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Time Courses and Value of Circulating Microparticles in Patients with Operable Stage Non-small Cell Lung Cancer Undergoing Surgical Intervention

Overview
Journal Tumour Biol
Publisher Sage Publications
Specialty Oncology
Date 2016 Apr 10
PMID 27059732
Citations 2
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Abstract

Microparticles (MPs) are substantially increased in patients with operable stage non-small cell lung cancer (NSCLC) prior to lung resection surgery. This study tested the hypothesis that there is a decrease in MPs after surgical intervention. Between March 2012 and January 2015, 33 patients who had operable stage NSCLC were consecutively and prospectively enrolled into the study. Additionally, 31 healthy subjects who were consecutively enrolled in the study period served as age- and gender-matched controls. Circulating MPs (EDAc-MPs, EDAp-MPs, PDAc-MPs, PDAp-MPs) were measured by flow cytometry once in control subjects and twice (i.e., prior to and three months later after surgical intervention) in NSCLC patients. Compared with control subjects, these four types of circulating MPs were significantly higher in NSCLC patients prior to operation (all P < 0.005), but did not differ among the controls and NSCLC patients at 3 months after surgery (all P > 0.2). Additionally, a receiver operating characteristic curve (ROC) showed that these four types of MPs were significantly valuable predictors for detecting early stage NSCLC (all P < 0.004). Circulating MPs which were remarkably increased in the operable stage of NSCLC prior to surgery were substantially decreased 3 months later after surgery. These findings show that circulating MPs might be an accessory biomarker for monitoring those of NSCLC after receiving lung resection surgery.

Citing Articles

Circulating microparticles are prognostic biomarkers in advanced non-small cell lung cancer patients.

Wang C, Tseng C, Chang H, Huang K, Fang W, Chen Y Oncotarget. 2017; 8(44):75952-75967.

PMID: 29100283 PMC: 5652677. DOI: 10.18632/oncotarget.18372.


Clinical significance of circulating microparticles in Ph myeloproliferative neoplasms.

Zhang W, Qi J, Zhao S, Shen W, Dai L, Han W Oncol Lett. 2017; 14(2):2531-2536.

PMID: 28789461 PMC: 5530094. DOI: 10.3892/ol.2017.6459.

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