High expression of the mismatch repair protein MSH6 is associated with poor patient survival in melanoma

The outcome of patients with primary melanoma (PM) cannot be completely explained based on currently adopted clinical-histopathologic criteria. In this study, we evaluated the potential prognostic value of mismatch repair protein expression in PMs. We examined the immunohistochemical staining of mis...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:American journal of clinical pathology 2014-07, Vol.142 (1), p.121-132
Hauptverfasser: Alvino, Ester, Passarelli, Francesca, Cannavò, Elda, Fortes, Cristina, Mastroeni, Simona, Caporali, Simona, Jiricny, Josef, Cappellini, Gian Carlo Antonini, Scoppola, Alessandro, Marchetti, Paolo, Modesti, Andrea, D'Atri, Stefania
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The outcome of patients with primary melanoma (PM) cannot be completely explained based on currently adopted clinical-histopathologic criteria. In this study, we evaluated the potential prognostic value of mismatch repair protein expression in PMs. We examined the immunohistochemical staining of mismatch repair proteins in 18 benign nevi and 101 stage I to III PMs and investigated their association with tumor clinicopathologic variables and melanoma mortality. Expression of MSH2, MLH1, and PMS2 was high in benign nevi and reduced in a subset of PMs. Conversely, MSH6 expression was absent or extremely low in benign nevi and increased in a subset of PMs. In the multivariate analysis, including sex, age, Breslow thickness, and ulceration, high MSH6 expression in PMs (ie, immunostaining in >20% of tumor cells) was significantly associated with an increased risk of melanoma mortality (relative risk, 3.76; 95% confidence interval, 1.12-12.70). MSH6 protein expression can be a valuable marker to improve prognosis assessment in PMs.
ISSN:0002-9173
1943-7722
DOI:10.1309/AJCPCX2D9YULBBLG