PMID- 32284620 OWN - NLM STAT- MEDLINE DCOM- 20210426 LR - 20210426 IS - 1804-7521 (Electronic) IS - 1213-8118 (Linking) VI - 164 IP - 2 DP - 2020 Jun TI - Gene rearrangement detection by next-generation sequencing in patients with non-small cell lung carcinoma. PG - 127-132 LID - 10.5507/bp.2020.015 [doi] AB - Non-small cell lung carcinoma (NSCLC) is the leading cause of cancer-related deaths worldwide. Various molecular markers in NSCLC patients have been developed, including gene rearrangements, currently used in therapeutic strategies. With increasing number of these molecular biomarkers of NSCLC, there is a demand for highly efficient methods for detecting mutations and translocations in treatable targets. Those currently available U.S. Food and Drug Administration (FDA) approved approaches, for example imunohistochemisty (IHC) and fluorescence in situ hybridization (FISH), are inadequate, due to sufficient quantity of material and long time duration. Next-generation massive parallel sequencing (NGS), with the ability to perform and capture data from millions of sequencing reactions simultaneously could resolve the problem. Thanks to gradual NGS introduction into clinical laboratories, screening time should be considerably shorter, which is very important for patients with advanced NSCLC. Moreover, only a minimum sample input is needed for achieving adequate results. NGS was compared to the current detection methods of ALK, ROS1, c-RET and c-MET rearrangements in NSCLC and a significant match, between IHC, FISH and NGS results, was found. Recent available researches have been carried out on a small numbers of patients. Verifying these results on larger patients cohort is important. This review sumarizes the literature on this subject and compares current possibilities of predictive gene rearrangements detection in patients with NSCLC. FAU - Brisudova, Aneta AU - Brisudova A AD - Department of Clinical and Molecular Pathology, Faculty of Medicine and Dentistry, Palacky University Olomouc, Czech Republic. FAU - Skarda, Jozef AU - Skarda J AD - Department of Clinical and Molecular Pathology, Faculty of Medicine and Dentistry, Palacky University Olomouc, Czech Republic. LA - eng PT - Journal Article PT - Review DEP - 20200406 PL - Czech Republic TA - Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub JT - Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia JID - 101140142 RN - 0 (Proto-Oncogene Proteins) RN - EC 2.7.10.1 (ALK protein, human) RN - EC 2.7.10.1 (Anaplastic Lymphoma Kinase) RN - EC 2.7.10.1 (MET protein, human) RN - EC 2.7.10.1 (Protein-Tyrosine Kinases) RN - EC 2.7.10.1 (Proto-Oncogene Proteins c-met) RN - EC 2.7.10.1 (Proto-Oncogene Proteins c-ret) RN - EC 2.7.10.1 (RET protein, human) RN - EC 2.7.10.1 (ROS1 protein, human) SB - IM MH - Anaplastic Lymphoma Kinase/genetics MH - Carcinoma, Non-Small-Cell Lung/diagnosis/*genetics MH - Gene Rearrangement/genetics MH - High-Throughput Nucleotide Sequencing/*methods MH - Humans MH - Immunohistochemistry MH - In Situ Hybridization, Fluorescence MH - Lung Neoplasms/diagnosis/*genetics MH - Molecular Targeted Therapy MH - Mutation/genetics MH - Oncogene Fusion/*genetics MH - Protein-Tyrosine Kinases/genetics MH - Proto-Oncogene Proteins/genetics MH - Proto-Oncogene Proteins c-met/genetics MH - Proto-Oncogene Proteins c-ret/genetics MH - Sequence Analysis, DNA MH - Sequence Analysis, RNA MH - Translocation, Genetic/genetics OTO - NOTNLM OT - fluorescence in situ hybridization OT - gene rearrangement OT - immunohistochemistry OT - next-generation sequencing OT - non-small cel lung carcinoma EDAT- 2020/04/15 06:00 MHDA- 2021/04/27 06:00 CRDT- 2020/04/15 06:00 PHST- 2019/11/11 00:00 [received] PHST- 2020/03/19 00:00 [accepted] PHST- 2020/04/15 06:00 [pubmed] PHST- 2021/04/27 06:00 [medline] PHST- 2020/04/15 06:00 [entrez] AID - 10.5507/bp.2020.015 [doi] PST - ppublish SO - Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2020 Jun;164(2):127-132. doi: 10.5507/bp.2020.015. Epub 2020 Apr 6.