Deciphering tumour tissue organization by 3D electron microscopy and machine learning.

Journal: Communications biology
Published Date:

Abstract

Despite recent progress in the characterization of tumour components, the tri-dimensional (3D) organization of this pathological tissue and the parameters determining its internal architecture remain elusive. Here, we analysed the spatial organization of patient-derived xenograft tissues generated from hepatoblastoma, the most frequent childhood liver tumour, by serial block-face scanning electron microscopy using an integrated workflow combining 3D imaging, manual and machine learning-based semi-automatic segmentations, mathematics and infographics. By digitally reconstituting an entire hepatoblastoma sample with a blood capillary, a bile canaliculus-like structure, hundreds of tumour cells and their main organelles (e.g. cytoplasm, nucleus, mitochondria), we report unique 3D ultrastructural data about the organization of tumour tissue. We found that the size of hepatoblastoma cells correlates with the size of their nucleus, cytoplasm and mitochondrial mass. We also found anatomical connections between the blood capillary and the planar alignment and size of tumour cells in their 3D milieu. Finally, a set of tumour cells polarized in the direction of a hot spot corresponding to a bile canaliculus-like structure. In conclusion, this pilot study allowed the identification of bioarchitectural parameters that shape the internal and spatial organization of tumours, thus paving the way for future investigations in the emerging onconanotomy field.

Authors

  • Baudouin Denis de Senneville
    CNRS, University of Bordeaux, "Institut de Mathématiques de Bordeaux" (IMB), UMR5251, 351 cours Libération, F-33400, Talence, France.
  • Fatma Zohra Khoubai
    Univ. Bordeaux, INSERM, Biotherapy of Genetic Diseases, Inflammatory Disorders and Cancer, BMGIC, U1035, MIRCADE team, 146 rue Léo Saignat, 33076, Bordeaux, France.
  • Marc Bevilacqua
    Univ. Bordeaux, CNRS, INSERM, Bordeaux Imaging Centre, BIC, UMS 3420, US 4, F-33000, Bordeaux, France.
  • Alexandre Labedade
    Alexandre Labedade, freelance, F-33870, Vayres, France.
  • Kathleen Flosseau
    XenTech Company, Genopole Campus 3, 4 Rue Pierre Fontaine, F-91000, Évry-Courcouronnes, France.
  • Christophe Chardot
    Chirurgie Pédiatrique-Transplantation, Hôpital Necker-Enfants Malades, Assistance Publique Hôpitaux de Paris, 149 rue de Sèvres, F-75015, Paris, France.
  • Sophie Branchereau
    Paediatric Surgery and Liver Transplant unit, Hôpital Bicêtre, Assistance Publique Hôpitaux de Paris - Université Paris Saclay, 78 rue du Général Leclerc, F-94270, Le Kremlin-Bicêtre, France.
  • Jean Ripoche
    Univ. Bordeaux, INSERM, retired, 146 rue Léo Saignat, 33076, Bordeaux, France.
  • Stefano Cairo
    XenTech Company, Genopole Campus 3, 4 Rue Pierre Fontaine, F-91000, Évry-Courcouronnes, France.
  • Etienne Gontier
    Univ. Bordeaux, CNRS, INSERM, Bordeaux Imaging Centre, BIC, UMS 3420, US 4, F-33000, Bordeaux, France. etienne.gontier@u-bordeaux.fr.
  • Christophe F Grosset
    Univ. Bordeaux, INSERM, Biotherapy of Genetic Diseases, Inflammatory Disorders and Cancer, BMGIC, U1035, MIRCADE team, 146 rue Léo Saignat, 33076, Bordeaux, France. christophe.grosset@inserm.fr.