TY - JOUR
T1 - Establishment and characterization of novel patient-derived cell lines from giant cell tumor of bone
AU - Yoshimatsu, Yuki
AU - Noguchi, Rei
AU - Tsuchiya, Ryuto
AU - Ono, Takuya
AU - Sin, Yooksil
AU - Akane, Sei
AU - Sugaya, Jun
AU - Mori, Tomoaki
AU - Fukushima, Suguru
AU - Yoshida, Akihiko
AU - Kawai, Akira
AU - Kondo, Tadashi
N1 - Funding Information:
We appreciate the technical support provided by Mesdames Yu Kuwata and Rina Sasaki (Division of Rare Cancer Research, National Cancer Center). We would like to thank Drs. F Nakatani, S. Iwata, E Kobayashi, M Nakagawa, T Komatsubara, M Saito, C Sato (Department of Musculoskeletal Oncology, National Cancer Center Hospital), Drs. T Shibayama, and H Tanaka (Department of Diagnostic Pathology, National Cancer Center Hospital) for sampling tumor tissue specimens from curetted materials. (Division of Rare Cancer Research). We appreciate the technical support provided by Ms. Y Shiotani, Mr. N Uchiya, and Dr. T Imai (Central Animal Division, National Cancer Center Research Institute). We would also like to thank Editage (www.editage.jp ) for their help with English language editing and their constructive comments on the manuscript. This research was technically assisted by the Fundamental Innovative Oncology Core at the National Cancer Center This research was supported by the Japan Agency for Medical Research and Development (Grant number 20ck0106537h0001).
Funding Information:
We appreciate the technical support provided by Mesdames Yu Kuwata and Rina Sasaki (Division of Rare Cancer Research, National Cancer Center). We would like to thank Drs. F Nakatani, S. Iwata, E Kobayashi, M Nakagawa, T Komatsubara, M Saito, C Sato (Department of Musculoskeletal Oncology, National Cancer Center Hospital), Drs. T Shibayama, and H Tanaka (Department of Diagnostic Pathology, National Cancer Center Hospital) for sampling tumor tissue specimens from curetted materials. (Division of Rare Cancer Research). We appreciate the technical support provided by Ms. Y Shiotani, Mr. N Uchiya, and Dr. T Imai (Central Animal Division, National Cancer Center Research Institute). We would also like to thank Editage ( www.editage.jp ) for their help with English language editing and their constructive comments on the manuscript. This research was technically assisted by the Fundamental Innovative Oncology Core at the National Cancer Center This research was supported by the Japan Agency for Medical Research and Development (Grant number 20ck0106537h0001).
Publisher Copyright:
© 2021, Japan Human Cell Society.
PY - 2021/11
Y1 - 2021/11
N2 - Giant cell tumor of bone (GCTB) is a locally aggressive and rarely metastasizing tumor. GCTB is characterized by the presence of unique giant cells and a recurrent mutation in the histone tail of the histone variant H3.3, which is encoded by H3F3A on chromosome 1. GCTB accounts for ~ 5% of primary bone tumors. Although GCTB exhibits an indolent course, it has the potential to develop aggressive behaviors associated with local recurrence and distant metastasis. Currently, complete surgical resection is the only curative treatment, and novel therapeutic strategies are required. Patient-derived cancer cell lines are critical tools for basic and pre-clinical research. However, only a few GCTB cell lines have been reported, and none of them are available from public cell banks. Therefore, we aimed to establish novel GCTB cell lines in the present study. Using curetted tumor tissues of GCTB, we established two cell lines and named them NCC-GCTB2-C1 and NCC-GCTB3-C1. These cells harbored a typical mutation in histones and exhibited slow but constant growth, formed spheroids, and had invasive capabilities. We demonstrated the utility of these cell lines for high-throughput drug screening using 214 anticancer agents. We concluded that NCC-GCTB2-C1 and NCC-GCTB3-C1 cell lines were useful for the in vitro study of GCTB.
AB - Giant cell tumor of bone (GCTB) is a locally aggressive and rarely metastasizing tumor. GCTB is characterized by the presence of unique giant cells and a recurrent mutation in the histone tail of the histone variant H3.3, which is encoded by H3F3A on chromosome 1. GCTB accounts for ~ 5% of primary bone tumors. Although GCTB exhibits an indolent course, it has the potential to develop aggressive behaviors associated with local recurrence and distant metastasis. Currently, complete surgical resection is the only curative treatment, and novel therapeutic strategies are required. Patient-derived cancer cell lines are critical tools for basic and pre-clinical research. However, only a few GCTB cell lines have been reported, and none of them are available from public cell banks. Therefore, we aimed to establish novel GCTB cell lines in the present study. Using curetted tumor tissues of GCTB, we established two cell lines and named them NCC-GCTB2-C1 and NCC-GCTB3-C1. These cells harbored a typical mutation in histones and exhibited slow but constant growth, formed spheroids, and had invasive capabilities. We demonstrated the utility of these cell lines for high-throughput drug screening using 214 anticancer agents. We concluded that NCC-GCTB2-C1 and NCC-GCTB3-C1 cell lines were useful for the in vitro study of GCTB.
KW - Cell lines
KW - Giant cell tumor of bone
KW - High-throughput screening
KW - Patient-derived cancer model
KW - Spheroids
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U2 - 10.1007/s13577-021-00579-z
DO - 10.1007/s13577-021-00579-z
M3 - Article
C2 - 34304386
AN - SCOPUS:85111128210
SN - 0914-7470
VL - 34
SP - 1899
EP - 1910
JO - Human Cell
JF - Human Cell
IS - 6
ER -