Abstract

Ameloblastoma is a benign tumor of the odontogenic epithelium with several histological subtypes. All subtypes of ameloblastoma contain abundant stroma; the tumor cells invade collectively into the surrounding tissues without losing intratumor cell attachments. However, the molecular mechanisms mediating ameloblastoma invasion remain unclear. Here, we evaluated the functional significance of the interactions between ameloblastoma tumor cells and stromal fibroblasts on collective cellular invasion using a three‐dimensional cultivation method, double‐layered collagen gel hemisphere (DL‐CGH) culture. The AM‐1 plexiform and AM‐3 follicular human ameloblastoma cell lines and HFF‐2 human fibroblasts were labeled with GFP and DsRed, respectively. Collective cellular invasion of ameloblastoma cells was assessed in the presence or absence of fibroblasts. Notably, without fibroblasts, AM‐1 cells formed sharp, plexiform‐like invasive processes, whereas AM‐3 cells formed a series of blunt processes often observed during collective migration. In comparison, under the cocultures with HFF‐2 fibroblasts, AM‐3 cells formed tuft‐like invasive processes and collectively invaded into outer layer more than that observed with AM‐1 cells. Moreover, HFF‐2 fibroblasts localized to the tips of the invasive tumor processes. These findings suggest that tumor‐associated cells assist tumor cell invasion. Microscopic analysis of sectioned three‐dimensional cultures revealed that AM‐3/HFF‐2 hemispheres were histologically similar to follicular ameloblastoma tumor samples. Therefore, our findings suggest that ameloblastoma subtypes exhibit distinct invasion patterns and that fibroblasts promote collective tumor invasion in follicular ameloblastoma.

Highlights

  • Takao Fuchigami1, Hirofumi Koyama2, Michiko Kishida2, Yoshiaki Nishizawa2, Mikio Iijima2, Toshiro Kibe1, Masahiro Ueda2, Tohru Kiyono3, Yoshimasa Maniwa4, Norifumi Nakamura1 and Shosei Kishida2

  • Virus titers were estimated by quantitative real-time reverse transcription polymerase chain reaction (RT-qPCR) and an appropriate volume of viral supernatant was added to ameloblastoma (AM-1 and AM-3) and HFF-2 cell cultures in the presence of G418 (400 lgÁmLÀ1) and puromycin (10 lgÁmLÀ1), to generate GFP-expressing ameloblastoma cells and DsRed-expressing HFF-2 fibroblasts, respectively

  • Ameloblastoma is an odontogenic tumor that can be classified into several types with distinct invasive growth patterns based on histopathological findings [1]

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Summary

METHOD

Fibroblasts promote the collective invasion of ameloblastoma tumor cells in a 3D coculture model. Keywords 3D culture; ameloblastoma; collective cellular invasion; odontogenic tumor; stromal fibroblast. We evaluated the functional significance of the interactions between ameloblastoma tumor cells and stromal fibroblasts on collective cellular invasion using a three-dimensional cultivation method, double-layered collagen gel hemisphere (DL-CGH) culture. We have shown that different types of ameloblastoma cells have characteristic properties in gene expression pattern and invasion activity [19]. Based on these findings, we hypothesized that intercellular interactions between ameloblastoma cells and the neighboring stroma could affect the collective invasion of ameloblastoma cells. While several studies have focused on ameloblastoma tumor classification, little is known on their molecular pathophysiology, which has substantially hindered clinical decision making Clarification of these biological mechanisms will provide a foundation to develop new treatment strategies for this disease

Materials and methods
Discussion

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