1969
DOI: 10.1073/pnas.64.4.1172
|View full text |Cite
|
Sign up to set email alerts
|

Induction of Transmissible Lymphomas in Syrian Hamsters by Application of Dna From Viral Hamster Papovavirus-Induced Tumors and by Cell-Free Filtrates From Human Tumors

Abstract: Abstract.-DNA isolated from skin epitheliomas containing papovavirus induced lymphomas within four to eight weeks in 40 to 50 per cent of newborn Syrian hamsters injected. This DNA effect was eliminated by DNase but not by RNase and was not induced by DNA preparations of transplanted epitheliomas or the induced lymphomas. Lymphomas were similarly induced by cellfree filtrates from certain human tumors such as gastric carcinomas and ovarian tumors. Little or no lymphoma effects were observed following injection… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

1
19
1

Year Published

1977
1977
2015
2015

Publication Types

Select...
5
4

Relationship

0
9

Authors

Journals

citations
Cited by 25 publications
(21 citation statements)
references
References 3 publications
1
19
1
Order By: Relevance
“…Similarly, papillomavirus vegetative replication occurs sporadically in only the most superficial terminally differentiated epidermal cells of a wart (Howley 1990). A third possibility is that the agent that causes GTFP is present in tumors primarily as episomal genetic material which is infectious under experimental conditions as shown for severai papovaviruses, including hamster polyomavirus (Graffi et al 1969) and cottontail rabbit papillomavirus (Ito & Evans 1961, Brandsma & Xiao 1993. Several oncogenic viruses, including papillomaviruses (Howley 1983) and retroviruses (Benjamin & Vogt 1990), cause neoplastic lesions in tissues that are not permissive to vegetative viral replication.…”
Section: Discussionmentioning
confidence: 99%
“…Similarly, papillomavirus vegetative replication occurs sporadically in only the most superficial terminally differentiated epidermal cells of a wart (Howley 1990). A third possibility is that the agent that causes GTFP is present in tumors primarily as episomal genetic material which is infectious under experimental conditions as shown for severai papovaviruses, including hamster polyomavirus (Graffi et al 1969) and cottontail rabbit papillomavirus (Ito & Evans 1961, Brandsma & Xiao 1993. Several oncogenic viruses, including papillomaviruses (Howley 1983) and retroviruses (Benjamin & Vogt 1990), cause neoplastic lesions in tissues that are not permissive to vegetative viral replication.…”
Section: Discussionmentioning
confidence: 99%
“…Although polyomavirus infection has been associated with skin tumors in hamsters and with Merkel cell carcinoma in humans, the relationship between polyomavirus infection and the glossal fibropapilloma in this sea lion is not clear. 6,20 In Merkel cell carcinomas, viral DNA can be detected within tumor cells but not in nonneoplastic cells. 20 As viral particles were noted within only endothelial cells and not within epithelial or stromal cells within the glossal mass, it is possible that neoplasia and severe renal disease caused reactivation of latent viral infection.…”
mentioning
confidence: 99%
“…15 Hamster polyomavirus is associated with skin tumors. 6,7 In contrast, polyomavirus infection in avian species can cause acute and chronic diseases such as budgerigar fledgling disease caused by Psittacine polyomavirus and hemorrhagic nephritis and enteritis of geese caused by Goose hemorrhagic polyomavirus. 10 The purpose of the current report is to describe the histopathologic and molecular features of polyomavirus infection and intestinal T-cell lymphoma in a free-ranging California sea lion (Zalophus californianus), both of which have not been previously reported in any marine mammal species.…”
mentioning
confidence: 99%
“…23 A second disease course is seen when HaPV infects naive young hamsters in which it readily induces multicentric lymphoma originating from the mesentery and metastasizing to the liver, kidney, and thymus. 3,10,19,22 The ability of HaPV to infect both undifferentiated keratinocytes and lymphocytes is unique among the papovaviruses and led to its initial misclassification as a papillomavirus. However, characterization of virus genomic sequence and gene structure definitively identifies HaPV as a polyomavirus.…”
mentioning
confidence: 99%