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J Oral Pathol Med ; 45(3): 180-8, 2016 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-26399460

RESUMO

BACKGROUND: CD44 and aldehyde dehydrogenase 1 (ALDH1) have been shown to be useful markers for identification of cancer stem cells (CSCs). We previously reported that glycogen synthase kinase 3ß (GSK3ß) is involved in regulation of the self-renewal ability of head and neck squamous cell carcinoma (HNSCC) CSCs. The purpose of the present study was to clarify the role of GSK3ß in CD44(high) /ALDH1(high) HNSCC cells. METHODS: Cells with greater expression of CD44 and higher ALDH1 enzymatic activity were FACS sorted from the OM-1 HNSCC cell line. The self-renewal ability of CD44(high) /ALDH1(high) cells was then examined using a tumor sphere formation assay. mRNA expressions of the stem cell markers Sox2, Oct4, and Nanog, as well as GSK3ß were evaluated by real-time RT-PCR. RESULTS: CD44(high) /ALDH1(high) cells exhibited higher tumor sphere forming ability and increased expression of stem cell markers as compared with CD44(high) /ALDH1(low) cells. Interestingly, spindle-shaped cells positive for vimentin were found in the CD44(high) /ALDH1(high) but not the CD44(high) /ALDH1(low) cell population. In addition, the ALDH1 activity and sphere forming ability of CD44(high) /ALDH1(high) cells was significantly inhibited by GSK3ß knockdown. On the other hand, CD44(high) /ALDH1(low) cells exhibited high epidermal growth factor receptor (EGFR) expression and increased cell growth. CONCLUSIONS: Our results show that GSK3ß plays a major role in maintenance of stemness of CD44(high) /ALDH1(high) HNSCC cells. Additionally, they indicate a close relationship between CSC and mesenchymal characteristics in HNSCC.


Assuntos
Carcinoma de Células Escamosas/metabolismo , Glicogênio Sintase Quinase 3 beta/metabolismo , Neoplasias de Cabeça e Pescoço/metabolismo , Receptores de Hialuronatos/biossíntese , Isoenzimas/efeitos dos fármacos , Células-Tronco Neoplásicas/metabolismo , Retinal Desidrogenase/efeitos dos fármacos , Família Aldeído Desidrogenase 1 , Biomarcadores Tumorais/biossíntese , Carcinoma de Células Escamosas/enzimologia , Linhagem Celular Tumoral , Ativação Enzimática , Receptores ErbB/biossíntese , Neoplasias de Cabeça e Pescoço/enzimologia , Humanos , Receptores de Hialuronatos/efeitos dos fármacos , Isoenzimas/biossíntese , Isoenzimas/metabolismo , Células-Tronco Mesenquimais/enzimologia , Células-Tronco Mesenquimais/metabolismo , Proteína Homeobox Nanog/biossíntese , Células-Tronco Neoplásicas/enzimologia , Fatores de Transcrição de Octâmero/biossíntese , RNA Mensageiro/biossíntese , RNA Interferente Pequeno/genética , Retinal Desidrogenase/biossíntese , Retinal Desidrogenase/metabolismo , Fatores de Transcrição SOXB2/biossíntese , Carcinoma de Células Escamosas de Cabeça e Pescoço
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