Please use this identifier to cite or link to this item:
https://doi.org/10.1038/s41598-017-17628-z
DC Field | Value | |
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dc.title | Non-malignant epithelial cells preferentially proliferate from nasopharyngeal carcinoma biopsy cultured under conditionally reprogrammed conditions | |
dc.contributor.author | Yu F. | |
dc.contributor.author | Lu Y. | |
dc.contributor.author | Tao L. | |
dc.contributor.author | Jiang Y.-Y. | |
dc.contributor.author | Lin D.-C. | |
dc.contributor.author | Wang L. | |
dc.contributor.author | Petersson F. | |
dc.contributor.author | Yoshiyama H. | |
dc.contributor.author | Koeffler P.H. | |
dc.contributor.author | Goh B.-C. | |
dc.contributor.author | Loh K.S. | |
dc.date.accessioned | 2020-09-09T03:15:48Z | |
dc.date.available | 2020-09-09T03:15:48Z | |
dc.date.issued | 2017 | |
dc.identifier.citation | Yu F., Lu Y., Tao L., Jiang Y.-Y., Lin D.-C., Wang L., Petersson F., Yoshiyama H., Koeffler P.H., Goh B.-C., Loh K.S. (2017). Non-malignant epithelial cells preferentially proliferate from nasopharyngeal carcinoma biopsy cultured under conditionally reprogrammed conditions. Scientific Reports 7 (1) : 17359. ScholarBank@NUS Repository. https://doi.org/10.1038/s41598-017-17628-z | |
dc.identifier.issn | 20452322 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/175087 | |
dc.description.abstract | Nasopharyngeal carcinoma (NPC) is an invasive cancer with particularly high incidence in Southern China and Southeast Asia. The study of NPC is greatly hampered by the lack of reliable cell lines due to the loss of EBV genome and HeLa cell contamination. Conditional reprogramming (CR) cell culture technique has been reported for rapid and efficient establishment of patient derived normal and tumor cell cultures. The purpose of this study was to assess this method to culture NPC patient derived primary tumor cells. Using CR protocol, we demonstrated that epithelial cells could be efficiently cultured from normal (70%) and cancerous nasopharyngeal (46%) biopsies. However, by comparing with original tumors in terms of mutation and methylation profiles, epithelial cells derived from cancerous biopsy represented non malignant cells. Further, they exhibited stem like characteristics based on their cell surface proteins and could differentiate into pseudostratified epithelium in an air-liquid interface culture system. We conclude that CR method is a highly selective and useful method for growing non malignant nasopharyngeal epithelial cells. © 2017 The Author(s). | |
dc.source | Unpaywall 20200831 | |
dc.subject | 3T3 cell line | |
dc.subject | adult | |
dc.subject | aged | |
dc.subject | animal | |
dc.subject | biopsy | |
dc.subject | cell proliferation | |
dc.subject | coculture | |
dc.subject | dna mutational analysis | |
dc.subject | epithelium cell | |
dc.subject | evaluation study | |
dc.subject | feeder cell | |
dc.subject | female | |
dc.subject | genetics | |
dc.subject | human | |
dc.subject | male | |
dc.subject | middle aged | |
dc.subject | mouse | |
dc.subject | mutation | |
dc.subject | nasopharynx carcinoma | |
dc.subject | nasopharynx tumor | |
dc.subject | nuclear reprogramming | |
dc.subject | pathology | |
dc.subject | physiology | |
dc.subject | primary cell culture | |
dc.subject | procedures | |
dc.subject | tumor cell culture | |
dc.subject | 3T3 Cells | |
dc.subject | Adult | |
dc.subject | Aged | |
dc.subject | Animals | |
dc.subject | Biopsy | |
dc.subject | Cell Proliferation | |
dc.subject | Cellular Reprogramming | |
dc.subject | Coculture Techniques | |
dc.subject | DNA Mutational Analysis | |
dc.subject | Epithelial Cells | |
dc.subject | Feeder Cells | |
dc.subject | Female | |
dc.subject | Humans | |
dc.subject | Male | |
dc.subject | Mice | |
dc.subject | Middle Aged | |
dc.subject | Mutation | |
dc.subject | Nasopharyngeal Carcinoma | |
dc.subject | Nasopharyngeal Neoplasms | |
dc.subject | Primary Cell Culture | |
dc.subject | Tumor Cells, Cultured | |
dc.type | Article | |
dc.contributor.department | OTOLARYNGOLOGY | |
dc.contributor.department | CANCER SCIENCE INSTITUTE OF SINGAPORE | |
dc.contributor.department | PHARMACY | |
dc.contributor.department | PATHOLOGY | |
dc.contributor.department | PHARMACOLOGY | |
dc.description.doi | 10.1038/s41598-017-17628-z | |
dc.description.sourcetitle | Scientific Reports | |
dc.description.volume | 7 | |
dc.description.issue | 1 | |
dc.description.page | 17359 | |
Appears in Collections: | Elements Staff Publications |
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