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The Role of Melanocyte in Basal Cell Carcinoma

Conditions
Basal Cell Carcinoma
Interventions
Other: No intervention
Registration Number
NCT02576769
Lead Sponsor
Universidad Autonoma de San Luis Potosí
Brief Summary

Basal cell carcinoma (BCC) is the most frequent neoplasia worldwide. There are more than 30 histopathologic subtypes, however the nodular subtype is the most common. Pigmented varieties are common in darker skin types, therefore in our country. Previous studies have shown an increase number and size of melanocytes. Melanogenesis were increased at the expense of hyperfunctioning melanocytes as well. The aim of the study was to describe the characteristics of melanocytes in pigmented and non-pigmented variants of basal cell carcinoma.

Detailed Description

Melanocytes are highly specialized dendritic cells that performs multiple functions through autocrine, paracrine and endocrine mechanisms. These cells are part of a complex system of intercellular communication along with keratinocytes, Langerhans cells and fibroblasts. This intricate network of cellular communication is possible thanks to interaction with cytokines, growth factors and neurotransmitters. Although melanocytes perform brilliantly immunoregulatory and neuroendocrine functions, their fundamental role is to offer protection against the harmful effects of UV radiation through production and transference of melanin to keratinocytes, a process better known as melanogenesis. The latter requires 3 basic proteins to ensure photoprotection: MC1R (activation), MITF (traduction) and TYR (melanin synthesis).

If one of the main features of melanocytes is to avoid UV radiation injurious effect, thus it raises many questions regarding the possible relation between these cells and skin cancer. Currently a great number of melanocytic alterations have been described in melanoma; however in non-melanoma skin cancer the role of melanocytes is less clear. Basal cell carcinoma (BCC) is the most frequent neoplasia worldwide. There are more than 30 histopathologic subtypes, however the nodular subtype is the most common. Pigmented varieties are common in darker skin types, therefore in our country. Previous studies have shown an increase number and size of melanocytes. Melanogenesis were increased at the expense of hyperfunctioning melanocytes as well. In our experience we have noticed the clinical course regarding pigmented nodular basal cell carcinoma is more benign when compared to those without pigment. Most studies regarding the role of melanocytes and pigmentation in basal cell carcinoma have been conducted in caucasian populations, and therefore not representative of what may occur in mestizo population. The aim of the study was to describe the characteristics of melanocytes in pigmented and non-pigmented variants of basal cell carcinoma. Quantify the expression of melanocytic maturation: transcription factors (SOX9 and SOX10), focal adhesion kinase (FAK125) and receptor tyrosine kinase (c-KIT) and melanogenesis such as melanocortin 1 receptor (MC1R), microphthalmia-associated transcription factor (MITF) and tyrosinase (TYR) markers. Investigate the tumoral microenvironment through the quantification of melanin, mast cells, angiogenesis and solar elastosis.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
30
Inclusion Criteria
  • Mexican subjects
  • Age between 40 and 90 years
  • Both genders
  • Sign informed consent
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Exclusion Criteria
  • Sign informed consent withdrawal
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Basal cell carcinomaNo interventionBasal cell carcinoma
Primary Outcome Measures
NameTimeMethod
Melanocyte numberUp to 1 year

To quantify the number of melanocytes in basal cell carcinoma

Melanocyte phenotypeUp to 1 year

To quantify melanocyte maturation stages in basal cell carcinoma through markers

Melanogenesis characteristicsUp to 1 year

To quantify the expression of melanogenic markers in basal cell carcinoma

Secondary Outcome Measures
NameTimeMethod
Melanin presenceUp to 1 year

To quantify melanin deposition in basal cell carcinoma using special histologic stains (Fontana-Masson)

Vessels number (angiogenesis)Up to 1 year

To quantify number of vessels in basal cell carcinoma using special histologic stains (Elastic fibers)

Mast cells numberUp to 1 year

To quantify melanocytes in basal cell carcinoma using special histologic stains (Giemsa)

Solar elastosis quantityUp to 1 year

To quantify solar elastosis in basal cell carcinoma using special histologic stains (Elastic fibers)

Trial Locations

Locations (1)

Hospital Central Dr. Ignacio Morones Prieto

🇲🇽

San Luis Potosi, Mexico

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