Graphical abstract graphic file with name fx1.jpg [53]Open in a new tab Highlights * • Introduction of the GlyExo-Capture approach for isolating extracellular vesicles * • Identification and validation of five miRNAs with strong diagnostic performance for HCC * • Effective detection of early-stage HCC and differentiation from other malignancies * • Development of a high-throughput, rapid, and non-invasive method for early HCC diagnosis __________________________________________________________________ Li and colleagues present the GlyExo-Capture method for isolating fucosylated extracellular vesicles (Fu-EVs) and identify five miRNAs for early HCC diagnosis. The method effectively detects early-stage HCC and differentiates it from other cancers, offering a high-throughput, rapid, and non-invasive screening approach. Introduction Liver cancer is a leading cause of cancer-related death globally, estimated to cause over one million fatalities by 2025.[54]^1 Hepatocellular carcinoma (HCC) is the most prevalent class of liver cancer, accounting for approximately 85% of all primary hepatic malignancies.[55]^2 The survival rate for HCC patients is strikingly low, with only 18% surviving beyond five years of diagnosis. This high mortality rate is largely attributed to the lack of effective early diagnosis strategies.[56]^3 The prognosis for HCC depends on the stage of diagnosis. For patients with advanced-stage disease, the 5-year survival rate is below 5%, while it exceeds 70% for those diagnosed early.[57]^4 The current standard approach for HCC screening and surveillance in patients with cirrhosis and subgroups with chronic hepatitis B virus infection involves abdominal ultrasound with or without serum alpha-fetoprotein (AFP) measurements.[58]^5 In a meta-analysis of cohort investigations, ultrasound alone was found to have a sensitivity of only 45% for detecting early-stage HCC, rising to 63% alongside AFP.[59]^6 Furthermore, the utilization of HCC surveillance remains low, with under 20% of at-risk patients participating in early detection programs due to poor adherence to ultrasound screening.[60]^6 Therefore, there is an urgent need for a minimally invasive and highly accurate approach for detecting HCC. Liquid biopsy has been identified as a promising approach for early detection of HCC patients. It encompasses analyzing tumor components, primarily nucleic acids and tumor cells, which are released into the bloodstream by tumors.[61]^7 In the realm of nucleic acids, microRNAs (miRNAs) are a category of single-stranded, small non-coding RNAs, typically 18–22 nucleotides long.[62]^8 miRNAs, frequently dysregulated in multiple cancers, including HCC, are involved in various cancer biology processes, promoting tumor growth, apoptosis, progression, metastasis, immune evasion, and drug resistance.[63]^9^,[64]^10^,[65]^11^,[66]^12 Current research indicates that miRNAs show promise as potential candidates for liquid biopsy in the detection of human cancers.[67]^13^,[68]^14 In addition, circulating miRNAs have been improved to be promising molecules for early detection of HCC.[69]^15 In another study, four miRNAs were identified to be significantly deferentially expressed between individuals with HCC and non-cancerous healthy individuals, indicating their potential as biomarkers for HCC detection. However, the specificity of miRNA-based biomarkers is challenged by the observation that cell-free miRNAs (cf-miRNAs) can originate from various sources, like apoptotic and immune cells, not only tumor cells.[70]^16 Therefore, we infer that the potential heterogeneity associated with the origins of cf-miRNAs may limit the specificity of miRNA as a biomarker. Another promising liquid biopsy approach involves examining of extracellular vesicles (EVs), which are lipid bilayer membrane-enclosed structures 40–160 nm in size, excreted by the majority of cells, and stably circulated in body fluid.[71]^17^,[72]^18 EVs have diverse biochemical signals, including genetic material, proteins, and lipids, from their cells of origin. Various studies suggest that EVs participate in cell-to-cell communication by delivering molecular cargo to target cells in the tumor microenvironment, promoting tumorigenesis and growth.[73]^19 Furthermore, EVs have inherent stability due to their resilient lipid bilayers, allowing sustained circulation within the demanding tumor microenvironment and under physiological conditions.