Investigation of the Potential of Concomitant Radiation Therapy and Gold Nanoparticles for Pancreatic Cancer

1. Introduction

In 2020 the World Health Organization estimated that 495 773 new pancreatic cancer cases were diagnosed, and 466 003 patients died from this disease [1]. As a consequence of the frequent late diagnosis of this pathology and the low effectiveness of available treatments, especially in advanced stages, the prognosis is extremely poor, with five-year survival rates below 9% [2]. Thus, new treatment approaches that address the existing challenges are largely needed aiming to improve overall survival and patients’ quality of life. For patients with locally advanced pancreatic cancer, which represent about 30-40% of all pancreatic cancer cases, chemoradiotherapy or chemotherapy alone is recommended. However, none of the multiagent chemotherapy regimens are totally effective. Furthermore, pancreatic cancer is a deep-seated tumour surrounded by radiosensitive organs that limit the prescribed radiation dose. Despite the most recent advances in chemoradiotherapy, including cytotoxic agents and new RT techniques, pancreatic cancer is still one of the deadliest cancers [3].

Nanoparticles (NPs) with high atomic number (Z), such as gadolinium (Z=64), hafnium (Z=72), platinum (Z=78), and gold (Au) (Z=79) have been increasingly studied in the context of RT as radiation sensitizers due to their capacity to enhance radiation effects locally when introduced into tumour cells [4,5,6,7]. The basic principle is related to the high potential of these high-Z NPs to absorb low-energy X-rays, consequently leading to atomic excitation, and an increase of electrons released into the tumour tissue compared to soft tissue. Enhancement of electrons release translates into a local increase of energy deposition, which causes larger damage to tumour cells compared to RT alone.

Gold NPs (AuNPs) are the most studied NPs for RT due to their high-Z, good biocompatibility, and low production cost [4,5,6,7,8]. AuNPs are colloidal or clustered particles with diameters generally ranging from 1-200 nm that consist of a gold core with a surface coating. Owing to their synthetic versatility, it is possible to design AuNPs with different sizes, shapes, and surface coatings [9]. The manipulation of the size and shape allows the production of AuNPs with specific chemical, electrical, and optical properties. The coating offers the possibility to control particle solubility, stability, and interaction with the biological environment [5]. These are factors of great importance as they dictate the fate of the NPs and, consequently, their accumulation in the tumour.

Size and shape are decisive factors for AuNPs internalization into cells via receptor-mediated endocytosis (RME). Shape dependence is related to AuNPs surface area and local curvature, both interfering in the interaction of their ligands with the cell membrane receptors [7]. Spherical AuNPs are the most common gold-based nanotherapeutics as they are simple to produce, and alteration of size and surface chemistry is easily achieved [6].

Active targeting is the more efficient method to obtain an intratumoural accumulation of AuNPs. In this strategy, AuNPs’ surface is functionalized with peptides or antibodies that will later bind to cell surface proteins (receptors) preferentially overexpressed by cancer cells This translates into getting a higher concentration of AuNPs within tumour cells compared to healthy tissues, and a reduced amount of gold needed for radiosensitization [7].

Hyaluronic acid (HA) is a natural mucopolysaccharide, highly biocompatible, that specially binds CD44, a receptor overexpressed by a wide range of tumours [10,11], including pancreatic adenocarcinomas [12,13]. Thus, conjugating AuNPs with HA may lead to a preferred accumulation of NPs into pancreatic tumour cells via RME, which in turn would translate into further harm to these cells during RT. On the other hand, bombesin (BBN) derivatives have the ability to recognize the gastrin-releasing peptide receptor (GRPR) that is overexpressed in several human tumours, such as breast, prostate and pancreatic cancer [14]. For this reason, NPs decorated with BBN peptides might promote a receptor-mediated uptake by target tumour cells to enhance the radiosensitizing effects.

