5-Aminolevulinic acid for fluorescence-guided surgery in pancreatic cancer: Cellular transport and fluorescence quantification studies

被引:9
|
作者
Labib, P. L. [1 ]
Yaghini, E. [2 ]
Davidson, B. R. [2 ]
MacRobert, A. J. [2 ]
Pereira, S. P. [1 ]
机构
[1] UCL, UCL Inst Liver & Digest Hlth, Royal Free Campus,Rowland Hill St, London NW3 2PF, England
[2] UCL, UCL Div Surg & Intervent Sci, Royal Free Campus,Rowland Hill St, London NW3 2PF, England
来源
TRANSLATIONAL ONCOLOGY | 2021年 / 14卷 / 01期
关键词
OLIGOPEPTIDE TRANSPORTER; PEPTIDE TRANSPORTERS; PHOTODYNAMIC THERAPY; CELLS; EXPRESSION; GENOTYPE; MODEL; LINES;
D O I
10.1016/j.tranon.2020.100886
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
5-Aminolevulinic acid (ALA) is a potential contrast agent for fluorescence-guided surgery in pancreatic ductal adenocarcinoma (PDAC). However, factors influencing ALA uptake in PDAC have not been adequately assessed. We investigated ALA-induced porphyrin fluorescence in PDAC cell lines CFPAG1 and PANC-1 and pancreatic ductal cell line H6c7 following incubation with 0.25-1.0 mM ALA for 4-48 h. Fluorescence was assessed qualitatively by microscopy and quantitatively by plate reader and flow cytometry. Haem biosynthesis enzymes and transporters were measured by quantitative polymerase chain reaction (qPCR). CFPAC-1 cells exhibited intense fluorescence under microscopy at low concentrations whereas PANC-1 cells and pancreatic ductal cell line H6c7 showed much lower fluorescence. Quantitative fluorescence studies demonstrated fluorescence saturation in the two PDAC cell lines at 0.5 mM ALA, whereas H6c7 cells showed increasing fluorescence with increasing ALA. Based on the PDAC:H6c7 fluorescence ratio studies, lower ALA concentrations provide better contrast between PDAC and benign pancreatic cells. Studies with qPCR showed upregulation of ALA influx transporter PEPT1 in CFPAC-1, whereas PANG1 upregulated the efflux transporter ABCG2. We conclude that PEPT1 and ABCG2 expression may be key contributory factors for variability in ALA-induced fluorescence in PDAC.
引用
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页数:8
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