Evidence map›Paper›PMID 29151932›Full record

ArticleJournal of Cancer2017

Restoration of KLF4 Inhibits Invasion and Metastases of Lung Adenocarcinoma through Suppressing MMP2.

Shaoli Li, Lixia Huang, Jincui Gu, Jian Wu, Weijun Ou, Jinglun Feng, Baomo Liu, Xiaoxian Xu, Yanbin Zhou

Open access · goldAbstract read
In one paragraph

Article in Journal of Cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

17 citing papers in PubMed, 25 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

9 authors at 2 institutions in 1 country.

Shaoli LiDepartment of Respiratory Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Lixia HuangDepartment of Respiratory Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Jincui GuDepartment of Respiratory Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Jian WuDepartment of Respiratory Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Weijun OuCenter of Organ Transplantation, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Jinglun FengDepartment of Respiratory Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Baomo LiuDepartment of Respiratory Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Xiaoxian XuDepartment of Respiratory Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Yanbin ZhouDepartment of Respiratory Medicine, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Sun Yat-sen University · CNThe First Affiliated Hospital, Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundKLF4 is a zin-finger transcription factor that plays roles in differentiation, development, and proliferation. Recent studies show that KLF4 is involved in tumorigenesis and somatic cells reprogramming. Metastasis is the primary cause of death in patients with lung cancer, and its biological mechanisms are poorly understood. GOALS: In this study, we aim to explore the expression pattern and biological function of KLF4 in lung adenocarcinoma.

methodsWe determined KLF4 in lung adenocarcinoma tissue and cell lines, using immunohistochemistry and western blotting. And we further analyzed the correlation between KLF4 expression and clinicopathologic parameters. We restored KLF4 expression and studied its effect on lung adenocarcinoma cells in vivo and in vitro. Luciferase assay was used to study impact of KLF4 on activity of MMP2 promoter.

resultsKLF4 is dramatically down-regulated in lung adenocarcinoma tissue and cell lines. Promoter methylation contributes to the down-regulation of KLF4. Down-regulation of KLF4 in lung adenocarcinoma tissue is significantly associated with reduced survival time. Restoration of KLF4 inhibits migration and invasion of lung adenocarcinoma cells in vitro. Metastases to lungs significantly decrease in mice intravenously injected with tumor cells overexpressing KLF4. KLF4 inhibits invasion and metastasis via suppressing MMP2 promoter activity.

conclusionThe ability of KLF4 to inhibit migration, invasion, and metastasis of lung tumor cells indicates a potential role of KLF4 as therapeutic target in lung adenocarcinoma. KLF4 might be utilized as a favorable biomarker for prognosis of lung adenocarcinoma patients.

Indexed as

GKLFInvasionKrüppel-like factorMetastasisMMP2

Identifiers

PMID29151932
PMCPMC5687162
OpenAlexW2765149288

What OpenQuestion holds

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LicenceCC BY-NC
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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.