Evidence map›Paper›PMID 24272676›Full record

ArticlePathology oncology research : POR2014

NOB1 in non-small-cell lung cancer: expression profile and clinical significance.

Kun Liu, Ming-Ming Gu, Hong-Lin Chen, Qing-Sheng You

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Article in Pathology oncology research : POR, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

5 citing papers in PubMed.

  1. International journal of breast cancer · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Evaluation of NIN/RPN12 binding protein inhibits proliferation and growth in human renal cancer cells.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Article
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Kun LiuDepartment of Cardiothoracic Surgery, Affiliated Hospital of Nantong University, Xi Si Road 20#, Nantong City, Jiangsu Province, 226001, People's Republic of China.
Ming-Ming Gu
Hong-Lin Chen
Qing-Sheng You

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nin one binding (NOB1) gene has been reported up-regulated in several types of cancer. The aim of this study was to investigate the expression profile of NOB1 in non-small-cell lung cancer (NSCLC) and assess the clinical significance. qRT-PCR was used in the detection of NOB1 mRNA expression both in NSCLC tissue and in adjacent normal lung tissue. Western blot analysis and immunohistochemistry were used in the detection of NOB1 protein expression. The clinicopathological implications of NOB1 were analyzed statistically. It was confirmed by RT-qPCR that expression of NOB1 mRNA in NSCLC cells was higher than in human lung cells (P < 0.05), and NOB1 mRNA was also over-expressed in NSCLC tissue when compared with adjacent tissue and normal lung tissue (P < 0.05). Western blot analysis showed that NOB1 protein was significant increased in NSCLC cell lines compared with human lung cell line. Western blot analysis and immunohistochemistry showed that NOB1 protein was significant increased in NSCLC tissue compared with adjacent tissue and normal lung tissue (P < 0.05). There were significant associations between NOB1 expression and TNM stage, lymph node metastasis, and histopathological grade (P < 0.05), but not gender, age, smoke, or tumor diameter (P > 0.05). Our results suggest that enhanced expression of NOB1 gene plays an important role in the occurrence and development of NSCLC. NOB1 may be a potential therapeutic target in NSCLC.

Indexed as

Carcinoma, Non-Small-Cell LungCell Line, TumorFemaleHumansImmunohistochemistryLung NeoplasmsLymphatic MetastasisMaleMiddle AgedNuclear ProteinsRNA-Binding ProteinsRNA, MessengerTranscriptomeNOB1 protein, humanNuclear ProteinsRNA-Binding ProteinsRNA, Messenger

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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.