Abstract

BackgroundAlthough the human β-defensins hBDs today seem to have diverse functional activities in innate antimicrobial immunity, a few reports also indicated an altered expression of these antimicrobial peptides (AMPs) in tissues of cancers such as oral squamous cell carcinoma. The present work was aimed on the study of hBD gene expression in basal cell carcinoma (BCC) which is the most common cancer in humans.MethodsTwenty-two non-ulcerated BCCs (12 nodular type, 10 superficial type) have been analysed for the presence of hBD (1–3) mRNA by quantitative real-time RT-PCR. As controls, non-lesional skin specimens of BCC patients as well as samples of healthy subjects were assessed by RT-PCR.ResultshBD-1 levels in healthy controls and non-lesional skin of BCC patients were significantly (P < 0.05) higher than the levels observed in tumour tissue. Moreover, BCCs showed significantly (P < 0.05) increased mRNA expression of hBD-2 as compared to controls. There was no significant (P > 0.05) difference between lesional mRNA levels for hBD-3 and those levels observed in controls. The mRNA expression of hBDs (1–3) found in nodular and superficial BCCs did not significantly (P > 0.05) differ.ConclusionThe gene expression patterns of hBD-1 and hBD-2 are for the first time shown to be significantly altered in non-ulcerated BCCs as compared to intra-individual and inter-individual controls, respectively. The present findings may indicate that beside the antimicrobial activity of AMPs, hBDs may also play a role in the pathogenesis of BCC. However, functional and immunohistological studies investigating hBDs in patients with BCC are needed to confirm our data.

Highlights

  • The human β-defensins human beta-defensins (hBD) today seem to have diverse functional activities in innate antimicrobial immunity, a few reports indicated an altered expression of these antimicrobial peptides (AMPs) in tissues of cancers such as oral squamous cell carcinoma

  • HBD-1 levels in healthy controls and non-lesional skin were significantly (P < 0.05) higher than the hBD-1 levels observed in basal cell carcinoma (BCC)

  • There was no significant (P > 0.05) difference between lesional mRNA levels for hBD-3 and those levels observed in healthy controls and non-lesional skin

Read more

Summary

Introduction

The human β-defensins hBDs today seem to have diverse functional activities in innate antimicrobial immunity, a few reports indicated an altered expression of these antimicrobial peptides (AMPs) in tissues of cancers such as oral squamous cell carcinoma. The present work was aimed on the study of hBD gene expression in basal cell carcinoma (BCC) which is the most common cancer in humans. Basal cell carcinoma (BCC) is the most common cancer in humans. It is classified, together with squamous cell carcinoma, as non-melanoma skin cancer. The development of BCC is clearly associated with mutated p53 tumour-suppressor gene and constitutive activation of sonic hedgehog signalling molecules that regulate cell proliferation and cell fate determination. Risk factors for the development of BCC include advanced age, fair skin colour, chronic ultraviolet exposure, and immunosuppression [1,2]

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call