PMID- 35548167 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20220716 IS - 2046-2069 (Electronic) IS - 2046-2069 (Linking) VI - 8 IP - 49 DP - 2018 Aug 2 TI - Development of a high-throughput and sensitive assay of fusion genes in lung cancer by array-based MALDI-TOFMS. PG - 27935-27945 LID - 10.1039/c8ra05165h [doi] AB - ALK (anaplastic lymphoma kinase gene), ROS1 (ros proto-oncogene 1) and RET (ret proto-oncogene) fusions are oncogenic drivers in non-small cell lung cancer (NSCLC). Methods like fluorescence in situ hybridization (FISH) and immunohistochemistry (IHC) are highly sensitive but subjectively analyzed, labor intensive, expensive and unsuitable for multiple fusion gene screening. This study aimed to establish a high-throughput, sensitive and cost-effective screening method (array-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry, array-based MALDI-TOFMS) for ALK, ROS1 and RET fusion detection. This method was established with three fusion gene positive cell lines (H2228, ALK positive; HCC78, ROS1 positive; LC-2/AD, RET positive) and negative samples. Then, 34 clinical samples were selected and detected by Sanger sequencing, next generation sequencing (NGS) and array-based MALDI-TOFMS. The results were compared and analyzed and Sanger sequencing was considered the standard. 7 cases showed ALK fusions, 1 case showed ROS1 fusions, no case showed RET fusions and 4 cases were both ALK and ROS1 fusions. Results showed that array-based MALDI-TOFMS was 100% concordant with Sanger sequencing and NGS 82.3%. In this study, we reported the utility of array-based MALDI-TOFMS in the assessment of ALK, ROS1 and RET fusions in routine lung biopsies of FFPE and fresh tissue specimens. Besides, this method may also be applied to the diagnosis, monitoring and prognosis of illness. CI - This journal is (c) The Royal Society of Chemistry. FAU - Wu, Han-Tao AU - Wu HT AD - Institute of Antibody Engineering, School of Laboratory Medicine and Biotechnology, Southern Medical University Guangzhou 510515 Guangdong P. R. China wg@smu.edu.cn liutc@smu.edu.cn +86-20-37247604 +86-20-62789355. FAU - Li, Kun AU - Li K AD - Institute of Antibody Engineering, School of Laboratory Medicine and Biotechnology, Southern Medical University Guangzhou 510515 Guangdong P. R. China wg@smu.edu.cn liutc@smu.edu.cn +86-20-37247604 +86-20-62789355. FAU - Wang, Gang AU - Wang G AD - Institute of Antibody Engineering, School of Laboratory Medicine and Biotechnology, Southern Medical University Guangzhou 510515 Guangdong P. R. China wg@smu.edu.cn liutc@smu.edu.cn +86-20-37247604 +86-20-62789355. FAU - Yang, Xue-Xi AU - Yang XX AD - Institute of Antibody Engineering, School of Laboratory Medicine and Biotechnology, Southern Medical University Guangzhou 510515 Guangdong P. R. China wg@smu.edu.cn liutc@smu.edu.cn +86-20-37247604 +86-20-62789355. FAU - Zhu, Anna AU - Zhu A AD - Guangzhou Darui Biotechnology Co. Ltd. Guangzhou 510665 China. FAU - Xu, Xu-Ping AU - Xu XP AD - Guangzhou Darui Biotechnology Co. Ltd. Guangzhou 510665 China. FAU - Li, Ming AU - Li M AD - Institute of Antibody Engineering, School of Laboratory Medicine and Biotechnology, Southern Medical University Guangzhou 510515 Guangdong P. R. China wg@smu.edu.cn liutc@smu.edu.cn +86-20-37247604 +86-20-62789355. FAU - Wu, Ying-Song AU - Wu YS AD - Institute of Antibody Engineering, School of Laboratory Medicine and Biotechnology, Southern Medical University Guangzhou 510515 Guangdong P. R. China wg@smu.edu.cn liutc@smu.edu.cn +86-20-37247604 +86-20-62789355. FAU - Liu, Tian-Cai AU - Liu TC AUID- ORCID: 0000-0002-2985-3766 AD - Institute of Antibody Engineering, School of Laboratory Medicine and Biotechnology, Southern Medical University Guangzhou 510515 Guangdong P. R. China wg@smu.edu.cn liutc@smu.edu.cn +86-20-37247604 +86-20-62789355. LA - eng PT - Journal Article DEP - 20180806 PL - England TA - RSC Adv JT - RSC advances JID - 101581657 PMC - PMC9087866 COIS- None. EDAT- 2018/08/06 00:00 MHDA- 2018/08/06 00:01 PMCR- 2018/08/06 CRDT- 2022/05/13 11:22 PHST- 2018/06/16 00:00 [received] PHST- 2018/07/07 00:00 [accepted] PHST- 2022/05/13 11:22 [entrez] PHST- 2018/08/06 00:00 [pubmed] PHST- 2018/08/06 00:01 [medline] PHST- 2018/08/06 00:00 [pmc-release] AID - c8ra05165h [pii] AID - 10.1039/c8ra05165h [doi] PST - epublish SO - RSC Adv. 2018 Aug 6;8(49):27935-27945. doi: 10.1039/c8ra05165h. eCollection 2018 Aug 2.