Abstract |
Heparan sulfate (HS) with various sulfation patterns is one of important modulators of cancer cell fate through interacting with numerous growth factors. Here we found HS 2-O sulfotransferase 1 (HS2ST1) was downregulated at both mRNA and protein levels during granulocytic differentiation of SKM-1 leukemia cells and also HS ( glucosamine) 3-O sulfotransferase 3A (HS3ST3A) in epithelial-mesenchymal transition (EMT) of A549 lung cancer cells, meanwhile, cell-surface HS recognized by anti-HS antibody was also changed in both cancer cell lines. Further, HS3ST3A was negatively correlated with the in vitro cell metastasis capability of A549 cells confirmed by RNA interference technology, wound-healing assay and in vitro Matrigel invasion assay. Together, specific HS sulfotransferases may serve as molecular markers and targets for cancer treatment.
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Authors | Shancheng Zhao, Zhen Wang |
Journal | Glycoconjugate journal
(Glycoconj J)
Vol. 37
Issue 2
Pg. 151-164
(04 2020)
ISSN: 1573-4986 [Electronic] United States |
PMID | 31863309
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Heparitin Sulfate
- Sulfotransferases
- heparan-sulfate 2-sulfotransferase
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Topics |
- A549 Cells
- Cell Differentiation
- Cell Movement
- Epithelial-Mesenchymal Transition
- Granulocytes
(cytology, metabolism)
- Heparitin Sulfate
(metabolism)
- Humans
- Sulfotransferases
(genetics, metabolism)
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