Evidence map›Paper›PMID 30836988›Full record

ArticleJournal of experimental & clinical cancer research : CR2019

Overexpression of RNF38 facilitates TGF-β signaling by Ubiquitinating and degrading AHNAK in hepatocellular carcinoma.

Rui Peng, Peng-Fei Zhang, Xuan Yang, Chuan-Yuan Wei, Xiao-Yong Huang, Jia-Bin Cai, Jia-Cheng Lu, Chao Gao, Hai-Xiang Sun, Qiang Gao and 4 more

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

37 citing papers in PubMed, 69 citations in OpenAlex.

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  9. mInternational journal of oncology · 2024
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  10. E3 ubiquitin ligases in nasopharyngeal carcinoma and implications for therapies.Journal of molecular medicine (Berlin, Germany) · 2023
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  16. A comparative assessment ofInternational journal of reproductive biomedicine · 2022
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  17. Article
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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

14 authors at 4 institutions in 1 country.

Rui PengLiver Cancer Institute, Zhongshan Hospital, Fudan University; Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Ministry of Education, 180 Feng lin Road, Shanghai, 200032, People's Republic of China.
Peng-Fei ZhangLiver Cancer Institute, Zhongshan Hospital, Fudan University; Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Ministry of Education, 180 Feng lin Road, Shanghai, 200032, People's Republic of China.
Xuan YangLiver Cancer Institute, Zhongshan Hospital, Fudan University; Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Ministry of Education, 180 Feng lin Road, Shanghai, 200032, People's Republic of China.
Chuan-Yuan WeiLiver Cancer Institute, Zhongshan Hospital, Fudan University; Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Ministry of Education, 180 Feng lin Road, Shanghai, 200032, People's Republic of China.
Xiao-Yong HuangLiver Cancer Institute, Zhongshan Hospital, Fudan University; Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Ministry of Education, 180 Feng lin Road, Shanghai, 200032, People's Republic of China.
Jia-Bin CaiLiver Cancer Institute, Zhongshan Hospital, Fudan University; Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Ministry of Education, 180 Feng lin Road, Shanghai, 200032, People's Republic of China.
Jia-Cheng LuLiver Cancer Institute, Zhongshan Hospital, Fudan University; Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Ministry of Education, 180 Feng lin Road, Shanghai, 200032, People's Republic of China.
Chao GaoLiver Cancer Institute, Zhongshan Hospital, Fudan University; Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Ministry of Education, 180 Feng lin Road, Shanghai, 200032, People's Republic of China.
Hai-Xiang SunLiver Cancer Institute, Zhongshan Hospital, Fudan University; Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Ministry of Education, 180 Feng lin Road, Shanghai, 200032, People's Republic of China.
Qiang GaoLiver Cancer Institute, Zhongshan Hospital, Fudan University; Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Ministry of Education, 180 Feng lin Road, Shanghai, 200032, People's Republic of China.
Dou-Sheng BaiClinical Medical College, Yangzhou University, Yangzhou, 225009, Jiangsu, China.
Guo-Ming ShiLiver Cancer Institute, Zhongshan Hospital, Fudan University; Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Ministry of Education, 180 Feng lin Road, Shanghai, 200032, People's Republic of China. shi.guoming@zs-hospital.sh.cn.
Ai-Wu KeLiver Cancer Institute, Zhongshan Hospital, Fudan University; Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Ministry of Education, 180 Feng lin Road, Shanghai, 200032, People's Republic of China. ke.aiwu@zs-hospital.sh.cn.
Jia FanLiver Cancer Institute, Zhongshan Hospital, Fudan University; Key Laboratory of Carcinogenesis and Cancer Invasion (Fudan University), Ministry of Education, 180 Feng lin Road, Shanghai, 200032, People's Republic of China. fanjia-zs@hotmail.com.
Fudan University · CNZhongshan Hospital · CNYangzhou University · CNShanghai East Hospital · CN

Funding

Cancer Biology State Key Laboratory Project CBSKL201717National Natural Science Foundation of China 81302100National Natural Science Foundation of China 81472840National Natural Science Foundation of China 81702861National Natural Science Foundation of China 81871909National Natural Science Foundation of China (CN) 81502526National Natural Science Foundation of China (CN) 81672825
6 · The paper itself

Abstract

backgroundRING finger protein 38 (RNF38), a member of the RNF protein family, has just emerged as a vital driver of cancer progression. However, the oncogenic mechanisms of RNF38 remain unexplored.

methodsUsing frozen tumor tissue and tissue microarray from hepatocellular carcinoma (HCC) patients, we tried to probe the expression of RNF38 in HCC and its clinical value. Then the biological functions of RNF38 were analyzed in vivo and vitro. Stable isotope labeling with amino acids (SILAC) in cell culture and co-immunoprecipitation proteomic analyses were combined to reveal the potential mechanism of RNF38 in HCC progression.

resultsWe report that RNF38 expression was markedly higher in HCC tissues than in peritumor tissues. Correspondingly, RNF38 overexpression promoted the HCC cell migration and invasion and inhibited apoptosis both in vitro and in vivo. And elevated RNF38 expression induced HCC cell epithelial-mesenchymal transition by facilitating transforming growth factor-β (TGF-β) signaling via ubiquitinating and degrading neuroblast differentiation-associated protein (AHNAK), a well-established inhibitor of TGF-β signaling. Furthermore, AHNAK interference restored the HCC cell invasion and metastasis deprived by RNF38 downregulation. Clinically, elevated RNF38 and transforming growth factor beta receptor 1 (TGFBR1) expression was related to short overall survival (OS) and high cumulative recurrence rates in HCC patients.

conclusionsHigh levels of RNF38 promote HCC by facilitating TGF-β signaling and are a novel marker for predicting the prognosis of HCC patients and a potential therapeutic target in HCC.

Indexed as

AdultAnimalsCarcinogenesisCarcinoma, HepatocellularCarrier ProteinsDisease-Free SurvivalEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHumansIsotope LabelingLiver NeoplasmsMaleMembrane ProteinsMiceMiddle AgedAHNAK protein, humanCarrier ProteinsMembrane ProteinsNeoplasm ProteinsReceptor, Transforming Growth Factor-beta Type IRNF38 protein, humanTGFBR1 protein, humanTransforming Growth Factor betaUbiquitin-Protein LigasesAHNAKHepatocellular carcinomaPrognosisRNF38TGF-β signaling

Identifiers

PMID30836988
PMCPMC6402116
OpenAlexW2923631155

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.