Evidence map›Paper›PMID 26330328›Full record

ArticleScientific reports2015

High expression of SOX30 is associated with favorable survival in human lung adenocarcinoma.

Fei Han, Wenbin Liu, Hualiang Xiao, Yan Dong, Lei Sun, Chengyi Mao, Li Yin, Xiao Jiang, Lin Ao, Zhihong Cui and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

21 citing papers in PubMed, 29 citations in OpenAlex.

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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

12 authors at 3 institutions in 1 country.

Fei HanInstitute of Toxicology, College of Preventive Medicine, Third Military Medical University.
Wenbin LiuInstitute of Toxicology, College of Preventive Medicine, Third Military Medical University.
Hualiang XiaoDepartment of Pathology, Daping Hospital, Third Military Medical University, Chongqing, China.
Yan DongInstitute of Toxicology, College of Preventive Medicine, Third Military Medical University.
Lei SunInstitute of Toxicology, College of Preventive Medicine, Third Military Medical University.
Chengyi MaoDepartment of Pathology, Daping Hospital, Third Military Medical University, Chongqing, China.
Li YinInstitute of Toxicology, College of Preventive Medicine, Third Military Medical University.
Xiao JiangInstitute of Toxicology, College of Preventive Medicine, Third Military Medical University.
Lin AoInstitute of Toxicology, College of Preventive Medicine, Third Military Medical University.
Zhihong CuiInstitute of Toxicology, College of Preventive Medicine, Third Military Medical University.
Jia CaoInstitute of Toxicology, College of Preventive Medicine, Third Military Medical University.
Jinyi LiuInstitute of Toxicology, College of Preventive Medicine, Third Military Medical University.
Ministry of Education of the People's Republic of China · CNArmy Medical University · CNDaping Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In our previous study, we had identified SOX30 as a novel tumor suppressor that acts through direct regulation of p53 transcription in human lung cancer. Here, we sought to determine the clinical relevance of SOX30 expression in a series of surgically-resected non-small cell lung cancer (NSCLC) patients. Analysis of SOX30 expression and clinico-pathologic features reveal a significant correlation of SOX30 expression with histological type (n = 220, P = 0.008) and clinical stage (n = 220, P = 0.024). Kaplan-Meier analysis indicates an association of high SOX30 expression with better prognosis in NSCLC patients (n = 220, P = 0.007). Via multivariate Cox-regression analysis, SOX30 expression is revealed to be an independent prognostic factor for overall survival (OS) of NSCLC patients (n = 220, P = 0.014, hazard ratio (HR) = 0.816). In particular, SOX30 is a favorable and independent prognostic factor in one main subtype of NSCLC, lung adenocarcinoma (ADC) patients (n = 150, P = 0.000, HR = 0.405), but not in another main subtype of NSCLC, squamous cell carcinoma patients. Furthermore, high expression of SOX30 represents a favorable and independent factor for the prognosis of ADC patients at clinical stage II (P = 0.013), with positive lymph node (P = 0.003), at histological grade 2 (P = 0.000) or grade 3 (P = 0.025). In summary, SOX30 expression represents an important prognostic factor for survival time in ADC patients.

Indexed as

AdenocarcinomaAdenocarcinoma of LungApoptosisCarcinoma, Non-Small-Cell LungCarcinoma, Squamous CellCell CycleCell Line, TumorCell ProliferationHumansLung NeoplasmsLymph NodesMultivariate AnalysisNeoplasm StagingSOX Transcription FactorsSurvival AnalysisTime FactorsSOX30 protein, humanSOX Transcription FactorsTumor Suppressor Proteins

Identifiers

PMID26330328
PMCPMC4557060
OpenAlexW1260835739

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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.