ALK-rearrangement in non-small-cell lung cancer (NSCLC).
Xue DuYun ShaoHai-Feng QinYan-Hong TaiHong-Jun GaoPublished in: Thoracic cancer (2018)
The ALK gene encodes a transmembrane tyrosine kinase receptor. ALK is physiologically expressed in the nervous system during embryogenesis, but its expression decreases postnatally. ALK first emerged in the field of oncology in 1994 when it was identified to fuse to NPM1 in anaplastic large-cell lymphoma. Since then, ALK has been associated with other types of cancers, including non-small-cell lung cancer (NSCLC). More than 19 different ALK fusion partners have been discovered in NSCLC, including EML4, KIF5B, KLC1, and TPR. Most of these ALK fusions in NSCLC patients respond well to the ALK inhibitor, crizotinib. In this paper, we reviewed fusion partner genes with ALK, detection methods for ALK-rearrangement (ALK-R), and the ALK-tyrosine kinase inhibitor, crizotinib, used in NSCLC patients.
Keyphrases
- advanced non small cell lung cancer
- epidermal growth factor receptor
- tyrosine kinase
- small cell lung cancer
- end stage renal disease
- ejection fraction
- stem cells
- newly diagnosed
- prognostic factors
- genome wide
- acute myeloid leukemia
- dna methylation
- cell therapy
- bone marrow
- hepatitis c virus
- poor prognosis
- genome wide identification
- single cell
- copy number
- long non coding rna
- binding protein
- human immunodeficiency virus
- brain metastases
- real time pcr
- hiv testing
- men who have sex with men