Department of Oncology and Hematology, Jikei University School of Medicine, Minato‑Ku, Tokyo 105‑8471, Japan.
Oncol Rep. 2013 Sep;30(3):1053-8. doi: 10.3892/or.2013.2594. Epub 2013 Jul 5.
Various anticancer drugs, including camptothecins and indolocarbazoles, target DNA topoisomerase I (Top1). We previously described the camptothecin-resistant colon cancer cell line DLDSNR6, which has a Gly365Ser missense mutation in Top1. In the present study, we established highly camptothecin-resistant sublines from DLDSNR6 cells by continuous exposure to higher camptothecin concentrations. The established sublines grew in the presence of 30 µM of camptothecin, but exhibited markedly retarded growth. In addition to Gly365Ser, these sublines harbored a Top1 Gly717Arg mutation and some had also a Top1 Gln421Arg mutation. Top1 activity was reduced to approximately one-eighth in highly resistant cell lines compared with that in parental DLD-1 cells. Resistant clones with 3 Top1 mutations including Gln421RArg exhibited the highest resistance to the indolocarbazole J-107088 in terms of the effect on the cell cycle distribution. The Gln421 mutation was equivalent to a mutation recently found in camptothecin biosynthesizing plants, but it has not previously been found in mammalian cells.
多种抗癌药物,包括喜树碱类和吲哚卡唑类,靶向 DNA 拓扑异构酶 I(Top1)。我们之前描述了一种对喜树碱耐药的结肠癌细胞系 DLDSNR6,该细胞系中 Top1 的 Gly365Ser 错义突变。在本研究中,我们通过持续暴露于更高的喜树碱浓度,从 DLDSNR6 细胞中建立了高度耐药的亚系。所建立的亚系在 30µM 的喜树碱存在下生长,但生长明显延迟。除了 Gly365Ser,这些亚系还携带 Top1 Gly717Arg 突变,有些还携带 Top1 Gln421Arg 突变。与亲本 DLD-1 细胞相比,高度耐药细胞系中的 Top1 活性降低到约八分之一。具有 3 种 Top1 突变(包括 Gln421RArg)的耐药克隆在细胞周期分布方面对吲哚卡唑 J-107088 的抑制作用最强。Gln421 突变与喜树碱生物合成植物中最近发现的突变相当,但以前在哺乳动物细胞中尚未发现。