The possibility of combining AuNPs with RT for cancer treatment has been widely studied over the last years through simulation, in vitro and in vivo studies [4,5,6,7,15]. Monte Carlo simulations can be used to model the physical and physicochemical processes of radiation interactions with matter, including biological targets. This provides valuable insights into estimating AuNPs-induced dose enhancement and ionisations for a range of parameters, such as their size, shape, radiation source and energy, etc. Studies assessing dose enhancement by AuNPs using 80–120 kV beams obtained a dose enhancement factor near two [4]. Based solely on physical dose enhancement, radiosensitization with AuNPs is expected to be insignificant at megavoltage (MV) energies due to the minimal contribution of the photoelectric effect. However, experimental studies using MV beams with AuNPs showed an enhancement of RT effects that were significantly higher than those estimated by Monte Carlo simulations [5]. The discrepancies between theoretical predictions and experimental data opened the possibility of chemical and/or biological enhancement in addition to the physical mode of action. Thus, in vitro studies are strongly needed to characterize the effect of AuNPs including cell toxicity, uptake dynamics, radiation-induced cell survival, etc.

Promising results have been obtained with AuNPs plus RT using kV X-rays. However, low-energy photon beams are not suitable for external RT of deep-seated tumours. The greater penetration power of MV photon beams makes this energy range preferable for clinical RT of most pathologies. Given the treatment units available in RT departments nowadays, the in vitro radiosensitizer effect of AuNPs with MV beams has been investigated on various human tumour cell lines including breast, brain, colon, lung, and prostate [16]. Tudda et al. tested the irradiation of the MDA-MB-231 breast tumour cell line with 6 MV in the presence of 15 nm AuNPs. A Dose Enhancement Factor (DEF) of 1.14±0.06 and 1.33±0.06 was obtained for MV and kV X-rays, respectively [17]. For the same cell line, Jain et al. compared cell survival fractions after the irradiation with 160 kV, 6 MV and 15 MV X-ray beams using 1.9 nm AuNP. Sensitizer Enhancement Ratios (SER) of 1.41, 1.29 and 1.16 were obtained, respectively [18]. For the breast cancer cell line MCF-7 and using glucose-bound AuNPs of 16 nm, Soleymanifard et al. obtained smaller gains after the irradiation with 6 MV beams than with kV as quantified by the inhibition of cell proliferation (39% vs 64%, respectively) [19]. Using the HeLa cell line, Chithrani et al. tested the effect of AuNP of different sizes and different beam energies. Photon beams of 105 kV and 50 nm AuNP was the combination that showed the highest Radiosensitization Enhancement Factor (REF) of 1.66. This value was reduced to 1.17 when 6 MV photon beams was used [20]. These findings are consistent with those obtained for the MDA-MB-231 cell line incubated with 49 nm and 16 nm thioglucose-bound AuNP and irradiated with 6 MV beams. A significantly larger radiosensitization was obtained with 49 nm AuNPs than with 16 nm (1.86 vs 1.49, respectively, p<0.005) [21]. For other cell lines, the gain in irradiation in the presence of AuNPs, either expressed as DEF, SER or REF, up to 1.74 were obtained with different types of AuNPs combined with clinical beams [22,23,24,25,26,27].

For pancreatic cancer the in vitro and in vivo potential of AuNPs for RT using low energy photon beams has been assessed [28]. In this study, KPC and PANC-1 cells were incubated with poly(l-glutamic acid-co-l-lysine), or P(Glu-co-Lys)1:5, gold nanorods and irradiated with 250 kV X-rays under extracellular tumour acidosis and tumour microenvironment hypoxia. A DEF_10% of 1.24 and 1.1 was obtained for KPC and PANC-1 cells at a pH of 6.5, respectively. Interestingly, a similar radiosensitization was obtained for both cell lines under hypoxia conditions. The radiosensitization of pancreatic cancer in vivo was also evaluated in a subcutaneous tumour model performed in male mice using KPC cells. After establishment of tumour mass, animals were irradiated 24 h after intravenous administration of P(Glu-co-Lys)1:5 or PEGylated gold nanorods. The combination of RT plus P(Glu-co-Lys)1:5 gold nanorods showed the best treatment efficacy, compared to RT alone or RT plus PEGylated-gold nanorods, even in the presence of extensive hypoxic tumour regions.

