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首页> 外文期刊>Translational Oncology >5-Aminolevulinic acid for fluorescence-guided surgery in pancreatic cancer: Cellular transport and fluorescence quantification studies
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5-Aminolevulinic acid for fluorescence-guided surgery in pancreatic cancer: Cellular transport and fluorescence quantification studies

机译:胰腺癌中的荧光导向手术的5-氨基乙酰丙酸:细胞运输和荧光量化研究

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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 CFPAC-1 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 PANC-1 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.
机译:5-氨基乙酰丙酸(ALA)是胰腺导管腺癌(PDAC)中荧光导向手术的潜在造影剂。然而,影响PDAC中ALA摄取的因素尚未得到充分评估。在孵育0.25-1.0μmAla后,我们研究了在PDAC细胞系CFPAC-1和PANC-1和PANCERIC-1和PANCREATIC DV-1和PANCREATIC DV-1和胰腺导管细胞系H6C7中诱导的卟啉荧光。通过显微镜经典地评估荧光,并通过板读取器定量评估和流式细胞术。通过定量聚合酶链反应(QPCR)测量血清生物合成酶和转运蛋白。 CFPAC-1细胞在低浓度下在显微镜下表现出强烈的荧光,而Panc-1细胞和胰管线H6C7显示出大得多的荧光。定量荧光研究在0.5μAAla的两个PDAC细胞系中表现出荧光饱和度,而H6C7细胞随着ALA的增加显示荧光增加。基于PDAC:H6C7荧光比研究,下ALA浓度在PDAC和良性胰腺细胞之间提供更好的对比。 QPCR的研究表明,CFPAC-1中ALA流入转运蛋白PEPT1的上调,而PANC-1上调了流出转运蛋白ABCG2。我们得出结论,PEPT1和ABCG2表达可能是ALA诱导荧光在PDAC中的变异性的关键贡献因素。

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