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岩藻糖挽救途径抑制黑色素瘤细胞中的侵袭伪足形成和细胞外基质降解。

The fucose salvage pathway inhibits invadopodia formation and extracellular matrix degradation in melanoma cells.

机构信息

Department of Cellular and Molecular Physiology, Penn State College of Medicine, Hershey, Pennsylvania, United States of America.

University of South Florida Cancer Biology Graduate Program, Tampa, Florida, United States of America.

出版信息

PLoS One. 2018 Jun 20;13(6):e0199128. doi: 10.1371/journal.pone.0199128. eCollection 2018.

Abstract

The fucose salvage pathway is a two-step process in which mammalian cells transform L-fucose into GDP-L-fucose, a universal fucose donor used by fucosyltransferases to modify glycans. Emerging evidence indicates the fucose salvage pathway and the fucosylation of proteins are altered during melanoma progression and metastasis. However the underlying mechanisms are not completely understood. Here, we report that the fucose salvage pathway inhibits invadopodia formation and extracellular matrix degradation by promoting α-1,2 fucosylation. Chemically or genetically increasing the fucose salvage pathway decreases invadopodium numbers and inhibits the proteolytic activity of invadopodia in WM793 melanoma cells. Inhibiting fucosylation by depleting fucokinase abrogates L-fucose-mediated inhibition of invadopodia, suggesting dependence on the fucose salvage pathway. The inhibition of invadopodium formation by L-fucose or ectopically expressed FUK could be rescued by treatment with α-1,2, but not α-1,3/α-1,4 fucosidase, implicating an α-1,2 fucose linkage-dependent anti-metastatic effect. The expression of FUT1, an α-1,2 fucosyltransferase, is remarkably down-regulated during melanoma progression, and the ectopic expression of FUT1 is sufficient to inhibit invadopodium formation and ECM degradation. Our findings indicate that the fucose salvage pathway can inhibit invadopodium formation, and consequently, invasiveness in melanoma via α-1,2 fucosylation. Re-activation of this pathway in melanoma could be useful for preventing melanoma invasion and metastasis.

摘要

岩藻糖补救途径是一个两步过程,在此过程中哺乳动物细胞将 L-岩藻糖转化为 GDP-L-岩藻糖,这是一种通用的岩藻糖供体,被岩藻糖基转移酶用于修饰聚糖。新出现的证据表明,岩藻糖补救途径和蛋白质的岩藻糖化在黑色素瘤进展和转移过程中发生改变。然而,其潜在机制尚不完全清楚。在这里,我们报告岩藻糖补救途径通过促进α-1,2 岩藻糖基化来抑制侵袭小体的形成和细胞外基质的降解。化学或遗传上增加岩藻糖补救途径会减少侵袭小体的数量,并抑制 WM793 黑色素瘤细胞中侵袭小体的蛋白水解活性。通过耗尽岩藻激酶来抑制岩藻糖基化会消除 L-岩藻糖介导的侵袭小体抑制作用,表明对岩藻糖补救途径的依赖性。L-岩藻糖或过表达 FUK 对侵袭小体形成的抑制作用可以通过用α-1,2,但不是α-1,3/α-1,4 岩藻糖苷酶处理来挽救,这暗示了与岩藻糖补救途径有关的抗转移作用。在黑色素瘤进展过程中,FUT1(一种α-1,2 岩藻糖基转移酶)的表达显著下调,而过表达 FUT1 足以抑制侵袭小体的形成和 ECM 的降解。我们的研究结果表明,岩藻糖补救途径可以通过α-1,2 岩藻糖基化抑制黑色素瘤中侵袭小体的形成,从而抑制其侵袭性。在黑色素瘤中重新激活该途径可能有助于预防黑色素瘤的侵袭和转移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e515/6010265/0de1149d827a/pone.0199128.g001.jpg

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