Still for pancreatic cancer, Brero et al. tested 19.2 nm magnetic NPs (Fe₃O₄) in BxPC-3 cells that were irradiated with 6 MV photons, and concluded that these NPs at 50 μg/mL conferred a 50-60% additive effect on cell death compared to RT alone [29]. Detappe et al. evaluated 3.5 nm gadolinium-based NPs during irradiation with 220 kV of PANC-1 [30]. They concluded that 0.43 mg/mL of these NPs led to a SER of 1.37. Enhanced DNA damage and higher apoptosis were obtained in irradiated groups previously incubated with NPs compared to RT alone. Finally, Yoshida et al. assessed the radiosensitization effect of 190 nm AuNPs microgels in mice injected with MIAPaCa-2 human pancreatic cancer cells and concluded that tumour growth was effectively suppressed in mice injected with AuNPs microgels when 150 kV X-ray irradiation was performed [31].

Motivated by the challenges and difficulties found in pancreatic cancer therapy, this study reports an exploratory work involving the in vitro assessment of the radiation sensitizing potential of target-specific AuNPs during the RT treatment of human pancreatic adenocarcinoma cells, BxPC-3, with MV X-rays. For this purpose, AuNPs coated with hyaluronic acid and oleic acid (HAOA-AuNPs) or with a BBN coating (BBN-AuNPs) were used. The impact of these AuNPs formulations together with RT was assessed by viability assays.

2. Materials and Methods

2.1. Synthesis of HAOA-AuNPs and BBN-AuNPs

HAOA-AuNPs were prepared according to previous methods [10,32,33]. Gold (III) chloride trihydrate (HAuCl₄‧3H₂O), silver nitrate (A_gNO₃), L-ascorbic acid (L-AA), rosmarinic acid (RA), hyaluronic acid (HA) from Streptococcus Equi (MW ~1.5–1.8 x 10⁶ Da), and oleic acid (OA; MW = 282.46 g/mol) were supplied from Sigma-Aldrich (Steinheim, Germany). Briefly, fresh solutions of gold salt, silver nitrate, L-ascorbic acid, and rosmarinic acid were prepared [10,32,33]. The coating was previously prepared by mixing HA and OA, followed by stirring the suspension overnight at 400 rpm at 60 °C. The reaction of preparing uncoated AuNPs was carried out at 800 rpm for 15 min in a stirring plate (Fisherbrand ARE Hotplate Stirrer, Bradford, UK). On the next day, the coating suspension (HAOA) was added to the AuNPs core (proportion 1:1, v/v) and stirred for 30 min at 800 rpm at room temperature. Finally, HAOA-AuNPs were centrifuged (10,900× g for 10 min) stored at 4 °C and protected from the light [32].

BBN-AuNPs were prepared as described in Silva et al [34]. Firstly, AuNPs stabilized with 2-[4,7-bis(carboxymethyl)-10-[2-(3-sulfanylpropanoylamino) ethyl]- 1,4,7,10-tetrazacyclododec-1-yl] acetic acid (TDOTA) were synthesized. The final solution was centrifuged at 1000 rpm for 20 min and the pellet obtained was washed two times with methanol (MeOH) and two times with H₂O. NPs were then dried at reduced pressure. Thioctic acid terminated bombesin peptide (SS-BBN) was prepared in an automated peptide synthesizer. The final product was prepared by mixing AuNP-TDOTA with the thiolated peptide in a 1:2 ratio (w/w) at room temperature for 2 h. Briefly, 800 µL of MeOH was added to a 200 µL suspension of AuNP-TDOTA (5 mg/mL in deionized water) and then 1 mL of a solution of SS-BBN (2 mg, 1.77 µmol, in MeOH) was added. The mixtures were stirred at room temperature for 2 h. Then, centrifugation at 12000 rpm for 5 min was performed. The BBN-AuNPs were washed with MeOH and H₂O and lyophilised [34].

AuNPs were characterized in terms of morphology and mean particle size by AFM and Dynamic Light Scattering (DLS), respectively. For the mean size and polydispersity index (PdI), samples were diluted in water (1:10) and analysed through DLS (Zetasizer Nano S; Malvern Instruments, Malvern, UK), in three series of 11 measurements of each analyzed sample. For AFM, 40 μL of each sample was placed on a freshly cleaved mica surface and allowed to dry for one hour before analysis. Images were acquired by Multimode 8 HR coupled to Nanoscope V Controller (Bruker, Coventry, UK), using a peak force tapping and ScanAssist mode. The tip model used was scanasyst-air 0.4 N/m, Bruker.

