Karen Chiam, George C Mayne, Tingting Wang, David I Watson, Tanya S Irvine, Tim Bright, Lorelle T Smith,Imogen A Ball, Joanne M Bowen, Dorothy M Keefe, Sarah K Thompson, Damian J Hussey

Abstract

Key words: Biomarkers; Exosomes; Extracellular vesicles; Circulating microRNA;MicroRNAs; Plasma; Serum; Blood cells; Real-time polymerase chain reaction;Adenocarcinoma of esophagus

INTRODUCTION

MicroRNAs (miRNAs) are small non-coding RNA molecules (21-23 nucleotides) that can regulate gene expressionviavarious mechanisms including repression of messenger RNA translation. miRNAs are important regulators because a single miRNA can target multiple genes. Furthermore, specific miRNA expression signatures have been shown to be tissue-specific[1], and disease-specific[2-4]. miRNAs are found in a range of body fluids such as serum, plasma, whole blood, urine and saliva. These circulating miRNAs are highly stable in different conditions (e.g.,temperature, pH and storage period) and can be easily measured. For these reasons,circulating miRNAs have garnered significant research interest as potential biomarkers for diagnostic, prognostic and treatment prediction purposes.

However, there are many challenges in the process of biomarker discovery to clinical practice for circulating miRNAs. Various factors can influence the quality and outcome of biomarker studies, which include the choice of sample, processing conditions, biomarker detection and analysis methods[5,6]. There is also increasing awareness about the multiple origins of specific circulating miRNAs and the implications this has on how we should evaluate and interpret miRNAs biomarkers studies[7-10]. A study by Pritchardet al[8]highlighted that a large proportion of circulating miRNA cancer biomarkers identified in the literature overlapped with those that have been reported to be highly expressed in blood cells. This has raised concerns on factors such as hemolysis and whether different types of blood samples used in miRNA studies may vary in their content of miRNAs originating from bloodcells.

Small extracellular microvesicles (sEVs), are considered to be a more stable and disease-specific source of circulating miRNAs for biomarker development[11]. In cancers, circulating miRNAs encapsulated in sEVs have been shown to have critical functional roles such as regulating disease progression, metastasis and sensitivity to specific drugs[12]. Circulating miRNAs can also be found complexed with the Argonaute2 (Ago2) protein, which functions to protect the miRNAs against RNases and enhance their stability in the circulation[13,14]. Although these protein-associated circulating miRNAs have been found to be present in larger quantities than sEV miRNAs, their functional roles in disease pathogenesis and potential utility as biomarkers have not been investigated. Thus far, the focus remains on circulating sEV miRNAs as preferred candidates for biomarkers development and protocol-related studies[11,15-17].

A crucial step in the development of robust circulating miRNAs biomarkers is to determine which blood sample is optimum for the study. This is a challenging question to address due to the multiple origins of circulating miRNAs and experimental factors that can influence miRNA levels. Previous studies have endeavoured to address this question by comparing circulating miRNA profiles,mostly of cell-free miRNAs across different blood samples, and have reported inconsistent results[10,11,16,18,19]. There are only limited studies that have comprehensively investigated and reported sEV miRNAs profiles between different blood samples[11,13].In this study, we compared miRNA profiles between matched serum and plasma sEV preparations, collected from healthy controls and patients with esophageal adenocarcinoma, for the presence of reported specific vesicular and non-vesicular miRNAs. We also compared the performance of a previously identified multibiomarker panel (comprising of 5 sEV miRNA ratios)[20], between serum and plasma sEV preparations, to discriminate patients with esophageal adenocarcinoma from the healthy individuals.

MATERIALS AND METHODS

Patient recruitment and sample collection

Individuals visiting Flinders Medical Centre (Adelaide, South Australia) and the Royal Adelaide Hospital (Adelaide, South Australia) for endoscopy procedures and management of esophageal cancer were recruited for a biomarker research study.Ethical approval was obtained from the Southern Adelaide Clinical Human Research Ethics Committee and the Royal Adelaide Hospital Research Committee. All individuals provided written informed consent for blood and personal data collection for research purposes. The study was conducted in accordance with the Declaration of Helsinki’s (2008) statement for the ethical principles for medical research involving human subjects.

