Are there multiple cells of origin of Merkel cell carcinoma?

被引:92
|
作者
Sunshine, J. C. [1 ]
Jahchan, N. S. [2 ,3 ]
Sage, J. [2 ,3 ]
Choi, J. [1 ,4 ,5 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Dermatol, Chicago, IL 60611 USA
[2] Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Pediat, Sch Med, Stanford, CA 94305 USA
[4] Northwestern Univ, Feinberg Sch Med, Dept Biochem Mol Genet, Chicago, IL 60611 USA
[5] Northwestern Univ, Feinberg Sch Med, Ctr Genet Med, Chicago, IL 60611 USA
关键词
SMALL T-ANTIGEN; TRANSGENIC MOUSE MODEL; MUTATIONAL LANDSCAPE; PROSTATE-CANCER; LUNG-CANCER; ANTIANDROGEN RESISTANCE; LINEAGE PLASTICITY; TUMOR-DEVELOPMENT; STEM-CELLS; POLYOMAVIRUS;
D O I
10.1038/s41388-017-0073-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Merkel cell carcinoma (MCC) is a rare but lethal cancer with the highest case-by-case fatality rate among all skin cancers. Eighty percent of cancers are associated with the Merkel cell polyomavirus (MCPyV). Twenty percent of MCCs are virus negative. Recent epidemiological data suggest that there are important, clinically relevant differences between these two subtypes of MCC. Recent studies in cancer genomics, mouse genetics, and virology experiments have transformed our understanding of MCC pathophysiology. Importantly, dramatic differences in the genetics of these two MCC subtypes suggest fundamental differences in their pathophysiology. We review these recent works and find that they provocatively suggest that MCPyV-positive and MCPyV-negative MCCs arise from two different cells of origin: the MCPyV-negative MCC from epidermal keratinocytes and the MCPyV-positive MCC from dermal fibroblasts. If true, this would represent the first cancer that we are aware of that evolves from cells of origin from two distinct germ layers: MCPyV-negative MCCs from ectodermal keratinocytes and MCPyV-positive MCCs from mesodermal fibroblasts. Future epigenetic experiments may prove valuable in confirming these distinct lineages for these MCC subtypes, especially for the clinical importance the cell of origin has on MCC treatment and prevention.
引用
收藏
页码:1409 / 1416
页数:8
相关论文
共 50 条
  • [11] Update on Merkel Cell Carcinoma
    Harms, Paul W.
    CLINICS IN LABORATORY MEDICINE, 2017, 37 (03) : 485 - +
  • [12] Detection of Merkel Cell Carcinoma Polyomavirus in Mucosal Merkel Cell Carcinoma
    Wu, Karen N.
    McCue, Peter A.
    Berger, Adam
    Spiegel, Joseph R.
    Wang, Zi-Xuan
    Witkiewicz, Agnieszka K.
    INTERNATIONAL JOURNAL OF SURGICAL PATHOLOGY, 2010, 18 (05) : 342 - 346
  • [13] Merkel Cell Carcinoma: Aetiopathogenesis and Management
    Heitmann, J.
    Houben, R.
    Schrama, D.
    Goebeler, M.
    Gesierich, A.
    Schilling, B.
    AKTUELLE DERMATOLOGIE, 2019, 45 (1-2) : 60 - 66
  • [14] Prevalence of Merkel cell polyomavirus in Merkel cell carcinoma
    Duncavage, Eric J.
    Zehnbauer, Barbara A.
    Pfeifer, John D.
    MODERN PATHOLOGY, 2009, 22 (04) : 516 - 521
  • [15] Merkel cell carcinoma
    Nasseri, Eiman
    CANADIAN FAMILY PHYSICIAN, 2012, 58 (09) : 967 - 969
  • [16] Merkel Cell Carcinoma
    Strong, Jennifer
    Hallaert, Patrick
    Brownell, Isaac
    HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 2024, 38 (05) : 1133 - 1147
  • [17] Merkel cell carcinoma
    Drusio C.
    Becker J.C.
    Schadendorf D.
    Ugurel S.
    best practice onkologie, 2019, 14 (7-8) : 312 - 323
  • [18] Merkel Cell Carcinoma
    Ramahi, Emma
    Choi, Jehee
    Fuller, Clifton D.
    Eng, Tony Y.
    AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2013, 36 (03): : 299 - 309
  • [19] Merkel cell carcinoma
    Drusio, Christina
    Becker, Juergen C.
    Schadendorf, Dirk
    Ugurel, Selma
    ONKOLOGE, 2018, 24 (12): : 1037 - 1049
  • [20] Merkel cell carcinoma
    Becker, J. C.
    Schrama, D.
    Houben, R.
    CELLULAR AND MOLECULAR LIFE SCIENCES, 2009, 66 (01) : 1 - 8