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Merkel cell carcinoma - pathogenesis, clinical aspects and treatment

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TLDR
Recent findings of the pathogenesis of MCC are summarized, an overview of clinical aspects are presented and treatment options for MCCs are discussed.
Abstract
Merkel cell carcinoma (MCC) is a highly aggressive neuroendocrine carcinoma of the skin demonstrating a high rate of recurrence and metastasis. Indeed, 5-year rates for MCC specific survival are only about 60%. Although MCCs’ incidence is rapidly increasing, it is still a very rare tumour. In this regard, the American Cancer Society had estimated for 2008 almost 1500 new cases in the USA. Recently, the newly identified Merkel cell polyomavirus has been found associated with most of the MCC cases. Nevertheless, the pathogenesis of MCC is not yet fully understood. Here, we will summarize recent findings of the pathogenesis of MCC, present an overview of clinical aspects and discuss treatment options for MCCs.

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Citations
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Journal ArticleDOI

Merkel cell carcinoma: Epidemiology, prognosis, therapy and unmet medical needs.

TL;DR: Patients with advanced disease are encouraged to participate in clinical trials for treatment, indicating the largely unmet need for durable, safe treatment within this population.
Journal ArticleDOI

Merkel cell carcinoma: recent insights and new treatment options.

TL;DR: This review summarizes recent findings on MCC pathogenesis with a special emphasis on the impact of MCV, presents an overview of clinical aspects, and discusses treatment options.
Journal ArticleDOI

BET protein inhibitor JQ1 attenuates Myc-amplified MCC tumor growth in vivo

TL;DR: The results provide initial evidence, indicating the potential clinical utility of BET protein inhibitors in the treatment of MCC with pathologic activation of c-Myc, and JQ1 significantly attenuates tumor growth in xenograft MCC mouse models.
Journal ArticleDOI

Merkel Cell Carcinoma Dependence on Bcl-2 Family Members for Survival

TL;DR: It is established that concurrent inhibition of multiple pro-survival Bcl-2 proteins leads to effective induction of apoptosis, and strongly support the concept that targeting MCC addiction to these molecules may be useful therapeutically by reversing an intrinsic resistance to cell death.
References
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Journal ArticleDOI

Clonal integration of a polyomavirus in human Merkel cell carcinoma.

TL;DR: In six of eight MCV-positive MCCs, viral DNA was integrated within the tumor genome in a clonal pattern, suggesting that MCV infection and integration preceded clonal expansion of the tumor cells, and MCV may be a contributing factor in the pathogenesis of MCC.
Journal ArticleDOI

Trabecular carcinoma of the skin.

TL;DR: The histological features of these tumors are not sufficiently distinctive to permit differentiation from anaplastic metastatic carcinomas, and familiarity with their existence is of importance in the evaluation of cutaneous malignancy.
Journal ArticleDOI

Clinical characteristics of Merkel cell carcinoma at diagnosis in 195 patients: the AEIOU features

TL;DR: The most significant features can be summarized in an acronym: AEIOU (asymptomatic/lack of tenderness, expanding rapidly, immune suppression, older than 50 years, and ultraviolet-exposed site on a person with fair skin) and 89% of primary MCCs had 3 or more of these findings.
Journal ArticleDOI

Merkel Cell Carcinoma: Prognosis and Treatment of Patients From a Single Institution

TL;DR: The data demonstrate that the natural history of MCC is variable and dependent on the stage of disease at presentation, and pathologic nodal staging identifies a group of patients with excellent long-term survival.
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