4.6 Article

The polypeptide N-acetylgalactosaminyltransferase 4 exhibits stage-dependent expression in colorectal cancer and affects tumorigenesis, invasion and differentiation

Journal

FEBS JOURNAL
Volume 285, Issue 16, Pages 3041-3055

Publisher

WILEY
DOI: 10.1111/febs.14593

Keywords

colorectal cancer; glycosyltransferase; O-glycosylation; ppGalNAc-T4; stage-dependent expression

Funding

  1. National Natural Science Foundation of China [31370806, 31170771, 31570796, 31600643, 31670807, 31770850]
  2. National Basic Research Program of China [2012CB822103, 2011CB910603]
  3. Shanghai Municipal Commission of Health and Family Planning Program [201640030]
  4. Shanghai Translational Medicine Collaborative Innovation Center Program [TM201701]
  5. Shanghai Jiao Tong University Interdiscipline with Medicine Program [YG2013MS26]
  6. China Postdoctoral Science Foundation [2016M600310]

Ask authors/readers for more resources

The aberrant expression of mucin-type O-glycosylation plays important roles in cancer malignancy. The polypeptide N-acetylgalactosaminyltransferases (ppGalNAc-Ts) are a family of conserved enzymes that initiate the mucin-type O-glycosylation in cells. In human, consistent up- or down-regulation of ppGalNAc-Ts expression during cancer development has been frequently reported. Here, we provide evidence that ppGalNAc-T4 shows a stage-dependent expression at the different stages of colorectal cancer (CRC) in the 62 pair-matched tumor/normal tissues. In detail, ppGalNAc-T4 expression is significantly induced at stage I and II but not at stage III and IV. Overexpression of ppGalNAc-T4 in CRC cells enhances colony formation and sphere formation suggesting an important role of ppGalNAc-T4 in tumorigenesis. Conversely, knockdown of ppGalNAc-T4 in CRC cells increases the cell migration and invasion, and leads to an epithelial-mesenchymal transition-like transition. Further analysis suggests that loss of ppGalNAc-T4 contributes to the dedifferentiation of CRC and high expression of ppGalNAc-T4 correlates to a good prognosis of patients. Taken together, our results not only demonstrate a stage-dependent expression of ppGalNAc-T4 in CRC progression, but also suggest that such stage-dependent expression may contribute to the tumorigenesis at the early stage and promote cell migration and invasion at the advanced stage.

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