2.2. Cell Culture

Human pancreatic adenocarcinoma BxPC-3 (ATCC© CRL-1687TM) cells were cultured in RPMI-1640, supplemented with 10% fetal bovine serum and 100 IU/mL of penicillin and 100 μg/mL streptomycin (Gibco, Thermo Fisher Scientific, Waltham, MA, USA), further designated as complete medium. Cells were kept at 37 °C, under a 5% CO₂ atmosphere. Maintenance of cultures was performed every two to three days until cells reached a confluence of about 80%.

Before irradiation, BxPC-3 cells were trypsinized and suspensions with 4×10⁴ cells/mL were prepared. Cells were seeded in 96-well plates (200 μL) and allowed to adhere overnight. Then, the medium was discarded, and cells were incubated with AuNPs for 4 h to allow internalization or with complete medium (control) [10,35,36]. After incubation period the supernatant was discarded and 100 μL of the complete medium was added to each well to proceed to irradiation.

2.3. Irradiation Setup

All irradiations were performed on a Varian Edge medical LINAC (Varian Medical Systems, Inc., Palo Alto, CA, USA) from the Champalimaud Foundation. For irradiation, BxPC-3 cell plates were placed inside the phantom at a depth of 10 cm. The phantom was composed of a stack of polystyrene plates of 30 x 30 cm²; holding a set of PMMA plates mounted around the 96-well plate, designed to avoid the presence of air around the plate (Error! Reference source not found.). Five cm of polystyrene plates were placed above the cell plates to allow backscatter. A CT of this phantom was acquired in a Philips Brilliance Big Bore 16 Slice CT Simulator (Koninklijke Philips N.V.). Treatment planning for dosimetry was made using the treatment planning system Eclipse (Eclipse Software, Varian Medical Systems, Inc.). Irradiation was performed with a 6 MV photon beam produced by a standard flattening filter, with a 20 × 20 cm² field size at a dose rate of 600 MU/min with cells placed at the isocentre of the linac. A posterior beam was used to avoid the beam from having to pass through air before reaching the cells. Cells, in the absence and presence of AuNPs, were irradiated with doses ranging from 2 to 10 Gy.

Figure 1. CT of the phantom and dose distribution used for irradiation of BxPC-3 cells using a posterior 6 MV beam from a Varian Edge linac. Each 96-well plate was placed at the isocenter at 10 cm depth.

Figure 1. CT of the phantom and dose distribution used for irradiation of BxPC-3 cells using a posterior 6 MV beam from a Varian Edge linac. Each 96-well plate was placed at the isocenter at 10 cm depth.

2.4. Viability Assays

The viability of BxPC-3 cells after incubation and irradiation at pre-selected times was evaluated by the MTT (3-[4,5-dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide) assay. To validate the best MTT assay conditions for the subsequent assays, the influence of post-irradiation time on cell viability was first assessed. Cells were thus irradiated with 2, 5, and 10 Gy and cell viability was evaluated by MTT assay 24, 48, and 72 h post-irradiation. No AuNPs were used during this assay.

After irradiation, 100 μL of complete medium was added to each well. Then, after 24, 48 or 72h, medium was discarded followed by twice washing with PBS, and 50 μL of MTT reagent at a concentration of 0.5 mg/mL in medium was added to each well. Following an incubation period of 2 - 4 h, 100 μL of dimethyl sulfoxide (DMSO) was added to each well to solubilize the formazan crystals. After solubilization, absorbance was measured at 570 nm in a microplate reader (BioTek ELx800; BioTek Instruments, Inc.,Winooski, VT, USA) [36]. Cell plates transported to Champalimaud Foundation, but not irradiated nor incubated with AuNPs, were defined as the control group, corresponding to 100% cell viability. Results of the test groups (RT alone, AuNPs alone, and RT + AuNPs) were normalized to the control group.

To investigate the impact that AuNPs induced during RT, BxPC-3 cells were incubated with HAOA-AuNPs at different gold concentrations (50, 200, and 400 μM) and with BBN-AuNPs at 50 and 200 μM. Cells were irradiated using the described setup with 2.0, 3.5, and 5.0 Gy. After irradiation, cells were incubated for 48 and 72 h and cell viability was evaluated by MTT assay.

