Abstract | Objectives: Materials and Methods: Histopathological examination was performed using hematoxylin- eosin-stained surgical margin tissue sections in 235 OSCC patients. Axin2 and Snail expression at the surgical margin was detected by immunohistochemistry. The impact of the Axin2-Snail cascade on tumorigenesis of the immortalized human oral keratinocyte (IHOK) line was investigated in vivo. Results: The width and dysplasia of surgical margins were not significantly associated with the outcome of OSCC patients. In a multivariate analysis using variable clinicopathologic factors and with Axin2 and Snail expression as cofactors, higher age (hazard ratio [HR]:1.050; P=0.047), Axin2 (HR:6.883; P=0.014), and Snail abundance (HR:5.663; P=0.009) had independent impacts on worsened overall survival. Similarly, lesion site in retromolar trigone (HR:4.077; P=0.010), upper (HR:4.332; P=0.005) and lower gingiva (HR:3.545; P=0.012), presence of extranodal extension (HR:9.967; P<0.001), perineural invasion (HR:3.627; P=0.024), and Snail abundance (HR:3.587; P<0.001) had independent impacts on worsened recurrence-free survival. Furthermore, Axin2 knockdown induced decreased Snail expression and attenuated tumorigenesis in the IHOK line. Conclusion: Histopathological examination of surgical margins may not be reliable to predict OSCC patient outcome. Molecular analysis may provide a more accurate risk assessment of surgical margins in OSCC. In particular, Axin2 and Snail are potential predictive biomarkers for the risk assessment of surgical margins in OSCC.
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Authors | Meiling Pei, Dawool Han, Ki-Yeol Kim, Dong Wook Kim, Woong Nam, Hyung Jun Kim, Eunae Sandra Cho, Hyun Sil Kim, In-Ho Cha, Xianglan Zhang |
Journal | Frontiers in oncology
(Front Oncol)
Vol. 12
Pg. 930988
( 2022)
ISSN: 2234-943X [Print] Switzerland |
PMID | 35875099
(Publication Type: Journal Article)
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Copyright | Copyright © 2022 Pei, Han, Kim, Kim, Nam, Kim, Cho, Kim, Cha and Zhang. |