Literature DB >> 25601488

Identification of atypical ATRNL1 insertion to EML4-ALK fusion gene in NSCLC.

Blanka Robesova1, Monika Bajerova2, Jitka Hausnerova3, Jana Skrickova4, Marcela Tomiskova4, Dana Dvorakova2.   

Abstract

We herein present a rare case of an EML4-ALK positive patient. A 61-year-old man was diagnosed with locoregional non-small cell lung cancer (NSCLC). No EGFR mutations were detected, and therefore the ALK rearrangement was evaluated using immunohistochemistry (IHC), fluorescence in situ hybridization (FISH) and the reverse transcription PCR (RT-PCR) method for EML4-ALK. All methods showed a positive result and, therefore, the patient was treated with crizotinib with a good therapeutic response. However, a detailed RT-PCR analysis and sequencing revealed an unexpected 138 bp insertion of attractin-like 1 (ATRNL1) gene into the EML4-ALK fusion gene. In our case, the positive therapeutic response suggests that ATRNL1 insertion does not affect EML4-ALK's sensitivity to crizotinib. This case shows great EML4-ALK heterogeneity and also that basic detection methods (IHC, FISH) cannot fully specify ALK rearrangement but in many cases a full specification seems to be important for an effective TKI indication, and sequencing ALK variants might contribute to optimized patient selection.
Copyright © 2015 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  ATRNL1; Crizotinib; EML4-ALK; Lung cancer; NSCLC; Targeted therapy

Mesh:

Substances:

Year:  2015        PMID: 25601488     DOI: 10.1016/j.lungcan.2015.01.002

Source DB:  PubMed          Journal:  Lung Cancer        ISSN: 0169-5002            Impact factor:   5.705


  5 in total

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Journal:  Onco Targets Ther       Date:  2018-03-01       Impact factor: 4.147

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Journal:  Commun Biol       Date:  2021-11-22

5.  Circular RNA CpG island hypermethylation-associated silencing in human cancer.

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Journal:  Oncotarget       Date:  2018-06-26
  5 in total

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