Blood samples from 10 healthy controls (median age 56.5 ± 10) and 10 patients with locally advanced esophageal adenocarcinoma (median age 59.5 ± 7) were used. The individuals were previously part of a larger biomarker study for esophageal adenocarcinoma[20]. The “healthy controls” all underwent endoscopy with biopsies and were not identified as having Barrett’s esophagus, gastroesophageal reflux disease, or cancer. Only individuals with no endoscopic or histological abnormality were included in the control group. Matched serum and plasma samples from each individual was collected at the same time prior to their endoscopy procedure. Blood was collected from the patients with cancer prior to any treatment. Collection was performed with 8 mL Z Serum Separator Clot Activator tubes Vacuette?(cat# 455078)and 9 mL K3E K3EDTA tubes Vacuette?(cat# 455036) respectively.

Blood processing and extracellular vesicle isolation

All blood samples were left at room temperature for a period of 16-24 h before processing with a standardised protocol established in our laboratory. Serum was collectedviacentrifugation of blood at 650gfor 15 min and stored as 1 mL aliquots at-80 °C for later use. Plasma was collectedviacentrifugation at 650gfor 15 min to separate the plasma supernatant from the red blood cells and buffy coat containing white blood cells. The top clear layer of plasma supernatant was transferred to a fresh 10 mL tube (Techno-Plas Pty Ltd., Australia; cat# S9716-V06) for a second centrifugation at 650gfor 15 min and the supernatant was stored as 1 mL aliquots at -80 °C for later use.

For extracellular vesicle isolation, aliquots (1 mL) of the matched serum and plasma from the 10 healthy controls and 10 patients with esophageal adenocarcinoma were retrieved from -80 °C and quick thawed. The aliquots were centrifuged at 16000gat 4°C for 30 min to exclude large microparticles. Two hundred and fifty microliter supernatants from each sample was processed with the ExoQuickTMkit (System Biosciences, CA, United States; EXOQ20A-1) according to the manufacturer’s protocol. All samples were incubated with ExoQuickTMat 4 °C for 16 h. The extracellular vesicle pellet isolated from each sample was resuspended with 50 μL phosphate buffered saline.

Size distribution and quantification of extracellular vesicles

The size and concentration of extracellular vesicles isolated from each sample was measured using a NanoSight LM10 Nanoparticle Analysis System and Nanoparticle Tracking Analysis Software (NanoSight Ltd., Malvern, United Kingdom). One microliter of vesicle suspension was serially diluted in pre-filtered phosphate buffered saline to a dilution factor of 1:3200 for the NanoSight measurement. This dilution factor was determined in the laboratory to achieve an average particle concentration range of 108-109/mL for our samples, which is the optimal measurement range recommended by the manufacturer’s protocol. The diluted sample was injected into the NanoSight instrument sample inlet port and a 60 s video were captured for measurement. The measurements were performed in triplicate for each diluted sample by re-injecting the same sample into the sample inlet port. Average particle size and concentration for each sample was evaluated using the batch-processing settings within the NTA software.

Extracellular vesicle miRNA extraction and profiling

The miRNeasy Serum/Plasma kit (QIAGEN, #217184) was used according to the manufacturer’s protocol. After the addition of 500 μL QIAzol Lysis reagent to each vesicle pellet, 5 μL (0.1 picomole) of each of the synthetic RNA molecules ath-miR-159a and cel-miR-54 were added (Shanghai Genepharma Co. Ltd.). The final RNA elution from each sample was performed with 24 μL of RNase-free ultrapure water.

The Taqman?OpenArray?Human microRNA panel (Life technologies, #4461104)was used to profile the expression of 758 miRNAs. The detailed steps for the miRNA profiling were as previously described[20]. The profiling was performed using the Biotrove OpenArray NT cycler at the Flinders Genomics Facility (Flinders University,South Australia). The Realtime PCR Statminer?software (v4.5, Integromics) was used to assess the miRNA expression as cycle threshold (Ct) value per assay. The relative miRNA expression was calculated as 2(40-Ct). The data has been submitted to the Gene Expression Omnibus website (GSE142855).

