targeting cancer cells in head and neck squamous cell carcinoma hnscc by curcumin as potential nanomedicine an in vitro study
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Abstract
According to GLOBOCAN 2018 report, the incidence, mortality, and prevalence (5-
newlineyear) of head and neck squamous cell carcinoma (HNSCC) in India is 1/5th 1/3rd, and 1/2th of
newlinetotal HNSCC of world data respectively. The incidence, mortality, and prevalence are
newlinedecreasing globally over the past 4 years whereas, in India, HNSCC remains challenging
newlinebecause of failure in current therapies like surgery, radiation therapy, and chemotherapies.
newlineThe discovery of cancer stem cells (CSC) and certain chemotherapeutic drugs with their side
newlineeffects might lead to poor prognosis and ultimately failure of therapy. In recent years many
newlineinvestigators have shown the therapeutic potential of curcumin to target CSCs from several
newlineother cancers including breast cancer, colon cancer as a regulator of multiple pathways
newlineincluding self-renewal and differentiation pathways. However, due to its low aqueous
newlinesolubility, pervasive first-pass metabolism, and stability issues, the oral bioavailability of
newlinecurcumin is low.
newlineObjectives
newlineThe main objective of the current research study is to develop and evaluate the curcumin
newlinenanomicelles on cancer stem cells (CSCs) isolated from primary head and cancer tumors and
newlinealso on cisplatin drug-resistant cell lines.
newlineMethodology
newlineThe identification and cell sorting were done by Fluorescence-activated cell sorting
newline(FACS) using CD44, CD24 cell surface markers. We evaluated the self-renewal capacity and
newlineclonogenicity of CSCs using a Tumorsphere formation assay. We also analyzed the chemoresistance
newlineof CSC using cisplatin. Further, we were carried out RT-PCR to examine the
newlineexpression of stem cell markers. Immunofluorescence assay was done to analyze the surface
newlinemarker expression. Simultaneously we developed the cisplatin drug-resistant oral cancer cell
newlinelines with repeated exposure of parental cell (KB) with a stepwise dose incremental strategy.
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