|Table of Contents|

Gold nanoclusters assisted delivery of PD-L1 siRNA for anti-tumor activity in oral squamous cell carcinoma

Journal Of Modern Oncology[ISSN:1672-4992/CN:61-1415/R]

Issue:
2021 02
Page:
206-210
Research Field:
Publishing date:

Info

Title:
Gold nanoclusters assisted delivery of PD-L1 siRNA for anti-tumor activity in oral squamous cell carcinoma
Author(s):
CHEN ChuangmaoSONG JingqinCHEN ZhijunCHEN Wen
Maxillofacial Surgery,the Second Affiliated Hospital of Hainan Medical College,Hainan Haikou 570311,China.
Keywords:
oral squamous cell carcinomagold nanoclusterssiRNAPD-L1
PACS:
R739.8
DOI:
10.3969/j.issn.1672-4992.2021.02.006
Abstract:
Objective:To investigate whether PD-L1 siRNA delivered by gold nanoclusters can enhance the anti-tumor effect of lymphocytes on oral squamous cell carcinoma HSC-4 cells.Methods:The gold nanoclusters were reacted in one step,and the gold nanoclusters-siRNA complex was formed with PD-L1 siRNA.The free siRNA and gold nanoclusters siRNA complex were incubated with HSC-4 cells respectively.The knockdown of PD-L1 was detected by qPCR and Western blot.The secretion of cytokine IL-2 of T cells was detected by ELISA,and the anti-tumor activity was detected by establishing mouse tumor model.Results:Gold nanoclusters-siRNA complex was successfully produced and could effectively knock down the expression of PD-L1 in HSC-4 cells.After T cells were co-incubated with tumor cells,gold nanoclusters-siRNA could significantly increase the secretion of cytokine IL-2 compared with free siRNA.In vivo experiments showed that,compared with free siRNA,gold nanoclusters-siRNA can better target tumor tissue and enhance anti-tumor ability of T cells in HSC-4 tumors.Conclusion:The PD-L1 siRNA system delivered by gold nanoclusters can enhance the anti-tumor effect of PD-L1 siRNA in tumors and reduce the expression of PD-L1 in oral squamous cell carcinoma,thus enhancing the anti-tumor activity of T cells against oral squamous cell carcinoma.This suggests that this gold nanoclusters-PD-L1-siRNA complex may be a promising strategy for the treatment of oral squamous cell carcinoma.

References:

[1]SHIA BC,QIN L,LIN KC,et al.Outcomes for elderly patients aged 70 to 80 years or older with locally advanced oral cavity squamous cell carcinoma:A propensity score-matched,nationwide,oldest old patient-based cohort study[J].Cancers (Basel),2020,12(2):E258.
[2]DASKALOPOULOS AG,AVGOUSTIDIS D,CHAISUPARAT R,et al.Assessment of TLR4 and TLR9 signaling and correlation with human papillomavirus status and histopathologic parameters in oral tongue squamous cell carcinoma[J].Oral Surg Oral Med Oral Pathol Oral Radiol,2020,129(5):493-513.
[3]ACHARYA S,PRABHU P,PATIL V,et al.Tumor necrosis factor-like weak inducer of apoptosis expression in healthy oral mucosa,oral dysplasia and oral squamous cell carcinoma[J].J Oral Maxillofac Pathol,2019,23:369-377.
[4]LEE YS,JOHNSON DE,GRANDIS JR.An update:Emerging drugs to treat squamous cell carcinomas of the head and neck[J].Expert Opin Emerg Drugs,2018,23(4):283-299.
[5]HAZEKAWA M,NISHINAKAGAWA T,KAWAKUBO-YASUKOCHI T,et al.Glypican-3 gene silencing for ovarian cancer using siRNA-PLGA hybrid micelles in a murine peritoneal dissemination model[J].J Pharmacol Sci,2019,139:231-239.
[6]PENG S,LU Y,LI P,et al.The short interference RNA (siRNA) targeting NMUR2 relieves nociception in a bone cancer pain model of rat through PKC-ERK and PI3K-AKT pathways[J].Biochem Biophys Res Commun,2019,512:616-622.
[7]SHABANI S,MAHJOUBI F,MOOSAVI MA.A siRNA-based method for efficient silencing of PYROXD1 gene expression in the colon cancer cell line HCT116[J].J Cell Biochem,2019,120:19310-19317.
[8]GUAN ZJ,HU F,LI JJ,et al.Isomerization in alkynyl-protected gold nanoclusters[J].J Am Chem Soc,2020,142:2995-3001.
[9]HOBO W,MAAS F,ADISTY N,et al.siRNA silencing of PD-L1 and PD-L2 on dendritic cells augments expansion and function of minor histocompatibility antigen-specific CD8+ T cells[J].Blood,2010,116:4501-4511.
[10]HAYES RB,AHN J,FAN X,et al.Association of oral microbiome with risk for incident head and neck squamous cell cancer[J].JAMA Oncol,2018,4(3):358-365.
[11]MALASPINA TS,GASPAROTO TH,COSTA MR,et al.Enhanced programmed death 1 (PD-1) and PD-1 ligand (PD-L1) expression in patients with actinic cheilitis and oral squamous cell carcinoma[J].Cancer Immunol Immunother,2011,60:965-974.
[12]TROEITZSCH M,WOODLCK T,PIANKA A,et al.Is there evidence for the presence and relevance of the PD-1/PD-L1 pathway in oral squamous cell carcinoma?Hints from an immunohistochemical study[J].J Oral Maxillofac Surg,2017,75:969-977.
[13]SHARMA A,KUMAR P,AMBASTA RK.Cancer fighting SiRNA-RRM2 loaded nanorobots[J].Pharm Nanotechnol,2020,8(2):79-90.
[14]MAYSINGER D,GRAN ER,BERTORELLE F,et al.Gold nanoclusters elicit homeostatic perturbations in glioblastoma cells and adaptive changes of lysosomes[J].Theranostics,2020,10:1633-1648.
[15]PORRET E,LE GUEVEL X,COLL JL.Gold nanoclusters for biomedical applications:Toward in vivo studies[J].J Mater Chem B,2020,8(11):2216-2232.
[16]LIU Y,WU L,TONG R,et al.PD-1/PD-L1 inhibitors in cervical cancer[J].Front Pharmacol,2019,10:65.
[17]SHEN K,CUI J,WEI Y,et al.Effectiveness and safety of PD-1/PD-L1 or CTLA4 inhibitors combined with chemotherapy as a first-line treatment for lung cancer:A meta-analysis[J].J Thorac Dis,2018,10:6636-6652.

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海南省卫生健康行业科研项目(编号:19A200007)
Last Update: 1900-01-01