Cisplatin-Induced Giant Cells Formation Is Involved in Chemoresistance of Melanoma Cells
Melanoma is notoriously resistant to current cancer therapy. However, the chemoresistance mechanism of melanoma remains unclear. The present study unveiled that chemotherapy drug cisplatin induced the formation of giant cells, which exhibited enlargement in cell diameter and nucleus in mice and huma...
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doaj-ca74be2b88f440ab826e08b34d5372ea2020-11-25T03:59:03ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672020-10-01217892789210.3390/ijms21217892Cisplatin-Induced Giant Cells Formation Is Involved in Chemoresistance of Melanoma CellsChien-Hui Weng0Chieh-Shan Wu1Jian-Ching Wu2Mei-Lang Kung3Ming-Hsiu Wu4Ming-Hong Tai5Department of Biological Sciences, National Sun Yat-Sen University, Kaohsiung 80424, TaiwanDepartment of Dermatology, Kaohsiung Veterans General Hospital, Kaohsiung 81362, TaiwanBiobank and Tissue Bank, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung 83301, TaiwanDepartment of Medical Education and Research, Kaohsiung Veterans General Hospital, Kaohsiung 81362, TaiwanDepartment of Nutrition and Health Science, Fooyin University, Kaohsiung 83102, TaiwanDepartment of Biological Sciences, National Sun Yat-Sen University, Kaohsiung 80424, TaiwanMelanoma is notoriously resistant to current cancer therapy. However, the chemoresistance mechanism of melanoma remains unclear. The present study unveiled that chemotherapy drug cisplatin induced the formation of giant cells, which exhibited enlargement in cell diameter and nucleus in mice and human melanoma cells. Giant cells were positive with melanoma maker S100 and cancer stem cell markers including ABCB5 and CD133 in vitro and in vivo. Moreover, giant cells retained the mitotic ability with expression of proliferation marker Ki-67 and exhibited multiple drug resistance to doxorubicin and actinomycin D. The mitochondria genesis/activities and cellular ATP level were significantly elevated in giant cells, implicating the demand for energy supply. Application of metabolic blockers such as sodium azide or 2-deoxy glucose abolished the cisplatin-induced giant cells formation and expression of cancer stemness markers. The present study unveils a novel chemoresistance mechanism of melanoma cells via size alteration and the anti-neoplastic strategy by targeting giant cells.https://www.mdpi.com/1422-0067/21/21/7892melanomachemoresistancecisplatingiant cellstemness |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Chien-Hui Weng Chieh-Shan Wu Jian-Ching Wu Mei-Lang Kung Ming-Hsiu Wu Ming-Hong Tai |
spellingShingle |
Chien-Hui Weng Chieh-Shan Wu Jian-Ching Wu Mei-Lang Kung Ming-Hsiu Wu Ming-Hong Tai Cisplatin-Induced Giant Cells Formation Is Involved in Chemoresistance of Melanoma Cells International Journal of Molecular Sciences melanoma chemoresistance cisplatin giant cell stemness |
author_facet |
Chien-Hui Weng Chieh-Shan Wu Jian-Ching Wu Mei-Lang Kung Ming-Hsiu Wu Ming-Hong Tai |
author_sort |
Chien-Hui Weng |
title |
Cisplatin-Induced Giant Cells Formation Is Involved in Chemoresistance of Melanoma Cells |
title_short |
Cisplatin-Induced Giant Cells Formation Is Involved in Chemoresistance of Melanoma Cells |
title_full |
Cisplatin-Induced Giant Cells Formation Is Involved in Chemoresistance of Melanoma Cells |
title_fullStr |
Cisplatin-Induced Giant Cells Formation Is Involved in Chemoresistance of Melanoma Cells |
title_full_unstemmed |
Cisplatin-Induced Giant Cells Formation Is Involved in Chemoresistance of Melanoma Cells |
title_sort |
cisplatin-induced giant cells formation is involved in chemoresistance of melanoma cells |
publisher |
MDPI AG |
series |
International Journal of Molecular Sciences |
issn |
1661-6596 1422-0067 |
publishDate |
2020-10-01 |
description |
Melanoma is notoriously resistant to current cancer therapy. However, the chemoresistance mechanism of melanoma remains unclear. The present study unveiled that chemotherapy drug cisplatin induced the formation of giant cells, which exhibited enlargement in cell diameter and nucleus in mice and human melanoma cells. Giant cells were positive with melanoma maker S100 and cancer stem cell markers including ABCB5 and CD133 in vitro and in vivo. Moreover, giant cells retained the mitotic ability with expression of proliferation marker Ki-67 and exhibited multiple drug resistance to doxorubicin and actinomycin D. The mitochondria genesis/activities and cellular ATP level were significantly elevated in giant cells, implicating the demand for energy supply. Application of metabolic blockers such as sodium azide or 2-deoxy glucose abolished the cisplatin-induced giant cells formation and expression of cancer stemness markers. The present study unveils a novel chemoresistance mechanism of melanoma cells via size alteration and the anti-neoplastic strategy by targeting giant cells. |
topic |
melanoma chemoresistance cisplatin giant cell stemness |
url |
https://www.mdpi.com/1422-0067/21/21/7892 |
work_keys_str_mv |
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