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Establishment of PDX ‐derived salivary adenoid cystic carcinoma cell lines using organoid culture method
Author(s) -
Takada Kentaro,
Aizawa Yoshihiro,
Sano Daisuke,
Okuda Ryo,
Sekine Keisuke,
Ueno Yasuharu,
Yamanaka Shoji,
Aoyama Jun,
Sato Kaname,
Kuwahara Tatsu,
Hatano Takashi,
Takahashi Hideaki,
Arai Yasuhiro,
Nishimura Goshi,
Taniguchi Hideki,
Oridate Nobuhiko
Publication year - 2020
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.33315
Subject(s) - organoid , adenoid cystic carcinoma , cell culture , in vivo , in vitro , cancer research , pathology , biology , cancer , 3d cell culture , cell , carcinoma , medicine , microbiology and biotechnology , biochemistry , genetics
To generate a reliable preclinical model system exhibiting the molecular features of salivary adenoid cystic carcinoma (ACC) whose biology is still unclear due to the paucity of stable cell cultures. To develop new in vitro and in vivo models of ACC, the techniques of organoid culture and patient‐derived tumor xenograft (PDX), which have attracted attention in other malignancies in recent years, were applied. Tumor specimens from surgically resected salivary ACC were proceeded for the preparation of PDX and organoid culture. The orthotopic transplantation of patient‐derived or PDX‐derived organoids was demonstrated into submandibular glands of NSG mice and those histology was evaluated. PDX‐derived organoid cells were evaluated for the presence of MYB ‐mediated fusion genes and proceeded for in vitro drug sensitivity assay. Human ACC‐derived organoids were successfully generated in three‐dimensional culture and confirmed the ability of these cells to form tumors by orthotopic injection. Short‐term organoid cell cultures from two individual ACC PDX tumors were also established that maintain the characteristic MYBL1 translocation and histological features of the original parent and PDX tumors. Finally, the establishment of drug sensitivity tests on these short‐term cultured cells was confirmed using three different agents. This is the first to report an approach for the generation of human ACC‐derived organoids as in vitro and in vivo cancer models, providing insights into understanding of the ACC biology and creating personalized therapy design for patients with ACC.