Evidence map›Paper›PMID 25877751›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2015

JARID1B modulates lung cancer cell proliferation and invasion by regulating p53 expression.

Xudong Shen, Zhixiang Zhuang, Yusong Zhang, Zhigang Chen, Liqin Shen, Wangyang Pu, Lei Chen, Zhonghua Xu

Abstract read
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In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2015. 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
1.8field-weighted citation impact, top 15% 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, 35 citations in OpenAlex.

  1. Review
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  14. Prognostic value of elevated KDM5B expression in patients with laryngeal squamous cell carcinoma.International journal of clinical and experimental pathology · 2019
    Article
  15. Article
  16. Review
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  18. JARID1B modulates breast cancer cell apoptosis by regulating p53 expression.International journal of clinical and experimental pathology · 2018
    Article
  19. Article
  20. 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

8 authors at 2 institutions in 1 country.

Xudong ShenDepartment of Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Zhixiang ZhuangDepartment of Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Yusong ZhangDepartment of Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Zhigang ChenDepartment of Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Liqin ShenDepartment of Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Wangyang PuDepartment of Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Lei ChenDepartment of Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Zhonghua XuDepartment of Thoracic Surgery, The Second Affiliated Hospital of Soochow University, Suzhou, China. zhonghuaxutg@sina.cn.
Soochow University · CNSecond Affiliated Hospital of Soochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although three therapeutic modalities (surgical resection, chemotherapy, and radiotherapy) have been established, long-term survival for lung cancer patients is still generally poor. Until now, the mechanisms of lung cancer genesis remain elusive. The JARID1B is a histone demethylase that has been proposed as oncogene in several types of human cancer, but its clinical significance and functional role in human non-small cell lung cancer (NSCLC) remain unclear. In present study, we found that JARID1B was overexpressed in lung cancer cell lines and lung cancer tissues but not in normal lung tissues. The proliferation and invasive potential of lung cancer cells was significantly increased by ectopic expression of JARID1B. Contrarily, RNA interference targeting JARID1B in lung cancer cells significantly decreased the proliferation and invasive potential of cells. Moreover, we also found that the expression of p53 was modulated by JARID1B. Overexpressed JARID1B cell exhibited greatly decreased p53 expression, whereas silencing of JARID1B expression dramatically increased p53 expression at both the messenger RNA (mRNA) and protein levels. Inhibition of p53 by small interfering RNA (siRNA) reversed the shJARID1B-induced suppression of proliferation and invasion. Our results collectively suggested that JARID1B expressed in lung cancer played a role in lung cancer cells proliferation and invasion, which may be partly associated with the p53 expression.

Indexed as

AnimalsCarcinogenesisCarcinoma, Non-Small-Cell LungCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHumansJumonji Domain-Containing Histone DemethylasesMiceNeoplasm InvasivenessNuclear ProteinsRepressor ProteinsRNA InterferenceTumor Suppressor Protein p53Xenograft Model Antitumor AssaysJumonji Domain-Containing Histone DemethylasesKDM5B protein, humanNuclear ProteinsRepressor ProteinsTP53 protein, humanTumor Suppressor Protein p53InvasionJARID1BLung cancerp53Proliferation

Identifiers

PMID25877751
OpenAlexW2054133150

What OpenQuestion holds

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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.