Statistical analysis

Wilcoxon signed-rank test was used to investigate the pairwise differences between the matched serum and plasma samples of individual. This included comparisons on the particle concentrations, number of miRNAs detected and relative expression of specific miRNA. Correlation was assessed using the Spearman’s rank correlation coefficient. The diagnostic accuracy of a previously identified 5-miRNA ratio panel[20]was determined using leave-one-out cross-validation and receiver-operating characteristics (ROC) curve analysis. Statistical significance was defined by aPvalue＜ 0.05. Statistical analyses were performed using Stata software version 13.1(StataCorp, College station, TX, United States) and IBM?SPSS?Statistics software version 25.

RESULTS

Particle yield

The Nanosight system was used to compare the profiles of particles isolated from the matched serum and plasma of healthy individuals. The main population of particles isolated from serum and plasma were similar in size, at 97.7 ± 3.3 nm and 93.1 ± 3.1 nm respectively (Figure 1A). The range of particle sizes detected in the samples,including those from the cancer patients (Supplementary Figure 1A), were consistent with the reported sizes of exosomes (30-150 nm)[16,21,22]. To be consistent with the Minimal Information for Studies of Extracellular Vesicles 2018 guidelines, we refer here to the majority particle population in the preparations as “small extracellular vesicles (sEVs)” , while noting that a minor population of “medium-large extracellular vesicles (m/lEVs)” were also detected[23]. The average concentration of particles from healthy controls was 1.2-fold higher in the serum sEV preparations compared to the matched plasma sEV preparations (Wilcoxon signed-rank test,P= 0.047) (Figure 1B).However, there was no statistical difference in the yield of particles in the matched serum sEV preparations and plasma sEV preparations from the cancer patients(Wilcoxon signed-rank test,P= 0.56) (Supplementary Figure 1B).

miRNA content in serum and plasma sEV preparations

The number of miRNAs detected was greater in plasma sEV preparations than serum sEV preparations, either for those detected in each sample (total detectable), or for those detected in all samples (Figure 2A). In plasma sEV preparations, 480 miRNAs were detected, and 45.4% (218 miRNAs) of these were robustly expressed in all samples. In serum sEV preparations, 412 miRNAs were detected and 31.1% (128 miRNAs) of these were robustly expressed in all samples. Pairwise comparison of the number of total miRNAs that were detectable was consistently higher in the plasma sEV preparations (Wilcoxon signed-rank test,P= 0.005) (Figure 2B). The number of miRNAs unique to plasma sEV preparations was also greater than the number of miRNAs unique to serum sEV preparations (108vs40). Furthermore, a large proportion of the miRNAs unique to plasma sEV preparations were expressed in at least 50% of the cohort (at least 5 out of 10 samples) (Supplementary Table 1). While for miRNAs unique to serum sEV preparations, only 1 miRNA (hsa-miR-1233) was expressed in at least 50% of the cohort.

The majority of the miRNAs detected in serum sEV preparations were also detected in plasma sEV preparations. 372 miRNAs were commonly expressed between serum and plasma sEV preparations, which represented 90.3% of the total miRNA content in serum sEV preparations. Of these, 118 miRNAs were commonly expressed in all serum and plasma sEV preparations. The relative expression of the 372 commonly expressed miRNAs was significantly correlated (Spearman’s R = 0.87,P＜ 0.0001)(Figure 2C). There was a stronger correlation among the common 118 miRNAs expressed in all serum and plasma sEV preparations (Spearman’s R = 0.92,P＜ 0.0001)(Figure 2D). Similar observations of the overall miRNA content were found in the matched serum and plasma sEV preparations from the patients with esophageal adenocarcinoma (Supplementary Figure 2), although the overall number of miRNAs were higher in the sEV preparations from the cancer patients compared to healthy individuals.

Highly expressed miRNAs in serum and plasma sEV preparations

The top 20 most abundant miRNAs expressed in the serum and plasma sEV preparations were compared (Table 1). 16 out of 20 of the most abundant miRNAs were common between serum and plasma sEV preparations. However, the expression levels of the 16 common miRNAs were 2 to 11-fold higher in the plasma sEV preparations compared to serum sEV preparations (Wilcoxon signed-rank test,P＜0.05) (Figure 3). Of the 20 most highly expressed miRNAs in plasma sEV preparations,hsa-miR-484, hsa-miR-130a-3p, hsa-miR-30c-5p and hsa-miR-221-3p were not detected in serum sEV preparations. Of the 20 miRNAs that were highly expressed in serum sEV preparations, hsa-miR-1274b, RNU6-1, hsa-miR-517a-3p and hsa-miR-25-3p were not detected in plasma sEV preparations.

