In vitro investigation of head and neck cancer stem cell proportions and their changes following X-ray irradiation as a function of HPV status

被引:18
作者
Reid, Paul [1 ,2 ]
Wilson, Puthenparampil [3 ,4 ]
Li, Yanrui [2 ]
Marcu, Loredana G. [1 ,5 ]
Staudacher, Alexander H. [6 ,7 ,8 ]
Brown, Michael P. [6 ,7 ,8 ,9 ]
Bezak, Eva [1 ,2 ,10 ]
机构
[1] Univ South Australia, Sch Hlth Sci, Adelaide, SA, Australia
[2] Univ South Australia, Sansom Inst Hlth Res, Adelaide, SA, Australia
[3] Univ South Australia, Sch Engn, Adelaide, SA, Australia
[4] Royal Adelaide Hosp, Dept Med Phys, Adelaide, SA, Australia
[5] Univ Oradea, Fac Sci, Oradea, Romania
[6] SA Pathol, Ctr Canc Biol, Translat Oncol Lab, Adelaide, SA, Australia
[7] Univ South Australia, Adelaide, SA, Australia
[8] Univ Adelaide, Sch Med, Adelaide, SA, Australia
[9] Royal Adelaide Hosp, Canc Clin Trials Unit, Adelaide, SA, Australia
[10] Univ Adelaide, Sch Phys Sci, Adelaide, SA, Australia
关键词
HUMAN-PAPILLOMAVIRUS; CD44; EXPRESSION; POSITIVE HEAD; RADIOTHERAPY; CARCINOMA; MARKER; IDENTIFICATION; ASSOCIATION; RECURRENCE; BIOLOGY;
D O I
10.1371/journal.pone.0186186
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Introduction Some head and neck squamous cell carcinomas (HNSCC) have a distinct aetiology, which depends on the presence of oncogenic human papilloma virus (HPV). Also, HNSCC contains cancer stem cells (CSCs) that have greater radioresistance and capacity to change replication dynamics in response to irradiation compared to non-clonogenic cells. Since there is limited data on CSCs in HNSCC as a function of HPV status, better understanding of their radiobiology may enable improved treatment outcome. Methods Baseline and post-irradiation changes in CSC proportions were investigated by flow cytometry in a HPV-negative (UM-SCC-1) and a HPV-positive (UM-SCC-47) HNSCC cell line, using fluorescent staining with CD44/ALDH markers. CSC proportions in both irradiated and unirradiated cultures were compared for the two cell lines at various times post-irradiation. To assess repopulation of CSCs, untreated cultures were depleted of CD44+/ALDH+ cells and re-cultured for 3 weeks before flow cytometry analysis. Results CSC proportions in untreated cell lines were 0.57% (UM-SCC-1) and 2.87% (UM-SCC-47). Untreated cell lines depleted of CD44+/ALDH+ repopulated this phenotype to a mean of 0.15% (UM-SCC-1) and 6.76% (UM-SCC-47). All UM-SCC-47 generations showed elevated CSC proportions after irradiation, with the most significant increase at 2 days post-irradiation. The highest elevation in UM-SCC-1 CSCs was observed at 1 day post-irradiation in the 2 nd generation and at 3 days after irradiation in the 3 rd generation. When measured after 10 days, only the 3 rd generation of UM-SCC-1 showed elevated CSCs. Conclusions CSC proportions in both cell lines were elevated after exposure and varied with time post irradiation. UM-SCC-47 displayed significant plasticity in repopulating the CSC phenotype in depleted cultures, which was not seen in UM-SCC-1.
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页数:16
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