Evidence map›Paper›PMID 26622824›Full record

ArticleOncology letters2015

BRD4 induces cell migration and invasion in HCC cells through MMP-2 and MMP-9 activation mediated by the Sonic hedgehog signaling pathway.

Yong-Hui Wang, Xiao-Mei Sui, Ya-Na Sui, Qin-Wei Zhu, Kai Yan, Li-Shan Wang, Fei Wang, Jia-Hua Zhou

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.3field-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

35 citing papers in PubMed, 71 citations in OpenAlex.

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  4. Practical immunomodulatory landscape of glioblastoma multiforme (GBM) therapy.Journal of the Egyptian National Cancer Institute · 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

8 authors at 3 institutions in 1 country.

Yong-Hui WangDepartment of General Surgery, The Affiliated Zhongda Hospital, Medical School, Southeast University, Nanjing 210096, P.R. China.
Xiao-Mei SuiRadiotherapy Department of Affiliated Hospital of Weifang Medical University, Weifang, Shandong 261000, P.R. China.
Ya-Na SuiEmergency Department of Weifang Traditional Chinese Hospital, Weifang, Shandong 261041, P.R. China.
Qin-Wei ZhuEmergency Department of Weifang Traditional Chinese Hospital, Weifang, Shandong 261041, P.R. China.
Kai YanDepartment of General Surgery, The Affiliated Zhongda Hospital, Medical School, Southeast University, Nanjing 210096, P.R. China.
Li-Shan WangDepartment of General Surgery, The Affiliated Zhongda Hospital, Medical School, Southeast University, Nanjing 210096, P.R. China.
Fei WangDepartment of Hematology and Oncology (Key Department of Jiangsu Medicine), Medical School, Zhongda Hospital, Southeast University, Nanjing 210096, P.R. China.
Jia-Hua ZhouDepartment of General Surgery, The Affiliated Zhongda Hospital, Medical School, Southeast University, Nanjing 210096, P.R. China.
Zhongda Hospital Southeast University · CNWeifang Chinese Medicine Hospital · CNWeifang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is a highly aggressive form of carcinoma with poor prognosis, and HCC-associated mortality primarily occurs due to migration and invasion of HCC cells. The manipulation of epigenetic proteins, such as BRD4, has recently emerged as an alternative therapeutic strategy. The present study aimed to investigate the novel mechanism of BRD4 involvement in the migration and invasion of HCC cells. Reverse transcription-quantitative polymerase chain reaction was used to assess BRD4 mRNA expression levels in HCC cell lines. This analysis demonstrated that BRD4 was significantly overexpressed in HCC cell lines compared with a human immortalized normal liver cell line. A short hairpin RNA (shRNA) was then used to suppress BRD4 expression in HCC cells, and resulted in impaired HCC cell proliferation, migration and invasion. When the HepG2 HCC cell line was treated with recombinant human sonic hedgehog (SHH) peptide, the migration and invasion capabilities of HepG2 cells that were inhibited by BRD4 silencing were restored. BRD4 induced cell migration and invasion in HepG2 cells through the activation of matrix metalloproteinase (MMP)-2 and MMP-9, mediated by the SHH signaling pathway. Taken together, the results of the present study demonstrated the importance of BRD4 in HCC cell proliferation and metastasis. Thus, BRD4 is a potential novel target for the development of therapeutic approaches against HCC.

Indexed as

BRD4hepatocellular carcinomamatrix metalloproteinasemigration and invasionsonic hedgehog pathway

Identifiers

PMID26622824
PMCPMC4579919
OpenAlexW2147067540

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.