Horlad Hasita, Ohnishi Koji, Ma Chaoya, Fujiwara Yukio, Niino Daisuke, Ohshima Koichi, Jinushi Masahisa, Matsuoka Masao, Takeya Motohiro, Komohara Yoshihiro
Department of Cell Pathology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto 860-8556, Japan.
Department of Pathology, School of Medicine, Kurume University, Kurume, Fukuoka 839-0851, Japan.
Oncol Lett. 2016 Aug;12(2):1519-1524. doi: 10.3892/ol.2016.4774. Epub 2016 Jun 23.
Adult T-cell leukemia/lymphoma (ATLL), an aggressive type of malignant lymphoma, is highly resistant to chemotherapy. However, the detailed mechanisms of the chemoresistance of ATLL have never been elucidated. We previously demonstrated that direct cell-cell interaction between macrophages and lymphoma cells was significantly associated with lymphoma progression in patients with ATLL. The present study aimed to further analyze the effects of cell-cell interaction between macrophages and ATLL cells by means of cell culture studies and immunohistochemical analysis using human ATLL samples. It was found that direct co-culture with macrophages induced chemoresistance in the ATLL ATN-1 cell line, but not in other cell lines, including TL-Mor, ED and ATL-2S. It was also found that expression of the T cell Ig and mucin domain-containing molecule-3 (TIM-3) was induced in ATN-1 cells by their long-term co-culture with macrophages. TIM-3 gene transfection induced chemoresistance in the ATN-1 cells. Immunostaining of ATLL tissues showed TIM-3 expression in 25 out of 58 ATLL cases. Although TIM-3 expression was not associated with overall survival or T classification, it was associated with resistance to chemotherapy. TIM-3 expression is therefore considered to be a marker for predicting the efficacy of chemotherapy, and TIM-3-associated signals may be a therapeutic target for patients with ATLL.
成人T细胞白血病/淋巴瘤(ATLL)是一种侵袭性恶性淋巴瘤,对化疗具有高度抗性。然而,ATLL化疗耐药的详细机制尚未阐明。我们之前证明,巨噬细胞与淋巴瘤细胞之间的直接细胞间相互作用与ATLL患者的淋巴瘤进展显著相关。本研究旨在通过细胞培养研究和使用人ATLL样本的免疫组织化学分析,进一步分析巨噬细胞与ATLL细胞之间细胞间相互作用的影响。研究发现,与巨噬细胞直接共培养可诱导ATLL的ATN-1细胞系产生化疗耐药性,但对包括TL-Mor、ED和ATL-2S在内的其他细胞系则无此作用。还发现,ATN-1细胞与巨噬细胞长期共培养可诱导其表达含T细胞免疫球蛋白和粘蛋白结构域分子-3(TIM-3)。TIM-3基因转染可诱导ATN-1细胞产生化疗耐药性。ATLL组织的免疫染色显示,58例ATLL病例中有25例存在TIM-3表达。虽然TIM-3表达与总生存期或T分类无关,但与化疗耐药相关。因此,TIM-3表达被认为是预测化疗疗效的一个标志物,TIM-3相关信号可能是ATLL患者的一个治疗靶点。