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DOI 10.1038/modpathol.2016.226

Медицинская библиотека · Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2017

High ALDH1 expression correlates with better prognosis in tumorigenic malignant melanoma.

Taylor Laura A, Abraham Ronnie M, Tahirovic Emin, van Belle Patricia, Li Bin, Huang Linfang, Elder David E, Gimotty Phyllis, Xu Xiaowei

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Аннотация

Aldehyde dehydrogenase 1 (ALDH1) has been proposed as biomarker of stem cells for certain human cancers. ALDH1 expression has been correlated with poor patient outcomes in a variety of malignancies but better patient outcomes in others, and its prognostic significance in malignant melanoma is unclear. Thus, 68 melanoma patients with comprehensive clinical and pathologic follow-up data were used to construct a tissue microarray. A modified histological score (H-score) with a maximum score of 300 was used to quantify immunohistochemical staining for ALDH1. Survival time was defined as the time between diagnosis and melanoma-specific death. Using univariate logistic regression, a low (<80 H-score) ALDH1 score showed 3.7-fold increase in risk for melanoma-specific death within 10 years when compared with high (>80) ALDH1 levels (P=0.017). Odds of MSD were lower by a factor of ~0.9 for each 10-point increase in H-Score. Median survival time was 44.1 months and 180.9 months for patients with low and high ALDH1 expression, respectively. Using multivariate analysis, ALDH1 H-score was found to be an independent prognostic factor. These findings suggest that ALDH1 expression in malignant melanoma has a favorable effect on patient survival. Further study is needed elucidate the function of this enzymatic protein in melanoma progression.

Для цитирования: Taylor Laura A, Abraham Ronnie M, Tahirovic Emin, van Belle Patricia, Li Bin, Huang Linfang, Elder David E, Gimotty Phyllis, Xu Xiaowei. High ALDH1 expression correlates with better prognosis in tumorigenic malignant melanoma.. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc. 2017. DOI: 10.1038/modpathol.2016.226.

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