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转铁蛋白受体和 ABC 转运蛋白 ABCB6 和 ABCB7 在青蒿琥酯耐药和肿瘤细胞分化中的作用。

Role of transferrin receptor and the ABC transporters ABCB6 and ABCB7 for resistance and differentiation of tumor cells towards artesunate.

机构信息

Oncotest GmbH, Institute of Experimental Oncology, Freiburg, Germany.

出版信息

PLoS One. 2007 Aug 29;2(8):e798. doi: 10.1371/journal.pone.0000798.

Abstract

The anti-malarial artesunate also exerts profound anti-cancer activity. The susceptibility of tumor cells to artesunate can be enhanced by ferrous iron. The transferrin receptor (TfR) is involved in iron uptake by internalization of transferrin and is over-expressed in rapidly growing tumors. The ATP-binding cassette (ABC) transporters ABCB6 and ABCB7 are also involved in iron homeostasis. To investigate whether these proteins play a role for sensitivity towards artesunate, Oncotest's 36 cell line panel was treated with artesunate or artesunate plus iron(II) glycine sulfate (Ferrosanol). The majority of cell lines showed increased inhibition rates, for the combination of artesunate plus iron(II) glycine sulfate compared to artesunate alone. However, in 11 out of the 36 cell lines the combination treatment was not superior. Cell lines with high TfR expression significantly correlated with high degrees of modulation indicating that high TfR expressing tumor cells would be more efficiently inhibited by this combination treatment than low TfR expressing ones. Furthermore, we found a significant relationship between cellular response to artesunate and TfR expression in 55 cell lines of the National Cancer Institute (NCI), USA. A significant correlation was also found for ABCB6, but not for ABCB7 in the NCI panel. Artesunate treatment of human CCRF-CEM leukemia and MCF7 breast cancer cells induced ABCB6 expression but repressed ABCB7 expression. Finally, artesunate inhibited proliferation and differentiation of mouse erythroleukemia (MEL) cells. Down-regulation of ABCB6 by antisense oligonucleotides inhibited differentiation of MEL cells indicating that artesunate and ABCB6 may cooperate. In conclusion, our results indicate that ferrous iron improves the activity of artesunate in some but not all tumor cell lines. Several factors involved in iron homeostasis such as TfR and ABCB6 may contribute to this effect.

摘要

抗疟药青蒿琥酯也具有显著的抗癌活性。亚铁离子可增强肿瘤细胞对青蒿琥酯的敏感性。转铁蛋白受体(TfR)参与转铁蛋白的内化摄取,在快速生长的肿瘤中过度表达。ATP 结合盒(ABC)转运蛋白 ABCB6 和 ABCB7 也参与铁稳态。为了研究这些蛋白是否与青蒿琥酯的敏感性有关,Oncotest 的 36 个细胞系面板用青蒿琥酯或青蒿琥酯加甘氨酸亚铁(Ferrosanol)进行了处理。与单独使用青蒿琥酯相比,大多数细胞系对青蒿琥酯加甘氨酸亚铁的组合治疗显示出更高的抑制率。然而,在 36 个细胞系中有 11 个组合治疗并不优越。TfR 表达高的细胞系与高调节程度显著相关,表明高 TfR 表达的肿瘤细胞比低 TfR 表达的肿瘤细胞更能被这种组合治疗有效地抑制。此外,我们在来自美国国立癌症研究所(NCI)的 55 个细胞系中发现了青蒿琥酯与 TfR 表达之间的显著关系。在 NCI 面板中也发现了与 ABCB6 的显著相关性,但与 ABCB7 无关。青蒿琥酯处理人 CCRF-CEM 白血病和 MCF7 乳腺癌细胞诱导 ABCB6 表达,但抑制 ABCB7 表达。最后,青蒿琥酯抑制了小鼠红白血病(MEL)细胞的增殖和分化。反义寡核苷酸下调 ABCB6 抑制了 MEL 细胞的分化,表明青蒿琥酯和 ABCB6 可能协同作用。总之,我们的结果表明,亚铁离子可提高一些但不是所有肿瘤细胞系中青蒿琥酯的活性。铁稳态中涉及的几个因素,如 TfR 和 ABCB6,可能有助于这种效应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67c3/1949049/fd9e404d48bb/pone.0000798.g001.jpg

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