Pathophysiological relationship between hypoxia associated oxidative stress, Epithelial-mesenchymal transition, stemness acquisition and alteration of Shh/ Gli-1 axis during oral sub-mucous fibrosis and oral squamous cell carcinoma

• Published in: European journal of cell biology Vol. 100; no. 1; p. 151146
• Main Authors: Chatterjee, Ritam, Ghosh, Biswajoy, Mandal, Mousumi, Nawn, Debaleena, Banerjee, Satarupa, Pal, Mousumi, Paul, Ranjan Rashmi, Banerjee, Swarnabindu, Chatterjee, Jyotirmoy
• Format: Journal Article
• Language: English
• Published: Germany Elsevier GmbH 01.01.2021; Elsevier
• Subjects: Epithelial-mesenchymal transition; Oral squamous cell carcinoma; Oral sub-mucous fibrosis; Oxidative stress; Stemness; Oxidative stress; Epithelial-mesenchymal transition; Stemness; Oral sub-mucous fibrosis; Oral squamous cell carcinoma; epithelial-mesenchymal transition; oral squamous cell carcinoma; oral sub-mucous fibrosis; oxidative stress; stemness
• ISSN: 0171-9335; 1618-1298
• DOI: 10.1016/j.ejcb.2020.151146

[Display omitted] •Oxidative stress in association with hypoxia promotes EMT in OSF and OSCC.•Oxidative stress mediated EMT is associated with p-ERK up-regulation.•EMT in OSF promotes sub-epithelial fibrosis and in OSCC associates metastasis.•Acquisition of stemness in OSCC associated with EMT.•Hypoxia associated Shh/ Gli-1 signaling promotes disease pathophysiologies. Oral sub-mucous fibrosis (OSF) is a pathophysiological state of oral cavity or oropharynx having a high chance of conversion to oral squamous cell carcinoma (OSCC). It involves fibrotic transformation of sub-epithelial matrix along with epithelial abnormalities. The present work aims to unveil the mechanistic domain regarding OSF to OSCC conversion exploring the scenario of hypoxia associated oxidative stress, epithelial-mesenchymal transition (EMT), metastasis and stemness acquisition. The study involves histopathological analysis of the diseased condition along with the exploration of oxidative stress status, assessment of mitochondrial condition, immunohistochemical analysis of HIF-1α, E-cadherin, vimentin, ERK, ALDH-1, CD133, Shh, Gli-1 and survivin expressions in the oral epithelial region together with the quantitative approach towards collagen deposition in the sub-epithelial matrix. Oxidative stress was found to be associated with type-II EMT in case of OSF attributing the development of sub-epithelial fibrosis and type-III EMT in case of OSCC favoring malignancy associated metastasis. Moreover, the acquisition of stemness during OSCC can also be correlated with EMT. Alteration of Shh and Gli-1 expression pattern revealed the mechanistic association of hypoxia with the phenotypic plasticity and disease manifestation in case of OSF as well as OSCC. Shh/ Gli-1 signaling can also be correlated with survivin mediated cytoprotective phenomenon under oxidative stress. Overall, the study established the correlative network of hypoxia associated oxidative stress, EMT and manifestation of oral pre-cancerous and cancerous condition in a holistic approach that may throw rays of hope in the therapeutic domain of the concerned diseases.