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Phylogenetic analysis of metastatic progression in breast cancer using somatic mutations and copy number aberrations

Author

Listed:
  • David Brown

    (Breast Cancer Translational Research Laboratory, Institut Jules Bordet, Université Libre de Bruxelles)

  • Dominiek Smeets

    (Laboratory of Translational Genetics, Vesalius Research Center, VIB
    Laboratory of Translational Genetics, Katholieke Universiteit Leuven)

  • Borbála Székely

    (Semmelweis University)

  • Denis Larsimont

    (Institut Jules Bordet)

  • A. Marcell Szász

    (Semmelweis University)

  • Pierre-Yves Adnet

    (Breast Cancer Translational Research Laboratory, Institut Jules Bordet, Université Libre de Bruxelles)

  • Françoise Rothé

    (Breast Cancer Translational Research Laboratory, Institut Jules Bordet, Université Libre de Bruxelles)

  • Ghizlane Rouas

    (Breast Cancer Translational Research Laboratory, Institut Jules Bordet, Université Libre de Bruxelles)

  • Zsófia I. Nagy

    (Semmelweis University)

  • Zsófia Faragó

    (Semmelweis University)

  • Anna-Mária Tőkés

    (Semmelweis University
    MTA-SE Tumor Progression Research Group, Semmelweis University)

  • Magdolna Dank

    (Semmelweis University Cancer Center, Semmelweis University)

  • Gyöngyvér Szentmártoni

    (Semmelweis University Cancer Center, Semmelweis University)

  • Nóra Udvarhelyi

    (Surgical and Molecular Tumor Pathology Centre, National Institute of Oncology)

  • Gabriele Zoppoli

    (University of Genova and Istituto di Cura a Carattere Clinico e Scientifico Azienda Ospedaliera Universitaria San Martino—Instituto Nazionale Tumori)

  • Lajos Pusztai

    (Yale University)

  • Martine Piccart

    (Institut Jules Bordet, Université Libre de Bruxelles)

  • Janina Kulka

    (Semmelweis University)

  • Diether Lambrechts

    (Laboratory of Translational Genetics, Vesalius Research Center, VIB
    Laboratory of Translational Genetics, Katholieke Universiteit Leuven)

  • Christos Sotiriou

    (Breast Cancer Translational Research Laboratory, Institut Jules Bordet, Université Libre de Bruxelles)

  • Christine Desmedt

    (Breast Cancer Translational Research Laboratory, Institut Jules Bordet, Université Libre de Bruxelles)

Abstract

Several studies using genome-wide molecular techniques have reported various degrees of genetic heterogeneity between primary tumours and their distant metastases. However, it has been difficult to discern patterns of dissemination owing to the limited number of patients and available metastases. Here, we use phylogenetic techniques on data generated using whole-exome sequencing and copy number profiling of primary and multiple-matched metastatic tumours from ten autopsied patients to infer the evolutionary history of breast cancer progression. We observed two modes of disease progression. In some patients, all distant metastases cluster on a branch separate from their primary lesion. Clonal frequency analyses of somatic mutations show that the metastases have a monoclonal origin and descend from a common ‘metastatic precursor’. Alternatively, multiple metastatic lesions are seeded from different clones present within the primary tumour. We further show that a metastasis can be horizontally cross-seeded. These findings provide insights into breast cancer dissemination.

Suggested Citation

  • David Brown & Dominiek Smeets & Borbála Székely & Denis Larsimont & A. Marcell Szász & Pierre-Yves Adnet & Françoise Rothé & Ghizlane Rouas & Zsófia I. Nagy & Zsófia Faragó & Anna-Mária Tőkés & Magdol, 2017. "Phylogenetic analysis of metastatic progression in breast cancer using somatic mutations and copy number aberrations," Nature Communications, Nature, vol. 8(1), pages 1-13, April.
  • Handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_ncomms14944
    DOI: 10.1038/ncomms14944
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