Evidence map›Paper›PMID 25126166›Full record

ArticleInternational journal of clinical and experimental medicine2014

FRAS1 knockdown reduces A549 cells migration and invasion through downregulation of FAK signaling.

Qiong Zhan, Ruo-Fan Huang, Xiao-Hua Liang, Meng-Xi Ge, Jing-Wei Jiang, Hao Lin, Xin-Li Zhou

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.2field-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

18 citing papers in PubMed, 24 citations in OpenAlex.

  1. The therapeutic potential of RNA m(6)A in lung cancer.Cell communication and signaling : CCS · 2024
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  7. Methylation silencing of ULK2 via epithelial-mesenchymal transition causes transformation to poorly differentiated gastric cancers.Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association · 2022
    Article
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  9. Frontiers in genetics · 2022
    Article
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  12. Article
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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

7 authors at 1 institution in 1 country.

Qiong ZhanDepartment of Oncology, Huashan Hospital, Fudan University Shanghai, China.
Ruo-Fan HuangDepartment of Oncology, Huashan Hospital, Fudan University Shanghai, China.
Xiao-Hua LiangDepartment of Oncology, Huashan Hospital, Fudan University Shanghai, China.
Meng-Xi GeDepartment of Oncology, Huashan Hospital, Fudan University Shanghai, China.
Jing-Wei JiangDepartment of Oncology, Huashan Hospital, Fudan University Shanghai, China.
Hao LinDepartment of Oncology, Huashan Hospital North, Fudan University Shanghai, China.
Xin-Li ZhouDepartment of Oncology, Huashan Hospital, Fudan University Shanghai, China.
Huashan Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Distal metastasis is the major cause of death for the vast majority of lung cancer patients. Many extracellular matrix (ECM)-related molecules are proposed to be associated with the migration and invasion of cancer cells. FRAS1 encodes an ECM protein, however, little is known about its function on tumorigenesis and metastasis of lung cancer. In this work, FRAS1 was silenced by shRNA in non-small cell lung cancer (NSCLC) A549 cell line. The capacities of A549 cells to migrate and invade were decreased markedly after FRAS1 knockdown. The shRNA knockdown of FRAS1 was found to be specific and had no effect on A549 cells proliferation. Western blot experiments demonstrated that FRAS1 knockdown inhibited FAK signaling but not Src signaling. Overall, we found that FRAS1 knockdown reduces A549 cells migration and invasion ability through downregulation of FAK signaling.

Indexed as

FAK signalingFRAS1Lung cancer metastasismigration and invasion

Identifiers

PMID25126166
PMCPMC4132130
OpenAlexW1421924677

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.