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Overexpression of iASPP is required for autophagy in response to oxidative stress in choriocarcinoma

BACKGROUND: Gestational trophoblastic disease (GTD) is a heterogeneous group of diseases developed from trophoblasts. ASPP (Ankyrin-repeat, SH3-domain and proline-rich region containing protein) family proteins, ASPP1 and ASPP2, have been reported to be dysregulated in GTD. They modulate p53 activit...

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Autores principales: Chan, Ka-Kui, Wong, Esther Shuk-Ying, Wong, Ivy Tsz-Lo, Cheung, Claire Ling-Yang, Wong, Oscar Gee-Wan, Ngan, Hextan Yuen-Sheung, Cheung, Annie Nga-Yin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6792270/
https://www.ncbi.nlm.nih.gov/pubmed/31615473
http://dx.doi.org/10.1186/s12885-019-6206-z
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author Chan, Ka-Kui
Wong, Esther Shuk-Ying
Wong, Ivy Tsz-Lo
Cheung, Claire Ling-Yang
Wong, Oscar Gee-Wan
Ngan, Hextan Yuen-Sheung
Cheung, Annie Nga-Yin
author_facet Chan, Ka-Kui
Wong, Esther Shuk-Ying
Wong, Ivy Tsz-Lo
Cheung, Claire Ling-Yang
Wong, Oscar Gee-Wan
Ngan, Hextan Yuen-Sheung
Cheung, Annie Nga-Yin
author_sort Chan, Ka-Kui
collection PubMed
description BACKGROUND: Gestational trophoblastic disease (GTD) is a heterogeneous group of diseases developed from trophoblasts. ASPP (Ankyrin-repeat, SH3-domain and proline-rich region containing protein) family proteins, ASPP1 and ASPP2, have been reported to be dysregulated in GTD. They modulate p53 activities and are responsible for multiple cellular processes. Nevertheless, the functional role of the ASPP family inhibitory member, iASPP, is not well characterized in GTD. METHODS: To study the functional role of iASPP in GTD, trophoblastic tissues from normal placentas, hydatidiform mole (HM) and choriocarcinoma were used for immunohistochemistry, whereas siRNAs were used to manipulate iASPP expression in choriocarcinoma cell lines and study the subsequent molecular changes. RESULTS: We demonstrated that iASPP was overexpressed in both HM and choriocarcinoma when compared to normal placenta. Progressive increase in iASPP expression from HM to choriocarcinoma suggests that iASPP may be related to the development of trophoblastic malignancy. High iASPP expression in HM was also significantly associated with a high expression of autophagy-related protein LC3. Interestingly, iASPP silencing retarded the growth of choriocarcinoma through senescence instead of induction of apoptosis. LC3 expression decreased once iASPP was knocked down, suggesting a downregulation on autophagy. This may be due to iASPP downregulation rendered decrease in Atg5 expression and concomitantly hindered autophagy in choriocarcinoma cells. Autophagy inhibition per se had no effect on the growth of choriocarcinoma cells but increased the susceptibility of choriocarcinoma cells to oxidative stress, implying a protective role of iASPP against oxidative stress through autophagy in choriocarcinoma. CONCLUSIONS: iASPP regulates growth and the cellular responses towards oxidative stress in choriocarcinoma cells. Its overexpression is advantageous to the pathogenesis of GTD. (266 words).
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spelling pubmed-67922702019-10-21 Overexpression of iASPP is required for autophagy in response to oxidative stress in choriocarcinoma Chan, Ka-Kui Wong, Esther Shuk-Ying Wong, Ivy Tsz-Lo Cheung, Claire Ling-Yang Wong, Oscar Gee-Wan Ngan, Hextan Yuen-Sheung Cheung, Annie Nga-Yin BMC Cancer Research Article BACKGROUND: Gestational trophoblastic disease (GTD) is a heterogeneous group of diseases developed from trophoblasts. ASPP (Ankyrin-repeat, SH3-domain and proline-rich region containing protein) family proteins, ASPP1 and ASPP2, have been reported to be dysregulated in GTD. They modulate p53 activities and are responsible for multiple cellular processes. Nevertheless, the functional role of the ASPP family inhibitory member, iASPP, is not well characterized in GTD. METHODS: To study the functional role of iASPP in GTD, trophoblastic tissues from normal placentas, hydatidiform mole (HM) and choriocarcinoma were used for immunohistochemistry, whereas siRNAs were used to manipulate iASPP expression in choriocarcinoma cell lines and study the subsequent molecular changes. RESULTS: We demonstrated that iASPP was overexpressed in both HM and choriocarcinoma when compared to normal placenta. Progressive increase in iASPP expression from HM to choriocarcinoma suggests that iASPP may be related to the development of trophoblastic malignancy. High iASPP expression in HM was also significantly associated with a high expression of autophagy-related protein LC3. Interestingly, iASPP silencing retarded the growth of choriocarcinoma through senescence instead of induction of apoptosis. LC3 expression decreased once iASPP was knocked down, suggesting a downregulation on autophagy. This may be due to iASPP downregulation rendered decrease in Atg5 expression and concomitantly hindered autophagy in choriocarcinoma cells. Autophagy inhibition per se had no effect on the growth of choriocarcinoma cells but increased the susceptibility of choriocarcinoma cells to oxidative stress, implying a protective role of iASPP against oxidative stress through autophagy in choriocarcinoma. CONCLUSIONS: iASPP regulates growth and the cellular responses towards oxidative stress in choriocarcinoma cells. Its overexpression is advantageous to the pathogenesis of GTD. (266 words). BioMed Central 2019-10-15 /pmc/articles/PMC6792270/ /pubmed/31615473 http://dx.doi.org/10.1186/s12885-019-6206-z Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Chan, Ka-Kui
Wong, Esther Shuk-Ying
Wong, Ivy Tsz-Lo
Cheung, Claire Ling-Yang
Wong, Oscar Gee-Wan
Ngan, Hextan Yuen-Sheung
Cheung, Annie Nga-Yin
Overexpression of iASPP is required for autophagy in response to oxidative stress in choriocarcinoma
title Overexpression of iASPP is required for autophagy in response to oxidative stress in choriocarcinoma
title_full Overexpression of iASPP is required for autophagy in response to oxidative stress in choriocarcinoma
title_fullStr Overexpression of iASPP is required for autophagy in response to oxidative stress in choriocarcinoma
title_full_unstemmed Overexpression of iASPP is required for autophagy in response to oxidative stress in choriocarcinoma
title_short Overexpression of iASPP is required for autophagy in response to oxidative stress in choriocarcinoma
title_sort overexpression of iaspp is required for autophagy in response to oxidative stress in choriocarcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6792270/
https://www.ncbi.nlm.nih.gov/pubmed/31615473
http://dx.doi.org/10.1186/s12885-019-6206-z
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