[74]^20^,[75]^21^,[76]^22 This exceptional biological stability ensures reliable EV isolation and detection while allowing for extended specimen storage.[77]^23 These advantages make EVs a reliable source of biomarkers for cancers like HCC.[78]^24^,[79]^25^,[80]^26 According to previous studies, we inferred that miRNAs within EVs are highly promising candidate biomarkers for the initial screening of liver cancer. However, challenges in efficiently isolating and specifically detecting EVs due to their small size and heterogeneity pose obstacles.[81]^27^,[82]^28 As cancer-derived EVs make up only a small fraction of the total EVs in bodily fluids, achieving ultra-sensitive and specific identification is imperative for advancing EV-based cancer diagnostics. Various methods have been developed for EV isolation and nucleic acids detection demonstrating progress.[83]^29^,[84]^30^,[85]^31 However, challenges persist, including limited sensitivity and specificity, as well as issues linked to low purity and throughput, influencing both academic research and practical applications.[86]^32^,[87]^33 Therefore, developing an effective approach to extracting and enriching tumor-derived EVs from serum is the pivotal challenge in leveraging EV cargo contents for tumor screening. Fortunately, tumor cells frequently produce surface glycans with distinct structures and expression levels compared to normal counterparts.[88]^34 Therefore, the membrane surface of tumor-derived EVs should exhibit a significant abundance of fucosylated proteins, linked to the shared similarity in glycosylation structures between EVs and their secreted parent cells. Moreover, the excessive expression of “core” fucosylation is a crucial event in the development and progression of human HCC.[89]^35 In this study, we developed an innovative method for EV isolation, termed GlyExo-Capture technology, leveraging the affinity of lectins for fucose on the EV membranes. This method can enrich fucosylated EVs (Fu-EVs) from liquid samples with high throughput and rapid turnaround times, enhancing the potential of EVs-based diagnostics in cancer. We performed an extensive small RNA transcriptomic profiling on a substantial quantity of clinical samples from patients with HCC, cirrhosis, and hepatitis and healthy controls. The primary objective was to identify an EV-miRNA signature capable of distinguishing HCC from non-HCC conditions. Subsequent to the identification of potential biomarkers, we confirmed our classifier model across multiple independent clinical cohorts, advancing HCC detection methods. Results The GlyExo-Capture approach substantially enriches Fu-EVs We developed a GlyExo-Capture method to specifically capture Fu-EVs from liquid samples, utilizing lectin immobilized on hydroxyl macromolecular magnetic beads ([90]Figure S1). Notably, this method enabled the entire process of preparing 96 samples to be completed in 11 min. We conducted a comprehensive evaluation of Fu-EVs isolated by GlyExo-Capture with EVs isolated by ultracentrifugation (UC) (referred to as UC-EVs). Transmission electron microscopy analysis uncovered that both Fu-EVs and UC-EVs exhibited oval or bowl-like shapes ([91]Figure 1A). Fu-EVs exhibited a smaller mean size (106.5 ± 6.7 nm) compared to UC-EVs (137.5 ± 0.4 nm) yet had a broader size distribution ([92]Figure 1B). Further validation through immunoblot and ExoView analyses confirmed the presence of EV membrane protein markers, including CD81, CD63, and CD9, as well as tetraspanins like TSG101 and ALIX ([93]Figures 1C and 1D). These findings collectively confirm the successful isolation of Fu-EVs. To further characterize Fu-EVs, we evaluated their uptake dynamics using flow cytometry. Both Fu-EVs and UC-EVs were labeled with 1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate (DiD). As illustrated, Fu-EVs exhibited time- and dose-dependent uptake patterns ([94]Figures S2A and S2B). Notably, Fu-EVs exhibited increased uptake efficiency compared to UC-EVs ([95]Figures S2C–S2F). Consistent with this, the enhanced uptake efficiency of Fu-EVs was reduced to levels similar to UC-EVs upon enzymatic removal of N-glycans using peptide-N-glycosidase F (PNGase F). Figure 1. [96]Figure 1 [97]Open in a new tab Characterization and comparative analysis of EVs isolated using GlyExo and UC methods (A) Wide-field electron microscopy images of