Evidence map›Paper›PMID 25970780›Full record

ArticleOncotarget2015

BCL6B expression in hepatocellular carcinoma and its efficacy in the inhibition of liver damage and fibrogenesis.

Weilin Wang, Pengfei Huang, Panyisha Wu, Rong Kong, Jiang Xu, Lufei Zhang, Qifan Yang, Qingsong Xie, Linshi Zhang, Xiaohu Zhou and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

13 citing papers in PubMed, 19 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

14 authors at 1 institution in 1 country.

Weilin WangKey Lab of Combined Multi-Organ Transplantation, Ministry of Public Health, Hangzhou 310003, China.
Pengfei HuangKey Lab of Combined Multi-Organ Transplantation, Ministry of Public Health, Hangzhou 310003, China.
Panyisha WuDivision of Hepatobiliary and Pancreatic Surgery, Department of Surgery, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China.
Rong KongKey Lab of Combined Multi-Organ Transplantation, Ministry of Public Health, Hangzhou 310003, China.
Jiang XuKey Lab of Combined Multi-Organ Transplantation, Ministry of Public Health, Hangzhou 310003, China.
Lufei ZhangKey Lab of Combined Multi-Organ Transplantation, Ministry of Public Health, Hangzhou 310003, China.
Qifan YangKey Lab of Combined Multi-Organ Transplantation, Ministry of Public Health, Hangzhou 310003, China.
Qingsong XieKey Lab of Combined Multi-Organ Transplantation, Ministry of Public Health, Hangzhou 310003, China.
Linshi ZhangDivision of Hepatobiliary and Pancreatic Surgery, Department of Surgery, First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310003, China.
Xiaohu ZhouKey Lab of Combined Multi-Organ Transplantation, Ministry of Public Health, Hangzhou 310003, China.
Linghui ChenKey Lab of Combined Multi-Organ Transplantation, Ministry of Public Health, Hangzhou 310003, China.
Haiyang XieKey Lab of Combined Multi-Organ Transplantation, Ministry of Public Health, Hangzhou 310003, China.
Lin ZhouKey Lab of Combined Multi-Organ Transplantation, Ministry of Public Health, Hangzhou 310003, China.
Shusen ZhengKey Lab of Combined Multi-Organ Transplantation, Ministry of Public Health, Hangzhou 310003, China.
First Affiliated Hospital Zhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

B cell CLL/lymphoma 6 member B (BCL6B) is expressed in many normal tissues but expressed at very low levels in cancer tissues. It was reported that BCL6B inhibits hepatocellular carcinoma (HCC) metastases, but the exact role of BCL6B in HCC remains to be investigated. BCL6B expression was significantly decreased in HCC tissues compared with paired non-cancer tissues. Low BCL6B expression in tumors was correlated with shorter overall survival in patients, and multivariate Cox regression analysis revealed that BCL6B expression was an independent prognostic factor for human HCC patients. Moreover, a positive correlation between BCL6B expression and hepatic cirrhosis was found in an analysis of HCC clinicopathological characteristics. BCL6B expression was increased in rat fibrotic liver samples in response to liver injury. BCL6B transgenic rats were less susceptible to hepatocellular damage, inflammation and fibrosis. In vitro studies demonstrated that BCL6B inhibited the activation of hepatic stellate cells though upregulation of hepatocyte growth factor. In addition, transcriptomic microarray analysis was performed to explore the mechanisms in which BCL6B confers protection from tumorigenesis. In conclusion, BCL6B plays a pivotal role as a prognostic biomarker for HCC, and the restoration of BCL6B may be a novel strategy as an anti-fibrogenic therapy for human HCC.

Indexed as

AnimalsCarcinoma, HepatocellularFemaleHumansLiver CirrhosisLiver NeoplasmsMaleMiddle AgedPrognosisRatsRats, Sprague-DawleyRepressor ProteinsBCL6B protein, humanRepressor ProteinsBCL6Bhepatocellular carcinomaliver fibrosisprognostic biomarker

Identifiers

PMID25970780
PMCPMC4653002
OpenAlexW1884430658

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.