Hedgehog signaling pathway mediates tongue tumorigenesis in wild-type mice but not in Gal3-deficient mice

Débora de Oliveira Santos, Adriano Mota Loyola, Sérgio Vitorino Cardoso, Roger Chammas, Fu-Tong Liu, Paulo Rogério de Faria

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Oral squamous cell carcinoma (OSCC) is one of the most aggressive cancers of the oral cavity and an important cause of death worldwide. Currently, there are limited clinical tools aiding clinicians to establish its early diagnosis, and genetic and epigenetic events leading to the pathogenesis of OSCC remain unsolved. The use of carcinogen-induced knocked out mouse models would help to improve its early detection and also determine the role of proteins such as galectin-3 (Gal3) in this process. Here we used a mouse model of oral carcinogenesis employing two mouse genotypes: wild-type (Gal3. +/+) and galectin-3-deficient mice (Gal3. -/-) challenged by the carcinogen 4NQO for 16. weeks. After induction, the expression of Wnt1, Wnt3A, Shh and Gli3 proteins in tongue samples was evaluated using an immunohistochemistry approach. All samples of dysplasia and carcinoma were negative for Wnt1. Wnt3A expression was detected in both Gal3. +/+ and Gal3. -/- mice, at similar levels. Wnt3A expression did not predict tongue tumorigenesis in either genotype. Dysplastic- and carcinoma-expressing Shh was statistically significantly higher in Gal3. +/+ mice than Gal3. -/- mice (p. <. 0.0001), and was associated with tongue tumorigenesis only in the former. Gli3 expression decreased and increased from dysplasia to carcinoma in Gal3. +/+ and Gal3. -/- mice, respectively, although the difference was not significant. The results suggest that activated Wnt signaling is present in both mice, and that the Hh signaling pathway might play a role in tongue carcinoma development in Gal3. +/+ mice.

Original languageEnglish (US)
Pages (from-to)332-337
Number of pages6
JournalExperimental and Molecular Pathology
Volume97
Issue number3
DOIs
StatePublished - Sep 16 2014

Fingerprint

Galectin 3
Hedgehogs
Tongue
Carcinogenesis
Carcinoma
Carcinogens
Squamous Cell Carcinoma
Genotype
Mouth Neoplasms
Epigenomics
Mouth
Early Diagnosis
Cause of Death
Proteins
Immunohistochemistry

Keywords

  • Galectin-3
  • Mice
  • Oral carcinogenesis
  • Sonic hedgehog
  • Tongue
  • Wnt signaling

ASJC Scopus subject areas

  • Clinical Biochemistry
  • Molecular Biology
  • Pathology and Forensic Medicine
  • Medicine(all)

Cite this

de Oliveira Santos, D., Loyola, A. M., Cardoso, S. V., Chammas, R., Liu, F-T., & de Faria, P. R. (2014). Hedgehog signaling pathway mediates tongue tumorigenesis in wild-type mice but not in Gal3-deficient mice. Experimental and Molecular Pathology, 97(3), 332-337. https://doi.org/10.1016/j.yexmp.2014.09.018

Hedgehog signaling pathway mediates tongue tumorigenesis in wild-type mice but not in Gal3-deficient mice. / de Oliveira Santos, Débora; Loyola, Adriano Mota; Cardoso, Sérgio Vitorino; Chammas, Roger; Liu, Fu-Tong; de Faria, Paulo Rogério.

In: Experimental and Molecular Pathology, Vol. 97, No. 3, 16.09.2014, p. 332-337.

Research output: Contribution to journalArticle

de Oliveira Santos, D, Loyola, AM, Cardoso, SV, Chammas, R, Liu, F-T & de Faria, PR 2014, 'Hedgehog signaling pathway mediates tongue tumorigenesis in wild-type mice but not in Gal3-deficient mice', Experimental and Molecular Pathology, vol. 97, no. 3, pp. 332-337. https://doi.org/10.1016/j.yexmp.2014.09.018
de Oliveira Santos, Débora ; Loyola, Adriano Mota ; Cardoso, Sérgio Vitorino ; Chammas, Roger ; Liu, Fu-Tong ; de Faria, Paulo Rogério. / Hedgehog signaling pathway mediates tongue tumorigenesis in wild-type mice but not in Gal3-deficient mice. In: Experimental and Molecular Pathology. 2014 ; Vol. 97, No. 3. pp. 332-337.
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