NEU4L sialidase overexpression promotes β-catenin signaling in neuroblastoma cells, enhancing stem-like malignant cell growth

Cristina Tringali, Federica Cirillo, Giuseppe Lamorte, Nadia Papini, Luigi Anastasia, Barbara Lupo, Ilaria Silvestri, Guido Tettamanti, Bruno Venerando

Research output: Contribution to journalArticle

15 Citations (Scopus)

Abstract

Neuroblastoma (NB) is a frequently lethal tumor that occurs in childhood and originates from embryonic neural crest cells. The malignant and aggressive phenotype of NB is strictly related to the deregulation of pivotal pathways governing the proliferation/differentiation status of neural crest precursor cells, such as MYCN, Delta/Notch and Wnt/β-catenin (CTNNB1) signaling. In this article, we demonstrate that sialidase NEU4 long (NEU4L) influences the differentiation/proliferation behavior of NB SK-N-BE cells by determining hyperactivation of the Wnt/β-catenin signaling pathway. NEU4L overexpression in SK-N-BE cells induced significant increases in active, nonphosphorylated β-catenin content, β-catenin/TCF transcriptional activity and β-catenin gene target expression including MYCN, MYC, CCND2 (cyclin D2) and CDC25A. In turn, these molecular features strongly modified the behavior of NEU4L SK-N-BE overexpressing cells, promoting the following: (1) an enhanced proliferation rate, mainly due to a faster transition from G1 to S phase in the cell cycle; (2) a more undifferentiated cell phenotype, which was similar to stem-like NB cells and possibly mediated by an increase of the expression of the pluripotency genes, MYC, NANOG, OCT-4, CD133 and NES (nestin); (3) the failure of NB cell differentiation after serum withdrawal. The molecular link between NEU4L and Wnt/β-catenin signaling appeared to rely most likely on the capability of the enzyme to modify the sialylation level of cell glycoproteins. These findings could provide a new candidate for therapeutic treatment.

Original languageEnglish
Pages (from-to)1768-1778
Number of pages11
JournalInternational Journal of Cancer
Volume131
Issue number8
DOIs
Publication statusPublished - Oct 15 2012

Fingerprint

Catenins
Neuraminidase
Neuroblastoma
Stem Cells
Growth
Neural Crest
Cyclin D2
Phenotype
Gene Expression
Nestin
Wnt Signaling Pathway
S Phase
Cell Differentiation
Glycoproteins
Cell Cycle
Enzymes
Serum
Neoplasms

Keywords

  • β-catenin
  • cancer stem cells
  • neuroblastoma
  • sialidase
  • sialoglycoproteins

ASJC Scopus subject areas

  • Cancer Research
  • Oncology

Cite this

NEU4L sialidase overexpression promotes β-catenin signaling in neuroblastoma cells, enhancing stem-like malignant cell growth. / Tringali, Cristina; Cirillo, Federica; Lamorte, Giuseppe; Papini, Nadia; Anastasia, Luigi; Lupo, Barbara; Silvestri, Ilaria; Tettamanti, Guido; Venerando, Bruno.

In: International Journal of Cancer, Vol. 131, No. 8, 15.10.2012, p. 1768-1778.

Research output: Contribution to journalArticle

Tringali, Cristina ; Cirillo, Federica ; Lamorte, Giuseppe ; Papini, Nadia ; Anastasia, Luigi ; Lupo, Barbara ; Silvestri, Ilaria ; Tettamanti, Guido ; Venerando, Bruno. / NEU4L sialidase overexpression promotes β-catenin signaling in neuroblastoma cells, enhancing stem-like malignant cell growth. In: International Journal of Cancer. 2012 ; Vol. 131, No. 8. pp. 1768-1778.
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AU - Tringali, Cristina

AU - Cirillo, Federica

AU - Lamorte, Giuseppe

AU - Papini, Nadia

AU - Anastasia, Luigi

AU - Lupo, Barbara

AU - Silvestri, Ilaria

AU - Tettamanti, Guido

AU - Venerando, Bruno

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AB - Neuroblastoma (NB) is a frequently lethal tumor that occurs in childhood and originates from embryonic neural crest cells. The malignant and aggressive phenotype of NB is strictly related to the deregulation of pivotal pathways governing the proliferation/differentiation status of neural crest precursor cells, such as MYCN, Delta/Notch and Wnt/β-catenin (CTNNB1) signaling. In this article, we demonstrate that sialidase NEU4 long (NEU4L) influences the differentiation/proliferation behavior of NB SK-N-BE cells by determining hyperactivation of the Wnt/β-catenin signaling pathway. NEU4L overexpression in SK-N-BE cells induced significant increases in active, nonphosphorylated β-catenin content, β-catenin/TCF transcriptional activity and β-catenin gene target expression including MYCN, MYC, CCND2 (cyclin D2) and CDC25A. In turn, these molecular features strongly modified the behavior of NEU4L SK-N-BE overexpressing cells, promoting the following: (1) an enhanced proliferation rate, mainly due to a faster transition from G1 to S phase in the cell cycle; (2) a more undifferentiated cell phenotype, which was similar to stem-like NB cells and possibly mediated by an increase of the expression of the pluripotency genes, MYC, NANOG, OCT-4, CD133 and NES (nestin); (3) the failure of NB cell differentiation after serum withdrawal. The molecular link between NEU4L and Wnt/β-catenin signaling appeared to rely most likely on the capability of the enzyme to modify the sialylation level of cell glycoproteins. These findings could provide a new candidate for therapeutic treatment.

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