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The family of apoptosis-stimulating proteins of p53 is dysregulated in colorectal cancer patients

The apoptosis-stimulating protein of p53 (ASPP) family is a newly identified family protein including ASPP1, ASPP2 and inhibitor of ASPP (iASPP), by which the tumor protein 53 (TP53)-mediated apoptotic process is selectively regulated. Downregulation of ASPP1/ASPP2 and upregulation of iASPP were rev...

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Autores principales: Yin, Libin, Lin, Yuyang, Wang, Xu, Su, Yanzhuo, Hu, Han, Li, Chao, Wang, Lei, Jiang, Yanfang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921073/
https://www.ncbi.nlm.nih.gov/pubmed/29731851
http://dx.doi.org/10.3892/ol.2018.8151
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author Yin, Libin
Lin, Yuyang
Wang, Xu
Su, Yanzhuo
Hu, Han
Li, Chao
Wang, Lei
Jiang, Yanfang
author_facet Yin, Libin
Lin, Yuyang
Wang, Xu
Su, Yanzhuo
Hu, Han
Li, Chao
Wang, Lei
Jiang, Yanfang
author_sort Yin, Libin
collection PubMed
description The apoptosis-stimulating protein of p53 (ASPP) family is a newly identified family protein including ASPP1, ASPP2 and inhibitor of ASPP (iASPP), by which the tumor protein 53 (TP53)-mediated apoptotic process is selectively regulated. Downregulation of ASPP1/ASPP2 and upregulation of iASPP were revealed to be associated with a poor prognosis and metastasis in several types of cancer. However, to the best of our knowledge, the expression of ASPP in colorectal cancer (CRC) has not previously been investigated. The present study analyzed ASPP expression in human CRC tissues with multiple clinical and pathological profiles. A total of 41 patients diagnosed with CRC were enrolled in the present study. The expression of ASPP was detected by immunohistochemistry, immunofluorescence and reverse transcription-quantitative polymerase chain reaction. In addition, the variation in ASPP expression was examined in a number of pathological groups. The associations among ASPP expression, and the expression of TP53, plasma carcinoembryonic antigen (CEA) levels and α-fetoprotein (AFP) levels were also investigated. ASPP1 and ASPP2 expression was significantly reduced, while iASPP expression was elevated in CRC samples compared with expression in adjacent non-cancerous tissues. Downregulation of ASPP1 was detected in the TP53-positive group compared with the TP53-negative group. The increase in iASPP expression was correlated with the grade of malignancy, but not with regional lymph node status or metastases. The expression of ASPP2 was negatively correlated with plasma CEA levels. The results of the present study, not only enrich CRC epidemic and pathological data, but also provide valuable indices for CRC clinical treatment and prognosis.
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spelling pubmed-59210732018-05-04 The family of apoptosis-stimulating proteins of p53 is dysregulated in colorectal cancer patients Yin, Libin Lin, Yuyang Wang, Xu Su, Yanzhuo Hu, Han Li, Chao Wang, Lei Jiang, Yanfang Oncol Lett Articles The apoptosis-stimulating protein of p53 (ASPP) family is a newly identified family protein including ASPP1, ASPP2 and inhibitor of ASPP (iASPP), by which the tumor protein 53 (TP53)-mediated apoptotic process is selectively regulated. Downregulation of ASPP1/ASPP2 and upregulation of iASPP were revealed to be associated with a poor prognosis and metastasis in several types of cancer. However, to the best of our knowledge, the expression of ASPP in colorectal cancer (CRC) has not previously been investigated. The present study analyzed ASPP expression in human CRC tissues with multiple clinical and pathological profiles. A total of 41 patients diagnosed with CRC were enrolled in the present study. The expression of ASPP was detected by immunohistochemistry, immunofluorescence and reverse transcription-quantitative polymerase chain reaction. In addition, the variation in ASPP expression was examined in a number of pathological groups. The associations among ASPP expression, and the expression of TP53, plasma carcinoembryonic antigen (CEA) levels and α-fetoprotein (AFP) levels were also investigated. ASPP1 and ASPP2 expression was significantly reduced, while iASPP expression was elevated in CRC samples compared with expression in adjacent non-cancerous tissues. Downregulation of ASPP1 was detected in the TP53-positive group compared with the TP53-negative group. The increase in iASPP expression was correlated with the grade of malignancy, but not with regional lymph node status or metastases. The expression of ASPP2 was negatively correlated with plasma CEA levels. The results of the present study, not only enrich CRC epidemic and pathological data, but also provide valuable indices for CRC clinical treatment and prognosis. D.A. Spandidos 2018-05 2018-03-01 /pmc/articles/PMC5921073/ /pubmed/29731851 http://dx.doi.org/10.3892/ol.2018.8151 Text en Copyright: © Yin et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Yin, Libin
Lin, Yuyang
Wang, Xu
Su, Yanzhuo
Hu, Han
Li, Chao
Wang, Lei
Jiang, Yanfang
The family of apoptosis-stimulating proteins of p53 is dysregulated in colorectal cancer patients
title The family of apoptosis-stimulating proteins of p53 is dysregulated in colorectal cancer patients
title_full The family of apoptosis-stimulating proteins of p53 is dysregulated in colorectal cancer patients
title_fullStr The family of apoptosis-stimulating proteins of p53 is dysregulated in colorectal cancer patients
title_full_unstemmed The family of apoptosis-stimulating proteins of p53 is dysregulated in colorectal cancer patients
title_short The family of apoptosis-stimulating proteins of p53 is dysregulated in colorectal cancer patients
title_sort family of apoptosis-stimulating proteins of p53 is dysregulated in colorectal cancer patients
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5921073/
https://www.ncbi.nlm.nih.gov/pubmed/29731851
http://dx.doi.org/10.3892/ol.2018.8151
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