TAF1L promotes development of oral squamous cell carcinoma via decreasing autophagy-dependent apoptosis
Identifieur interne : 000041 ( Main/Curation ); précédent : 000040; suivant : 000042TAF1L promotes development of oral squamous cell carcinoma via decreasing autophagy-dependent apoptosis
Auteurs : Daiwei Wang [République populaire de Chine] ; Hong Qi [République populaire de Chine] ; Haoxing Zhang [République populaire de Chine] ; Wei Zhou [République populaire de Chine] ; Yanpeng Li [République populaire de Chine] ; Ang Li [République populaire de Chine] ; Qiong Liu [République populaire de Chine] ; Yun Wang [République populaire de Chine]Source :
- International Journal of Biological Sciences [ 1449-2288 ] ; 2020.
Abstract
This study focused on investigating the relationships of TAF1L expression and clinical features or pathological stages of oral squamous cell carcinoma (OSCC), and its potential roles of TAF1L on OSCC development. Western blot and immunohistochemical staining were used to detect TAF1L expression in OSCC tissues and cells. Effects of TAF1L on OSCC cells
Url:
DOI: 10.7150/ijbs.41148
PubMed: 32174793
PubMed Central: 7053316
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<front><div type="abstract" xml:lang="en"><p>This study focused on investigating the relationships of TAF1L expression and clinical features or pathological stages of oral squamous cell carcinoma (OSCC), and its potential roles of TAF1L on OSCC development. Western blot and immunohistochemical staining were used to detect TAF1L expression in OSCC tissues and cells. Effects of TAF1L on OSCC cells<italic> in vitro</italic>
were examined by cell proliferation assay, wound healing assay, transwell chamber assay, flow cytometry analysis and siRNA technique. Cellular key proteins related to cell autophagy and apoptosis were evaluated by Western blot and immunofluorescent staining. Moreover, functions of TAF1L on OSCC process were observed in nude mouse model. Testing results showed that expression of TAF1L protein was higher in OSCC tissues than that in normal oral epithelial or paracancerous tissues. Additionally, the level of TAF1L protein expression was upregulated in OSCC cell lines, compared to that in normal oral epithelial cells. Furthermore, cell proliferation, migration, autophagy and apoptosis were modulated post siRNA-<italic>TAF1L</italic>
treatment <italic>in vitro</italic>
. Especially, TAF1L knockdown-induced apoptotic activation on OSCC cells could be rescued by autophagic activator (Rapamycin). Moreover, that overexpression of TAF1L protein could promote the growth of OSCC cell xenografts was confirmed in nude mouse model. Taken together, it suggests that TAF1L may facilitate OSCC cells to escape cell apoptosis via autophagic activation for enhancing OSCC development.</p>
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