Evidence map›Paper›PMID 25880371›Full record

ArticleCancer biology & therapy2015

Bmi-1 expression modulates non-small cell lung cancer progression.

Dan Xiong, Yunlin Ye, Yujie Fu, Jinglong Wang, Bohua Kuang, Hongbo Wang, Xiumin Wang, Lidong Zu, Gang Xiao, Mingang Hao and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer biology & therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

20 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Lung Cancer Stage Prediction Using Multi-Omics Data.Computational and mathematical methods in medicine · 2022
    Article
  11. Article
  12. New 1,3-Disubstituted Benzo[Molecules (Basel, Switzerland) · 2020
    Article
  13. Article
  14. Article
  15. Article
  16. A novel BMI-1 inhibitor QW24 for the treatment of stem-like colorectal cancer.Journal of experimental & clinical cancer research : CR · 2019
    Article
  17. Article
  18. Article
  19. Article
  20. Expression of microRNA-452 via adenoviral vector inhibits non-small cell lung cancer cells proliferation and metastasis.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
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

11 authors at 3 institutions in 2 countries.

Dan Xionga Department of Biochemistry and Molecular & Cell Biology; Shanghai Key Laboratory of Tumor Microenvironment and Inflammation ; Shanghai Jiaotong University School of Medicine ; Shanghai , PR China.
Yunlin Ye
Yujie Fu
Jinglong Wang
Bohua Kuang
Hongbo Wang
Xiumin Wang
Lidong Zu
Gang Xiao
Mingang Hao
Jianhua Wang
Shanghai Jiao Tong University · CNSun Yat-sen University · CNRenji Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous studies indicate that the role of B lymphoma Mo-MLV insertion region 1 homolog (Bmi-1) is responsible for multiple cancer progression. However, Bmi-1 in controlling gene expression in non-small cell lung cancer (NSCLC) development is not well explored. Here we report that the Bmi-1 level is highly increased in primary NSCLC tissues compared to matched adjacent non-cancerous tissues and required for lung tumor growth in xenograft model. Furthermore, we also demonstrate that Bmi-1 level is lower in matched involved lymph node cancerous tissues than the respective primary NSCLC tissues. We find that Bmi-1 does not affect cell cycle and apoptosis in lung cancer cell lines as it does not affect the expression of p16/p19, Pten, AKT and P-AKT. Mechanistic analyses note that reduction of Bmi-1 expression inversely regulates invasion and metastasis of NSCLC cells in vitro and in vivo, followed by induction of epithelial-mesenchymal transition (EMT). Using genome microarray assays, we find that RNAi-mediated silence of Bmi-1 modulates some important molecular genetics or signaling pathways, potentially associated with NSCLC development. Taken together, our findings disclose for the first time that Bmi-1 level accumulates strongly in early stage and then declines in late stage, which is potentially important for NSCLC cell invasion and metastasis during progression.

Indexed as

AdultAgedAged, 80 and overAnimalsCarcinoma, Non-Small-Cell LungCell Line, TumorDisease ProgressionEpithelial-Mesenchymal TransitionHumansLung NeoplasmsMiceMice, Inbred BALB CMice, NudeMicroarray AnalysisMiddle AgedPolycomb Repressive Complex 1BMI1 protein, humanPolycomb Repressive Complex 1Bmi-1Bmi-1, B lymphoma Mo-MLV insertion region 1 homologEMTEMT, epithelial-mesenchymal transitionFBS, fetal calf serumIHC, immunohistochemistryinvasionmetastasisNSCLCNSCLC, non-small cell lung cancerprogressionqRT-PCR, quantitative real-time PCR.

Identifiers

PMID25880371
PMCPMC4622534
OpenAlexW1569049710

What OpenQuestion holds

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Read underepoch 390

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.