2.5. Statistical Analysis

Cell viability measurements of BxPC-3 cells were presented as the mean ± standard deviation (SD). Data analysis was performed using GraphPad Prism version 9.4.0 (GraphPad Software, Inc., San Diego, CA, USA) and a p-value < 0.05 was considered statistically significant. Cell viabilities were compared by two-way ANOVA followed by Tukey’s multiple comparisons test.

The Coefficient of treatment Interaction (CI) was calculated using the expression,

$$CI=\frac{{VC}_{RT+AuNP}}{{VC}_{RT}{VC}_{AuNP}}$$

Where VC_RT+AuNP is the percentage of viable cells after the combined treatment, VC_RT is the percentage of viable cells after RT alone and VC_AuNP is the percentage of viable cells after the treatment with the AuNP alone. It was considered that for CI values below one there was synergy between the two treatments while for values equal to one or larger than one the effect was additive or antagonistic, respectively [37].

3. Results

3.1. Characterization of HAOA-AuNPs and BBN-AuNPs

AuNPs were evaluated in terms of their morphology by AFM and in terms of their mean particle size by AFM and DLS (Table 1). AFM technique demonstrated that both AuNPs presented a spherical morphology (Error! Reference source not found.) with a mean particle size of 83 ± 20 nm and 49 ± 12 nm for HAOA-AuNPs and BBN-AuNPs, respectively. By DLS, a mean particle size of 118 nm for HAOA-AuNPs (PdI < 0.3) was obtained while for BBN-AuNPs a mean particle size of 78.2 nm was reported by Silva et al [38].

Figure 2. 3D Atomic Force Microscopy images with corresponding cross-section profiles for the two AuNPs formulations: (a) HAOA-AuNPs and (b) BBN-AuNPs.

Figure 2. 3D Atomic Force Microscopy images with corresponding cross-section profiles for the two AuNPs formulations: (a) HAOA-AuNPs and (b) BBN-AuNPs.

3.2. Influence of Post-Irradiation Assessment Time

The influence of radiation dose on cell viability was assessed at 24, 48, and 72 h post-irradiation by MTT assay. Three different radiation doses were used: 2, 5, and 10 Gy. For the 24 h post-irradiation time, no significant differences were noted between the control (i.e., cells non-irradiated) and cells irradiated (Error! Reference source not found.). For the 48 h post-irradiation time, a statistically significant difference was obtained only for cells irradiated with 2 Gy with a reduction in cell viability of 13 ± 10% compared to the control group (p = 0.002). Neither 5 Gy nor 10 Gy led to the expected larger loss in cell viability (p > 0.09). For the 72 h post-irradiation time, statistically significant reductions in cell viability of about 20 ± 13%, 22 ± 11%, and 33 ± 12% were obtained after irradiation with 2, 5, and 10 Gy, respectively (p = 0.004; p = 0.001; p < 0.0001).

Figure 3. Cell viability of BxPC-3 cell line 24, 48, and 72 h after irradiation. **p < 0.01, ****p < 0.0001 compared to control at the same incubation time.

Figure 3. Cell viability of BxPC-3 cell line 24, 48, and 72 h after irradiation. **p < 0.01, ****p < 0.0001 compared to control at the same incubation time.

Figure 4. Cell viability of BxPC-3 cell line 48 and 72 h after treatment with HAOA-AuNPs and BBN-AuNPs and MV photon irradiation. *p < 0.05, **p < 0.01, ***p < 0.001 and **** p < 0.0001 compared to control, i.e., non-treated cells. ## p < 0.01, ### p < 0.001 and #### p < 0.0001 compared to RT alone at the same radiation dose. $ p < 0.05, $$ p < 0.01, $$$ p < 0.001 and $$$$ p < 0.0001 compared to AuNPs alone at the same concentration.

