Abstract
Background
Lung combined neuroendocrine carcinomas (NECs) comprise NEC and non-NEC components, such as adenocarcinoma and squamous cell carcinoma. Mutation of epidermal growth factor receptor (EGFR) often is observed in non-NEC but is very rare in sporadic NEC, which almost always has p53 mutation. Therefore, we hypothesized the following research concept: mutation analysis of EGFR and p53 in each component of combined NEC tissues can provide important information on whether such components originate from the same tumor cells or incidentally arise as collision cancers.
Methods
We compared the mutations of EGFR and p53 in laser-microdissected NEC and non-NEC from lungs of eight cases affected by combined NEC. We examined the expression of EGFR and NEC markers in the combined NECs by immunohistochemistry.
Results
Five of eight cases of combined NEC had the same mutations of EGFR and/or p53 in both non-NEC and NEC. One case had EGFR mutation in only the non-NEC component, and two cases did not have these mutations. Replacement transformation was observed in borderline areas between non-NEC and NEC. The signal of activated EGFR in non-NEC with the same EGFR mutation was more intense than that in NEC components.
Conclusions
Our study suggests the mechanism behind the carcinogenesis of lung combined NEC, which is partially caused by the transformation from epithelial carcinoma of non-NEC to NEC.
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Acknowledgment
The authors thank Ms. Yukie Saito, Ms. Mariko Nakamura, Ms. Sayaka Okada, and Ms. Sawa Nagayama for their excellent assistance. Grants-in-Aid for Scientific Research from the Japan Society for the Promotion of Science (JSPS): Grant numbers 17K19893 and 18K07665.
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Iijima, M., Yokobori, T., Mogi, A. et al. Genetic and Immunohistochemical Studies Investigating the Histogenesis of Neuroendocrine and Carcinomatous Components of Combined Neuroendocrine Carcinoma. Ann Surg Oncol 26, 1744–1750 (2019). https://doi.org/10.1245/s10434-019-07268-0
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DOI: https://doi.org/10.1245/s10434-019-07268-0