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Expression of Stem Cell Markers and Dopamine D2 Receptors in Human and Rat Prolactinomas
BACKGROUND: Dopamine agonists (DAs) are the first-line treatment for prolactinomas. DAs primarily target the dopamine D2 receptor (D2R). Tumor stem-like cells (TSLCs) are associated with the tolerance to radiotherapy and chemotherapy. TSLCs have also been identified in pituitary adenomas. We aimed t...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402840/ https://www.ncbi.nlm.nih.gov/pubmed/28411401 http://dx.doi.org/10.12659/MSM.901154 |
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author | Gao, Zhichao Cai, Lin Lu, Jianglong Wang, Chengde Li, Qun Chen, Jian Song, Xiaoxiao Chen, Xianbin Zhang, Linlin Zheng, Weiming Su, Zhipeng |
author_facet | Gao, Zhichao Cai, Lin Lu, Jianglong Wang, Chengde Li, Qun Chen, Jian Song, Xiaoxiao Chen, Xianbin Zhang, Linlin Zheng, Weiming Su, Zhipeng |
author_sort | Gao, Zhichao |
collection | PubMed |
description | BACKGROUND: Dopamine agonists (DAs) are the first-line treatment for prolactinomas. DAs primarily target the dopamine D2 receptor (D2R). Tumor stem-like cells (TSLCs) are associated with the tolerance to radiotherapy and chemotherapy. TSLCs have also been identified in pituitary adenomas. We aimed to characterize the expression pattern of stem cell markers and D2R in human and rat prolactinomas. MATERIAL/METHODS: Human prolactinoma specimens (n=14) were obtained from patients with surgical resection. The xenograft model of rat prolactinomas was generated by endermically injecting MMQ cells, HE and PRL were confirmed by immunohistochemical staining of tumor sections, and the expression of serum PRL was measured by ELISA. The expression of stem cell markers (CD133, Nestin, Oct4, and Sox2) and D2R in prolactinomas was detected by immunofluorescence. The proportion of CD133-expressing cells after DA treatment was evaluated by flow cytometry in vitro. RESULTS: We found that a small subpopulation of cells expressing stem cell markers existed both in human and rat prolactinomas. Furthermore, the CD133-expressing cells showed negative D2R expression. Conversely, the D2R-expressing cells showed negative CD133 expression. The proportion of CD133-expressing cells in surviving tumor cells was significantly increased after DA treatment. CONCLUSIONS: Our results confirmed the existence of cells expressing stem cell markers in human and rat prolactinomas. Additionally, the CD133-expressing cells might resist DA therapy due to the lack of D2R expression. |
format | Online Article Text |
id | pubmed-5402840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54028402017-05-03 Expression of Stem Cell Markers and Dopamine D2 Receptors in Human and Rat Prolactinomas Gao, Zhichao Cai, Lin Lu, Jianglong Wang, Chengde Li, Qun Chen, Jian Song, Xiaoxiao Chen, Xianbin Zhang, Linlin Zheng, Weiming Su, Zhipeng Med Sci Monit Lab/In Vitro Research BACKGROUND: Dopamine agonists (DAs) are the first-line treatment for prolactinomas. DAs primarily target the dopamine D2 receptor (D2R). Tumor stem-like cells (TSLCs) are associated with the tolerance to radiotherapy and chemotherapy. TSLCs have also been identified in pituitary adenomas. We aimed to characterize the expression pattern of stem cell markers and D2R in human and rat prolactinomas. MATERIAL/METHODS: Human prolactinoma specimens (n=14) were obtained from patients with surgical resection. The xenograft model of rat prolactinomas was generated by endermically injecting MMQ cells, HE and PRL were confirmed by immunohistochemical staining of tumor sections, and the expression of serum PRL was measured by ELISA. The expression of stem cell markers (CD133, Nestin, Oct4, and Sox2) and D2R in prolactinomas was detected by immunofluorescence. The proportion of CD133-expressing cells after DA treatment was evaluated by flow cytometry in vitro. RESULTS: We found that a small subpopulation of cells expressing stem cell markers existed both in human and rat prolactinomas. Furthermore, the CD133-expressing cells showed negative D2R expression. Conversely, the D2R-expressing cells showed negative CD133 expression. The proportion of CD133-expressing cells in surviving tumor cells was significantly increased after DA treatment. CONCLUSIONS: Our results confirmed the existence of cells expressing stem cell markers in human and rat prolactinomas. Additionally, the CD133-expressing cells might resist DA therapy due to the lack of D2R expression. International Scientific Literature, Inc. 2017-04-15 /pmc/articles/PMC5402840/ /pubmed/28411401 http://dx.doi.org/10.12659/MSM.901154 Text en © Med Sci Monit, 2017 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Lab/In Vitro Research Gao, Zhichao Cai, Lin Lu, Jianglong Wang, Chengde Li, Qun Chen, Jian Song, Xiaoxiao Chen, Xianbin Zhang, Linlin Zheng, Weiming Su, Zhipeng Expression of Stem Cell Markers and Dopamine D2 Receptors in Human and Rat Prolactinomas |
title | Expression of Stem Cell Markers and Dopamine D2 Receptors in Human and Rat Prolactinomas |
title_full | Expression of Stem Cell Markers and Dopamine D2 Receptors in Human and Rat Prolactinomas |
title_fullStr | Expression of Stem Cell Markers and Dopamine D2 Receptors in Human and Rat Prolactinomas |
title_full_unstemmed | Expression of Stem Cell Markers and Dopamine D2 Receptors in Human and Rat Prolactinomas |
title_short | Expression of Stem Cell Markers and Dopamine D2 Receptors in Human and Rat Prolactinomas |
title_sort | expression of stem cell markers and dopamine d2 receptors in human and rat prolactinomas |
topic | Lab/In Vitro Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5402840/ https://www.ncbi.nlm.nih.gov/pubmed/28411401 http://dx.doi.org/10.12659/MSM.901154 |
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