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LKB1 消除了 Snail 的稳定性,并抑制了二甲双胍治疗后的胰腺癌转移。

LKB1 obliterates Snail stability and inhibits pancreatic cancer metastasis in response to metformin treatment.

机构信息

Key Laboratory of Food Safety Research, Institute for Nutritional Sciences, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.

University of the Chinese Academy of Sciences, Shanghai, China.

出版信息

Cancer Sci. 2018 May;109(5):1382-1392. doi: 10.1111/cas.13591.

Abstract

Metastasis to distant organs is a particularly ominous feature of malignant cancer. LKB1 (also known as STK11) has been identified as a tumor suppressor in several types of cancers. Here, we show that LKB1 is at low levels and is negatively associated with poor clinical outcomes in pancreatic cancer (PC). LKB1 is inversely correlated with Snail protein in PC, in which the loss of LKB1 facilitates metastasis through elevating Snail protein level. Furthermore, LKB1 boosts Snail's interaction with E3 ligase FBXL14, leading to increasing ubiquitin-mediated Snail degradation. Notably, metformin could increase Snail protein ubiquitination via augmenting the location of LKB1 at cytoplasm as well as increasing LKB1 expression. Altogether, our data established that LKB1 impedes invasion and metastasis by decreasing the Snail protein level in PC. Targeting the LKB1/FBXL14/Snail axis may represent a promising therapeutic strategy and metformin might be beneficial for PC therapy through activating the LKB1-mediated Snail ubiquitination pathway.

摘要

远处器官转移是恶性癌症的一个特别危险的特征。LKB1(也称为 STK11)已被确定为几种类型癌症的肿瘤抑制因子。在这里,我们表明 LKB1 在胰腺癌(PC)中水平较低,与不良的临床结局呈负相关。LKB1 在 PC 中与 Snail 蛋白呈负相关,其中 LKB1 的缺失通过提高 Snail 蛋白水平促进转移。此外,LKB1 增强了 Snail 与 E3 连接酶 FBXL14 的相互作用,导致泛素介导的 Snail 降解增加。值得注意的是,二甲双胍可以通过增加 LKB1 在细胞质中的位置以及增加 LKB1 的表达来增加 Snail 蛋白的泛素化。总的来说,我们的数据表明 LKB1 通过降低 PC 中的 Snail 蛋白水平来抑制侵袭和转移。针对 LKB1/FBXL14/Snail 轴可能代表一种有前途的治疗策略,二甲双胍可能通过激活 LKB1 介导的 Snail 泛素化途径对 PC 治疗有益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dedf/5980291/f77963066675/CAS-109-1382-g001.jpg

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