Figure 4. Cell viability of BxPC-3 cell line 48 and 72 h after treatment with HAOA-AuNPs and BBN-AuNPs and MV photon irradiation. *p < 0.05, **p < 0.01, ***p < 0.001 and **** p < 0.0001 compared to control, i.e., non-treated cells. ## p < 0.01, ### p < 0.001 and #### p < 0.0001 compared to RT alone at the same radiation dose. $ p < 0.05, $$ p < 0.01, $$$ p < 0.001 and $$$$ p < 0.0001 compared to AuNPs alone at the same concentration.

3.3. Impact of AuNPs during RT

The potential effect of AuNPs during RT of BxPC-3 cancer cells was evaluated by MTT assay 48 and 72 h post-irradiation. Cell viability was assessed for HAOA-AuNPs at 50, 200, and 400 µM and BBN-AuNPs at 50 and 200 µM using radiation doses ranging from 2 to 5 Gy. For the 48 h post-irradiation time, a statistically significant reduction in cell viability was obtained with 400 μM of HAOA-AuNPs alone and 50 μM or 200 μM of BBN-AuNPs alone, compared to control cells (p < 0.0001, indicated by the stars in the left panels of Error! Reference source not found.). Neither 50 μM, or 200 μM, of HAOA-AuNPs alone induced a significant difference in cell viability compared to the control (p = 0.055; p = 0.165, respectively). For RT alone, 5 Gy was required to significanty reduce cell viability compared to the control group (p = 0.001).

For the 48 h post-irradiation time, the combined treatment of 2 Gy+50 μM of HAOA-AuNPs induced a reduction in cell viability of 22 ± 3% and 2 Gy+200 μM a loss in cell viability of approximately 30 ± 5% compared to control (p < 0.0001). However, the cytotoxic effect of the combined treatment with radiation doses of 3.5 and 5.0 Gy was not enhanced compared to that obtained at 2 Gy. Overall, an higher cell viability for higher radiation doses was obtained. This validates above findings and therefore the need for longer post-irradiation times to evaluate the biological effects of RT.

The results of MTT assays performed 72 h post-irradiation are shown on Error! Reference source not found. (right panels). Within the range of radiation doses tested, RT alone reduced cell viability from 21 to 31 ± 5% (p < 0.0001). No significant difference in cell viability was obtained between 50 µM HAOA-AuNPs alone and the control (p = 0.26). On the other hand, a statistically significant reduction in cell viability of approximately 20 ± 4% and 35 ± 4% for HAOA-AuNPs alone at 200 and 400 µM, respectively, was obtained compared to control cells (p < 0.0001). Similarly, for cells incubated with BBN-AuNPs alone, a statistically significant loss in cell viability of 25 ± 3% and 37 ± 3% was obtained for 50 and 200 µM AuNPs, respectively, when compared with control cells (p < 0.0001).

The combined treatment of RT with HAOA-AuNPs at 50, 200 and 400 µM induced a loss in cell viability of 28-35%, 37-43% and 45%-51%, respectively, compared to the control (p < 0.0001). For RT+HAOA-AuNPs, an almost linear relation was obtained between cell viability and concentration of HAOA-AuNPs for the combined treatment (Error! Reference source not found. – Supplementary Material). Furthermore, statistically significant reductions in cell viability were obtained between RT with HAOA-AuNPs (200 µM and 400 µM) and RT alone for the same radiation dose (comparison represented by the cardinal symbols in Error! Reference source not found.), but not for 50 µM of AuNPs (p > 0.6). Also, a statistically significant reduction in cell viability was obtained between RT + HAOA-AuNPs at 50 and 200 μM and AuNPs alone at the same concentration (indicated by the dollar signs in Error! Reference source not found.). Finally, a statistically significant loss in cell viability was obtained when combining a radiation dose of 5 Gy with HAOA-AuNPs at 400 μM compared to the same nanoparticle concentration. For the tested AuNPs concentrations, and within the range of estimated uncertainties, the effects caused by the combined treatment were mainly caused by an additive effect between RT and AuNPs, as demonstrated by the calculated CI value (Error! Reference source not found.).

Figure 5. Results of the coefficient of treatment interaction (CI) for the NPs tested 72 h post-irradiation.

Figure 5. Results of the coefficient of treatment interaction (CI) for the NPs tested 72 h post-irradiation.

