Evidence map›Paper›PMID 32198183›Full record

ArticleThe Journal of biological chemistry2020

The FKH domain in FOXP3 mRNA frequently contains mutations in hepatocellular carcinoma that influence the subcellular localization and functions of FOXP3.

Jianwei Ren, Yi Liu, Shanshan Wang, Yu Wang, Wende Li, Siyu Chen, Dexuan Cui, Shengli Yang, Ming-Yue Li, Bo Feng and 2 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

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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 7 institutions in 3 countries.

Jianwei RenDepartment of Surgery, Chinese University of Hong Kong, Hong Kong, China; Shenzhen Research Institute (SZRI), Chinese University of Hong Kong, Shenzhen 518057, China.
Yi LiuDepartment of Surgery, Chinese University of Hong Kong, Hong Kong, China; Guangdong Key Laboratory for Research and Development of Natural Drugs, Guangdong Medical University, Zhanjiang, Guangdong 524023, China.
Shanshan WangSchool of Life Sciences and Biopharmaceutics, Guangdong Pharmaceutical University, Guangzhou 510006, China.
Yu WangDivision of Cellular & Molecular Research, National Cancer Centre, Singapore 169610.
Wende LiGuangdong Laboratory Animals Monitoring Institute, Guangzhou 510663, China.
Siyu ChenGuangdong Laboratory Animals Monitoring Institute, Guangzhou 510663, China.
Dexuan CuiSchool of Biomedical Sciences, Chinese University of Hong Kong, Hong Kong, China.
Shengli YangUnion Hospital Tumour Center, Wuhan 430022, China.
Ming-Yue LiDepartment of Surgery, Chinese University of Hong Kong, Hong Kong, China; Guangzhou Regenerative Medicine and Health Guangdong Laboratory, Guangzhou 510320, China.
Bo FengSchool of Biomedical Sciences, Chinese University of Hong Kong, Hong Kong, China.
Paul B S LaiDepartment of Surgery, Chinese University of Hong Kong, Hong Kong, China. Electronic address: paullai@surgery.cuhk.edu.hk.
George G ChenDepartment of Surgery, Chinese University of Hong Kong, Hong Kong, China; Shenzhen Research Institute (SZRI), Chinese University of Hong Kong, Shenzhen 518057, China; Guangdong Key Laboratory for Research and Development of Natural Drugs, Guangdong Medical University, Zhanjiang, Guangdong 524023, China; Department of Otorhinolaryngology, Head and Neck Surgery, Chinese University of Hong Kong, Hong Kong, China. Electronic address: gchen@cuhk.edu.hk.
Chinese University of Hong Kong · HKGuangdong Laboratory Animals Monitoring Institute · CNGuangdong Medical College · CNGuangdong Pharmaceutical University · CNGuangzhou University of Chinese Medicine · CNNational Cancer Centre Singapore · SGUnion Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transcription factor forkhead box P3 (FOXP3) is a biomarker for regulatory T cells and can also be expressed in cancer cells, but its function in cancer appears to be divergent. The role of hepatocyte-expressed FOXP3 in hepatocellular carcinoma (HCC) is unknown. Here, we collected tumor samples and clinical information from 115 HCC patients and used five human cancer cell lines. We examined

Indexed as

MutationActive Transport, Cell NucleusAnimalsCarcinoma, HepatocellularCell NucleusFemaleForkhead Transcription FactorsHepatocytesHumansLiver NeoplasmsMaleMCF-7 CellsMiceMice, SCIDMiddle AgedProtein DomainsForkhead Transcription FactorsFOXP3 protein, humanRNA, MessengerFKH domainforkhead box P3 (FOXP3)gene transcriptionhepatocellular carcinoma (HCC)liver cancermutagenesismutationssignal transductionsubcellular locationsuppressiontranscriptional mutagenesistranscription factortranslocationtumor suppressor

Identifiers

PMID32198183
PMCPMC7170510
OpenAlexW3010994153

What OpenQuestion holds

Textmetadata
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.