Presence of blood-cell specific miRNAs

The presence of miRNAs reported by Wanget al[10], 2012, and Pritchardet al[8], 2012, to be highly expressed or uniquely expressed in blood cells was examined in our serum and plasma derived sEV preparations. Both Wanget al[10]and Pritchardet al[8]identified hsa-miR-223-3p and hsa-miR-451a as highly abundant in blood cells. Wanget al[10]reported 27 miRNAs that were uniquely expressed in blood cells. Pritchardet al[8]2012 reported 44 additional miRNAs that were highly expressed in blood cells.

Figure 1 NanoSight measurements of isolated vesicles from matched serum and plasma samples. A: The overall size distribution of particles (SEM indicated by shaded areas) was similar between the matched serum (n = 10) and plasma samples (n = 10); B: Pairwise comparison of the average concentration (± SEM) of particles demonstrated higher particle yields in serum (Wilcoxon signed-rank test, aP = 0.047).

Both hsa-miR-223-3p and hsa-miR-451a were found to be among the top 20 most highly expressed miRNAs in our serum and plasma sEV preparations (Figure 3).Compared to serum sEV preparations, hsa-miR-223-3p was expressed at 9.6-fold higher in plasma sEV preparations (Wilcoxon signed-rank test,P= 0.0051), while hsamiR-451a was expressed at 2.5-fold higher in plasma sEV preparations (Wilcoxon signed-rank test,P= 0.01). An additional 6 blood-cell miRNAs were identified in the top 20 most highly expressed miRNAs as consistently expressed at higher levels in plasma sEV preparations compared to serum sEV preparations (2.7 to 5.6 fold; hsamiR-19b-3p, hsa-miR-17-5p, hsa-miR-30b-5p, hsa-miR-106a-5p, hsa-miR-150-5p and hsa-miR-92a-3p; Figure 3). In addition, we identified 4 blood-cell miRNAs (hsa-miR-98-5p, hsa-miR-30d-3p, hsa-miR-146b-3p and hsa-miR-19b-1-5p) that were robustly expressed in at least 50% of the plasma sEV preparations, that were not expressed in the serum sEV preparations (Supplementary Table 1).

Presence of reported vesicular miRNAs and protein-associated miRNAs

The presence of unique vesicular miRNAs, whole blood miRNAs (blood-cell miRNAs) and cell-free miRNAs (protein-associated miRNAs) reported by Chenget al[11]were compared in our plasma and serum sEV preparations (Figure 4). Overall,we detected 12 of Chenget al[11]’s unique vesicular miRNAs in our serum sEV preparations, and 14 of Chenget al[11]’s unique vesicular miRNAs in our plasma sEV preparations (Figure 4). Smaller numbers of Chenget al[11]’s unique whole blood miRNAs and cell-free miRNAs were detected in our plasma and serum sEV preparations (Figure 4). Several of these unique miRNAs were detected in only a small number of serum or plasma sEV preparations. We therefore identified those that were more reliably and robustly expressed in at least 50% of samples. In serum derived preparations, 6 unique vesicular miRNAs and only 1 unique whole blood miRNA were robustly expressed. In comparison, there were more unique vesicular miRNAs (11 miRNAs) and cell-free miRNAs (5 miRNAs) robustly expressed in plasma derived preparations. These observations were consistent in the matched samples from patients with esophageal adenocarcinoma (Supplementary Table 2).

We next evaluated for the presence of vesicle-associated miRNAs and proteinassociated miRNAs reported by Arroyoet al[13](Figure 5). The list of miRNAs that were assessable on the TaqMan OpenArray platform are provided in Supplementary Tables 3 and 4. To investigate the relative expression levels of these miRNAs in serum and plasma sEV preparations, we partitioned them into the following 5 bins using their qPCR Ct’s: bin-1, not detected; bin-2, 40 > Ct ≥ 30; bin-3, 30 > Ct ≥ 25; bin-4, 25 >Ct ≥ 20; bin-5, Ct ＜ 20. The percentage of the total number of vesicle-associated miRNAs, and protein-associated miRNAs, was then determined for each bin, for serum sEV preparations and for plasma sEV preparations.

