Novel ex vivo disease model for extramammary Paget's disease using the cancer tissue-originated spheroid method

J Dermatol Sci. 2020 Sep;99(3):185-192. doi: 10.1016/j.jdermsci.2020.07.006. Epub 2020 Aug 5.

Abstract

Background: Extramammary Paget's disease (EMPD) is a rare skin cancer that frequently occurs in the anogenital region in the elderly. Prognosis in patients with metastatic EMPD is poor as EMPD treatment has advanced little in recent years, primarily because no EMPD cell line has been established.

Objective: We aimed to establish an ex vivo EMPD disease model using the cancer tissue-originated spheroid (CTOS) method, which is used to prepare and culture primary cancer cells while maintaining cell-cell contact.

Methods: Thirteen samples from 12 EMPD patients were obtained. CTOSs were prepared and cultured using CTOS method. Histopathological examination of the CTOSs was performed. We investigated optimum medium conditions and effects of growth factors for CTOS growth. Chemo-sensitivity assays were conducted.

Results: CTOSs were successfully prepared from 3 primary lesions and 2 metastatic lymph nodes. Of these, 2 CTOSs (EMPD-3 and EMPD-4) could be maintained and passaged long term ex vivo. Following transplantation of CTOSs to NOD/Scid mice, CTOS-derived xenotumors exhibited ductal formation, indicating that CTOSs retained the original tumor characteristics. Chemo-sensitivity assays revealed that docetaxel significantly inhibited EMPD-3 growth in a dose-dependent manner, whereas EMPD-4 was not clearly inhibited. These findings indicate the heterogeneity of EMPD and potential use of chemosensitivity assays with patient-derived CTOS to select the most effective drugs for each patient.

Conclusion: To our knowledge, this study represents the first establishment of an ex vivo-EMPD disease model involving conventional cell lines. EMPD CTOSs might be useful for developing new therapeutic strategies.

Keywords: CTOS; Chemosensitivity assay; Ex vivo disease model; Extramammary Paget’s disease; HRG–HER3 signaling.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Antineoplastic Agents / administration & dosage
  • Culture Media / metabolism
  • Docetaxel / administration & dosage
  • Dose-Response Relationship, Drug
  • Feasibility Studies
  • Female
  • Humans
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Male
  • Paget Disease, Extramammary / drug therapy
  • Paget Disease, Extramammary / pathology*
  • Penile Neoplasms / drug therapy
  • Penile Neoplasms / pathology*
  • Primary Cell Culture / methods*
  • Skin Neoplasms / drug therapy
  • Skin Neoplasms / pathology*
  • Spheroids, Cellular
  • Tumor Cells, Cultured
  • Vulvar Neoplasms / drug therapy
  • Vulvar Neoplasms / pathology*
  • Xenograft Model Antitumor Assays

Substances

  • Antineoplastic Agents
  • Culture Media
  • Intercellular Signaling Peptides and Proteins
  • Docetaxel