Suzuki Masayo, Toki Hiroe, Furuya Akiko, Ando Hiroshi
R&D Division, Tokyo Research Park, Kyowa Hakko Kirin Co., Ltd, Machida-shi, Tokyo, Japan.
R&D Division, Tokyo Research Park, Kyowa Hakko Kirin Co., Ltd, Machida-shi, Tokyo, Japan.
Biochem Biophys Res Commun. 2017 Jan 22;482(4):651-657. doi: 10.1016/j.bbrc.2016.11.089. Epub 2016 Nov 16.
Human alanine-serine-cysteine transporter 2 (ASCT2; SLC1A5) is a major transporter of the amino acid glutamine that is known to be overexpressed in certain malignant tumors. In this study, we generated specific monoclonal antibodies (MAbs) against ASCT2 by establishing an ASCT2-expressing Chinese hamster ovary cell line that was used to immunize mice and rats. The MAbs KM4008, KM4012, and KM4018 against ASCT2 were isolated through a cell-based screen; these specifically bound to ASCT2-positive cells, as determined by flow cytometry and immunoprecipitation. In addition, the antibodies suppressed glutamine-dependent growth of WiDr colorectal cancer cells. These results provide evidence supporting the use of MAbs against ASCT2 as an effective therapeutic strategy for cancer treatment.
人丙氨酸 - 丝氨酸 - 半胱氨酸转运蛋白2(ASCT2;SLC1A5)是氨基酸谷氨酰胺的主要转运蛋白,已知在某些恶性肿瘤中过表达。在本研究中,我们通过建立表达ASCT2的中国仓鼠卵巢细胞系来免疫小鼠和大鼠,从而产生了针对ASCT2的特异性单克隆抗体(MAb)。通过基于细胞的筛选分离出了针对ASCT2的单克隆抗体KM4008、KM4012和KM4018;通过流式细胞术和免疫沉淀法确定,这些抗体特异性结合ASCT2阳性细胞。此外,这些抗体抑制了WiDr结肠癌细胞的谷氨酰胺依赖性生长。这些结果提供了证据,支持使用针对ASCT2的单克隆抗体作为癌症治疗的有效策略。