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Human Polyomaviruses Are Not Frequently Present in Cancer of the Salivary Glands.

Abstract Malignant tumors of the salivary glands are rare and heterogeneous, with more than 20 subtypes, and classified mainly by histopathology. Their diagnosis is often challenging and their etiology unknown. Here, the possible association between human polyomaviruses (PyVs) and one or more salivary gland tumor subtypes was examined.
PMID
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Authors

Mayor MeshTerms
Keywords

Merkel cell polyomavirus

Salivary gland tumors

polyomavirus

tumor viruses

Journal Title anticancer research
Publication Year Start




PMID- 29715110
OWN - NLM
STAT- MEDLINE
DCOM- 20180515
LR  - 20180515
IS  - 1791-7530 (Electronic)
IS  - 0250-7005 (Linking)
VI  - 38
IP  - 5
DP  - 2018 May
TI  - Human Polyomaviruses Are Not Frequently Present in Cancer of the Salivary Glands.
PG  - 2871-2874
AB  - BACKGROUND/AIM: Malignant tumors of the salivary glands are rare and
      heterogeneous, with more than 20 subtypes, and classified mainly by
      histopathology. Their diagnosis is often challenging and their etiology unknown. 
      Here, the possible association between human polyomaviruses (PyVs) and one or
      more salivary gland tumor subtypes was examined. MATERIALS AND METHODS:
      Ninety-one primary tumors, including 12 subtypes and eight corresponding
      metastases, were analyzed for the presence of DNA of 10 different human PyV
      species by a bead-based multiplex assay using polymerase chain reaction and
      Luminex analyses. RESULTS: Three samples, one adenocarcinoma (not otherwise
      specified), one adenoid cystic carcinoma, and one mucoepidermoid carcinoma were
      found to be positive. However, the amount of MCPyV DNA in these tumors was
      estimated to be less than one genome per tumor cell. CONCLUSION: The analysis of 
      DNA from 10 human PyVs in a large number of malignant salivary gland cancers did 
      not implicate any of these human PyVs as an important causative agent in any of
      the 12 subtypes studied.
CI  - Copyright(c) 2018, International Institute of Anticancer Research (Dr. George J. 
      Delinasios), All rights reserved.
FAU - Ramqvist, Torbjorn
AU  - Ramqvist T
AD  - Department of Oncology-Pathology, Karolinska Institute, Karolinska University
      Hospital, Stockholm, Sweden.
FAU - Ursu, Ramona Gabriela
AU  - Ursu RG
AD  - Discipline of Microbiology, Grigore T. Popa University of Medicine and Pharmacy, 
      Iasi, Romania.
FAU - Haeggblom, Linnea
AU  - Haeggblom L
AD  - Department of Oncology-Pathology, Karolinska Institute, Karolinska University
      Hospital, Stockholm, Sweden.
FAU - Mirzaie, Leila
AU  - Mirzaie L
AD  - Department of Oncology-Pathology, Karolinska Institute, Karolinska University
      Hospital, Stockholm, Sweden.
FAU - Gahm, Caroline
AU  - Gahm C
AD  - Department of Clinical Science and Technology, Karolinska Institute, Karolinska
      University Hospital, Stockholm, Sweden.
FAU - Hammarstedt-Nordenvall, Lalle
AU  - Hammarstedt-Nordenvall L
AD  - Department of Clinical Science and Technology, Karolinska Institute, Karolinska
      University Hospital, Stockholm, Sweden.
FAU - Dalianis, Tina
AU  - Dalianis T
AD  - Department of Oncology-Pathology, Karolinska Institute, Karolinska University
      Hospital, Stockholm, Sweden.
FAU - Nasman, Anders
AU  - Nasman A
AD  - Department of Oncology-Pathology, Karolinska Institute, Karolinska University
      Hospital, Stockholm, Sweden [email protected]
LA  - eng
PT  - Journal Article
PL  - Greece
TA  - Anticancer Res
JT  - Anticancer research
JID - 8102988
SB  - IM
MH  - Adolescent
MH  - Adult
MH  - Aged
MH  - Aged, 80 and over
MH  - Carcinoma/*virology
MH  - Female
MH  - Humans
MH  - Male
MH  - Middle Aged
MH  - Polyomavirus
MH  - Polyomavirus Infections/*epidemiology
MH  - Salivary Gland Neoplasms/*virology
MH  - Tumor Virus Infections/*epidemiology
MH  - Young Adult
OTO - NOTNLM
OT  - *Merkel cell polyomavirus
OT  - *Salivary gland tumors
OT  - *polyomavirus
OT  - *tumor viruses
EDAT- 2018/05/02 06:00
MHDA- 2018/05/16 06:00
CRDT- 2018/05/02 06:00
PHST- 2018/02/26 00:00 [received]
PHST- 2018/03/16 00:00 [revised]
PHST- 2018/03/20 00:00 [accepted]
PHST- 2018/05/02 06:00 [entrez]
PHST- 2018/05/02 06:00 [pubmed]
PHST- 2018/05/16 06:00 [medline]
AID - 38/5/2871 [pii]
AID - 10.21873/anticanres.12532 [doi]
PST - ppublish
SO  - Anticancer Res. 2018 May;38(5):2871-2874. doi: 10.21873/anticanres.12532.