Evidence map›Paper›PMID 29717200›Full record

ArticleBritish journal of cancer2018

Chemerin suppresses hepatocellular carcinoma metastasis through CMKLR1-PTEN-Akt axis.

Jing-Jing Li, Hong-Kun Yin, Dong-Xian Guan, Jiang-Sha Zhao, Yu-Xiong Feng, Yue-Zhen Deng, Xiang Wang, Nan Li, Xiao-Fan Wang, Shu-Qun Cheng and 2 more

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
3.1field-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

50 citing papers in PubMed, 1 synthesis or guideline pooled it, 70 citations in OpenAlex.

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  9. Survival disparities among racial groups with hepatic malignant tumors.World journal of gastrointestinal oncology · 2024
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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

12 authors at 5 institutions in 2 countries.

Jing-Jing LiKey Laboratory of Nutrition, Metabolism and Food Safety, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 320 Yueyang Road, Shanghai, 200031, China.
Hong-Kun YinKey Laboratory of Nutrition, Metabolism and Food Safety, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 320 Yueyang Road, Shanghai, 200031, China.
Dong-Xian GuanKey Laboratory of Nutrition, Metabolism and Food Safety, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 320 Yueyang Road, Shanghai, 200031, China.
Jiang-Sha ZhaoKey Laboratory of Nutrition, Metabolism and Food Safety, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 320 Yueyang Road, Shanghai, 200031, China.
Yu-Xiong FengKey Laboratory of Nutrition, Metabolism and Food Safety, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 320 Yueyang Road, Shanghai, 200031, China.
Yue-Zhen DengKey Laboratory of Nutrition, Metabolism and Food Safety, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 320 Yueyang Road, Shanghai, 200031, China.
Xiang WangDepartment of Surgery, First People's Hospital Affiliated, Huzhou University, Huzhou, 313000, China.
Nan LiEastern Hepatobililary Surgery Hospital, Second Military Medical University, 225 Changhai Road, Shanghai, 200433, China.
Xiao-Fan WangDepartment of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC, 27710, USA.
Shu-Qun ChengEastern Hepatobililary Surgery Hospital, Second Military Medical University, 225 Changhai Road, Shanghai, 200433, China.
Ying BaoDepartment of Surgery, First People's Hospital Affiliated, Huzhou University, Huzhou, 313000, China. baoying2222@126.com.
Dong XieKey Laboratory of Nutrition, Metabolism and Food Safety, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 320 Yueyang Road, Shanghai, 200031, China. dxie@sibs.ac.cn.
Shanghai Institutes for Biological Sciences · CNHuzhou University · CNChinese Academy of Sciences · CNSecond Military Medical University · CNShanghaiTech University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChemerin, a known chemoattractant, participates in multiple biological events. However, its role in cancer remains largely unknown.

methodsChemerin expression was evaluated by real-time PCR, western blot and immunohistochemistry. Forced expression, RNAi, immunoprecipitation, etc. were used in function and mechanism study. Mouse models of extrahepatic and intrahepatic metastasis were employed to evaluate the therapeutic potential of chemerin.

resultsChemerin expression was significantly downregulated in hepatocellular carcinoma, and associated with poor prognosis of HCC patients. Forced expression of chemerin inhibited in vitro migration, invasion and in vivo metastasis of HCC cells. Administration of chemerin effectively suppressed extrahepatic and intrahepatic metastases of HCC cells, resulting in prolonged survival of tumour-bearing nude mice. Chemerin upregulated expression and phosphatase activity of PTEN by interfering with PTEN-CMKLR1 interaction, leading to weakened ubiquitination of PTEN and decreased p-Akt (Ser473) level, which was responsible for suppressed migration, invasion and metastasis of HCC cells. Positive correlation between chemerin and PTEN, and reverse correlation between chemerin and p-Akt (Ser473) were also observed in HCC clinical samples and intrahepatic mouse model in vivo.

conclusionsOur study has revealed the suppressive role and therapeutic potential of chemerin in HCC metastasis, providing both a prognostic marker and drug candidate for HCC.

Indexed as

AnimalsCarcinoma, HepatocellularCell MovementCell ProliferationChemokinesGene Expression Regulation, NeoplasticHep G2 CellsHumansIntercellular Signaling Peptides and ProteinsLiver NeoplasmsMiceNeoplasm InvasivenessNeoplasm MetastasisOncogene Protein v-aktPTEN PhosphohydrolaseReceptors, ChemokineChemokinesCMKLR1 protein, humanIntercellular Signaling Peptides and ProteinsOncogene Protein v-aktPTEN PhosphohydrolasePTEN protein, humanRARRES2 protein, humanReceptors, Chemokine

Identifiers

PMID29717200
PMCPMC5959946
OpenAlexW2803033229

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.