TY - JOUR
T1 - Apport des puces à ADN dans le diagnostic étiologique des pleurésies
T2 - Étude de faisabilité
AU - Greillier, L.
AU - Roll, P.
AU - Barlesi, F.
AU - Robaglia-Schlupp, A.
AU - Fraticelli, A.
AU - Cau, P.
AU - Astoul, P.
N1 - Funding Information:
This study is supported by grants from the National Natural Science Foundation of China (no. 81401618 ).
PY - 2007/1/1
Y1 - 2007/1/1
N2 - Introduction: Establishing the cause of exudative pleural effusions is sometimes difficult, especially in the context of possible malignant pleural mesothelioma (MPM). Therefore, the development of new biological tools is necessary. The aim of this study was to determine the feasibility and the diagnostic contribution of genomic analysis of cells contained in pleural fluid, using DNA microarray techniques. Methods: Patients with pleural effusion requiring diagnostic thoracocentesis were eligible to participate in the study. Five hundred mls of pleural fluid were then collected. RNA was extracted from pleural fluid cells and its integrity was assessed. Gene expression was studied using pangenomic DNA microarrays. Results: Seventeen patients were included (4 MPM, 8 secondary malignant pleurisies, 5 benign pleurisies). Three patients offered fully exploitable samples. Taking into account the results of control experiments, gene expression study from pleural fluid was reproducible. The comparison of samples showed significant differences in gene expression. Samples from 14 patients were not exploitable because of RNA degradation. Conclusions: Gene expression study of cells from pleural fluid is feasible but remains difficult, essentially in relationship with RNA weakness.
AB - Introduction: Establishing the cause of exudative pleural effusions is sometimes difficult, especially in the context of possible malignant pleural mesothelioma (MPM). Therefore, the development of new biological tools is necessary. The aim of this study was to determine the feasibility and the diagnostic contribution of genomic analysis of cells contained in pleural fluid, using DNA microarray techniques. Methods: Patients with pleural effusion requiring diagnostic thoracocentesis were eligible to participate in the study. Five hundred mls of pleural fluid were then collected. RNA was extracted from pleural fluid cells and its integrity was assessed. Gene expression was studied using pangenomic DNA microarrays. Results: Seventeen patients were included (4 MPM, 8 secondary malignant pleurisies, 5 benign pleurisies). Three patients offered fully exploitable samples. Taking into account the results of control experiments, gene expression study from pleural fluid was reproducible. The comparison of samples showed significant differences in gene expression. Samples from 14 patients were not exploitable because of RNA degradation. Conclusions: Gene expression study of cells from pleural fluid is feasible but remains difficult, essentially in relationship with RNA weakness.
KW - DNA microarray
KW - Diagnosis
KW - Exudate
KW - Gene expression profiling
KW - Malignant pleural mesothelioma
UR - http://www.scopus.com/inward/record.url?scp=34548851500&partnerID=8YFLogxK
U2 - 10.1016/S0761-8425(07)91388-1
DO - 10.1016/S0761-8425(07)91388-1
M3 - Article
C2 - 17925668
AN - SCOPUS:34548851500
SN - 0761-8425
VL - 24
SP - 859
EP - 867
JO - Revue des Maladies Respiratoires
JF - Revue des Maladies Respiratoires
IS - 7
ER -