Comparison of Breast Fine-Needle Aspiration Cytology and Tissue Sampling for High-Throughput Proteomic Analysis and Cancer Biomarker Detection

被引:3
|
作者
Park, Hye Eun [1 ,8 ]
Han, Dohyun [2 ,3 ]
Lee, Jae Seok [4 ]
Nikas, Ilias P. [5 ]
Kim, Hyeyoon [6 ]
Yang, Sohyeon [7 ,8 ]
Lee, Hyebin [9 ]
Ryu, Han Suk [7 ,8 ,10 ]
机构
[1] Seoul Natl Univ, Boramae Hosp, Dept Pathol, Seoul, South Korea
[2] Seoul Natl Univ Hosp, Transdisciplinary Dept Med & Adv Technol, Seoul, South Korea
[3] Seoul Natl Univ Hosp, Biomed Res Inst, Prote Core Facil, Seoul, South Korea
[4] Sungkyunkwan Univ, Samsung Changwon Hosp, Sch Med, Dept Pathol, Seoul, South Korea
[5] European Univ Cyprus, Sch Med, Nicosia, Cyprus
[6] Pacific Northwest Natl Lab, Biol Sci Div, Richland, WA USA
[7] Seoul Natl Univ Hosp, Dept Pathol, Seoul, South Korea
[8] Seoul Natl Univ, Coll Med, Dept Pathol, Seoul, South Korea
[9] Sungkyunkwan Univ, Sch Med, Kangbuk Samsung Hosp, Dept Radiat Oncol, Seoul, South Korea
[10] Seoul Natl Univ, Canc Res Inst, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
Fine-needle aspiration cytology; Proteomics; Breast cancer; Biomarker; Tissue sample; Targeted therapy; Cytopathology; COMPUTATIONAL PLATFORM; MASS SPECTROMETRY; LUNG-CANCER; FNA SMEARS; ENRICHMENT; MUTATIONS; DNA;
D O I
10.1159/000539478
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Introduction: Fine-needle aspiration cytology (FNAC) specimens are widely utilized for the diagnosis and molecular testing of various cancers. We performed a comparative proteomic analysis of three different sample types, including breast FNAC, core needle biopsy (CNB), and surgical resection tissues. Our goal was to evaluate the suitability of FNAC for in-depth proteomic analysis and for identifying potential therapeutic biomarkers in breast cancer. Methods: High-throughput proteomic analysis was conducted on matched FNAC, CNB, and surgical resection tissue samples obtained from breast cancer patients. The protein identification, including currently established or promising therapeutic targets, was compared among the three different sample types. Gene Ontology (GO) enrichment analysis was also performed on all matched samples. Results: Compared to tissue samples, FNAC testing revealed a comparable number of proteins (7,179 in FNAC; 7,196 in CNB; and 7,190 in resection samples). Around 85% of proteins were mutually identified in all sample types. FNAC, along with CNB, showed a positive correlation between the number of enrolled tumor cells and identified proteins. In the GO analysis, the FNAC samples demonstrated a higher number of genes for each pathway and GO terms than tissue samples. CCND1, CDK6, HER2, and IGF1R were found in higher quantities in the FNAC compared to tissue samples, while TUBB2A was only detected in the former. Conclusion: FNAC is suitable for high-throughput proteomic analysis, in addition to an emerging source that could be used to identify and quantify novel cancer biomarkers.
引用
收藏
页码:359 / 369
页数:11
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