How glycosylation aids tumor angiogenesis: An updated review

被引:31
作者
Cheng, Wei Kang [1 ]
Oon, Chern Ein [1 ]
机构
[1] Univ Sains Malaysia, Inst Res Mol Med INFORMM, George Town 11800, Malaysia
关键词
Glycosylation; Glycans; Tumor; Angiogenesis; HEPARAN-SULFATE; O-GLCNACYLATION; CELL-ADHESION; CANCER; GLYCANS; VEGF; METASTASIS; METABOLISM; ACTIVATION; PATHWAYS;
D O I
10.1016/j.biopha.2018.04.119
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Glycosylation is an enzymatic process in which a carbohydrate is attached to a functional group from another molecule. Glycosylation is a crucial post translational process in protein modification. The tumor micro-environment produces altered glycans that contribute to cancer progression and aggressiveness. Abnormal glycosylation is widely observed in tumor angiogenesis. Despite many attempts to decipher the role of glycosylation in different aspects of cancer, little is known regarding the roles of glycans in angiogenesis. The blood vessels in tumors are often used to transport oxygen and nutrients for tumor progression and metastasis. The crosstalk within the tumor microenvironment can induce angiogenesis by manipulating these glycans to hijack the normal angiogenesis process, thus promoting tumor growth. Abnormal glycosylation has been shown to promote tumor angiogenesis by degrading the extracellular matrix to activate the angiogenic signaling pathways. This review highlights the latest update on how glycosylation can contribute to tumor angiogenesis that may affect treatment outcomes.
引用
收藏
页码:1246 / 1252
页数:7
相关论文
共 70 条
[1]   Atu027, a Liposomal Small Interfering RNA Formulation Targeting Protein Kinase N3, Inhibits Cancer Progression [J].
Aleku, Manuela ;
Schulz, Petra ;
Keil, Oliver ;
Santel, Ansgar ;
Schaeper, Ute ;
Dieckhoff, Britta ;
Janke, Oliver ;
Endruschat, Jens ;
Durieux, Birgit ;
Roeder, Nadine ;
Loeffler, Kathrin ;
Lange, Christian ;
Fechtner, Melanie ;
Moepert, Kristin ;
Fisch, Gerald ;
Dames, Sibylle ;
Arnold, Wolfgang ;
Jochims, Karin ;
Giese, Klaus ;
Wiedenmann, Bertram ;
Scholz, Arne ;
Kaufmann, Joerg .
CANCER RESEARCH, 2008, 68 (23) :9788-9798
[2]   Organelle Specific O-Glycosylation Drives MMP14 Activation, Tumor Growth, and Metastasis [J].
Anh Tuan Nguyen ;
Chia, Joanne ;
Ros, Manon ;
Hui, Kam Man ;
Saltel, Frederic ;
Bard, Frederic .
CANCER CELL, 2017, 32 (05) :639-+
[3]  
[Anonymous], 2014, ROBBINS COTRAN PATHO
[4]   Notch signaling: Cell fate control and signal integration in development [J].
Artavanis-Tsakonas, S ;
Rand, MD ;
Lake, RJ .
SCIENCE, 1999, 284 (5415) :770-776
[5]   The Notch Ligands Dll4 and Jagged1 Have Opposing Effects on Angiogenesis [J].
Benedito, Rui ;
Roca, Cristina ;
Soerensen, Inga ;
Adams, Susanne ;
Gossler, Achim ;
Fruttiger, Marcus ;
Adams, Ralf H. .
CELL, 2009, 137 (06) :1124-1135
[6]   Matrix metalloproteinase-9 triggers the angiogenic switch during carcinogenesis [J].
Bergers, G ;
Brekken, R ;
McMahon, G ;
Vu, TH ;
Itoh, T ;
Tamaki, K ;
Tanzawa, K ;
Thorpe, P ;
Itohara, S ;
Werb, Z ;
Hanahan, D .
NATURE CELL BIOLOGY, 2000, 2 (10) :737-744
[7]   Jagged mediates differences in normal and tumor angiogenesis by affecting tip-stalk fate decision [J].
Boareto, Marcelo ;
Jolly, Mohit Kumar ;
Ben-Jacob, Eshel ;
Onuchic, Jose N. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2015, 112 (29) :E3836-E3844
[8]   Metabolic Enzymes Moonlighting in the Nucleus: Metabolic Regulation of Gene Transcription [J].
Boukouris, Aristeidis E. ;
Zervopoulos, Sotirios D. ;
Michelakis, Evangelos D. .
TRENDS IN BIOCHEMICAL SCIENCES, 2016, 41 (08) :712-730
[9]   Insights into the role of sulfated glycans in cancer cell adhesion and migration through use of branched peptide probe [J].
Brunetti, Jlenia ;
Depau, Lorenzo ;
Falciani, Chiara ;
Gentile, Mariangela ;
Mandarini, Elisabetta ;
Riolo, Giulia ;
Lupetti, Pietro ;
Pini, Alessandro ;
Bracci, Luisa .
SCIENTIFIC REPORTS, 2016, 6
[10]   Computational Identification and Modeling of Crosstalk between Phosphorylation, O-β-glycosylation and Methylation of FoxO3 and Implications for Cancer Therapeutics [J].
Butt, Azeem Mehmood ;
Feng, Dandan ;
Idrees, Muhammad ;
Tong, Yigang ;
Lu, Jun .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2012, 13 (03) :2918-2938