EVs isolated by GlyExo and UC methods, with representative EVs highlighted by arrows (scale bar: 100 nm). (B) Size distribution measurements of EVs using nanoparticle tracking analysis (NTA). (C) Western blot analysis showing Fu-EVs, UC-EVs, and whole-cell lysates (WCLs). (D) Analysis of EVs through ExoView using the specified antibodies. (E) Comparison of EV capture approaches using lectin- or BSA-immobilized beads; the captured EVs are quantified as the bound fraction relative to the UC-EVs loaded. (F) Comparison between EVs isolated from the cancer cell line HepG2 and the non-cancerous MIHA cell line. Experiments were performed in triplicate, with statistical significance determined using two-tailed Student’s t tests. ∗, p < 0.05; ∗∗, p < 0.01; ∗∗∗, p < 0.001. To assess the efficacy of lectin-immobilized beads, UC-EVs were separately incubated with lectin- or BSA-immobilized beads. Further quantitative analysis of the unbound fractions revealed a 40% reduction in the number of UC-EVs particles in the unbound fraction following incubation with lectin-immobilized beads ([98]Figure 1E). In addition, the enrichment of Fu-EVs secreted by HepG2 cells was significantly higher relative to those obtained from non-cancerous immortalized human hepatocyte cell line (MIHA) ([99]Figure 1F). Overall, the GlyExo-Capture method is a rapid and reliable approach for the high-throughput isolation of Fu-EVs. EV-miRNA expression profiles of the discovery cohort identify five HCC-specific miRNA signatures Given the increased presence of glycans on EVs originating from cancer cells, there is substantial promise in identifying miRNA cargos within enriched Fu-EVs for discovering more specific and sensitive cancer biomarkers. To assess this potential, we obtained a cohort of 88 patients diagnosed with HCC and 179 non-HCC controls, including 49 healthy individuals, 62 hepatitis, 54 cirrhosis, and 14 benign hepatic tumor patients. Next-generation sequencing (NGS) was employed to compare the Fu-EVs miRNA expression files across 88 HCC patients and 179 non-HCC controls. The quality of the NGS data is displayed in [100]Figures S3A and S3B. A total of 2,278 known miRNAs were identified ([101]Figure 2A). Differential analysis between the HCC group and the non-HCC group was conducted using the R software package DESeq2, leading to the identification of 112 miRNAs with significant differences ([102]Figure S4). Moreover, linear discriminant analysis was conducted using the 112 differentially expressed miRNAs (DEMs) across the five groups. These five groups could be effectively segregated beginning from a healthy state, progressing to hepatitis and cirrhosis, and culminating in HCC ([103]Figure 2B). Using the same approach, we conducted differential expression analysis for multiple comparisons, revealing a common set of DEMs common across the four non-healthy groups and the healthy group ([104]Figure 2C). Interestingly, all 28 miRNAs in this common intersection were part of the 122 DEMs between the HCC and non-HCC groups. However, no overlap was detected in the DEMs between the HCC group and the three non-cancerous liver disease groups ([105]Figure 2D). Figure 2. [106]Figure 2 [107]Open in a new tab Analysis of EVs-miRNA profiles in various cohorts (A) Distribution of annotated miRNA counts in healthy, hepatitis, and HCC groups. The values 0.01 and 0.041 within the figure represent the p values from the Wilcoxon's rank-sum test (B) Linear discriminant analysis of significantly different miRNAs among five populations. (C) Venn diagram showing deferentially expressed miRNAs across disease groups compared to the healthy cohort. (D) Venn diagram illustrating differentially expressed miRNAs in benign liver disease compared to the HCC group. We narrowed down the aforementioned 112 miRNAs to 35 miRNAs utilizing recursive feature elimination. From these, we identified the ten miRNAs based on their significance in the random forest feature importance analysis. The expression comparison of the ten miRNAs in both the HCC and non-HCC control groups is illustrated in [108]Figures S5A–S5J. Thereafter, we validated these ten miRNAs using quantitative reverse-transcription PCR (RT-qPCR) and refined our selection to five miRNAs exhibiting significant signaling disparities. Since pairs of miRNAs can mitigate experimental system errors and enhance the signal-to-noise ratio, these five DEMs were selected