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核心岩藻糖基化聚糖在人肺鳞状细胞癌中的表达增加。

Increased expression of core-fucosylated glycans in human lung squamous cell carcinoma.

作者信息

Ma Tianran, Wang Yan, Jia Liyuan, Shu Jian, Yu Hanjie, Du Haoqi, Yang Jiajun, Liang Yiqian, Chen Mingwei, Li Zheng

机构信息

Laboratory for Functional Glycomics, College of Life Sciences, Northwest University No. 229 Taibai Beilu Xi'an 710069 China

Department of Respiratory and Critical Care Medicine, The First Affiliated Hospital of School of Medicine of Xi'an, Jiaotong University Xi'an 710061 China

出版信息

RSC Adv. 2019 Jul 16;9(38):22064-22073. doi: 10.1039/c9ra04341a. eCollection 2019 Jul 11.

Abstract

Lung cancer is the most frequent cancer and the leading cause of cancer around the world. As one of the major types of lung cancer, lung squamous cell carcinoma (LUSC) is closely associated with smoking and shows poor sensitivity to therapy and prognosis. Although alteration of glycopatterns are reliable indicators of cancer, little is known about the alterations of protein glycosylation related to LUSC. In this study, we compared the differential expression levels of glycopatterns in seven pairs of LUSC tissues and normal pericarcinomatous tissues (PCTs) using lectin microarrays. Fluorescence-based lectin histochemistry and lectin blotting were utilized to validate and assess the expression and distribution of certain glycans in LUSC tissues and PCTs. And we further analyzed their total -linked glycans using MALDI-TOF/TOF-MS to provide more information about the aberrant glycopatterns. The results showed that the expression level of the core fucosylation recognized by agglutinin (PSA) and agglutinin (LCA) was significantly increased in LUSC tissues compared with PCTs. There were 10 and 15 fucosylated -linked glycans that were detected in PCTs and LUSC tissues respectively, 10 fucosylated -glycans were common, while five fucosylated -glycans were unique to LUSC tissues. And the abundance of the fucosylated -glycans was increased from 40.9% (PCTs) to 48.3% (LUSC). These finding is helpful to elucidate the molecular mechanisms underlying the lung diseases and develop new treatment strategies.

摘要

肺癌是全球最常见的癌症,也是癌症的主要致死原因。作为肺癌的主要类型之一,肺鳞状细胞癌(LUSC)与吸烟密切相关,对治疗和预后的敏感性较差。尽管糖模式的改变是癌症的可靠指标,但关于与LUSC相关的蛋白质糖基化改变却知之甚少。在本研究中,我们使用凝集素微阵列比较了7对LUSC组织和正常癌旁组织(PCT)中糖模式的差异表达水平。利用基于荧光的凝集素组织化学和凝集素印迹法来验证和评估LUSC组织和PCT中某些聚糖的表达和分布。并且我们进一步使用基质辅助激光解吸电离飞行时间串联质谱(MALDI-TOF/TOF-MS)分析了它们的全连接聚糖,以提供更多关于异常糖模式的信息。结果表明,与PCT相比,LUSC组织中由荆豆凝集素(PSA)和小扁豆凝集素(LCA)识别的核心岩藻糖基化表达水平显著增加。在PCT和LUSC组织中分别检测到10种和15种岩藻糖基化的N-连接聚糖,10种岩藻糖基化的N-聚糖是常见的,而5种岩藻糖基化的N-聚糖是LUSC组织特有的。并且岩藻糖基化的N-聚糖的丰度从40.9%(PCT)增加到48.3%(LUSC)。这些发现有助于阐明肺部疾病的分子机制并开发新的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7165/9066710/20014d4d0792/c9ra04341a-f1.jpg

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