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DOI 10.1046/j.1365-2133.2002.04579.x

Медицинская библиотека · The British journal of dermatology · 2002

Expression of tyrosinase, MIA and MART-1 in sentinel lymph nodes of patients with malignant melanoma.

Ait Hamdan Youssef, El Amerany Fatima, Desbrières Jacques, Aghrinane Abdessadek, Oudadesse Hassane, Rhazi Mohammed

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

BACKGROUND

Regional lymph node status is an important predictor of survival in patients with malignant melanoma. Mapping of sentinel lymph nodes using sensitive molecular techniques has recently been introduced. Malignant melanoma is heterogeneous in terms of its biological, immunological and metastatic properties, and melanoma cells exhibit a polymorphous expression of tumour markers. Thus, assays that include multiple markers appear to be more sensitive than single-marker assays.

OBJECTIVES

To characterize the molecular profiles of melanoma cells in sentinel lymph nodes employing the mRNA expression of tyrosinase, MIA and MART-1 as markers.

METHODS

Samples of sentinel lymph nodes from 17 melanoma patients and 18 control nodes from non-melanoma patients were assayed by reverse transcriptase-polymerase chain reaction, using specific primers for each marker.

RESULTS

We found that both tyrosinase and MIA expression were sensitive indicators of micrometastases in sentinel lymph nodes that were negative on routine histopathological examination, and that the finding of micrometastases expressing MART-1 in sentinel lymph nodes was negatively correlated with overall survival.

CONCLUSIONS

Characterization of the molecular profiles of melanoma cells constitutes a valid means of detecting metastatic melanoma cells in sentinel lymph nodes, and of predicting the survival of melanoma patients.

Для цитирования: Ait Hamdan Youssef, El Amerany Fatima, Desbrières Jacques, Aghrinane Abdessadek, Oudadesse Hassane, Rhazi Mohammed. Expression of tyrosinase, MIA and MART-1 in sentinel lymph nodes of patients with malignant melanoma.. The British journal of dermatology. 2002. DOI: 10.1046/j.1365-2133.2002.04579.x.

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