» Articles » PMID: 28822024

Glycosaminoglycans and Glycolipids As Potential Biomarkers in Lung Cancer

Overview
Journal Glycoconj J
Publisher Springer
Date 2017 Aug 20
PMID 28822024
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

In this report, we used liquid chromatography-mass spectrometry and Western blotting to analyze the content and structure of glycosaminoglycans, glycolipids and selected proteins to compare differences between patient-matched normal and cancerous lung tissues obtained from lung cancer patients. The cancer tissue samples contained over twice as much chondroitin sulfate (CS)/dermatan sulfate (DS) as did the normal tissue samples, while the amount of heparan sulfate (HS) and hyaluronan (HA) in normal and cancer tissues were not significantly different. In HS, several minor disaccharide components, including NS6S, NS2S and 2S were significantly lower in cancer tissues, while the levels of major disaccharides, TriS, NS and 0S disaccharides were not significantly different in normal and cancer tissues. In regards to CS/DS, the level of 4S disaccharide (the major component of CS-type A and DS) decreased and the level of 6S disaccharide (the major component of CS- type C) increased in cancer tissues. We also compared the content and structure of GAGs in lung tissues from smoking and non-smoking patients. Analysis of the glycolipids showed all lipids present in these lung tissues, with the exception of sphingomyelin were higher in cancer tissues than in normal tissues. Western analysis showed that syndecan 1 and 2 proteoglycans displayed much higher expression in cancer tissue/biopsy samples. This investigation begins to provide an understanding of patho-physiological roles on glycosaminoglycans and glycolipids and might be useful in identifying potential biomarkers in lung cancer.

Citing Articles

Targeting nanoparticles to lung cancer-derived A549 cells based on changes on interstitial stiffness in biomimetic models.

Kohon A, Man K, Hessami A, Mathis K, Webb J, Fang J iScience. 2024; 27(10):111015.

PMID: 39435151 PMC: 11492096. DOI: 10.1016/j.isci.2024.111015.


Discriminating Benign from Malignant Lung Diseases Using Plasma Glycosaminoglycans and Cell-Free DNA.

Qvick A, Bratulic S, Carlsson J, Stenmark B, Karlsson C, Nielsen J Int J Mol Sci. 2024; 25(18).

PMID: 39337265 PMC: 11431521. DOI: 10.3390/ijms25189777.


Biomarkers in Cancer Detection, Diagnosis, and Prognosis.

Das S, Dey M, Devireddy R, Gartia M Sensors (Basel). 2024; 24(1).

PMID: 38202898 PMC: 10780704. DOI: 10.3390/s24010037.


Compositional Analysis of Glycosaminoglycans in Different Lung Cancer Types-A Pilot Study.

Pal D, Toth G, Sugar S, Fugedi K, Szabo D, Kovalszky I Int J Mol Sci. 2023; 24(8).

PMID: 37108213 PMC: 10138872. DOI: 10.3390/ijms24087050.


Inter- and intratumoral proteomics and glycosaminoglycan characterization of ALK rearranged lung adenocarcinoma tissues: a pilot study.

Balbisi M, Sugar S, Schlosser G, Szeitz B, Fillinger J, Moldvay J Sci Rep. 2023; 13(1):6268.

PMID: 37069213 PMC: 10110559. DOI: 10.1038/s41598-023-33435-1.


References
1.
Shi X, Liang W, Yang W, Xia R, Song Y . Decorin is responsible for progression of non-small-cell lung cancer by promoting cell proliferation and metastasis. Tumour Biol. 2014; 36(5):3345-54. DOI: 10.1007/s13277-014-2968-8. View

2.
Yang B, Chang Y, Weyers A, Sterner E, Linhardt R . Disaccharide analysis of glycosaminoglycan mixtures by ultra-high-performance liquid chromatography-mass spectrometry. J Chromatogr A. 2012; 1225:91-8. PMC: 3268819. DOI: 10.1016/j.chroma.2011.12.063. View

3.
Yeat N, Lin C, Sager M, Lin J . Cancer proteomics: developments in technology, clinical use and commercialization. Expert Rev Proteomics. 2015; 12(4):391-405. DOI: 10.1586/14789450.2015.1051969. View

4.
Matsuda Y, Yamamoto T, Kudo M, Kawahara K, Kawamoto M, Nakajima Y . Expression and roles of lumican in lung adenocarcinoma and squamous cell carcinoma. Int J Oncol. 2008; 33(6):1177-85. View

5.
Couchman J, Pataki C . An introduction to proteoglycans and their localization. J Histochem Cytochem. 2012; 60(12):885-97. PMC: 3527888. DOI: 10.1369/0022155412464638. View