CD200: association with cancer stem cell features and response to chemoradiation in head and neck squamous cell carcinoma.

Yuh-Seog Jung, Paola D Vermeer, Daniel W Vermeer, Sang-Jin Lee, Ah Ra Goh, Hyun-Joo Ahn, John H Lee
Author Information
  1. Yuh-Seog Jung: Head and Neck Oncology Clinic, Center for Thyroid Cancer, Department of Otolaryngology, Research Institute and Hospital, National Cancer Center, Goyang, Korea.

Abstract

BACKGROUND: The purpose of this study was to characterize the expression of CD200, a membrane protein that functions in immune evasion, to examine its correlations with cancer stem cell (CSC)-like features and analyze its response to chemotherapy and radiation in human papillomavirus (HPV)-positive (+) and negative (-) head and neck squamous cell carcinomas (HNSCCs).
METHODS: CD200 expression was analyzed in several HNSCC cell lines. CD200 was overexpressed in HPV(+) murine tonsil epithelial cells, its effects on Shh and Bmi-1 were examined in vitro, and tumor growth and response to chemoradiation were analyzed in vitro and in vivo.
RESULTS: CD200 was diversely expressed and consistently associated with expression of Bmi-1 and Shh. Overexpression of CD200 induced Bmi-1 and Shh. Tumors grew similarly between C57BL/6 and Rag1(-/-) C57BL/6 mice. CD200 expression enhanced the resistance to chemoradiation only in vivo.
CONCLUSION: CD200 was related to CSC features and modulates response to chemoradiation in vivo. Attenuating this might be a potential therapeutic strategy.

Keywords

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Grants

  1. R01 DE018386/NIDCR NIH HHS
  2. 7R01DEO18386-03/PHS HHS

MeSH Term

Animals
Antigens, CD
Carcinoma, Squamous Cell
Cell Line, Tumor
Cell Proliferation
Chemoradiotherapy
Flow Cytometry
Gene Expression Regulation, Neoplastic
Head and Neck Neoplasms
Humans
Immunoblotting
Mice
Mice, Inbred C57BL
Neoplasms, Experimental
Neoplastic Stem Cells
Squamous Cell Carcinoma of Head and Neck
Transfection
Treatment Outcome

Chemicals

Antigens, CD
antigens, CD200

Word Cloud

Created with Highcharts 10.0.0CD200cellexpressionresponsechemoradiationcancerstemfeaturesShhBmi-1vivoimmuneCSChumanpapillomavirusHPV+headnecksquamousanalyzedcellsvitroC57BL/6BACKGROUND:purposestudycharacterizemembraneproteinfunctionsevasionexaminecorrelations-likeanalyzechemotherapyradiation-positivenegative-carcinomasHNSCCsMETHODS:severalHNSCClinesoverexpressedmurinetonsilepithelialeffectsexaminedtumorgrowthRESULTS:diverselyexpressedconsistentlyassociatedOverexpressioninducedTumorsgrewsimilarlyRag1-/-miceenhancedresistanceCONCLUSION:relatedmodulatesAttenuatingmightpotentialtherapeuticstrategyCD200:associationcarcinomatoleranceneoplasticoropharyngeal

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