Evidence map›Paper›PMID 27670699›Full record

ArticleCell research2016

Identification of TRA2B-DNAH5 fusion as a novel oncogenic driver in human lung squamous cell carcinoma.

Fei Li, Zhaoyuan Fang, Jian Zhang, Chen Li, Hongyan Liu, Jufeng Xia, Hongwen Zhu, Chenchen Guo, Zhen Qin, Fuming Li and 12 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

20 citing papers in PubMed, 31 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

22 authors at 7 institutions in 2 countries.

Fei LiKey Laboratory of Systems Biology, Shanghai 200031, China.
Zhaoyuan FangKey Laboratory of Computational Biology, CAS-MPG Partner Institute for Computational Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.
Jian ZhangKey Laboratory of Systems Biology, Shanghai 200031, China.
Chen LiKey Laboratory of Systems Biology, Shanghai 200031, China.
Hongyan LiuKey Laboratory of Systems Biology, Shanghai 200031, China.
Jufeng XiaKey Laboratory of Systems Biology, Shanghai 200031, China.
Hongwen ZhuKey Laboratory of Systems Biology, Shanghai 200031, China.
Chenchen GuoKey Laboratory of Systems Biology, Shanghai 200031, China.
Zhen QinKey Laboratory of Systems Biology, Shanghai 200031, China.
Fuming LiKey Laboratory of Systems Biology, Shanghai 200031, China.
Xiangkun HanKey Laboratory of Systems Biology, Shanghai 200031, China.
Yuetong WangKey Laboratory of Systems Biology, Shanghai 200031, China.
Yan FengKey Laboratory of Systems Biology, Shanghai 200031, China.
Ye WangKey Laboratory of Systems Biology, Shanghai 200031, China.
Wenjing ZhangKey Laboratory of Systems Biology, Shanghai 200031, China.
Zuoyun WangKey Laboratory of Systems Biology, Shanghai 200031, China.
Yujuan JinKey Laboratory of Systems Biology, Shanghai 200031, China.
Yihua SunDepartment of Thoracic Surgery, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Wenyi WeiDepartment of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115, USA.
Rong ZengKey Laboratory of Systems Biology, Shanghai 200031, China.
Haiquan ChenDepartment of Thoracic Surgery, Fudan University Shanghai Cancer Center, Shanghai 200032, China.
Hongbin JiKey Laboratory of Systems Biology, Shanghai 200031, China.
Center for Excellence in Molecular Cell Science · CNUniversity of Chinese Academy of Sciences · CNChinese Academy of Sciences · CNFudan University Shanghai Cancer Center · CNHarvard University · USShanghai Medical College of Fudan University · CNShanghaiTech University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung squamous cell carcinoma (SCC) is one of the major subtypes of lung cancer. Our current knowledge of oncogenic drivers in this specific subtype of lung cancer is largely limited compared with lung adenocarcinoma (ADC). Through exon array analyses, molecular analyses and functional studies, we here identify the TRA2B-DNAH5 fusion as a novel oncogenic driver in lung SCC. We found that this gene fusion occurs exclusively in lung SCC (3.1%, 5/163), but not in lung ADC (0/119). Through mechanistic studies, we further revealed that this TRA2B-DNAH5 fusion promotes lung SCC malignant progression through regulating a SIRT6-ERK1/2-MMP1 signaling axis. We show that inhibition of ERK1/2 activation using selumetinib efficiently inhibits the growth of lung SCC with TRA2B-DNAH5 fusion expression. These findings improve our current knowledge of oncogenic drivers in lung SCC and provide a potential therapeutic strategy for lung SCC patients with TRA2B-DNAH5 fusion.

Indexed as

AnimalsAxonemal DyneinsBenzimidazolesCarcinoma, Squamous CellCell LineCell ProliferationGene FusionHumansIntracellular Signaling Peptides and ProteinsLung NeoplasmsMatrix Metalloproteinase 1MiceMice, NudeMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Nerve Tissue ProteinsAxonemal DyneinsAZD 6244BenzimidazolesDNAH5 protein, humanIntracellular Signaling Peptides and ProteinsMatrix Metalloproteinase 1Mitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Nerve Tissue ProteinsOncogene Proteins, FusionRIN1 protein, humanSerine-Arginine Splicing FactorsSIRT6 protein, humanSirtuinsT-Lymphoma Invasion and Metastasis-inducing Protein 1TRA2B protein, human

Identifiers

PMID27670699
PMCPMC5113306
OpenAlexW2525102755

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.