Evidence map›Paper›PMID 25628935›Full record

ArticleAmerican journal of cancer research2015

BCL6 is a negative prognostic factor and exhibits pro-oncogenic activity in ovarian cancer.

Yi-Qin Wang, Mi-Die Xu, Wei-Wei Weng, Ping Wei, Yu-Si Yang, Xiang Du

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

31 citing papers in PubMed, 48 citations in OpenAlex.

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  14. Overexpression ofOncoTargets and therapy · 2022
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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

6 authors at 1 institution in 1 country.

Yi-Qin WangDepartment of Pathology, Fudan University Shanghai Cancer Center Shanghai, 200032, China ; Department of Oncology, Fudan University Shanghai Cancer Center Shanghai, 200032, China ; Institute of Pathology, Fudan University Shanghai 200032, China ; Institute of Biomedical Sciences, Fudan University Shanghai, 200032, China ; Department of Pathology, Obstetrics and Gynecology Hospital of Fudan University Shanghai, 200032, China ; Department of Pathology, Shanghai Medical College, Fudan University Shanghai, 200032, China.
Mi-Die XuDepartment of Pathology, Fudan University Shanghai Cancer Center Shanghai, 200032, China ; Department of Oncology, Fudan University Shanghai Cancer Center Shanghai, 200032, China ; Institute of Pathology, Fudan University Shanghai 200032, China ; Institute of Biomedical Sciences, Fudan University Shanghai, 200032, China.
Wei-Wei WengDepartment of Pathology, Fudan University Shanghai Cancer Center Shanghai, 200032, China ; Department of Oncology, Fudan University Shanghai Cancer Center Shanghai, 200032, China ; Institute of Pathology, Fudan University Shanghai 200032, China ; Institute of Biomedical Sciences, Fudan University Shanghai, 200032, China.
Ping WeiDepartment of Pathology, Fudan University Shanghai Cancer Center Shanghai, 200032, China ; Department of Oncology, Fudan University Shanghai Cancer Center Shanghai, 200032, China ; Institute of Pathology, Fudan University Shanghai 200032, China ; Institute of Biomedical Sciences, Fudan University Shanghai, 200032, China.
Yu-Si YangDepartment of Pathology, Fudan University Shanghai Cancer Center Shanghai, 200032, China ; Department of Oncology, Fudan University Shanghai Cancer Center Shanghai, 200032, China ; Institute of Pathology, Fudan University Shanghai 200032, China ; Institute of Biomedical Sciences, Fudan University Shanghai, 200032, China.
Xiang DuDepartment of Pathology, Fudan University Shanghai Cancer Center Shanghai, 200032, China ; Department of Oncology, Fudan University Shanghai Cancer Center Shanghai, 200032, China ; Institute of Pathology, Fudan University Shanghai 200032, China ; Institute of Biomedical Sciences, Fudan University Shanghai, 200032, China.
Fudan University Shanghai Cancer Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDysregulation of BCL6 plays critical oncogenic roles and facilitates tumorigenesis in various malignancies. However, whether the aberrant expression of BCL6 in ovarian carcinoma is associated with malignancy, metastasis or prognosis remains unknown. Our study aimed to investigate the expression of BCL6 in ovarian carcinoma and its possible correlation with clinicopathological features as well as patient survival to reveal its biological effects in ovarian tumor progression.

methodsImmunochemistry analysis was performed in 105 cases of ovarian carcinoma covering the histological types of serous, endometrioid and clear cell. Spearman analysis was used to calculate the correlation between pathological parameters and the expression of BCL6. Kaplan-Meier method and Cox proportional hazards analysis were used to analyze the disease-specific survival (DSS) and disease-free survival (DFS). We also assessed whether overexpression and knockdown of BCL6 influence in vitro cell proliferation, cell cycle progression, as well as tumor cell invasion and migration.

resultsThe expression of BCL6 was higher in all three major kinds of ovarian cancer in comparison with paratumorous epithelium. BCL6 expression was tightly correlated with FIGO staging, lymph node metastasis and recurrence. Higher expression of BCL6 led to a significantly poorer DSS and DFS and multivariate analysis revealed that BCL6 was an independent risk factor of DSS and DFS. Enforced overexpression of BCL6 in ovarian tumor cells stimulated proliferation by inducing G1-S transition, and promoted tumor cell invasion and migration. Conversely, RNA interference-mediated silencing BCL6 expression inhibited proliferation by altered cell cycle progression and reduced the ability of the cells to migrate, and invade the extracellular matrix in culture.

conclusionsOur study suggests that the inappropriate activation of BCL6 predicts poor prognosis and promotes tumor progression in ovarian carcinoma. Targeting BCL6 could be a novel therapeutic choice for treating ovarian carcinoma patients.

Indexed as

BCL6invasionovarian carcinomaprognosisproliferation

Identifiers

PMID25628935
PMCPMC4300693
OpenAlexW1516923698

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.