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HIV fragments detected in Kaposi sarcoma tumor cells in HIV-infected patients
Kaposi sarcoma (KS) is a malignant vascular neoplasm caused by KS-associated herpesvirus (KSHV) infection. HIV plays a major role in KS pathogenesis. KS in HIV usually produces more malignant features than classic KS. Despite the close KS–HIV relationship, no study has reported the existence of HIV...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622637/ https://www.ncbi.nlm.nih.gov/pubmed/36316837 http://dx.doi.org/10.1097/MD.0000000000031310 |
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author | Chen, Tung-Ying Yang, Horng-Woei Lin, Dar-Shong Huang, Zo-Darr Chang, Lung |
author_facet | Chen, Tung-Ying Yang, Horng-Woei Lin, Dar-Shong Huang, Zo-Darr Chang, Lung |
author_sort | Chen, Tung-Ying |
collection | PubMed |
description | Kaposi sarcoma (KS) is a malignant vascular neoplasm caused by KS-associated herpesvirus (KSHV) infection. HIV plays a major role in KS pathogenesis. KS in HIV usually produces more malignant features than classic KS. Despite the close KS–HIV relationship, no study has reported the existence of HIV in KS tissue. We used ddPCR to detect HIV and KSHV in HIV(+) KS samples and classic KS control. We verified KS cell types through immunohistochemistry and applied hypersensitive in situ hybridization (ISH) to detect HIV and KSHV in tumor cells. Furthermore, we co-stained samples with ISH and immunohistochemistry to identify HIV and KSHV in specific cell types. Regarding pathological stages, the KS were nodular (58.3%), plaque (33.3%), and patch (8.3%) tumors. Moreover, ddPCR revealed HIV in 58.3% of the KS samples. ISH revealed positive Pol/Gag mRNA signals in CD34 (+) tumor cells from HIV (+) patients (95.8%). HIV signals were absent in macrophages and other inflammatory cells. Most HIV (+) KS cells showed scattered reactive particles of HIV and KSHV. We demonstrated that HIV could infect CD34 (+) tumor cells and coexist with KSHV in KS, constituting a novel finding. We hypothesized that the direct KSHV–HIV interaction at the cellular level contributes to KS oncogenesis. |
format | Online Article Text |
id | pubmed-9622637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-96226372022-11-03 HIV fragments detected in Kaposi sarcoma tumor cells in HIV-infected patients Chen, Tung-Ying Yang, Horng-Woei Lin, Dar-Shong Huang, Zo-Darr Chang, Lung Medicine (Baltimore) 4900 Kaposi sarcoma (KS) is a malignant vascular neoplasm caused by KS-associated herpesvirus (KSHV) infection. HIV plays a major role in KS pathogenesis. KS in HIV usually produces more malignant features than classic KS. Despite the close KS–HIV relationship, no study has reported the existence of HIV in KS tissue. We used ddPCR to detect HIV and KSHV in HIV(+) KS samples and classic KS control. We verified KS cell types through immunohistochemistry and applied hypersensitive in situ hybridization (ISH) to detect HIV and KSHV in tumor cells. Furthermore, we co-stained samples with ISH and immunohistochemistry to identify HIV and KSHV in specific cell types. Regarding pathological stages, the KS were nodular (58.3%), plaque (33.3%), and patch (8.3%) tumors. Moreover, ddPCR revealed HIV in 58.3% of the KS samples. ISH revealed positive Pol/Gag mRNA signals in CD34 (+) tumor cells from HIV (+) patients (95.8%). HIV signals were absent in macrophages and other inflammatory cells. Most HIV (+) KS cells showed scattered reactive particles of HIV and KSHV. We demonstrated that HIV could infect CD34 (+) tumor cells and coexist with KSHV in KS, constituting a novel finding. We hypothesized that the direct KSHV–HIV interaction at the cellular level contributes to KS oncogenesis. Lippincott Williams & Wilkins 2022-10-28 /pmc/articles/PMC9622637/ /pubmed/36316837 http://dx.doi.org/10.1097/MD.0000000000031310 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | 4900 Chen, Tung-Ying Yang, Horng-Woei Lin, Dar-Shong Huang, Zo-Darr Chang, Lung HIV fragments detected in Kaposi sarcoma tumor cells in HIV-infected patients |
title | HIV fragments detected in Kaposi sarcoma tumor cells in HIV-infected patients |
title_full | HIV fragments detected in Kaposi sarcoma tumor cells in HIV-infected patients |
title_fullStr | HIV fragments detected in Kaposi sarcoma tumor cells in HIV-infected patients |
title_full_unstemmed | HIV fragments detected in Kaposi sarcoma tumor cells in HIV-infected patients |
title_short | HIV fragments detected in Kaposi sarcoma tumor cells in HIV-infected patients |
title_sort | hiv fragments detected in kaposi sarcoma tumor cells in hiv-infected patients |
topic | 4900 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622637/ https://www.ncbi.nlm.nih.gov/pubmed/36316837 http://dx.doi.org/10.1097/MD.0000000000031310 |
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