We found that serum sEV preparations had a greater percentage of vesicleassociated miRNAs expressed at relatively high levels (Ct’s ＜ 25) than plasma sEV preparations (60%vs44%), whereas plasma sEV preparations had a greater percentage of protein-associated miRNAs expressed at relatively high levels than serum sEV preparations (62%vs31%; Figure 5). Plasma sEV preparations also had a greater percentage, than serum sEV preparations, of protein-associated miRNAs expressed at very high levels (Ct’s ＜ 20; 22%vs0%), and plasma sEV preparations had a higher percentage of undetected vesicle-associated miRNAs than serum sEVpreparations (33%vs10%). We observed similar distributions of vesicle-associated and protein-associated miRNAs in serum and plasma sEV preparations from patients with esophageal adenocarcinoma (Supplementary Figure 3). Overall these results indicated that serum sEV preparations contained higher levels of vesicle associated miRNAs, and lower levels of protein associated miRNAs, compared with plasma sEV preparations.

Table 1 Top 20 abundant microRNAs expressed in plasma and serum small extracellular vesicle preparations

Diagnostic performance of multi-biomarker panel in serum and plasma

To investigate whether the above observed differences in proportions of non-vesicular to vesicular miRNAs in serum and plasma sEV preparations may influence outcomes of biomarker studies, we compared the diagnostic performance of a previously identified multi-biomarker panel[20]in the matched sEV preparations from serum and plasma samples (Figure 6). The multi-biomarker panel consisted of 5 specific miRNA ratios (RNU6-1/hsa-miR-16-5p, hsa-miR-25-3p/hsa-miR-320a, hsa-let-7e-5p/hsa-miR-15b-5p, hsa-miR-30a-5p/hsa-miR-324-5p, hsa-miR-17-5p/hsa-miR-194-5p) that discriminated esophageal adenocarcinoma patients from healthy controls and nondysplastic Barrett’s esophagus[20]. When assessed in the serum sEV preparations, the multi-biomarker panel achieved a good prediction accuracy (AUROC = 0.95) and remained robust in leave-one-out cross validation (AUROC = 0.90). When assessed in the matched plasma sEV preparations, the multi-biomarker panel was less accurate in predicting which patients had esophageal adenocarcinoma (AUROC = 0.80) and performed considerably worse in leave-one-out cross validation (AUROC = 0.54).

DISCUSSION

To date, there have only been limited studies investigating sEV miRNA profiles concurrently in serum and plasma sEV preparations to determine their suitability for biomarker studies[11,16]. Based on our overall study findings, we observed significant differences in the proportion of reported sEV associated miRNAs between serum and plasma sEV preparations. Our results suggest that there is a greater concern for potential contamination of non-vesicular miRNAs in the plasma sEV preparations,and that this may influence biomarker studies. Therefore, we propose serum to be the preferred choice over plasma for future sEV miRNA biomarkers studies.

Figure 2 Comparison of the microRNA content between serum and plasma small extracellular vesicles. A: The number of total detectable microRNA (miRNAs)(top Venn diagram), and the number of miRNAs detected in all serum or plasma samples (bottom Venn diagram), were higher in plasma; B: Pairwise comparison of the number of total detectable miRNAs was significantly higher in the plasma (Wilcoxon signed-rank test, bP = 0.005); C: Correlation of the average relative expression of the 372 common total detectable miRNAs (Spearman’s R = 0.87, cP ＜ 0.001); D: Correlation of the average relative expression of the 118 common miRNAs detected in all serum or plasma samples (Spearman’s R = 0.92, cP ＜ 0.001). miRNA: MicroRNA.

Under our specific study conditions, we isolated similar sEV yields yet overall higher miRNA content in plasma compared to serum sEV preparations. These findings are in contrast with previous studies that reported an overall higher miRNA content in serum sEV preparations compared to plasma sEV preparations[11,16]. In Chenget al[11], next generation sequencing was used to profile a larger number of miRNAs than our TaqMan OpenArray platform. However, the study only utilised matched samples from 3 healthy individuals and used different methods than us for sEV isolation. The number of miRNAs detected was also marginally higher in the serum sEV preparations compared to plasma sEV preparations (412vs386 miRNAs).Although Dinget al[16]used the same sEV isolation and quantification techniques as us, the blood processing and miRNA detection methods were different to our study.The authors reported higher sEV yield, higher albumin contamination, larger microvesicles and higher number of miRNAs detected in the serum compared to plasma sEV preparations[16]. However, blood samples used for the sEV quantification and sEV miRNA profiles were derived from different individuals (5 and 20 healthy individuals respectively). Despite the disparities among these studies, the evidence that miRNA profiles differ between matched serum and plasma sEV preparations is consistent.

