515, P.R. China.
Qiao-Dan LiuDepartment of Radiation Oncology, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai 519001, Guangdong Province, China.
Kailin WangDepartment of Oncology, The First Affiliated Hospital of Guangdong Pharmaceutical University, Guangdong Pharmaceutical University, Guangzhou 510062, China.
Xiuyu CaiDepartment of Integrated Therapy in Oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou 510060, P. R. China.
Jun DongDepartment of Integrated Therapy in Oncology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou 510060, P. R. China.
Sun Yat-sen University · CNFirst Affiliated Hospital of Guangdong Pharmaceutical University · CNFirst Affiliated Hospital of Guangzhou University of Chinese Medicine · CNSouthern Medical University · CNState Key Laboratory of Oncology in South ChinaSun Yat-sen University Cancer Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionWe aimed to characterize the expression of major facilitator superfamily domain-containing protein 2A (MFSD2A) in hepatocellular carcinoma (HCC) patients and analyze its prognostic value.

resultsImmunohistochemistry revealed that low expression of MFSD2A was present in 37 of 79 cases (46.84%), which was significantly correlated with poor histological differentiation (

conclusionThe current study indicate MFSD2A may be an optimal diagnostic and prognostic biomarker for HCC.

methodsFirst, we examined MFSD2A expression in 24 paired HCC and nontumorous tissues by real-time quantitative PCR (RT-qPCR). Second, the protein levels of MFSD2A in 11 paired HCC and nontumorous tissues were investigated by western blotting (WB). Moreover, MFSD2A protein expression was evaluated by immunohistochemistry in 79 HCC patients. In addition, we detected the plasma level of MFSD2A in HCC patients and healthy individuals and investigated the relationship between MFSD2A expression and clinicopathological parameters or prognosis of HCC patients.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsSymportersBiomarkers, TumorChinaDown-RegulationFemaleGene Expression Regulation, NeoplasticHumansImmunohistochemistryMaleMembrane Transport ProteinsMiddle AgedPredictive Value of TestsPrognosisBiomarkers, TumorMembrane Transport ProteinsMFSD2A protein, humanSymportershepatocellular carcinomaMFSD2Apoor differentiationprognosis

Identifiers

PMID31584009
PMCPMC6814593
OpenAlexW2978230874

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.