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Associations of sirtuins with clinicopathological parameters and prognosis in non–small cell lung cancer

Overview of attention for article published in Cancer Management and Research, September 2018
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Title
Associations of sirtuins with clinicopathological parameters and prognosis in non–small cell lung cancer
Published in
Cancer Management and Research, September 2018
DOI 10.2147/cmar.s166946
Pubmed ID
Authors

Jian Gong, Huiyan Wang, Wenwen Lou, Guiye Wang, Hongqun Tao, Huaikai Wen, Yu Liu, Qipeng Xie

Abstract

Lung cancer is the leading cause of cancer-related death worldwide and it is critical to discover specific biomarkers to provide better individualized treatment and subsequently better prognosis. The sirtuins (SIRT1-7) have been reported to be involved in cancers including non-small cell lung cancer (NCSLC), however, the results are not consistent and not all the seven sirtuins are explored and compared. TCGA data was downloaded and used to investigate and compare the associations of sirtuins mRNA levels with clinicopathological parameters and prognosis in NSCLC. Our results suggested SIRT1, SIRT3, SIRT4, and SIRT7 were highly expressed in adeno-carcinoma (ADC) patients and female patients while SIRT5 were highly expressed in squamous cell carcinoma (SCC) patients and male patients. Associations of high SIRT7 with younger onset age, high SIRT1 with distant metastasis and low T stage, and high SIRT4 with high T stage and TNM stage were also found. Kaplan-Meier plot curves and univariate Cox proportional regression analyses indicated that high SIRT2, SIRT4, and SIRT6 expressions were associated with longer overall survival (OS) time. Multivariate analyses indicated that SIRT2 and SIRT6 were still associated with OS. For recurrence-free survival (RFS), high SIRT1 expression was significantly associated with shorter RFS time while high SIRT2-3 and SIRT5-7 expressions were associated with longer RFS time in univariate analyses. After adjusting the confounding factors, significant associations were still found in SIRT1-2 and SIRT5-7 but not in SIRT3. We also stratified the patients by combining SIRT1 and SIRT2 and revealed that the combination of SIRT1 and SIRT2 was a better prediction model for RFS in NSCLC. To preliminarily understand the potential mechanisms of sirtuins in NSCLC carcinogenesis, the genes co-expressed with sirtuins were analyzed and annotated. sirtuins might be the potential therapy targets and prognostic biomarkers in NSCLC.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 20 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 20 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 3 15%
Student > Ph. D. Student 3 15%
Student > Bachelor 2 10%
Student > Doctoral Student 2 10%
Researcher 2 10%
Other 2 10%
Unknown 6 30%
Readers by discipline Count As %
Pharmacology, Toxicology and Pharmaceutical Science 3 15%
Biochemistry, Genetics and Molecular Biology 3 15%
Medicine and Dentistry 3 15%
Chemistry 2 10%
Immunology and Microbiology 1 5%
Other 2 10%
Unknown 6 30%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 11 September 2018.
All research outputs
#20,533,292
of 23,103,436 outputs
Outputs from Cancer Management and Research
#1,406
of 2,019 outputs
Outputs of similar age
#292,456
of 335,776 outputs
Outputs of similar age from Cancer Management and Research
#79
of 110 outputs
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We're also able to compare this research output to 110 others from the same source and published within six weeks on either side of this one. This one is in the 1st percentile – i.e., 1% of its contemporaries scored the same or lower than it.