to establish biologically relevant target pairs. Using five specific miRNAs, including hsa-let7a, hsa-miR-21, hsa-miR-200a, hsa-miR-150, and hsa-miR-125a, we identified three pairs of miRNAs. The resulting miRNA ratio signatures, acquired via both NGS ([109]Figures 3A–3C) and RT-qPCR ([110]Figures 3D–3F), consistently demonstrated significant differences between HCC and non-HCC control groups. Figure 3. [111]Figure 3 [112]Open in a new tab Comparison of the miRNA ratio signatures distinguishing HCC from controls using NGS and RT-qPCR Control groups, designated as non-HCC, include individuals with cirrhosis, hepatitis, benign hepatic tumors, and healthy controls. (A–C) Expression ratio signatures measured by NGS: (A) hsa-let-7a/hsa-miR-21, (B) hsa-miR-200a/hsa-miR-150, and (C) hsa-let-7a/hsa-miR-21. (D–F) Expression ratio signatures measured by RT-qPCR: (D) hsa-let-7a/hsa-miR-21, (E) hsa-miR-200a/hsa-miR-150, and (F) hsa-let-7a/hsa-miR-21. Each experiment was conducted with biological replicates. The p values represent those from the t test. The HCC prediction model using three miRNA ratios is successfully constructed and validated throughout multiple cohorts To assess the efficacy of these candidate miRNA ratios as biomarker panels, logistic regression models were constructed using NGS data from a discovery cohort of 267 individuals and RT-qPCR data from training and validation cohorts totaling 779 individuals. Receiver operating characteristic (ROC) curve analysis demonstrated an area under the curve (AUC) of 0.959 ([113]Figure 4A), while precision-recall curve (PRC) analysis had a precision-recall area under the curve (PRAUC) of 0.916 ([114]Figure 4B) for the NGS data. The confusion matrix ([115]Figure 4C) from the discovery cohort exhibited a sensitivity of 94.32% and a specificity of 87.71%, highlighting the model’s robust diagnostic performance. Utilizing the RT-qPCR data for the same three candidate miRNA ratios, the model was trained using a training cohort and validated on two distinct cohorts: one from the same center (within-center) and another including multiple centers (multi-center). Across these cohorts, the model achieved AUCs of 0.978, 0.947, and 0.930 in the training, within-center, and multi-center cohorts, respectively ([116]Figure 4D), whereas the corresponding PRAUCs were 0.929, 0.872, and 0.878 ([117]Figure 4E). Sensitivity and specificity values were computed according to all RT-qPCR data, with values of 92% and 90%, respectively. Moreover, the model’s performance metrics were calculated across the three cohorts and outlined in [118]Table 1. Notably, within the non-HCC group, specificity exceeded 97% in healthy control samples and surpassed 80% in cases of benign hepatic diseases. Furthermore, during external validation over multiple centers, the model demonstrated robust performance, attaining a sensitivity of 86.90% and a specificity of 89.25% at the established optimal cutoff derived from the training set. Figure 4. [119]Figure 4 [120]Open in a new tab Evaluation of the EVs-miRNA signature performance in clinical cohorts (A–C) Receiver operating characteristic (ROC) analysis, precision-recall curve (PRC) analysis, and confusion matrix analysis of prediction models using a three-miRNA ratio signature measured by NGS with 1,000 bootstrap sampling in 267 samples. (D–F) ROC analysis, PRC analysis, and confusion matrix for prediction models utilizing a three-miRNA ratio signature measured by RT-qPCR in training, within-center, and multi-center cohorts (n = 606). Table 1. Summary of diagnostic performance of classifier mode in the training and validation cohorts Train In-center validation Multi-center validation HCC Non-HCC HCC Non-HCC HCC Non-HCC Non-healthy Healthy Non-healthy Healthy Non-healthy Healthy miRNA model Pre-HCC 42 3 0 59 10 1 73 18 2 Pre-non-HCC 3 42 44 6 62 64 11 81 85 Sensitivity/ specificity 93.33% 93.33% 100% 90.77% 86.11% 98.46% 86.90% 81.82% 97.70% 96.63% 91.97% 89.25% miRNA & AFP model Pre-HCC 44 3 0 60 9 1 75 16 0 Pre-non-HCC 1 42 44 5 63 64 9 83 87 Sensitivity/ specificity 97.78% 93.33% 100% 92.31% 87.50% 98.46% 89.29% 83.84% 100% 96.63% 92.70% 91.40% [121]Open in a new tab To identify the specificity of the three-miRNA ratio signature for HCC, we obtained data from 173 cases of various malignancies, including gastric, lung, breast, and colorectal cancers ([122]Table S1). Analysis of the three-miRNA ratio