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脂联素 2 通过抑制肌动蛋白谷胱甘肽化促进侵袭和迁移。

Lipocalin 2 inhibits actin glutathionylation to promote invasion and migration.

机构信息

Cell and Tumor Biology, Advanced Centre for Treatment Research and Education in Cancer (ACTREC), Tata Memorial Centre, Navi Mumbai, India.

Homi Bhabha National Institute, Mumbai, India.

出版信息

FEBS Lett. 2023 Apr;597(8):1086-1097. doi: 10.1002/1873-3468.14572. Epub 2023 Jan 17.

Abstract

Invasive and metastatic tumor cells show an increase in migration and invasion, making the processes contributing to these phenotypes potential therapeutic targets. Lipocalin 2 (LCN2; also known as neutrophil gelatinase-associated lipocalin) is a putative therapeutic target in multiple tumor types and promotes invasion and migration, although the mechanisms underlying these phenotypes are unclear. The data in this report demonstrate that LCN2 promotes actin polymerization, invasion, and migration by inhibiting actin glutathionylation. LCN2 inhibits actin glutathionylation by decreasing the levels of reactive oxygen species (ROS) and by reducing intracellular iron levels. Inhibiting LCN2 function leads to increased actin glutathionylation, decreased migration, and decreased invasion. These results suggest that LCN2 is a potential therapeutic target in invasive tumors.

摘要

侵袭和转移的肿瘤细胞表现出迁移和侵袭能力的增强,使这些表型相关的过程成为潜在的治疗靶点。载脂蛋白 L2(LCN2;也称为中性粒细胞明胶酶相关载脂蛋白)是多种肿瘤类型的潜在治疗靶点,可促进侵袭和迁移,尽管这些表型的机制尚不清楚。本报告中的数据表明,LCN2 通过抑制肌动球蛋白的谷胱甘肽化来促进肌动球蛋白的聚合、侵袭和迁移。LCN2 通过降低活性氧(ROS)水平和减少细胞内铁水平来抑制肌动球蛋白的谷胱甘肽化。抑制 LCN2 功能会导致肌动球蛋白的谷胱甘肽化增加、迁移减少和侵袭减少。这些结果表明,LCN2 是侵袭性肿瘤的一个潜在治疗靶点。

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