IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v11y2020i1d10.1038_s41467-020-19855-x.html
   My bibliography  Save this article

Tumor evolutionary trajectories during the acquisition of invasiveness in early stage lung adenocarcinoma

Author

Listed:
  • Siwei Wang

    (Nanjing Medical University Affiliated Cancer Hospital & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research)

  • Mulong Du

    (Nanjing Medical University
    Harvard T. H. Chan School of Public Health
    Harvard T. H. Chan School of Public Health
    Massachusetts General Hospital/Harvard Medical School)

  • Jingyuan Zhang

    (Nanjing Medical University Affiliated Cancer Hospital & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research)

  • Weizhang Xu

    (Nanjing Medical University Affiliated Cancer Hospital & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research)

  • Qianyu Yuan

    (Harvard T. H. Chan School of Public Health
    Harvard T. H. Chan School of Public Health
    Massachusetts General Hospital/Harvard Medical School)

  • Ming Li

    (Nanjing Medical University Affiliated Cancer Hospital & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research)

  • Jie Wang

    (Nanjing Medical University Affiliated Cancer Hospital & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research
    Jiangsu Biobank of Clinical Resources)

  • Hongyu Zhu

    (Nanjing Medical University Affiliated Cancer Hospital & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research)

  • Yuzhuo Wang

    (Nanjing Medical University Affiliated Cancer Hospital & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research
    Nanjing Medical University)

  • Cheng Wang

    (Nanjing Medical University)

  • Yuhua Gong

    (Geneplus-Beijing Institute)

  • Xiaonan Wang

    (Geneseeq-Nanjing Technology Inc.)

  • Zhibin Hu

    (Nanjing Medical University)

  • David C. Christiani

    (Harvard T. H. Chan School of Public Health
    Harvard T. H. Chan School of Public Health
    Massachusetts General Hospital/Harvard Medical School)

  • Lin Xu

    (Nanjing Medical University Affiliated Cancer Hospital & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research
    Nanjing Medical University)

  • Hongbing Shen

    (Nanjing Medical University)

  • Rong Yin

    (Nanjing Medical University Affiliated Cancer Hospital & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research
    Nanjing Medical University Affiliated Cancer Hospital & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research
    Jiangsu Biobank of Clinical Resources
    Nanjing Medical University)

Abstract

The evolutionary trajectories of early lung adenocarcinoma (LUAD) have not been fully elucidated. We hypothesize that genomic analysis between pre-invasive and invasive components will facilitate the description of LUAD evolutionary patterns. We micro-dissect malignant pulmonary nodules (MPNs) into paired pre-invasive and invasive components for panel-genomic sequencing and recognize three evolutionary trajectories. Evolutionary mode 1 (EM1) demonstrates none of the common driver events between paired components, but another two modes, EM2A and EM2B, exhibit critical private alterations restricted to pre-invasive and invasive components, respectively. When ancestral clones harbor EGFR mutations, truncal mutation abundance significantly decrease after the acquisition of invasiveness, which may be associated with the intratumoral accumulation of infiltrated B cells. Harboring EGFR mutations is critical to the selective pressure and further impacts the prognosis. Our findings extend the understanding of evolutionary trajectories during invasiveness acquisition in early LUAD.

Suggested Citation

  • Siwei Wang & Mulong Du & Jingyuan Zhang & Weizhang Xu & Qianyu Yuan & Ming Li & Jie Wang & Hongyu Zhu & Yuzhuo Wang & Cheng Wang & Yuhua Gong & Xiaonan Wang & Zhibin Hu & David C. Christiani & Lin Xu , 2020. "Tumor evolutionary trajectories during the acquisition of invasiveness in early stage lung adenocarcinoma," Nature Communications, Nature, vol. 11(1), pages 1-8, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-19855-x
    DOI: 10.1038/s41467-020-19855-x
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-020-19855-x
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-020-19855-x?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-19855-x. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.