For the 72 h post-irradiation time, the combined treatment of RT with 50 µM of BBN-AuNP induced a maximum loss in cell viability of 47±1% when compared to control (p < 0.0001) and 22% compared to BBN-AuNP alone for the same concentration (p < 0.0001). A similar loss in cell viability was obtained with RT plus BBN-AuNPs at 200 μM, but this difference was not significantly different from the group of cells incubated with these AuNPs alone for the same concentration (p > 0.3). For the lowest concentration of BBN-AuNP tested, the combined effects with irradiation presented an additive effect (Error! Reference source not found.).

4. Discussion

In the last two decades, important advances in cytotoxic agents and RT techniques have occurred without a clinical translation into significant overall survival benefits for pancreatic cancer patients [3]. These difficulties are partly due to the generally late detection of this pathology, reflecting also the inability to deliver higher doses of RT locally without causing severe toxicity to nearby healthy tissues [39,40]. The ability to successfully improve local tumour response may lead to an extension of overall survival. As pancreatic tumour response is radiation dose-dependent [40], improving RT by allowing a local dose escalation while maintaining or reducing the dose in nearby organs at risk, could potentially result in a better treatment outcome.

In this study, the potential of RT in combination with AuNPs for the treatment of locally advanced pancreatic cancer was investigated in vitro by evaluation of the effects on cell viability via the MTT assay. This assay was used due to its multiple advantages: high reproducibility, rapid semi-automated reading, and comparatively low cost [41]. For MTT assays, preliminary studies were performed aiming to determine optimal irradiation conditions. It was found that for treatments with RT alone a 72 h post-irradiation time was the time point when significant changes in cell viability were measured. Masoudi-Khoram et al. obtained similar results after the irradiation of the human breast tumour cell line MDA-MB-231 where reductions in cell viability were only observed 72 h following irradiation with 6 and 10 Gy when compared to control [42]. For shorter periods, in general cell viability increased with radiation dose contradicting the expected biological effects of RT (Error! Reference source not found.). These results are consistent with the findings from others. Kong et al. did not obtain the expected reduction in cell viability of the human breast cancer cell line (MCF-7) 48 h following irradiation with 10 Gy. Indeed, the authors reported an 11.5% increase in cell viability when compared to the control [43].

This increase in cell viability obtained for short post-irradiation periods with increasing radiation dose (Error! Reference source not found.), might be related to the lag period of cells after irradiation. This delay is probably due to the time frame of cell death following irradiation, reflecting a damage repair that is cell-line dependent [41]. If cell viability is measured during the lag phase (i.e., too early), results are overestimated. For BxPC-3 cells, used in the present work, cell doubling time is 48 h to 60 h [44]. Thus, for incubation times lower than this period, cell viability may be overestimated. Additionally, the lag period is also influenced by the dose of radiation. Increasing the dose leads to an increased lag period and, consequently, it is necesssary to consider longest post-irradiation time points to accurately observe the losses in cell viability [41]. However, the feasibility of increasing post-irradiation time is limited by the possible overgrowth of the cells in the microplate, that is quite likely to occur for long incubation times. Thus, in this study, as the highest difference in cell viability between irradiated and control groups was observed for the 72 h post-irradiation time, this experimental condition was selected as the most appropriate for further assays.

Within the range of tested conditions, single treatment, either by RT or AuNPs, led to a maximum loss in cell viability of 31 ± 5% and 37 ± 4%, respectively, compared to the control. Aiming to assess the advantages of concomitant RT with AuNPs, pancreatic cancer cells were irradiated after 4 h of incubation with NPs. RT plus AuNPs induced a maximum loss in cell viability of 47 ± 1% with BBN-AuNP at 50 μM and of 51 ± 3% for RT plus HAOA-AuNP at 400 μM. For HAOA-AuNPs a linear relationship between concentration and cell viability was obtained (Error! Reference source not found.-Supplementary Material). Higher concentrations of HAOA-AuNPs concomitantly delivered with RT could potentially result in even better outcomes provided these concentrations could be safely delivered to patients.

