CD24, CD44 and EpCAM enrich for tumour-initiating cells in a newly established patient-derived xenograft of nasopharyngeal carcinoma
Subpopulations of nasopharyngeal carcinoma (NPC) contain cells with differential tumourigenic properties. Our study evaluates the tumourigenic potential of CD24, CD44, EpCAM and combination of EpCAM/CD44 cells in NPC. CD44br and EpCAMbr cells enriched for higher S-phase cell content, fastergrowing t...
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my.sunway.eprints.8302019-05-13T08:42:32Z http://eprints.sunway.edu.my/830/ CD24, CD44 and EpCAM enrich for tumour-initiating cells in a newly established patient-derived xenograft of nasopharyngeal carcinoma Hoe, Susan Ling Ling Tan, Lu Ping Abdul Aziz, Norazlin Liew, Kitson Teow, Sin Yeang * Abdul Razak, Fazlyn Reeny Chin, Yoon Ming Mohamed Shahrehan, Nurul Ashikin Chu, Tai Lin Mohd Kornain, Noor Kaslina Peh, Suat Cheng * Koay, Cheng Eng Lo, Kwok-Wai Ahmad, Munirah Ng, Ching-Ching Khoo, Alan Soo Beng RC0254 Neoplasms. Tumors. Oncology (including Cancer) Subpopulations of nasopharyngeal carcinoma (NPC) contain cells with differential tumourigenic properties. Our study evaluates the tumourigenic potential of CD24, CD44, EpCAM and combination of EpCAM/CD44 cells in NPC. CD44br and EpCAMbr cells enriched for higher S-phase cell content, fastergrowing tumourigenic cells leading to tumours with larger volume and higher mitotic figures. Although CD44br and EpCAMbr cells significantly enriched for tumour-initiating cells (TICs), all cells could retain self-renewal property for at least four generations. Compared to CD44 marker alone, EpCAM/CD44dbr marker did not enhance for cells with faster-growing ability or higher TIC frequency. Cells expressing high CD44 or EpCAM had lower KLF4 and p21 in NPC subpopulations. KLF4-overexpressed EpCAMbr cells had slower growth while Kenpaullone inhibition of KLF4 transcription increased in vitro cell proliferation. Compared to non-NPC, NPC specimens had increased expression of EPCAM, of which tumours from advanced stage of NPC had higher expression. Together, our study provides evidence that EpCAM is a potentially important marker in NPC. Nature Publishing Group 2017-09-28 Article PeerReviewed text en cc_by_nc_4 http://eprints.sunway.edu.my/830/1/Ronald%20Teow%20CD24%20CD44.pdf Hoe, Susan Ling Ling and Tan, Lu Ping and Abdul Aziz, Norazlin and Liew, Kitson and Teow, Sin Yeang * and Abdul Razak, Fazlyn Reeny and Chin, Yoon Ming and Mohamed Shahrehan, Nurul Ashikin and Chu, Tai Lin and Mohd Kornain, Noor Kaslina and Peh, Suat Cheng * and Koay, Cheng Eng and Lo, Kwok-Wai and Ahmad, Munirah and Ng, Ching-Ching and Khoo, Alan Soo Beng (2017) CD24, CD44 and EpCAM enrich for tumour-initiating cells in a newly established patient-derived xenograft of nasopharyngeal carcinoma. Scientific Reports, 7 (1). p. 12372. ISSN 2045-2322 http://doi.org/10.1038/s41598-017-12045-8 doi:10.1038/s41598-017-12045-8 |
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RC0254 Neoplasms. Tumors. Oncology (including Cancer) Hoe, Susan Ling Ling Tan, Lu Ping Abdul Aziz, Norazlin Liew, Kitson Teow, Sin Yeang * Abdul Razak, Fazlyn Reeny Chin, Yoon Ming Mohamed Shahrehan, Nurul Ashikin Chu, Tai Lin Mohd Kornain, Noor Kaslina Peh, Suat Cheng * Koay, Cheng Eng Lo, Kwok-Wai Ahmad, Munirah Ng, Ching-Ching Khoo, Alan Soo Beng CD24, CD44 and EpCAM enrich for tumour-initiating cells in a newly established patient-derived xenograft of nasopharyngeal carcinoma |
