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Primary effect of chemotherapy on the transcription profile of AIDS-related Kaposi's sarcoma

BACKGROUND: Drugs & used in anticancer chemotherapy have severe effects upon the cellular transcription and replication machinery. From in vitro studies it has become clear that these drugs can affect specific genes, as well as have an effect upon the total transcriptome. METHODS: Total mRNA fro...

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Autores principales: van der Kuyl, Antoinette C, van den Burg, Remco, Zorgdrager, Fokla, Dekker, John T, Maas, Jolanda, van Noesel, Carel JM, Goudsmit, Jaap, Cornelissen, Marion
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC126247/
https://www.ncbi.nlm.nih.gov/pubmed/12204098
http://dx.doi.org/10.1186/1471-2407-2-21
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author van der Kuyl, Antoinette C
van den Burg, Remco
Zorgdrager, Fokla
Dekker, John T
Maas, Jolanda
van Noesel, Carel JM
Goudsmit, Jaap
Cornelissen, Marion
author_facet van der Kuyl, Antoinette C
van den Burg, Remco
Zorgdrager, Fokla
Dekker, John T
Maas, Jolanda
van Noesel, Carel JM
Goudsmit, Jaap
Cornelissen, Marion
author_sort van der Kuyl, Antoinette C
collection PubMed
description BACKGROUND: Drugs & used in anticancer chemotherapy have severe effects upon the cellular transcription and replication machinery. From in vitro studies it has become clear that these drugs can affect specific genes, as well as have an effect upon the total transcriptome. METHODS: Total mRNA from two skin lesions from a single AIDS-KS patient was analyzed with the SAGE (Serial Analysis of Gene Expression) technique to assess changes in the transcriptome induced by chemotherapy. SAGE libraries were constructed from material obtained 24 (KS-24) and 48 (KS-48) hrs after combination therapy with bleomycin, doxorubicin and vincristine. KS-24 and KS-48 were compared to SAGE libraries of untreated AIDS-KS, and to libraries generated from normal skin and from isolated CD4+ T-cells, using the programs USAGE and HTM. SAGE libraries were also compared with the SAGEmap database. RESULTS: In order to assess the primary response of AIDS-related Kaposi's sarcoma (AIDS-KS) to chemotherapy in vivo, we analyzed the transcriptome of AIDS-KS skin lesions from a HIV-1 seropositive patient at two time points after therapy. The mRNA profile was found to have changed dramatically within 24 hours after drug treatment. There was an almost complete absence of transcripts highly expressed in AIDS-KS, probably due to a transcription block. Analysis of KS-24 suggested that mRNA pool used in its construction originated from poly(A) binding protein (PABP) mRNP complexes, which are probably located in nuclear structures known as interchromatin granule clusters (IGCs). IGCs are known to fuse after transcription inhibition, probably affecting poly(A)+RNA distribution. Forty-eight hours after chemotherapy, mRNA isolated from the lesion was largely derived from infiltrating lymphocytes, confirming the transcriptional block in the AIDS-KS tissue. CONCLUSIONS: These in vivo findings indicate that the effect of anti-cancer drugs is likely to be more global than up- or downregulation of specific genes, at least in this single patient with AIDS-KS. The SAGE results obtained 24 hrs after chemotherapy can be most plausibly explained by the isolation of a fraction of more stable poly(A)+RNA.
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spelling pubmed-1262472002-09-20 Primary effect of chemotherapy on the transcription profile of AIDS-related Kaposi's sarcoma van der Kuyl, Antoinette C van den Burg, Remco Zorgdrager, Fokla Dekker, John T Maas, Jolanda van Noesel, Carel JM Goudsmit, Jaap Cornelissen, Marion BMC Cancer Research Article BACKGROUND: Drugs & used in anticancer chemotherapy have severe effects upon the cellular transcription and replication machinery. From in vitro studies it has become clear that these drugs can affect specific genes, as well as have an effect upon the total transcriptome. METHODS: Total mRNA from two skin lesions from a single AIDS-KS patient was analyzed with the SAGE (Serial Analysis of Gene Expression) technique to assess changes in the transcriptome induced by chemotherapy. SAGE libraries were constructed from material obtained 24 (KS-24) and 48 (KS-48) hrs after combination therapy with bleomycin, doxorubicin and vincristine. KS-24 and KS-48 were compared to SAGE libraries of untreated AIDS-KS, and to libraries generated from normal skin and from isolated CD4+ T-cells, using the programs USAGE and HTM. SAGE libraries were also compared with the SAGEmap database. RESULTS: In order to assess the primary response of AIDS-related Kaposi's sarcoma (AIDS-KS) to chemotherapy in vivo, we analyzed the transcriptome of AIDS-KS skin lesions from a HIV-1 seropositive patient at two time points after therapy. The mRNA profile was found to have changed dramatically within 24 hours after drug treatment. There was an almost complete absence of transcripts highly expressed in AIDS-KS, probably due to a transcription block. Analysis of KS-24 suggested that mRNA pool used in its construction originated from poly(A) binding protein (PABP) mRNP complexes, which are probably located in nuclear structures known as interchromatin granule clusters (IGCs). IGCs are known to fuse after transcription inhibition, probably affecting poly(A)+RNA distribution. Forty-eight hours after chemotherapy, mRNA isolated from the lesion was largely derived from infiltrating lymphocytes, confirming the transcriptional block in the AIDS-KS tissue. CONCLUSIONS: These in vivo findings indicate that the effect of anti-cancer drugs is likely to be more global than up- or downregulation of specific genes, at least in this single patient with AIDS-KS. The SAGE results obtained 24 hrs after chemotherapy can be most plausibly explained by the isolation of a fraction of more stable poly(A)+RNA. BioMed Central 2002-09-02 /pmc/articles/PMC126247/ /pubmed/12204098 http://dx.doi.org/10.1186/1471-2407-2-21 Text en Copyright © 2002 van der Kuyl et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Research Article
van der Kuyl, Antoinette C
van den Burg, Remco
Zorgdrager, Fokla
Dekker, John T
Maas, Jolanda
van Noesel, Carel JM
Goudsmit, Jaap
Cornelissen, Marion
Primary effect of chemotherapy on the transcription profile of AIDS-related Kaposi's sarcoma
title Primary effect of chemotherapy on the transcription profile of AIDS-related Kaposi's sarcoma
title_full Primary effect of chemotherapy on the transcription profile of AIDS-related Kaposi's sarcoma
title_fullStr Primary effect of chemotherapy on the transcription profile of AIDS-related Kaposi's sarcoma
title_full_unstemmed Primary effect of chemotherapy on the transcription profile of AIDS-related Kaposi's sarcoma
title_short Primary effect of chemotherapy on the transcription profile of AIDS-related Kaposi's sarcoma
title_sort primary effect of chemotherapy on the transcription profile of aids-related kaposi's sarcoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC126247/
https://www.ncbi.nlm.nih.gov/pubmed/12204098
http://dx.doi.org/10.1186/1471-2407-2-21
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