Evidence map›Paper›PMID 30409062›Full record

ArticleCancer biology & therapy2019

Knockdown of FOXP1 promotes the development of lung adenocarcinoma.

Hua Sheng, Xiangyang Li, Yi Xu

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.0field-weighted citation impact, top 29% 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

23 citing papers in PubMed, 33 citations in OpenAlex.

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  14. Single nucleotide polymorphisms inTranslational lung cancer research · 2022
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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

3 authors at 1 institution in 1 country.

Hua Shenga Department of Pulmonary and Critical Care Medicine, Huadong Hospital, Fudan University , Shanghai , China.
Xiangyang Lia Department of Pulmonary and Critical Care Medicine, Huadong Hospital, Fudan University , Shanghai , China.
Yi Xua Department of Pulmonary and Critical Care Medicine, Huadong Hospital, Fudan University , Shanghai , China.
Huadong Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer is one of the most common cancers in the world, which accounts for about 27% of all cancer deaths. However, the mechanisms underlying the pathogenesis of lung cancer cells remain largely elusive. In this study, we examined the role of the Forkhead box protein P1 (FOXP1) in lung cancer development. Our Oncomine analysis shows that FOXP1 is downregulated in lung adenocarcinoma compared with normal lung tissue. Knockdown of FOXP1 promotes the growth and invasion of PC9 and A549 cells by regulating genes of chemokine signaling molecules, including CCR1, ADCY5, GNG7, VAV3, and PLCB1. Simultaneous knockdown of CCR1 and FOXP1 attenuated FOXP1 knockdown-induced increase of lung cancer cell growth. Finally, knockdown of FOXP1 in PC9 cells promotes the tumorigenesis via CCR1 signaling in xenograft mouse model. Taken together, our data suggest that FOXP1 plays important roles in preventing lung adenocarcinoma development via suppressing chemokine signaling pathways.

Indexed as

Gene Expression Regulation, NeoplasticAdenocarcinoma of LungAnimalsApoptosisBiomarkers, TumorCarcinogenesisCell ProliferationFemaleForkhead Transcription FactorsHumansLung NeoplasmsMiceMice, NudeNeoplasm InvasivenessPrognosisReceptors, CCR1Biomarkers, TumorCCR1 protein, humanForkhead Transcription FactorsFOXP1 protein, humanReceptors, CCR1Repressor ProteinsRNA, Small Interferingchemokine signalingFOXP1lung cancerproliferation

Identifiers

PMID30409062
PMCPMC6422458
OpenAlexW2899647343

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.