Evidence map›Paper›PMID 25228009›Full record

ArticleCellular oncology (Dordrecht, Netherlands)2014

Short hairpin RNA-mediated down-regulation of CENP-A attenuates the aggressive phenotype of lung adenocarcinoma cells.

Qing Wu, Yong-Feng Chen, Jie Fu, Qi-Han You, Shou-Mei Wang, Xue Huang, Xiao-Jun Feng, Shu-Hui Zhang

Abstract read
In one paragraph

Article in Cellular oncology (Dordrecht, Netherlands), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 25% 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

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

  1. Pooled it
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  6. CENP-A Regulation and Cancer.Frontiers in cell and developmental biology · 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

8 authors at 5 institutions in 1 country.

Qing WuDepartment of Respiratory Medicine, Guangxing Hospital, Hangzhou Hospital of Traditional Chinese Medicine, Zhejiang University of Traditional Chinese Medicine, Hangzhou, People's Republic of China, qingwuzj@126.com.
Yong-Feng Chen
Jie Fu
Qi-Han You
Shou-Mei Wang
Xue Huang
Xiao-Jun Feng
Shu-Hui Zhang
Shanghai University · CNHangzhou Hospital of Traditional Chinese Medicine · CNMaternal and Child Health Hospital of Xinjiang Uygur Autonomous Region · CNShanghai Jiao Tong University · CNZhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDeregulation of centromere protein (CENP)-A, a centromere-specific histone variant, has in the past been linked to cancer initiation and progression. Additionally, our previous work has shown that CENP-A upregulation predicts a poor overall survival in patients with lung adenocarcinoma. The aim of this study was to uncover the biological role of CENP-A in lung adenocarcinoma growth and invasion, including its underlying molecular mechanisms.

methodsCENP-A expression was knocked down in human lung adenocarcinoma A549 and PC-9 cells using a short hairpin RNA (shRNA) technology. Subsequently, the effects of this knock down on the proliferation, apoptosis, cell cycle progression, colony formation, migration, invasion and tumorigenicity were assessed. Additionally, Western blot analyses were performed to examine concomitant expression changes in key proteins involved in cell cycle regulation and apoptosis.

resultsWe found that shRNA-mediated knock down of CENP-A significantly inhibited the in vitro proliferation and colony formation of A549 and PC-9 cells as compared to control shRNA-transfected cells. In addition, CENP-A down-regulation was found to induce G0/G1 cell cycle arrest and apoptosis, and to inhibit the in vitro migration and invasion of A549 and PC-9 cells. Down-regulation of CENP-A was also found to significantly suppress the in vivo growth of xenografted A549 cells. At the protein level, we found that the expression of p21, p27, CHK2 and Bax was markedly increased and that the expression of CCNG1, Skp2, Cks1 and Bcl-2 was markedly decreased in CENP-A down-regulated cells.

conclusionBased on our results we conclude that down-regulation of CENP-A may attenuate the aggressive phenotype of lung adenocarcinoma cells. As such, CENP-A may serve as a promising therapeutic target for lung adenocarcinoma.

Indexed as

AdenocarcinomaAdenocarcinoma of LungApoptosisAutoantigensbcl-2-Associated X ProteinCDC2-CDC28 KinasesCell Cycle CheckpointsCell Line, TumorCentromere Protein ACheckpoint Kinase 2Chromosomal Proteins, Non-HistoneCyclin-Dependent Kinase Inhibitor p27Cyclin G1HumansLung NeoplasmsProto-Oncogene Proteins c-bcl-2Autoantigensbcl-2-Associated X ProteinCCNG1 protein, humanCDC2-CDC28 KinasesCENPA protein, humanCentromere Protein ACheckpoint Kinase 2CHEK2 protein, humanChromosomal Proteins, Non-HistoneCKS1B protein, humanCyclin-Dependent Kinase Inhibitor p27Cyclin G1Proto-Oncogene Proteins c-bcl-2rho GTP-Binding ProteinsRNA, Small InterferingS-Phase Kinase-Associated Proteins

Identifiers

PMID25228009
PMCPMC13004451
OpenAlexW2010208370

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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.