Department of Molecular Cytogenetics, Medical Research Institute, Tokyo Medical and Dental University, Bunkyo-ku, Tokyo, Japan.
Department of Obstetrics and Gynecology, Graduate School, Tokyo Medical and Dental University, Yushima, Bunkyo-ku, Tokyo, Japan.
Carcinogenesis. 2018 May 28;39(6):758-766. doi: 10.1093/carcin/bgy033.
Amino acids (AAs) are biologically important nutrient compounds necessary for the survival of any cell. Of the 20 AAs, cancer cells depend on the uptake of several extracellular AAs for survival. However, which extracellular AA is indispensable for the survival of cancer cells and the molecular mechanism involved have not been fully defined. In this study, we found that the reduction of cell survival caused by glutamine (Gln) depletion is inversely correlated with the expression level of glutamine synthetase (GS) in ovarian cancer (OVC) cells. GS expression was downregulated in 45 of 316 OVC cases (14.2%). The depletion of extracellular Gln by treatment with l-asparaginase, in addition to inhibiting Gln uptake via the knockdown of a Gln transporter, led to the inhibition of cell growth in OVC cells with low expression of GS (GSlow-OVC cells). Furthermore, the re-expression of GS in GSlow-OVC cells induced the inhibition of tumor growth in vitro and in vivo. Thus, these findings provide novel insight into the development of an OVC therapy based on the requirement of Gln.
氨基酸(AAs)是生物中非常重要的营养化合物,是任何细胞生存所必需的。在 20 种氨基酸中,癌细胞依赖于摄取几种细胞外氨基酸来生存。然而,哪种细胞外氨基酸对于癌细胞的生存是不可或缺的,以及涉及的分子机制尚未完全确定。在这项研究中,我们发现谷氨酰胺(Gln)耗尽引起的细胞存活率降低与卵巢癌细胞(OVC)中谷氨酰胺合成酶(GS)的表达水平呈负相关。在 316 例 OVC 病例中,有 45 例(14.2%)GS 表达下调。用 L-天冬酰胺酶处理以耗尽细胞外 Gln,除了通过敲低 Gln 转运蛋白抑制 Gln 摄取外,还导致 GS 低表达的 OVC 细胞(GSlow-OVC 细胞)的细胞生长受到抑制。此外,在 GSlow-OVC 细胞中重新表达 GS 诱导了体外和体内肿瘤生长的抑制。因此,这些发现为基于 Gln 需求的 OVC 治疗的开发提供了新的见解。