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A clear cancer cell line (150057) derived from human endometrial carcinoma harbors two novel mutations

BACKGROUND: Cell lines are extremely useful for both basic and clinical research. Thus, establishing endometrial cancer cell lines with malignant histology is important. This study aimed to extensively characterize an endometrial clear cell carcinoma cell line. METHODS: This cell line, named 150,057...

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Autores principales: Chang, Yu-Hsun, Ding, Dah-Ching
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607743/
https://www.ncbi.nlm.nih.gov/pubmed/33143664
http://dx.doi.org/10.1186/s12885-020-07567-w
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author Chang, Yu-Hsun
Ding, Dah-Ching
author_facet Chang, Yu-Hsun
Ding, Dah-Ching
author_sort Chang, Yu-Hsun
collection PubMed
description BACKGROUND: Cell lines are extremely useful for both basic and clinical research. Thus, establishing endometrial cancer cell lines with malignant histology is important. This study aimed to extensively characterize an endometrial clear cell carcinoma cell line. METHODS: This cell line, named 150,057, was derived from the endometrial clear cell cancer of a 63-year-old woman. The morphology, chromosomes, chemosensitivity, tumor markers, xenotransplantation characteristics, and cancer-related genes of the cell line were characterized. RESULTS: This cell line exhibited adequate growth, being passaged more than 70 times. The morphology of the cells was polygonal with a cobblestone-like appearance. Karyotyping of the cell line revealed a hypodiploid chromosomal number. 150057 cells expressed CA19–9 and CA125. The cell line was sensitive to doxorubicin, paclitaxel, carboplatin, and cisplatin. After the cells were transplanted into the subcutaneous region of non-obese diabetic-severe combined immunodeficiency mice, they generated xenograft tumors with similar histology as the original tumor. A total of 59 somatic nucleotide mutations were identified in 25 of the 53 examined tumor suppressor genes and oncogenes. Two novel mutations were found in FGFR3 and ARID1A. CONCLUSION: We established and characterized an endometrial clear cell carcinoma cell line that may be useful in carcinogenesis and treatment research for endometrial cancer. SUPPLEMENTARY INFORMATION: Supplementary information accompanies this paper at10.1186/s12885-020-07567-w.
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spelling pubmed-76077432020-11-03 A clear cancer cell line (150057) derived from human endometrial carcinoma harbors two novel mutations Chang, Yu-Hsun Ding, Dah-Ching BMC Cancer Research Article BACKGROUND: Cell lines are extremely useful for both basic and clinical research. Thus, establishing endometrial cancer cell lines with malignant histology is important. This study aimed to extensively characterize an endometrial clear cell carcinoma cell line. METHODS: This cell line, named 150,057, was derived from the endometrial clear cell cancer of a 63-year-old woman. The morphology, chromosomes, chemosensitivity, tumor markers, xenotransplantation characteristics, and cancer-related genes of the cell line were characterized. RESULTS: This cell line exhibited adequate growth, being passaged more than 70 times. The morphology of the cells was polygonal with a cobblestone-like appearance. Karyotyping of the cell line revealed a hypodiploid chromosomal number. 150057 cells expressed CA19–9 and CA125. The cell line was sensitive to doxorubicin, paclitaxel, carboplatin, and cisplatin. After the cells were transplanted into the subcutaneous region of non-obese diabetic-severe combined immunodeficiency mice, they generated xenograft tumors with similar histology as the original tumor. A total of 59 somatic nucleotide mutations were identified in 25 of the 53 examined tumor suppressor genes and oncogenes. Two novel mutations were found in FGFR3 and ARID1A. CONCLUSION: We established and characterized an endometrial clear cell carcinoma cell line that may be useful in carcinogenesis and treatment research for endometrial cancer. SUPPLEMENTARY INFORMATION: Supplementary information accompanies this paper at10.1186/s12885-020-07567-w. BioMed Central 2020-11-03 /pmc/articles/PMC7607743/ /pubmed/33143664 http://dx.doi.org/10.1186/s12885-020-07567-w Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research Article
Chang, Yu-Hsun
Ding, Dah-Ching
A clear cancer cell line (150057) derived from human endometrial carcinoma harbors two novel mutations
title A clear cancer cell line (150057) derived from human endometrial carcinoma harbors two novel mutations
title_full A clear cancer cell line (150057) derived from human endometrial carcinoma harbors two novel mutations
title_fullStr A clear cancer cell line (150057) derived from human endometrial carcinoma harbors two novel mutations
title_full_unstemmed A clear cancer cell line (150057) derived from human endometrial carcinoma harbors two novel mutations
title_short A clear cancer cell line (150057) derived from human endometrial carcinoma harbors two novel mutations
title_sort clear cancer cell line (150057) derived from human endometrial carcinoma harbors two novel mutations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607743/
https://www.ncbi.nlm.nih.gov/pubmed/33143664
http://dx.doi.org/10.1186/s12885-020-07567-w
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