Evidence map›Paper›PMID 29927028›Full record

ArticleCancer science2018

Resistin facilitates metastasis of lung adenocarcinoma through the TLR4/Src/EGFR/PI3K/NF-κB pathway.

Wei-Jing Gong, Jun-Yan Liu, Ji-Ye Yin, Jia-Jia Cui, Di Xiao, Wei Zhuo, Chao Luo, Rui-Jie Liu, Xi Li, Wei Zhang and 2 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Cancer science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

34 citing papers in PubMed, 54 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Wei-Jing GongDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, China.
Jun-Yan LiuDepartment of orthopaedics, The First Affiliated Hospital of the University of South China, Hengyang, China.
Ji-Ye YinDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, China.
Jia-Jia CuiDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, China.
Di XiaoDepartment of Pharmacy, Xiangya Hospital, Central South University, Changsha, China.
Wei ZhuoDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, China.
Chao LuoDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, China.
Rui-Jie LiuDepartment of Pathology, Xiangya Hospital, Central South University, Changsha, China.
Xi LiDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, China.
Wei ZhangDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, China.ORCID http://orcid.org/0000-0002-6190-3129
Hong-Hao ZhouDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, China.
Zhao-Qian LiuDepartment of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, China.ORCID http://orcid.org/0000-0003-0428-3928
Central South University · CNFirst Affiliated Hospital of University of South China · CNUnion Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metastasis is the main cause of lung cancer-related death. The tumor microenvironment greatly contributes to tumor metastasis. Resistin, mainly secreted by tumor-associated macrophages in tumor tissues, is a 12.5-kDa cysteine-rich secretory protein that is found at significantly higher levels in the serum or plasma of cancer patients compared with healthy controls. In this study, we explored the expression and role of resistin in lung adenocarcinoma. Our study showed that resistin was strongly expressed in lung adenocarcinoma tissues and promoted the migration and invasion of lung adenocarcinoma cells in a dose-dependent manner. Toll-like receptor 4 (TLR4) was the functional receptor of resistin for migration and invasion in A549 cells. Src/epidermal growth factor receptor (EGFR) was involved in resistin-induced migration and invasion. Resistin increased the phosphorylation of EGFR through the TLR4/Src pathway. We also found that PI3K/nuclear factor (NF)-κB were the intracellular downstream effectors mediating resistin-induced migration and invasion. Taken together, our results suggested that resistin promoted lung adenocarcinoma metastasis through the TLR4/Src/EGFR/PI3K/NF-κB pathway.

Indexed as

A549 CellsAdenocarcinomaAdenocarcinoma of LungCell Line, TumorCell MovementErbB ReceptorsHumansLung NeoplasmsNeoplasm MetastasisNF-kappa BPhosphatidylinositol 3-KinasesResistinSignal Transductionsrc-Family KinasesToll-Like Receptor 4U937 CellsEGFR protein, humanErbB ReceptorsNF-kappa BPhosphatidylinositol 3-KinasesResistinsrc-Family KinasesTLR4 protein, humanToll-Like Receptor 4invasionlung adenocarcinomamigrationresistinTLR4

Identifiers

PMID29927028
PMCPMC6113506
OpenAlexW2809610421

What OpenQuestion holds

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Registered trials

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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.