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Protein C receptor maintains cancer stem cell properties via activating lipid synthesis in nasopharyngeal carcinoma

Metastasis and recurrence account for 95% of deaths from nasopharyngeal carcinoma (NPC). Cancer stem cells (CSCs) are regarded as one of the main reasons for tumor cell resistance to clinical therapy, and cancer metastasis or recurrence, while little is known about CSCs in NPC. The present study unc...

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Autores principales: Zhang, Panpan, He, Qiuping, Wang, Yaqin, Zhou, Guanqun, Chen, Yupei, Tang, Linglong, Zhang, Yuan, Hong, Xiaohong, Mao, Yanping, He, Qingmei, Yang, Xiaojing, Liu, Na, Ma, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8847456/
https://www.ncbi.nlm.nih.gov/pubmed/35169126
http://dx.doi.org/10.1038/s41392-021-00866-z
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author Zhang, Panpan
He, Qiuping
Wang, Yaqin
Zhou, Guanqun
Chen, Yupei
Tang, Linglong
Zhang, Yuan
Hong, Xiaohong
Mao, Yanping
He, Qingmei
Yang, Xiaojing
Liu, Na
Ma, Jun
author_facet Zhang, Panpan
He, Qiuping
Wang, Yaqin
Zhou, Guanqun
Chen, Yupei
Tang, Linglong
Zhang, Yuan
Hong, Xiaohong
Mao, Yanping
He, Qingmei
Yang, Xiaojing
Liu, Na
Ma, Jun
author_sort Zhang, Panpan
collection PubMed
description Metastasis and recurrence account for 95% of deaths from nasopharyngeal carcinoma (NPC). Cancer stem cells (CSCs) are regarded as one of the main reasons for tumor cell resistance to clinical therapy, and cancer metastasis or recurrence, while little is known about CSCs in NPC. The present study uncovers a subpopulation of cells labeled as CD45(−)EPCAM(+)PROCR(+) in NPC biopsy samples that exhibit stem cell-like characteristics. A relatively low number of these cells initiate xenograft tumors in mice. Functional analysis reveals that protein C receptor (PROCR) not only serves as a stem cell marker in NPC, but also maintains tumor cells’ stemness potential through regulating lipid metabolism and mitochondrial fission. Epistatic studies reveal that cAMP-protein kinase A stimulates Ca2(+) release to manipulate lipid metabolism related genes’ expression. Finally, in a cohort of 207 NPC samples, PROCR expression is correlated with tumor metastasis or recurrence, and predicts poor prognosis. These novel findings link PROCR labeled CSCs with lipid metabolism and mitochondrial plasticity, and provides new clinical target against metastatic or recurrent NPC.
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spelling pubmed-88474562022-03-04 Protein C receptor maintains cancer stem cell properties via activating lipid synthesis in nasopharyngeal carcinoma Zhang, Panpan He, Qiuping Wang, Yaqin Zhou, Guanqun Chen, Yupei Tang, Linglong Zhang, Yuan Hong, Xiaohong Mao, Yanping He, Qingmei Yang, Xiaojing Liu, Na Ma, Jun Signal Transduct Target Ther Article Metastasis and recurrence account for 95% of deaths from nasopharyngeal carcinoma (NPC). Cancer stem cells (CSCs) are regarded as one of the main reasons for tumor cell resistance to clinical therapy, and cancer metastasis or recurrence, while little is known about CSCs in NPC. The present study uncovers a subpopulation of cells labeled as CD45(−)EPCAM(+)PROCR(+) in NPC biopsy samples that exhibit stem cell-like characteristics. A relatively low number of these cells initiate xenograft tumors in mice. Functional analysis reveals that protein C receptor (PROCR) not only serves as a stem cell marker in NPC, but also maintains tumor cells’ stemness potential through regulating lipid metabolism and mitochondrial fission. Epistatic studies reveal that cAMP-protein kinase A stimulates Ca2(+) release to manipulate lipid metabolism related genes’ expression. Finally, in a cohort of 207 NPC samples, PROCR expression is correlated with tumor metastasis or recurrence, and predicts poor prognosis. These novel findings link PROCR labeled CSCs with lipid metabolism and mitochondrial plasticity, and provides new clinical target against metastatic or recurrent NPC. Nature Publishing Group UK 2022-02-16 /pmc/articles/PMC8847456/ /pubmed/35169126 http://dx.doi.org/10.1038/s41392-021-00866-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zhang, Panpan
He, Qiuping
Wang, Yaqin
Zhou, Guanqun
Chen, Yupei
Tang, Linglong
Zhang, Yuan
Hong, Xiaohong
Mao, Yanping
He, Qingmei
Yang, Xiaojing
Liu, Na
Ma, Jun
Protein C receptor maintains cancer stem cell properties via activating lipid synthesis in nasopharyngeal carcinoma
title Protein C receptor maintains cancer stem cell properties via activating lipid synthesis in nasopharyngeal carcinoma
title_full Protein C receptor maintains cancer stem cell properties via activating lipid synthesis in nasopharyngeal carcinoma
title_fullStr Protein C receptor maintains cancer stem cell properties via activating lipid synthesis in nasopharyngeal carcinoma
title_full_unstemmed Protein C receptor maintains cancer stem cell properties via activating lipid synthesis in nasopharyngeal carcinoma
title_short Protein C receptor maintains cancer stem cell properties via activating lipid synthesis in nasopharyngeal carcinoma
title_sort protein c receptor maintains cancer stem cell properties via activating lipid synthesis in nasopharyngeal carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8847456/
https://www.ncbi.nlm.nih.gov/pubmed/35169126
http://dx.doi.org/10.1038/s41392-021-00866-z
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