Figure 3 Fold difference in abundance of the common most abundant microRNAs in plasma compared with serum small extracellular vesicles preparations. The fold change is calculated as the relative expression in the plasma divided by the relative expression in the serum. All common abundant microRNAs, including those previously reported as blood-cell microRNAs by Wang et al[10] and Pritchard et al[8], were significantly higher in the plasma than serum. (Wilcoxon signed-rank test, bP = 0.0051; dP = 0.007; aP = 0.01).

Possible explanations for the different miRNA profiles of sEV preparations from serum and plasma might include factors that impact upon the amount of proteinbound (non-vesicular) miRNAs present, and/or upon the sEVs produced from blood cells. These factors could include the different tubes with different additives that are used for producing plasma compared to serum, and that the production of serum involves blood clotting while the production of plasma specifically avoids this by using anti-coagulants. Blood clot formation involves trapping an array of proteins into the clot mesh, and this results in a significantly lower protein content in serum than in plasma[24], which may directly contribute towards an overall depletion of proteinbound miRNAs in serum compared to plasma. Besides Ago2 protein, high density lipoprotein (HDL) is another type of protein based vehicle for peripherally circulating miRNAs in plasma[25]. Of particular interest, it has been reported that HDL is trapped in the mesh that forms during clotting[26]. Therefore, it is possible that HDL-bound miRNAs are trapped in the clot, thereby resulting in lower numbers of HDL-bound miRNAs in serum than plasma. The method that we used for preparing sEVs involves the precipitation of membrane particles, and methods based upon this technique are known to result in co-precipitation of lipoproteins[27]. Taken together, it is possible that our serum sEV preparations contain less HDL-bound miRNAs than our plasma sEV preparations, and this may explain the lower overall miRNA abundance in our serum sEV preparations, as well as the tendency for our serum sEV preparations to contain a higher proportion of sEV associated miRNAs than our plasma sEV preparations.Different blood collection tube components have been shown to interfere with clinical chemistry assays in different ways[24]. The blood collection tubes used for plasma preparation in our study contained EDTA as the anti-coagulant. It has been reported that EDTA results in platelet activation, which increases the release of microvesicles,including sEVs, from platelets[28,29]. This might suggest that our plasma preparations would be more biased, than our serum sEV preparations, towards containing platelet derived / activated platelet sEV derived miRNAs. Consistent with this possibility, the top two miRNAs that were most heavily biased towards our plasma derived preparations were hsa-miR-223-3p, which is the most abundant miRNA in platelets,and hsa-miR-24-3p, which is a biomarker for platelet activation[30]. Another possibility is that the different blood tube components in the tubes used for preparing serum and plasma have different impacts upon the number of sEVs produced from blood cells,and / or the miRNA expression in blood cells, which translates into differences in the miRNA composition of sEVs derived from them[31]. It is also possible that the differences in blood tube components might impact upon the specific blood cell miRNAs that are sorted into sEVs[31].

One of the most significant differences between the miRNA profiles of our serum and plasma sEV preparations was the higher level of expression of reported blood cell miRNAs in plasma sEV preparations. In previous studies, circulating cell-free hsamiR-451a, hsa-miR-16-5p and hsa-miR-223-3p are among the most common miRNAs assessed as indicators of haemolysis or blood cells contamination[10,18,32-35]. Although we found several reported blood cell miRNAs, including hsa-miR-451a, hsa-miR-16-5p and hsa-miR-223-3p, to be abundant in both plasma and serum sEV preparations,they were all more highly expressed in plasma sEV preparations. The presence of higher blood cell contamination in plasma sEV preparations was further supported by the observation that several reported blood-cell miRNAs were uniquely expressed only in our plasma derived samples, and a greater number of unique cell-free miRNAs, reported by Cheng 2014, were detected in the plasma derived samples.

