Cargando…

Differential Susceptibility of Human Cancer Cell Lines to Wild-Type Tanapoxvirus Infection

Tanapoxvirus (TPV) is a member of the genus Yatapoxvirus in the family Poxviridae and is endemic to equatorial Africa. This disease is restricted to human and non-human primates, producing a mild febrile illness characterized by a single or more rarely additional pock-like lesions on the extremities...

Descripción completa

Detalles Bibliográficos
Autores principales: Lee, Hui Lin, Essani, Karim
Formato: Texto
Lenguaje:English
Publicado: Bentham Open 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2866450/
https://www.ncbi.nlm.nih.gov/pubmed/20461227
http://dx.doi.org/10.2174/1874357901004010001
_version_ 1782180911526182912
author Lee, Hui Lin
Essani, Karim
author_facet Lee, Hui Lin
Essani, Karim
author_sort Lee, Hui Lin
collection PubMed
description Tanapoxvirus (TPV) is a member of the genus Yatapoxvirus in the family Poxviridae and is endemic to equatorial Africa. This disease is restricted to human and non-human primates, producing a mild febrile illness characterized by a single or more rarely additional pock-like lesions on the extremities. While there are several studies elucidating the replication cycle and host range of TPV, there is currently no standardized investigation comparing the ability of TPV to successfully replicate in a variety of tumor cell lines. This study examined the cytopathic effect and calculated the efficiency of TPV replication in vitro using 14 different human cancer cell lines. TPV replicates efficiently in some human tumor cells, and is restricted in others when measured by viral titer at 7 days post infection. Results described here clearly demonstrate that TPV replication in one glioblastoma cell line (U-373), and one colorectal cancer cell line (HCT-116) is more productive than in owl monkey kidney cells (OMK). Replication in two renal cancer cell lines (ACHN and Caki-1) is also increased when compared to OMK. TPV infection produced the greatest change in cellular morphology in U-373 cells, and to a much lesser degree in the breast cancer cell lines T-47D and MCF-7, and in the ovarian cancer line SK-OV3. Negligible change was noted in glioblastoma line U-87, breast cancer line MDA-MB-435, osteosarcoma line HOS, melanoma line SK-MEL5, colorectal cancer line COLO205, and prostate cancer line PC3. The cell lines least permissive to TPV replication were the glioblastoma (U-87) and melanoma (SK-MEL5) cell lines.
format Text
id pubmed-2866450
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher Bentham Open
record_format MEDLINE/PubMed
spelling pubmed-28664502010-05-11 Differential Susceptibility of Human Cancer Cell Lines to Wild-Type Tanapoxvirus Infection Lee, Hui Lin Essani, Karim Open Virol J Article Tanapoxvirus (TPV) is a member of the genus Yatapoxvirus in the family Poxviridae and is endemic to equatorial Africa. This disease is restricted to human and non-human primates, producing a mild febrile illness characterized by a single or more rarely additional pock-like lesions on the extremities. While there are several studies elucidating the replication cycle and host range of TPV, there is currently no standardized investigation comparing the ability of TPV to successfully replicate in a variety of tumor cell lines. This study examined the cytopathic effect and calculated the efficiency of TPV replication in vitro using 14 different human cancer cell lines. TPV replicates efficiently in some human tumor cells, and is restricted in others when measured by viral titer at 7 days post infection. Results described here clearly demonstrate that TPV replication in one glioblastoma cell line (U-373), and one colorectal cancer cell line (HCT-116) is more productive than in owl monkey kidney cells (OMK). Replication in two renal cancer cell lines (ACHN and Caki-1) is also increased when compared to OMK. TPV infection produced the greatest change in cellular morphology in U-373 cells, and to a much lesser degree in the breast cancer cell lines T-47D and MCF-7, and in the ovarian cancer line SK-OV3. Negligible change was noted in glioblastoma line U-87, breast cancer line MDA-MB-435, osteosarcoma line HOS, melanoma line SK-MEL5, colorectal cancer line COLO205, and prostate cancer line PC3. The cell lines least permissive to TPV replication were the glioblastoma (U-87) and melanoma (SK-MEL5) cell lines. Bentham Open 2010-04-08 /pmc/articles/PMC2866450/ /pubmed/20461227 http://dx.doi.org/10.2174/1874357901004010001 Text en © Lee and Essani; Licensee Bentham Open. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Lee, Hui Lin
Essani, Karim
Differential Susceptibility of Human Cancer Cell Lines to Wild-Type Tanapoxvirus Infection
title Differential Susceptibility of Human Cancer Cell Lines to Wild-Type Tanapoxvirus Infection
title_full Differential Susceptibility of Human Cancer Cell Lines to Wild-Type Tanapoxvirus Infection
title_fullStr Differential Susceptibility of Human Cancer Cell Lines to Wild-Type Tanapoxvirus Infection
title_full_unstemmed Differential Susceptibility of Human Cancer Cell Lines to Wild-Type Tanapoxvirus Infection
title_short Differential Susceptibility of Human Cancer Cell Lines to Wild-Type Tanapoxvirus Infection
title_sort differential susceptibility of human cancer cell lines to wild-type tanapoxvirus infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2866450/
https://www.ncbi.nlm.nih.gov/pubmed/20461227
http://dx.doi.org/10.2174/1874357901004010001
work_keys_str_mv AT leehuilin differentialsusceptibilityofhumancancercelllinestowildtypetanapoxvirusinfection
AT essanikarim differentialsusceptibilityofhumancancercelllinestowildtypetanapoxvirusinfection