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Survivin Expression in Luminal Breast Cancer and Adjacent Normal Tissue for Immuno-Oncology Applications

Survivin (BIRC5) is a tumor-associated antigen (TAA) overexpressed in various tumors but present at low to undetectable levels in normal tissue. Survivin is known to have a high expression in breast cancer (e.g., Ductal Carcinoma in situ (DCIS) and triple negative breast cancer). Previous studies ha...

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Autores principales: Wright, Sharon, Burkholtz, Scott R., Zelinsky, Cathy, Wittman, Connor, Carback, Richard T., Harris, Paul E., Blankenberg, Tikoes, Herst, Charles V., Rubsamen, Reid M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10380623/
https://www.ncbi.nlm.nih.gov/pubmed/37511584
http://dx.doi.org/10.3390/ijms241411827
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author Wright, Sharon
Burkholtz, Scott R.
Zelinsky, Cathy
Wittman, Connor
Carback, Richard T.
Harris, Paul E.
Blankenberg, Tikoes
Herst, Charles V.
Rubsamen, Reid M.
author_facet Wright, Sharon
Burkholtz, Scott R.
Zelinsky, Cathy
Wittman, Connor
Carback, Richard T.
Harris, Paul E.
Blankenberg, Tikoes
Herst, Charles V.
Rubsamen, Reid M.
author_sort Wright, Sharon
collection PubMed
description Survivin (BIRC5) is a tumor-associated antigen (TAA) overexpressed in various tumors but present at low to undetectable levels in normal tissue. Survivin is known to have a high expression in breast cancer (e.g., Ductal Carcinoma in situ (DCIS) and triple negative breast cancer). Previous studies have not compared survivin expression levels in DCIS tumor samples to levels in adjacent, normal breast tissue from the same patient. To ensure the effective use of survivin as a target for T cell immunotherapy of breast cancer, it is essential to ascertain the varying levels of survivin expression between DCIS tumor tissue samples and the adjacent normal breast tissue taken from the same patient simultaneously. Next-generation sequencing of RNA (RNA-seq) in normal breast tissue and tumor breast tissue from five women presenting with DCIS for lumpectomy was used to identify sequence variation and expression levels of survivin. The identity of both tumor and adjacent normal tissue samples were corroborated by histopathology. Survivin was overexpressed in human breast tissue tumor samples relative to the corresponding adjacent human normal breast tissue. Wild-type survivin transcripts were the predominant species identified in all tumor tissue sequenced. This study demonstrates upregulated expression of wild type survivin in DCIS tumor tissue versus normal breast tissue taken from the same patient at the same time, and provides evidence that developing selective cytotoxic T lymphocyte (CTL) immunotherapy for DCIS targeting survivin warrants further study.
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spelling pubmed-103806232023-07-29 Survivin Expression in Luminal Breast Cancer and Adjacent Normal Tissue for Immuno-Oncology Applications Wright, Sharon Burkholtz, Scott R. Zelinsky, Cathy Wittman, Connor Carback, Richard T. Harris, Paul E. Blankenberg, Tikoes Herst, Charles V. Rubsamen, Reid M. Int J Mol Sci Article Survivin (BIRC5) is a tumor-associated antigen (TAA) overexpressed in various tumors but present at low to undetectable levels in normal tissue. Survivin is known to have a high expression in breast cancer (e.g., Ductal Carcinoma in situ (DCIS) and triple negative breast cancer). Previous studies have not compared survivin expression levels in DCIS tumor samples to levels in adjacent, normal breast tissue from the same patient. To ensure the effective use of survivin as a target for T cell immunotherapy of breast cancer, it is essential to ascertain the varying levels of survivin expression between DCIS tumor tissue samples and the adjacent normal breast tissue taken from the same patient simultaneously. Next-generation sequencing of RNA (RNA-seq) in normal breast tissue and tumor breast tissue from five women presenting with DCIS for lumpectomy was used to identify sequence variation and expression levels of survivin. The identity of both tumor and adjacent normal tissue samples were corroborated by histopathology. Survivin was overexpressed in human breast tissue tumor samples relative to the corresponding adjacent human normal breast tissue. Wild-type survivin transcripts were the predominant species identified in all tumor tissue sequenced. This study demonstrates upregulated expression of wild type survivin in DCIS tumor tissue versus normal breast tissue taken from the same patient at the same time, and provides evidence that developing selective cytotoxic T lymphocyte (CTL) immunotherapy for DCIS targeting survivin warrants further study. MDPI 2023-07-23 /pmc/articles/PMC10380623/ /pubmed/37511584 http://dx.doi.org/10.3390/ijms241411827 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wright, Sharon
Burkholtz, Scott R.
Zelinsky, Cathy
Wittman, Connor
Carback, Richard T.
Harris, Paul E.
Blankenberg, Tikoes
Herst, Charles V.
Rubsamen, Reid M.
Survivin Expression in Luminal Breast Cancer and Adjacent Normal Tissue for Immuno-Oncology Applications
title Survivin Expression in Luminal Breast Cancer and Adjacent Normal Tissue for Immuno-Oncology Applications
title_full Survivin Expression in Luminal Breast Cancer and Adjacent Normal Tissue for Immuno-Oncology Applications
title_fullStr Survivin Expression in Luminal Breast Cancer and Adjacent Normal Tissue for Immuno-Oncology Applications
title_full_unstemmed Survivin Expression in Luminal Breast Cancer and Adjacent Normal Tissue for Immuno-Oncology Applications
title_short Survivin Expression in Luminal Breast Cancer and Adjacent Normal Tissue for Immuno-Oncology Applications
title_sort survivin expression in luminal breast cancer and adjacent normal tissue for immuno-oncology applications
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10380623/
https://www.ncbi.nlm.nih.gov/pubmed/37511584
http://dx.doi.org/10.3390/ijms241411827
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