Figure 4 Presence of microRNAs reported to be uniquely expressed in whole blood, cell-free, or small extracellular vesicles, in serum and plasma. The lists of unique miRNAs were derived from Cheng et al[11]. miRNAs detected in at least 50% of each sample type are presented in bold.

Although the overall miRNA content was higher in our plasma sEV preparations,the concern was the high abundance of miRNAs in plasma sEV preparations that were reported to be from non-vesicular origins. Contrary to the consistently high miRNA content in plasma compared to serum derived sEV preparations, we observed a larger percentage of highly expressed vesicle-associated miRNAs in the serum sEV preparations, but a larger percentage of highly expressed protein-associated miRNAs in the matched plasma sEV preparations. We acknowledge that this conclusion is reliant on the findings of a single study (Arroyo 2011) and will require further validation. However, unlike blood-cell miRNAs, specific miRNAs that are highly expressed or uniquely expressed in sEVs or in protein-complexes with Ago2 are not as well-established. We identified only two studies, Cheng 2014[11], and Arroyo 2011[13],comprehensively reporting specific sEV miRNA profiles and protein-associated miRNA profiles in serum and plasma. Interestingly, RNU6-1, which has been reported to be enriched in sEVs, was also found to be abundant in our serum sEV preparations (top 20 most highly expressed miRNAs) but not in our plasma sEV preparations[36-39]. Altogether, these findings suggest that although a large proportion of miRNAs were consistently more highly expressed in plasma sEV preparations compared to serum sEV preparations, we identified a subset of miRNA candidates reported to be of sEV origin to be more highly expressed in serum sEV preparations.

Taking all these findings together, serum appears preferable to plasma for sEV miRNA biomarkers studies. As a proof-of-concept, we evaluated the diagnostic performance of a multi-biomarker panel to discriminate esophageal adenocarcinoma patients from the healthy controls in this study cohort when assessed in the serum sEV preparations compared to plasma sEV preparations. The diagnostic accuracy of the biomarker panel had higher cross validated prediction accuracy when assessed in the serum sEV preparations than in plasma sEV preparations. However, we recognise that our study findings are based on a small sample size and are specific to our study conditions, and further work is necessary to validate these findings. In particular,there is currently limited understanding on circulating miRNAs in protein-complexes,and a need to consider their role in future sEV miRNAs studies.

Research methods

Matched serum and plasma samples from 10 healthy controls and 10 patients with esophageal adenocarcinoma were used for this study. sEVs were isolated with using ExoquickTM. RNA extracted from the vesicles was profiled using the Taqman Openarray qPCR.

Research results

The overall miRNA content was higher in plasma sEV preparations (480 miRNAs) and contained 97.5% of the miRNAs found in the serum sEV preparations (412 miRNAs). The expression of commonly expressed miRNAs was highly correlated (Spearman’s R = 0.87,P＜ 0.0001) between the plasma and serum sEV preparations but was consistently higher in the plasma sEV preparations. Specific blood-cell miRNAs (hsa-miR-223-3p, hsa-miR-451a, miR-19b-3p, hsa-miR-17-5p, hsa-miR-30b-5p, hsa-miR-106a-5p, hsa-miR-150-5p and hsa-miR-92a-3p) were expressed at 2.7 to 9.6 fold higher levels in the plasma sEV preparations compared to serum sEV preparations (P＜ 0.05). In plasma sEV preparations, the percentage of protein-associated miRNAs expressed at relatively higher levels (cycle threshold 20-25) was greater than serum sEV preparations (50%vs31%). While the percentage of vesicle-associated miRNAs expressed at relatively higher levels was greater in the serum sEV preparations than plasma sEV preparations(70%vs44%). A 5-miRNA biomarker panel produced a higher cross validated accuracy for discriminating patients with esophageal adenocarcinoma from healthy controls using serum sEV preparations compared with plasma sEV preparations (AUROC 0.80vs0.54,P＜ 0.05).

Research conclusions

Although plasma sEV preparations contained more miRNAs than serum sEV preparations, they also contained more miRNAs from non-vesicle origins.

Research perspectives

Serum appears to be more suitable than plasma for sEV miRNAs biomarkers studies. Future studies on sEV associated cancer biomarkers may benefit from using serum as the sample type for analysis.

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