4.4 Article

Genetic variability and integration of Merkel cell polyomavirus in Merkel cell carcinoma

Journal

VIROLOGY
Volume 426, Issue 2, Pages 134-142

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.virol.2012.01.018

Keywords

Merkel cell polyomavirus; Viral integration; Oncogenic viruses; Genetic variability; Merkel cell carcinoma

Categories

Funding

  1. Institut Pasteur, the Association pour la Recherche sur le Cancer [A09/1/5041]
  2. La Ligue Nationale Contre le Cancer [RS10/75-1, RS11/75-63]
  3. Ministere de l'Enseignement Superieur et de la Recherche (MESR) of France
  4. Ile-de-France
  5. European Program EMPERIE

Ask authors/readers for more resources

Merkel cell polyomavirus (MCPyV) is associated to Merkel cell carcinoma (MCC). We studied 113 MCC tumoral skin lesions originating from 97 patients. MCPyV detection was higher in fresh-frozen (FF) biopsies (94%) than in formalin-fixed paraffin-embedded biopsies (39-47%). Mean viral load in FF tumor was of 7.5 copies per cell with a very wide range (0.01-95.4). Nineteen complete sequences of LTAg were obtained, mainly from FF biopsies when the viral load was high. Seventeen showed stop codons, all localized downstream of the pRb protein binding domain. Sequence comparison and phylogenetic analysis showed that all sequences clustered in the large C clade of MCPyV strains. MCPyV integration was demonstrated in 19 out of 27 FF MCC DNA biopsies without evidence of specific host cellular genome integration site. In 13/19 cases, the viral junction was located within the second exon of the LTAg, after the pRB binding domain. (C) 2012 Elsevier Inc. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available