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Correlation among metallothionein expression, intratumoural macrophage infiltration and the risk of metastasis in human cutaneous malignant melanoma
Author(s) -
Emri E.,
Egervari K.,
Varvolgyi T.,
Rozsa D.,
Miko E.,
Dezso B.,
Veres I.,
Mehes G.,
Emri G.,
Remenyik E.
Publication year - 2013
Publication title -
journal of the european academy of dermatology and venereology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.655
H-Index - 107
eISSN - 1468-3083
pISSN - 0926-9959
DOI - 10.1111/j.1468-3083.2012.04653.x
Subject(s) - cd68 , cd163 , immunohistochemistry , medicine , melanoma , tissue microarray , pathology , metastasis , metallothionein , immune system , infiltration (hvac) , macrophage , cancer research , cancer , immunology , biology , gene , biochemistry , physics , in vitro , thermodynamics
Background The formation of metastases and the efficacy of systemic therapies in cutaneous malignant melanoma (CMM) depend on the characteristics of the tumour cells and the host immune response. Aberrant expression of metallothionein (MT) has been observed in several types of cancers with poor prognoses. Objective To perform an immunohistochemical study on primary CMM comparing the MT expression of tumours without metastases ( n = 23) to that of samples with haematogenous metastases ( n = 23) and to examine the correlation between MT staining and immunological markers relevant in CMM progression. Methods The immunohistochemical labelling of different tumour sections was analysed using tissue microarrays for the evaluation of the suitability of this method in future studies. Results Our results suggest that MT overexpression is significantly more frequent in primary CMM with haematogenous metastases ( P = 0.018) and that the overexpression is independent of the Breslow tumour thickness (R = 0.102, P = 0.501). Interestingly, MT overexpression of the tumour cells was correlated with the presence of tumour‐infiltrating CD68 + macrophages ( P = 0.003), a known predictive factor for melanoma progression, thereby suggesting a role for MT in the development of a defective host immune response. Furthermore, the presence of CD163 + macrophages infiltrating the tumours correlated with metastasis formation ( P < 0.001), whereas the presence CD1a + dendritic cells surrounding the tumours was associated with a lower risk of haematogenous spread ( P = 0.003). Conclusion Our results demonstrate that MT may represent a suitable prognostic factor that can characterize the metastasising ability of CMM and the tumour‐promoting host immune response.