For BxPC-3 cells irradiated with MV beams, without AuNPs, cell survival fraction at 2 Gy, SF2, takes values of about 60%, and SF5 is around 20% [45]. In this study, for a radiation dose of 2 and 5 Gy cell viability, normalized to control, was 79 ± 5% and 69 ± 5%, respectively, while RT plus AuNPs reduced cell viability by an additional 15-26%. Discrepancies between the results obtained with MTT and clonogenic assays have been previously reported [46], [47] and for RT in the presence of AuNPs these discrepancies could be even more accentuated as there could be more DNA damage to be repaired. The CI indicates additive effects for most tested cases (Error! Reference source not found.), but the results obtained in this study may underestimate the true outcome of the combined treatment. The interaction between RT and the tested AuNPs on cell survival still needs to be thoroughly investigated.

The morphology of the NPs has a strong influence on their radiosensitizing capabilities. AFM has shown that both AuNP used in this study are spherical in shape, facilitating internalization into tumour cells [15],[20]. Ma et al. evaluated the radiosensitization effect in RT of three types of gold nanostructures: AuNPs with a spherical shape, gold nanorods and gold nanospikes. Radiosensitization was related to the ability of cellular internalization that was more efficient for spherical AuNPS followed by gold nanospikes and then gold nanorods (SER of 1.62, 1.37 and 1.21, respectively) [47].

Outcome for RT plus BBN-AuNPs at a low concentration and the combined treatment using HAOA-AuNPs at a high concentration was similar, indicating the influence of the size and/or coating of the NPs on the RT effect and, ultimately, in the potential of the combined treatment of RT with AuNPs. Successful nanoparticle internalization into target cells, and proximity to the cell nucleus, is paramount to achieve the desired tumour cell kill effect for which nanoparticle size is one of the key factors [15]. The presence of high atomic number NPs in tumour cells during RT mostly promotes the photoelectric effect, enhancing the number of Auger electrons released in the vicinity of AuNPs. While secondary electrons in the form of photoelectrons can travel up to a distance of several cells, low-energy Auger electrons have ranges of less than 10 nm in tissues. Consequently, these electrons offer a very precise and local dose deposition inside cells contributing to cell death while avoiding radiosensitization in nearby tissues [48]. For therapy, nanoparticles should primarily accumulate in the tumour and the distribution to non-target tissues should be minimized. However, some degree of diffusion or systemic distribution may occur depending on the specific characteristics of the nanoparticles and the tumour environment. Small nanoparticles (<20 nm) show better tumour penetration capabilities and diffuse more uniformly within tumour tissues. However, they can be easily pumped back into the bloodstream and rapidly expelled from the body, resulting in insufficient tumour accumulation [49,50]. But particle size also influences the NPs biodistribution. De Jong et al assessed AuNPs concentration in different organs after intravenous injection of male rats with spherical AuNPs ranging from 10-250 nm [51]. For 10 nm AuNPs, the percentage of gold in the kidneys, brain, reproductive organs, thymus and heart was much higher than for 50 to 250 nm AuNPs while no 100 and 250 nm particles were detected in the lung [51]. Larger AuNPs are advantageous due to their low toxicity, higher tumour retention and stability, which facilitate functionalization [9]. But AuNPs size and coating strongly impact on how many of Auger electrons can effectively escape from the nanoparticle as many can be stopped inside the nanoparticle itself [7,52]. Efforts are continually made to optimise nanoparticle design and delivery strategies to enhance their tumour-targeting capabilities while minimizing off-target effects.

5. Conclusion

The present study consisted of an exploratory analysis of the effect of AuNPs of different sizes and coatings, HAOA-AuNPs and BBN-AuNPs, on human pancreatic adenocarcinoma BxPC-3 cells irradiated with a clinical 6 MV photon beam. Cell viability assays showed that the effect of RT alone on BxPC-3 cells seems to be negligible for short post-irradiation times. The 72 h post-irradiation time proved to be more adequate to evaluate the effects of the combined treatment because it implied more significant differences on the cell viability values after treatment with low doses of RT and AuNP.

For the 72 h post-irradiation time, the combined treatment of RT either with HAOA-AuNPs at 200 μM or with BBN-AuNPs at 50 μM led to a mean cell viability reduction of around 45% compared to no treatment. In addition, the effect of the combined treatment seems to have originated from an additive effect caused by RT and AuNPs. Thus, there appears to be a potential benefit from the combined treatment for both formulations of AuNPs.