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Subpopulations of nasopharyngeal carcinoma (NPC) contain cells with differential tumourigenic properties. Our study evaluates the tumourigenic potential of CD24, CD44, EpCAM and combination of EpCAM/CD44 cells in NPC. CD44br and EpCAMbr cells enriched for higher S-phase cell content, fastergrowing tumourigenic cells leading to tumours with larger volume and higher mitotic figures. Although CD44br and EpCAMbr cells significantly enriched for tumour-initiating cells (TICs), all cells could retain self-renewal property for at least four generations. Compared to CD44 marker alone, EpCAM/CD44dbr marker did not enhance for cells with faster-growing ability or higher TIC frequency. Cells expressing high CD44 or EpCAM had lower KLF4 and p21 in NPC subpopulations. KLF4-overexpressed EpCAMbr cells had slower growth while Kenpaullone inhibition of KLF4 transcription increased in vitro cell proliferation. Compared to non-NPC, NPC specimens had increased expression of EPCAM, of which tumours from advanced stage of NPC had higher expression. Together, our study provides evidence that EpCAM is a potentially important marker in NPC. |
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Article |
author |
Hoe, Susan Ling Ling Tan, Lu Ping Abdul Aziz, Norazlin Liew, Kitson Teow, Sin Yeang * Abdul Razak, Fazlyn Reeny Chin, Yoon Ming Mohamed Shahrehan, Nurul Ashikin Chu, Tai Lin Mohd Kornain, Noor Kaslina Peh, Suat Cheng * Koay, Cheng Eng Lo, Kwok-Wai Ahmad, Munirah Ng, Ching-Ching Khoo, Alan Soo Beng |
author_facet |
Hoe, Susan Ling Ling Tan, Lu Ping Abdul Aziz, Norazlin Liew, Kitson Teow, Sin Yeang * Abdul Razak, Fazlyn Reeny Chin, Yoon Ming Mohamed Shahrehan, Nurul Ashikin Chu, Tai Lin Mohd Kornain, Noor Kaslina Peh, Suat Cheng * Koay, Cheng Eng Lo, Kwok-Wai Ahmad, Munirah Ng, Ching-Ching Khoo, Alan Soo Beng |
author_sort |
Hoe, Susan Ling Ling |
title |
CD24, CD44 and EpCAM enrich for tumour-initiating cells in a newly established patient-derived xenograft of nasopharyngeal carcinoma |
title_short |
CD24, CD44 and EpCAM enrich for tumour-initiating cells in a newly established patient-derived xenograft of nasopharyngeal carcinoma |
title_full |
CD24, CD44 and EpCAM enrich for tumour-initiating cells in a newly established patient-derived xenograft of nasopharyngeal carcinoma |
title_fullStr |
CD24, CD44 and EpCAM enrich for tumour-initiating cells in a newly established patient-derived xenograft of nasopharyngeal carcinoma |
title_full_unstemmed |
CD24, CD44 and EpCAM enrich for tumour-initiating cells in a newly established patient-derived xenograft of nasopharyngeal carcinoma |
title_sort |
cd24, cd44 and epcam enrich for tumour-initiating cells in a newly established patient-derived xenograft of nasopharyngeal carcinoma |
publisher |
Nature Publishing Group |
publishDate |
2017 |
url |
http://eprints.sunway.edu.my/830/1/Ronald%20Teow%20CD24%20CD44.pdf http://eprints.sunway.edu.my/830/ http://doi.org/10.1038/s41598-017-12045-8 |
_version_ |
1644324412104638464 |
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13.211869 |