Frontiers in Oncology (Apr 2019)

Germline Predisposition and Copy Number Alteration in Pre-stage Lung Adenocarcinomas Presenting as Ground-Glass Nodules

  • Yijiu Ren,
  • Shujun Huang,
  • Chenyang Dai,
  • Dong Xie,
  • Larry Zheng,
  • Huikang Xie,
  • Hui Zheng,
  • Yunlang She,
  • Fangyu Zhou,
  • Yue Wang,
  • Pengpeng Li,
  • Ke Fei,
  • Gening Jiang,
  • Yang Zhang,
  • Bo Su,
  • E. Alejandro Sweet-Cordero,
  • Nhan Le Tran,
  • Yanan Yang,
  • Jai N. Patel,
  • Christian Rolfo,
  • Gaetano Rocco,
  • Andrés Felipe Cardona,
  • Alessandro Tuzi,
  • Matteo B. Suter,
  • Ping Yang,
  • Wayne Xu,
  • Wayne Xu,
  • Wayne Xu,
  • Chang Chen

DOI
https://doi.org/10.3389/fonc.2019.00288
Journal volume & issue
Vol. 9

Abstract

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Objective: Synchronous multiple ground-glass nodules (SM-GGNs) are a distinct entity of lung cancer which has been emerging increasingly in recent years in China. The oncogenesis molecular mechanisms of SM-GGNs remain elusive.Methods: We investigated single nucleotide variations (SNV), insertions and deletions (INDEL), somatic copy number variations (CNV), and germline mutations of 69 SM-GGN samples collected from 31 patients, using target sequencing (TRS) and whole exome sequencing (WES).Results: In the entire cohort, many known driver mutations were found, including EGFR (21.7%), BRAF (14.5%), and KRAS (6%). However, only one out of the 31 patients had the same somatic missense or truncated events within SM-GGNs, indicating the independent origins for almost all of these SM-GGNs. Many germline mutations with a low frequency in the Chinese population, and genes harboring both germline and somatic variations, were discovered in these pre-stage GGNs. These GGNs also bore large segments of copy number gains and/or losses. The CNV segment number tended to be positively correlated with the germline mutations (r = 0.57). The CNV sizes were correlated with the somatic mutations (r = 0.55). A moderate correlation (r = 0.54) was also shown between the somatic and germline mutations.Conclusion: Our data suggests that the precancerous unstable CNVs with potentially predisposing genetic backgrounds may foster the onset of driver mutations and the development of independent SM-GGNs during the local stimulation of mutagens.

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