Evidence map›Paper›PMID 26676638›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

Overexpression of the transcription factor FOXP3 in lung adenocarcinoma sustains malignant character by promoting G1/S transition gene CCND1.

Yinan Li, Dong Li, Wei Yang, Haiying Fu, Yaqing Liu, Yi Li

Abstract read
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In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 24% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Identification of Key Transcription Factors Associated with Lung Squamous Cell Carcinoma.Medical science monitor : international medical journal of experimental and clinical research · 2017
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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 2 institutions in 1 country.

Yinan LiDepartment of Immunology, College of Basic Medical Science, Jilin University, Changchun, 130021, China.
Dong LiDepartment of Immunology, College of Basic Medical Science, Jilin University, Changchun, 130021, China.
Wei YangDepartment of Immunology, College of Basic Medical Science, Jilin University, Changchun, 130021, China.
Haiying FuDepartment of Immunology, College of Basic Medical Science, Jilin University, Changchun, 130021, China.
Yaqing LiuDepartment of Immunology, College of Basic Medical Science, Jilin University, Changchun, 130021, China.
Yi LiDepartment of Immunology, College of Basic Medical Science, Jilin University, Changchun, 130021, China. liyi@jlu.edu.cn.
Jilin University · CNJilin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Forkhead box P3 (FOXP3) transcription factor is the key driver of the differentiation and immunosuppressive function of regulatory T cells (Tregs). Additionally, FOXP3 has been reported to be expressed in many solid tumor cell lines and tissues. However, its role in tumorigenesis and tumor progression is conflicting, both tumor suppressive and promoting functions have been described. In this study, we demonstrated that FOXP3 was expressed in both lung adenocarcinoma tissues and the lung adenocarcinoma cell line A549. FOXP3 inhibition decreased cell proliferation, migration, and invasion as well as the secretion of inhibitory cytokines (e.g., transforming growth factor beta 1 (TGF-β1), interleukin 35 (IL-35), and heme oxygenase-1 (HMOX1)), suggesting a positive role for FOXP3 in tumor development. Importantly, we found that FOXP3 could enhance lung adenocarcinoma cell proliferation via upregulating the levels of the cell cycle G1/S checkpoint gene CCND1. These data demonstrated that FOXP3 could be regarded as a novel therapeutic target for inhibiting lung adenocarcinoma progression.

Indexed as

Gene Expression Regulation, NeoplasticA549 CellsAdenocarcinomaCarcinoma, Non-Small-Cell LungCell DivisionCyclin D1CytokinesForkhead Transcription FactorsG1 Phase Cell Cycle CheckpointsHumansLung NeoplasmsNeoplasm InvasivenessNeoplasm ProteinsRNA InterferenceRNA, NeoplasmRNA, Small InterferingCCND1 protein, humanCyclin D1CytokinesForkhead Transcription FactorsFOXP3 protein, humanNeoplasm ProteinsRNA, NeoplasmRNA, Small InterferingCCND1Cell proliferationFOXP3Lung adenocarcinoma

Identifiers

PMID26676638
OpenAlexW2199210770

What OpenQuestion holds

Textmetadata
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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.