Mutational Analysis of Merkel Cell Carcinoma
Merkel cell carcinoma (MCC) is an aggressive cutaneous neuroendocrine malignancy that is associated with a poor prognosis. The pathogenesis of MCC is not well understood, and despite a recent plethora of mutational analyses, we have yet to find a set of signature mutations implicated in the majority...
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doaj-93072b5f48694e2291cc1381f9d0cb042020-11-24T20:47:57ZengMDPI AGCancers2072-66942014-10-01642116213610.3390/cancers6042116cancers6042116Mutational Analysis of Merkel Cell CarcinomaDerek J. Erstad0James C. Cusack1Department of Surgery, Massachusetts General Hospital, 55 Fruit Street, Boston, MA 02114, USADivision of Surgical Oncology, Harvard Medical School, Massachusetts General Hospital, 55 Fruit Street, Boston, MA 02114, USAMerkel cell carcinoma (MCC) is an aggressive cutaneous neuroendocrine malignancy that is associated with a poor prognosis. The pathogenesis of MCC is not well understood, and despite a recent plethora of mutational analyses, we have yet to find a set of signature mutations implicated in the majority of cases. Mutations, including TP53, Retinoblastoma and PIK3CA, have been documented in subsets of patients. Other mechanisms are also likely at play, including infection with the Merkel cell polyomavirus in a subset of patients, dysregulated immune surveillance, epigenetic alterations, aberrant protein expression, posttranslational modifications and microRNAs. In this review, we summarize what is known about MCC genetic mutations and chromosomal abnormalities, and their clinical significance. We also examine aberrant protein function and microRNA expression, and discuss the therapeutic and prognostic implications of these findings. Multiple clinical trials designed to selectively target overexpressed oncogenes in MCC are currently underway, though most are still in early phases. As we accumulate more molecular data on MCC, we will be better able to understand its pathogenic mechanisms, develop libraries of targeted therapies, and define molecular prognostic signatures to enhance our clinicopathologic knowledge.http://www.mdpi.com/2072-6694/6/4/2116merkel cell carcinomamerkel cell polyomavirustumor suppressoroncogeneprognostic algorithmmutational analysis |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Derek J. Erstad James C. Cusack |
spellingShingle |
Derek J. Erstad James C. Cusack Mutational Analysis of Merkel Cell Carcinoma Cancers merkel cell carcinoma merkel cell polyomavirus tumor suppressor oncogene prognostic algorithm mutational analysis |
author_facet |
Derek J. Erstad James C. Cusack |
author_sort |
Derek J. Erstad |
title |
Mutational Analysis of Merkel Cell Carcinoma |
title_short |
Mutational Analysis of Merkel Cell Carcinoma |
title_full |
Mutational Analysis of Merkel Cell Carcinoma |
title_fullStr |
Mutational Analysis of Merkel Cell Carcinoma |
title_full_unstemmed |
Mutational Analysis of Merkel Cell Carcinoma |
title_sort |
mutational analysis of merkel cell carcinoma |
publisher |
MDPI AG |
series |
Cancers |
issn |
2072-6694 |
publishDate |
2014-10-01 |
description |
Merkel cell carcinoma (MCC) is an aggressive cutaneous neuroendocrine malignancy that is associated with a poor prognosis. The pathogenesis of MCC is not well understood, and despite a recent plethora of mutational analyses, we have yet to find a set of signature mutations implicated in the majority of cases. Mutations, including TP53, Retinoblastoma and PIK3CA, have been documented in subsets of patients. Other mechanisms are also likely at play, including infection with the Merkel cell polyomavirus in a subset of patients, dysregulated immune surveillance, epigenetic alterations, aberrant protein expression, posttranslational modifications and microRNAs. In this review, we summarize what is known about MCC genetic mutations and chromosomal abnormalities, and their clinical significance. We also examine aberrant protein function and microRNA expression, and discuss the therapeutic and prognostic implications of these findings. Multiple clinical trials designed to selectively target overexpressed oncogenes in MCC are currently underway, though most are still in early phases. As we accumulate more molecular data on MCC, we will be better able to understand its pathogenic mechanisms, develop libraries of targeted therapies, and define molecular prognostic signatures to enhance our clinicopathologic knowledge. |
topic |
merkel cell carcinoma merkel cell polyomavirus tumor suppressor oncogene prognostic algorithm mutational analysis |
url |
http://www.mdpi.com/2072-6694/6/4/2116 |
work_keys_str_mv |
AT derekjerstad mutationalanalysisofmerkelcellcarcinoma AT jamesccusack mutationalanalysisofmerkelcellcarcinoma |
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1716809486262337536 |