Integrin α11 is overexpressed by tumour stroma of head and neck squamous cell carcinoma and correlates positively with alpha smooth muscle actin expression. (4th October 2016)

• Record Type: Journal Article
• Authors: Parajuli, Himalaya; Teh, Muy‐Teck; Abrahamsen, Siren; Christoffersen, Ingrid; Neppelberg, Evelyn; Lybak, Stein; Osman, Tarig; Johannessen, Anne Chr.; Gullberg, Donald; Skarstein, Kathrine; Costea, Daniela Elena
• Is Part Of: Journal of oral pathology & medicine. Volume 46:Number 4(2017)
• Page Start: 267
• Page End: 275
• Publication Date: 2016-10-04
• Subjects: ACTA2 -- alpha smooth muscle actin -- immunohistochemistry -- integrin α11 -- ITGA11 -- tumour stroma; Dentistry -- Periodicals; Teeth -- Diseases -- Periodicals; 617
• DOI: 10.1111/jop.12493
• Languages: English
• ISSNs: 0904-2512

Abstract

Abstract : Background: Cancer‐associated fibroblasts (CAFs) were shown to be important for tumour progression in head and neck squamous cell carcinomas (HNSCCs). Their heterogeneity and lack of specific markers is increasingly recognized. Integrin α11 was recently shown to be expressed by CAFs and might serve as a specific CAF marker. Aim: To investigate integrin α11 expression and its correlation with the expression of a well‐known marker of CAF, alpha smooth muscle actin (α‐SMA), in HNSCC. Methods: Fresh frozen (FF) and formalin‐fixed paraffin‐embedded (FFPE) samples from healthy volunteers ( n = 24), oral lichen planus (OLP) ( n = 32) and HNSCC ( n = 106) were collected together with clinical data after ethical approval. Immunohistochemistry to detect integrin α11 and α‐SMA was performed on FF and FFPE samples. qPCR for integrin α11 (ITGA11) and α‐SMA (ACTA2) was performed on FF samples. Data were analysed using chi‐square test and Kaplan–Meier survival analysis. Results: Significantly higher levels of integrin α11 and α‐SMA at both protein and mRNA levels were found in HNSCC vs. normal controls and OLP. A strong correlation was found between integrin α11 and α‐SMA expression, and double staining showed their colocalization. Both integrin α11 and α‐SMA were detected surrounding metastatic islands. Expression of α‐SMA at tumour front but not tumour centre correlated with patient survival. Conclusion: Integrin α11 was overexpressed in HNSCC stroma and colocalized with α‐SMA. Expression of α‐SMA at tumour front but not tumour centre had prognostic value for survival, pinpointing the importance of assessing tumour front when evaluating stromal molecules as prognostic biomarkers.