Evidence map›Paper›PMID 35858900›Full record

ArticleMolecular cancer2022

CircGPR137B/miR-4739/FTO feedback loop suppresses tumorigenesis and metastasis of hepatocellular carcinoma.

Lianyong Liu, Mingjun Gu, Junhua Ma, Ying Wang, Miao Li, Hui Wang, Xin Yin, Xiangqi Li

Open access · goldAbstract read
In one paragraph

Article in Molecular cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed, 1 pooled it
16.7field-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

97 citing papers in PubMed, 1 synthesis or guideline pooled it, 195 citations in OpenAlex.

  1. Pooled it
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  17. The mMolecular biomedicine · 2025
    Review
  18. Article
  19. Chemically modified non-coding RNAs in cancer.Expert reviews in molecular medicine · 2025
    Review
  20. Review

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

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

8 authors at 4 institutions in 1 country.

Lianyong Liu *Department of Endocrinology and Metabolism, Punan Hospital, Pudong New District, Shanghai, 200125, China.
Mingjun Gu *Department of Endocrinology and Metabolism, Gongli Hospital, Naval Medical University, 200135, Shanghai, China.
Junhua MaDepartment of Endocrinology and Metabolism, Gongli Hospital, Naval Medical University, 200135, Shanghai, China.
Ying WangDepartment of Central Laboratory, Gongli Hospital, Naval Medical University, Shanghai, 200135, China.
Miao LiLiver Cancer Institute & Zhong Shan Hospital, Fudan University, Shanghai, 200032, China.
Hui WangYuxi Biotechnology, Shanghai co., Ltd, Shanghai, 201615, China.
Xin YinLiver Cancer Institute & Zhong Shan Hospital, Fudan University, Shanghai, 200032, China. yin.xin@zs-hospital.sh.cn.
Xiangqi LiDepartment of Endocrinology and Metabolism, Gongli Hospital, Naval Medical University, 200135, Shanghai, China. lixq@sibs.ac.cn.
Shanghai Pudong New Area Gongli Hospital · CNFudan University · CNPunan Hospital · CNSecond Military Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEmerging evidence indicates that circular RNAs (circRNAs) and m

methodsA novel hsa_circ_0017114 (circGPR137B) was identified from three pairs of primary HCC and adjacent normal tissues by circRNA expression profiling. The association of circGPR137B and miR-4739 with clinicopathological parameters and prognosis in patients with HCC was analyzed by RT-qPCR, fluorescence in situ hybridization and TCGA cohorts. The role of circGPR137B in HCC was estimated in vitro and in vivo. RT-qPCR, western blot, m

resultsWe identified a new dramatically downregulated circGPR137B in HCC tissues, and found that downregulation of circGPR137B or upregulation of miR-4739 was associated with poor prognosis in patients with HCC. Ectopic expression of circGPR137B strikingly repressed the proliferation, colony formation and invasion, whereas knockdown of circGPR137B harbored the opposite effects. Moreover, restored expression of circGPR137B inhibited tumor growth and lung metastasis in vivo. Further investigations showed that circGPR137B, co-localized with miR-4739 in the cytoplasm, acted as a sponge for miR-4739 to upregulate its target FTO, which mediated m

conclusionOur results demonstrate that circGPR137B inhibits HCC tumorigenesis and metastasis through the circGPR137B/miR-4739/FTO feedback loop. This positive feedback mechanism executed by functional coupling between a circRNA sponge and an m

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsMicroRNAsAlpha-Ketoglutarate-Dependent Dioxygenase FTOCarcinogenesisCell Line, TumorCell ProliferationCell Transformation, NeoplasticFeedbackGene Expression Regulation, NeoplasticHumansIn Situ Hybridization, FluorescenceRNA, CircularAlpha-Ketoglutarate-Dependent Dioxygenase FTOFTO protein, humanMicroRNAsRNA, CircularCircGPR137BDemethylationFTOHepatocellular carcinomam6AmiR-4739

Identifiers

PMID35858900
PMCPMC9297645
OpenAlexW4285988009

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Registered trials

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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.