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Targeted next-generation sequencing for analyzing the genetic alterations in atypical adenomatous hyperplasia and adenocarcinoma in situ

  • Original Article – Cancer Research
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Abstract

Purpose

Atypical adenomatous hyperplasia (AAH) and adenocarcinoma in situ (AIS) have been defined as preinvasive pulmonary adenocarcinoma lesions according to the 2015 World Health Organization lung adenocarcinoma classification. We aimed to search for the most common gene mutations in patients with AAH and AIS and investigate the distinctions between the two groups at the molecular level.

Methods

We performed targeted next-generation sequencing on 18 cases with AAH and 28 cases with AIS to screen for mutations with the Ion Torrent Oncomine Solid Tumor DNA panel. ALK and ROS1 fusions were detected by real-time PCR.

Results

Forty-six mutations were identified in 29 cases (76.1%), including 9 (50%) of 18 cases with AAH and 20 (71.4%) of 28 cases with AIS, in the following genes: EGFR, BRAF, KRAS, ERBB2, TP53, and FGFR3. The mutations in EGFR, BRAF, KRAS, ERBB2, and TP53 genes were more common in AIS lesions than in AAH lesions, whereas the FGFR3 gene was more frequently mutated in AAH compared to AIS. ALK and ROS1 fusions were not detected in any of the lesions.

Conclusions

Based on the molecular evidence, the proposal that AAH and AIS are preinvasive lesions of pulmonary adenocarcinomas is of great significance, and it is necessary to distinguish AAH from AIS. Our study provided insights into the genetic alterations in the early stage of lung adenocarcinoma, which could be beneficial for the pathologic diagnosis and early detection of these lesions.

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Acknowledgements

We acknowledge Youhui Hu, Shengji Ma, and Wenjie Ding for excellent technical help. This work was supported by the project of Shanghai Municipal Commission of Health and Family Planning (20164Y0046) and the “Five-New” Clinical and translational Project for Specialized Diseases (16CR3023A).

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Authors

Contributions

Author contributions

XX: sample processing, data analysis and manuscript preparation. NL: sample collection and clinical annotation. RZ: sample processing. LZ and JS: article revision. JZ: study conception and design, pathology assessment, and article revision.

Corresponding author

Correspondence to Jie Zhang.

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Conflict of interest

The authors declare no conflicts of interest.

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

Informed consent

Informed consent was obtained from all individual participants included in the study.

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Xu, X., Li, N., Zhao, R. et al. Targeted next-generation sequencing for analyzing the genetic alterations in atypical adenomatous hyperplasia and adenocarcinoma in situ. J Cancer Res Clin Oncol 143, 2447–2453 (2017). https://doi.org/10.1007/s00432-017-2500-9

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  • DOI: https://doi.org/10.1007/s00432-017-2500-9

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