Cargando…

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

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 rel...

Descripción completa

Detalles Bibliográficos
Autores principales: Ma, Tianran, Wang, Yan, Jia, Liyuan, Shu, Jian, Yu, Hanjie, Du, Haoqi, Yang, Jiajun, Liang, Yiqian, Chen, Mingwei, Li, Zheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9066710/
https://www.ncbi.nlm.nih.gov/pubmed/35518855
http://dx.doi.org/10.1039/c9ra04341a
_version_ 1784699851691261952
author Ma, Tianran
Wang, Yan
Jia, Liyuan
Shu, Jian
Yu, Hanjie
Du, Haoqi
Yang, Jiajun
Liang, Yiqian
Chen, Mingwei
Li, Zheng
author_facet Ma, Tianran
Wang, Yan
Jia, Liyuan
Shu, Jian
Yu, Hanjie
Du, Haoqi
Yang, Jiajun
Liang, Yiqian
Chen, Mingwei
Li, Zheng
author_sort Ma, Tianran
collection PubMed
description 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 N-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 Pisum sativum agglutinin (PSA) and Lens culinaris agglutinin (LCA) was significantly increased in LUSC tissues compared with PCTs. There were 10 and 15 fucosylated N-linked glycans that were detected in PCTs and LUSC tissues respectively, 10 fucosylated N-glycans were common, while five fucosylated N-glycans were unique to LUSC tissues. And the abundance of the fucosylated N-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.
format Online
Article
Text
id pubmed-9066710
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher The Royal Society of Chemistry
record_format MEDLINE/PubMed
spelling pubmed-90667102022-05-04 Increased expression of core-fucosylated glycans in human lung squamous cell carcinoma Ma, Tianran Wang, Yan Jia, Liyuan Shu, Jian Yu, Hanjie Du, Haoqi Yang, Jiajun Liang, Yiqian Chen, Mingwei Li, Zheng RSC Adv Chemistry 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 N-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 Pisum sativum agglutinin (PSA) and Lens culinaris agglutinin (LCA) was significantly increased in LUSC tissues compared with PCTs. There were 10 and 15 fucosylated N-linked glycans that were detected in PCTs and LUSC tissues respectively, 10 fucosylated N-glycans were common, while five fucosylated N-glycans were unique to LUSC tissues. And the abundance of the fucosylated N-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. The Royal Society of Chemistry 2019-07-16 /pmc/articles/PMC9066710/ /pubmed/35518855 http://dx.doi.org/10.1039/c9ra04341a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Ma, Tianran
Wang, Yan
Jia, Liyuan
Shu, Jian
Yu, Hanjie
Du, Haoqi
Yang, Jiajun
Liang, Yiqian
Chen, Mingwei
Li, Zheng
Increased expression of core-fucosylated glycans in human lung squamous cell carcinoma
title Increased expression of core-fucosylated glycans in human lung squamous cell carcinoma
title_full Increased expression of core-fucosylated glycans in human lung squamous cell carcinoma
title_fullStr Increased expression of core-fucosylated glycans in human lung squamous cell carcinoma
title_full_unstemmed Increased expression of core-fucosylated glycans in human lung squamous cell carcinoma
title_short Increased expression of core-fucosylated glycans in human lung squamous cell carcinoma
title_sort increased expression of core-fucosylated glycans in human lung squamous cell carcinoma
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9066710/
https://www.ncbi.nlm.nih.gov/pubmed/35518855
http://dx.doi.org/10.1039/c9ra04341a
work_keys_str_mv AT matianran increasedexpressionofcorefucosylatedglycansinhumanlungsquamouscellcarcinoma
AT wangyan increasedexpressionofcorefucosylatedglycansinhumanlungsquamouscellcarcinoma
AT jialiyuan increasedexpressionofcorefucosylatedglycansinhumanlungsquamouscellcarcinoma
AT shujian increasedexpressionofcorefucosylatedglycansinhumanlungsquamouscellcarcinoma
AT yuhanjie increasedexpressionofcorefucosylatedglycansinhumanlungsquamouscellcarcinoma
AT duhaoqi increasedexpressionofcorefucosylatedglycansinhumanlungsquamouscellcarcinoma
AT yangjiajun increasedexpressionofcorefucosylatedglycansinhumanlungsquamouscellcarcinoma
AT liangyiqian increasedexpressionofcorefucosylatedglycansinhumanlungsquamouscellcarcinoma
AT chenmingwei increasedexpressionofcorefucosylatedglycansinhumanlungsquamouscellcarcinoma
AT lizheng increasedexpressionofcorefucosylatedglycansinhumanlungsquamouscellcarcinoma