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EML4-ALK lung cancers are characterized by rare other mutations, a TTF-1 cell lineage, an acinar histology, and young onset
- Source :
- Modern Pathology. 22:508-515
- Publication Year :
- 2009
- Publisher :
- Elsevier BV, 2009.
-
Abstract
- A subset of lung cancers harbors a small inversion within chromosome 2p, giving rise to a transforming fusion gene, EML4-ALK (echinoderm microtubule-associated protein-like 4 gene and the anaplastic lymphoma kinase gene), which encodes an activated tyrosine kinase. We have earlier examined the presence of EML4-ALK by multiplex reverse transcription-polymerase chain reaction in 363 specimens of lung cancer, identifying 11 adenocarcinoma cases featuring the fusion gene. In this study, we clinicopathologically examined the characteristics of the EML4-ALK-positive cases, including the mutation status of EGFR, KRAS, and TP53, and whether they were of thyroid transcription factor-1 (TTF-1) cell lineage or not. Of 11 patients, 4 (36%) with EML4-ALK-positive lung adenocarcinomas who were below 50 years of age were affected by these diseases, as compared with 12 of 242 patients (5.0%) with EML4-ALK-negative lung adenocarcinomas (P=0.00038). EML4-ALK-positive lung adenocarcinomas were characterized by less-differentiated grade (P=0.0082) and acinar-predominant structure (P
- Subjects :
- Pathology
medicine.medical_specialty
Lung Neoplasms
EML4/ALK Fusion Gene
Oncogene Proteins, Fusion
Adenocarcinoma
Biology
Gene mutation
medicine.disease_cause
Polymerase Chain Reaction
Pathology and Forensic Medicine
Proto-Oncogene Proteins p21(ras)
Fusion gene
Proto-Oncogene Proteins
hemic and lymphatic diseases
medicine
Humans
Anaplastic lymphoma kinase
Cell Lineage
Age of Onset
Lung cancer
Polymorphism, Single-Stranded Conformational
ALK Gene Rearrangement
Genes, erbB-1
Middle Aged
medicine.disease
Immunohistochemistry
DNA-Binding Proteins
Mutation
ras Proteins
KRAS
Tumor Suppressor Protein p53
Transcription Factors
Subjects
Details
- ISSN :
- 08933952
- Volume :
- 22
- Database :
- OpenAIRE
- Journal :
- Modern Pathology
- Accession number :
- edsair.doi.dedup.....5eb7530f81b16b283318ab40a724c47a
- Full Text :
- https://doi.org/10.1038/modpathol.2009.2