Division of Otolaryngology-Head and Neck Surgery, Department of Surgery, University of Wisconsin-Madison, Madison, Wisconsin 53705-2275, USA.
Laryngoscope. 2013 Apr;123(4):960-5. doi: 10.1002/lary.23703. Epub 2013 Feb 12.
OBJECTIVES/ HYPOTHESIS: The use of molecular testing is becoming more significant for the diagnosis and classification of disease. The application of fine-needle aspiration (FNA) biopsy as the means of sampling lesions in union with molecular testing could be a powerful combination in laryngology. The objectives of this study were to investigate 1) if FNA was feasible to sample benign vocal fold lesions; 2) if FNA samples provided sufficient RNA quality for molecular analysis; and 3) if gene expression of FNA samples matched paired surgical excised specimens.
Prospective cross-sectional.
Fifteen vocal fold specimens were obtained from adult patients undergoing routine surgical removal for benign vocal fold lesions using FNA and surgical excision. Comparisons were made between FNA and excision biopsies for RNA quality. Correlative analysis was completed for RNA expression of nine genes, including decorin (DCN), connective tissue growth factor (CTGF), vascular endothelial growth factor (VEGF), collagen type VI alpha 3 (COL6A3), superoxide dismutase 1 (SOD1), glutathione S-transferase (GST2), collagen type I alpha 2 (COL1A2), ATP binding cassette (ABC), and procollagen I alpha 1 (COL1A1).
FNA and excision samples demonstrated similar RNA quality (P > 0.05). Per gene expression, four out of nine genes were moderately correlated between the paired samples (P < 0.05).
FNA of the vocal fold lamina propria is technically feasible to perform. Further improvement in the FNA technology is desirable to optimize RNA quality for reliable gene expression analysis.
目的/假设:分子检测在疾病的诊断和分类中变得越来越重要。将细针抽吸(FNA)活检作为取样病变的手段与分子检测相结合,可能是喉科学中的一种强大组合。本研究的目的是调查 1)FNA 是否可行用于取样良性声带病变;2)FNA 样本是否提供足够的 RNA 质量用于分子分析;3)FNA 样本的基因表达是否与配对的手术切除标本匹配。
前瞻性横断面研究。
使用 FNA 和手术切除从接受常规手术切除良性声带病变的成年患者中获得 15 个声带标本。比较 FNA 和切除活检的 RNA 质量。完成了九个基因的 RNA 表达的相关分析,包括核心蛋白聚糖(DCN)、结缔组织生长因子(CTGF)、血管内皮生长因子(VEGF)、胶原 VI 型 alpha3(COL6A3)、超氧化物歧化酶 1(SOD1)、谷胱甘肽 S-转移酶 2(GST2)、胶原 I 型 alpha2(COL1A2)、ATP 结合盒(ABC)和前胶原 I 型 alpha1(COL1A1)。
FNA 和切除样本的 RNA 质量相似(P>0.05)。对于每个基因的表达,九个基因中有四个在配对样本之间具有中度相关性(P<0.05)。
声带固有层的 FNA 技术上是可行的。进一步改进 FNA 技术,优化 RNA 质量,以进行可靠的基因表达分析是可取的。