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p63 inhibits CD44(+)/CD24(−) cell proliferation and chemoresistance in papillary thyroid carcinoma cells

Thyroid cancer typically has a good prognosis; however, the risks of recurrence and chemoresistance associated with thyroid cancer remain a cause for concern. Papillary thyroid carcinoma (PTC) comprises 80% of all cases of thyroid carcinoma. A previous study reported that cluster of differentiation...

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Detalles Bibliográficos
Autores principales: Guo, Jing-Jing, Xu, Hong-Shun, Wu, Gang, Ma, Zhen-Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5704253/
https://www.ncbi.nlm.nih.gov/pubmed/29201169
http://dx.doi.org/10.3892/etm.2017.5137
Descripción
Sumario:Thyroid cancer typically has a good prognosis; however, the risks of recurrence and chemoresistance associated with thyroid cancer remain a cause for concern. Papillary thyroid carcinoma (PTC) comprises 80% of all cases of thyroid carcinoma. A previous study reported that cluster of differentiation (CD) 44(+)/CD24(−) PTC cells may contribute to PTC recurrence and chemoresistance; however, the underlying molecular mechanisms remain elusive. In the present study, CD44(+)/CD24(−) cells were isolated from the TPC-1 PTC cell line and biological function assays revealed that CD44(+)/CD24(−) cells were significantly more proliferative and chemoresistant compared with CD44(−)/CD24(−) cells. Furthermore, the expression level of p63 was demonstrated to be negatively correlated with the expression of CD44 in PTC cells. The role of p63 in CD44(+)/CD24(−) cell proliferation and chemoresistance was investigated and, the ectopic expression of p63 was observed to significantly inhibit CD44(+)/CD24(−) cell proliferation and chemoresistance in vitro and in vivo. In conclusion, the present study indicated that CD44(+)/CD24(−) cells contribute to PTC proliferation and chemoresistance and that the suppression of p63 in CD44(+)/CD24(−) cells contributes to these effects.