Labib P L, Yaghini E, Davidson B R, MacRobert A J, Pereira S P
UCL Institute for Liver & Digestive Health, University College London, Royal Free Campus, Rowland Hill Street, London NW3 2PF, United Kingdom of Great Britain and Northern Ireland.
UCL Division of Surgery & Interventional Science, University College London, Royal Free Campus, Rowland Hill Street, London NW3 2PF, United Kingdom of Great Britain and Northern Ireland.
Transl Oncol. 2021 Jan;14(1):100886. doi: 10.1016/j.tranon.2020.100886. Epub 2020 Oct 12.
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.
5-氨基酮戊酸(ALA)是一种用于胰腺导管腺癌(PDAC)荧光引导手术的潜在造影剂。然而,影响PDAC中ALA摄取的因素尚未得到充分评估。我们在将0.25-1.0 mM ALA与CFPAC-1和PANC-1这两种PDAC细胞系以及胰腺导管细胞系H6c7孵育4-48小时后,研究了ALA诱导的卟啉荧光。通过显微镜进行定性荧光评估,并通过酶标仪和流式细胞术进行定量评估。通过定量聚合酶链反应(qPCR)测量血红素生物合成酶和转运蛋白。在显微镜下,CFPAC-1细胞在低浓度下显示出强烈荧光,而PANC-1细胞和胰腺导管细胞系H6c7的荧光则低得多。定量荧光研究表明,在0.5 mM ALA时,两种PDAC细胞系中的荧光达到饱和,而H6c7细胞的荧光随着ALA浓度的增加而增加。基于PDAC:H6c7荧光比率研究,较低的ALA浓度能在PDAC和良性胰腺细胞之间提供更好的对比度。qPCR研究表明,CFPAC-1中ALA流入转运蛋白PEPT1上调,而PANC-1中流出转运蛋白ABCG2上调。我们得出结论,PEPT1和ABCG2的表达可能是PDAC中ALA诱导荧光变异性的关键因素。