TK-ALCL1:一种新型NPM-ALK阳性无性大细胞淋巴瘤细胞系的建立和特征描述。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-07-01 Epub Date: 2024-05-16 DOI:10.1007/s13577-024-01077-8
Prin Sungwan, Jutatip Panaampon, Ryusho Kariya, Satoshi Kamio, Rumi Nakagawa, Toru Hirozane, Yukiko Ogura, Makoto Abe, Kaoru Hirabayashi, Yukio Fujiwara, Kazutaka Kikuta, Seiji Okada
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摘要

TK-ALCL1是一种新型无性淋巴瘤激酶(ALK)阳性无性大细胞淋巴瘤(ALK+ ALCL)细胞系,它是从一名59岁日本男性患者的原发肿瘤部位建立的。TK-ALCL1的免疫特征与原发性ALCL细胞的典型特征一致,即ALK、CD30、EMA和CD4阳性,但CD2、CD3、CD5、CD8a和EBV相关抗原阴性。T细胞受体-γ位点的重排表明,TK-ALCL1是从T系淋巴细胞中克隆衍生出来的。FISH和RT-PCR分析表明,TK-ALCL1具有核ophosmin(NPM)-ALK融合转录本,这是ALK+ ALCL细胞系的典型特征。将TK-ALCL1皮下接种到6周大的BALB/c Rag2-/Jak3-/-(BRJ)小鼠体内,4-6周内形成肿瘤块。形态学、免疫组化和分子遗传学检查证实,异种移植与原始 ALCL 肿瘤完全相同。ALK抑制剂Alectinib和Lorlatinib以剂量依赖的方式抑制增殖。因此,TK-ALCL1 为研究 ALK+ ALCLL 的生物学特性和针对 ALK 的新型治疗方法提供了一个有用的体外和体内模型。
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Establishment and characterization of TK-ALCL1: a novel NPM-ALK-positive anaplastic large-cell lymphoma cell line.

TK-ALCL1, a novel anaplastic lymphoma kinase (ALK)-positive anaplastic large-cell lymphoma (ALK+ ALCL) cell line, was established from the primary tumor site of a 59-year-old Japanese male patient. The immune profile of TK-ALCL1 corresponds to that seen typically in primary ALCL cells, i.e., positive for ALK, CD30, EMA, and CD4, but negative for CD2, CD3, CD5, CD8a, and EBV-related antigens. The rearrangement of the T cell receptor-gamma locus shows that TK-ALCL1 is clonally derived from T-lineage lymphoid cells. FISH and RT-PCR analysis revealed that TK-ALCL1 has the nucleophosmin (NPM)-ALK fusion transcript, which is typical for ALK+ ALCL cell lines. When TK-ALCL1 was subcutaneously inoculated into 6-week-old BALB/c Rag2-/-/Jak3-/- (BRJ) mice, it formed tumor masses within 4-6 weeks. Morphological, immunohistochemical, and molecular genetic investigations confirmed that the xenograft and the original ALCL tumor were identical. The ALK inhibitors Alectinib and Lorlatinib suppressed proliferation in a dose-dependent manner. Thus, TK-ALCL1 provides a useful in vitro and in vivo model for investigation of the biology of ALK+ ALCL and of novel therapeutic approaches targeting ALK.

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