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TK-DDCS1的建立与鉴定:一种新型异柠檬酸脱氢酶1(IDH1)突变的去分化软骨肉瘤细胞系

Establishment and characterization of TK-DDCS1: a novel IDH1 mutated dedifferentiated chondrosarcoma cell line.

作者信息

Saisuwan Krittamate, Boonnate Piyanard, Goto Hiroki, Nakagawa Rumi, Abe Makoto, Hirabayashi Kaoru, Fujiwara Yukio, Kikuta Kazutaka, Okada Seiji

机构信息

Division of Hematopoiesis, Joint Research Center for Human Retrovirus Infection & Graduate, School of Medical Sciences, Kumamoto University, 2-2-1 Honjo, Chuo-ku, Kumamoto, 860-0811, Japan.

Laboratory of Environmental and Toxicology, Chulabhorn Research Institute, Kamphaeng Phet 6 Rd, Talat Bang Khen, Lak Si, Bangkok, 10210, Thailand.

出版信息

Hum Cell. 2025 Jun 3;38(4):116. doi: 10.1007/s13577-025-01235-6.

Abstract

Dedifferentiated chondrosarcoma (DDCS) is a rare and aggressive subtype of chondrosarcoma, characterized by the coexistence of a high-grade spindle or pleomorphic tumor that lacks a substantial cartilaginous matrix. Notably, it shows a mutant IDH1 incidence of over 80%. This study established a novel DDCS cell line with an IDH1 mutation, TK-DDCS1, derived from the right ilium of a 67-year-old Japanese female patient. TK-DDCS1 cells maintain the undifferentiated DDCS phenotype with the IDH1p.R132L mutation. The IDH1R132 mutation is known to be associated with a poor prognosis for chondrosarcoma, and the p.R132L mutation is a novel variant among the registered DDCS cell lines in the Cellosaurus database. The mutant IDH1 inhibitor, DS-1001b, inhibited the proliferation of TK-DDCS1 in a dose-dependent manner in both two-dimensional and spheroid cultures. The tumorigenicity of TK-DDCS1 was demonstrated through xenografting into EGFP-transgenic BALB/c Rag2-/-/Jak3-/- (EGFP-BRJ) mice, where the tumors exhibited undifferentiated phenotypes of DDCS in both morphological and immunohistochemical features. Thus, TK-DDCS1 serves as a valuable model for investigating the characteristics of DDCS and exploring molecular targeted therapies.

摘要

去分化软骨肉瘤(DDCS)是软骨肉瘤中一种罕见且侵袭性强的亚型,其特征是存在高级别的梭形或多形性肿瘤,且缺乏大量软骨基质。值得注意的是,其异柠檬酸脱氢酶1(IDH1)突变发生率超过80%。本研究建立了一种具有IDH1突变的新型DDCS细胞系TK-DDCS1,该细胞系源自一名67岁日本女性患者的右髂骨。TK-DDCS1细胞维持着具有IDH1p.R132L突变的未分化DDCS表型。已知IDH1R132突变与软骨肉瘤的不良预后相关,且p.R132L突变是细胞osaurus数据库中已注册的DDCS细胞系中的一种新型变体。突变型IDH1抑制剂DS-1001b在二维和球体培养中均以剂量依赖方式抑制TK-DDCS1的增殖。通过将TK-DDCS1异种移植到增强型绿色荧光蛋白(EGFP)转基因BALB/c Rag2-/-/Jak3-/-(EGFP-BRJ)小鼠中,证实了TK-DDCS1的致瘤性,所形成的肿瘤在形态和免疫组化特征上均表现出DDCS的未分化表型。因此,TK-DDCS1是研究DDCS特征和探索分子靶向治疗的有价值模型。

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