signature model prediction scores uncovered that most individuals in this cohort exhibited positive scores below 0.5 ([123]Figure S6A). Notably, the highest specificity of 0.9 was observed for breast cancer, with the remaining three cancers also exhibiting specificity over 0.8 ([124]Figure S6B). In summary, our study has established a model capable of highly accurate clinical diagnosis for HCC. Five miRNAs and their target genes enriched in tumorigenic pathways are altered in HCC-EV-receiving cells To further confirm the alternation of the five miRNAs in Fu-EVs-receiving cells, human colon tumor cell line 116 (HCT-116)were treated with Fu-EVs isolated from HCC patients (HCC-EVs) or healthy controls (Ctr-EVs). Compared to cells treated with Ctr-EVs, the expression of the five miRNAs was significantly impacted in cells treated with HCC-EVs, determined by RT-qPCR ([125]Figure S7). NGS analysis was employed to identify genes with altered expression related to the five miRNAs. Significant transcriptional changes were identified in cells treated with HCC-EVs ([126]Table S2). We compared these changes with 234 predicted or reported target genes from the starBase database. The hypergeometric distribution test revealed a significant enrichment of differentially expressed genes within the 234 genes ([127]Table S2), demonstrating a notable overrepresentation of targets specifically related to these miRNAs. The regulatory network between the five miRNAs and their 82 targeted genes is illustrated in [128]Figure S8A. Pathway enrichment analysis of the identified 82 genes unveiled significant enrichment in tumorigenic pathways, especially the PI3K-Akt signaling pathway, cell-cycle regulation, and HCC pathway ([129]Figure S8B). EV-miRNAs combined with serum protein biomarkers enhance the diagnostic accuracy of HCC In clinical practice, AFP and des-gamma-carboxy prothrombin (DCP) serve as biomarkers for diagnosing HCC patients. However, their sensitivity and specificity for early detection in the general population remain inadequate. We hypothesized that integrating miRNAs with AFP and/or DCP could enhance clinical diagnostic efficacy for HCC. Consequently, we assessed the diagnostic performance of AFP and DCP alone, in combination with our miRNA ratio signatures. First, we conducted an analysis of model development and evaluation within the combined cohort of 706 samples from the three groups. As anticipated, developing the model using AFP or DCP alone resulted in AUC values of 0.79 and 0.81, respectively, significantly lower than the model based on the three-miRNA ratio signature, achieving an AUC of 0.95. Furthermore, combining AFP with miRNA signature enhanced overall diagnostic performance, yielding AUC values of 0.96 ([130]Figure 5A). The PRC supports this conclusion, with PRAUC increasing from 0.89 for miRNA to 0.91 with the addition of AFP ([131]Figure 5B). Additionally, we examined the detection outcomes of AFP, DCP, miRNA, and their combination (AFP+miRNAs, DCP+miRNAs, AFP+DCP+miRNAs) across all patients diagnosed with HCC ([132]Figure 5C). The miRNA-based classification model achieved an 88.06% detection rate in 67 AFP-negative patients, while the combined miRNA and AFP model achieved an overall recall rate of 90.70% over 194 HCC patients. This finding highlights the complementary nature of miRNA signatures and AFP, emphasizing the improved diagnostic performance achieved through combined detection. Further analyses specific to each cohort are shown in [133]Figures 5D–5F, 5G–5I, and 5J–5L, illustrating ROC, PRC, and HCC recall for the Fifth Medical Center of Chinese PLA General Hospital (cohort 1), the First Medical Center of Chinese PLA General Hospital (cohort 2), and Capital Medical University Affiliated Beijing Ditan Hospital (cohort 3), respectively. Cohort 2 exhibited superior metrics, while cohort 1 and cohort 3 showed slightly lower performance. Nevertheless, the combined analysis across all cohorts provides a larger sample size, enhancing the model’s capability for generalization. In summary, DCP exhibits superior specificity compared to AFP and miRNA features. In contrast, miRNA substantially enhances the sensitivity of HCC diagnosis compared to these protein biomarkers alone. Moreover, combining miRNA with AFP further enhances overall diagnostic accuracy ([134]Tables S3–S6). Figure 5. [135]Figure 5 [136]Open in a new tab Performance comparison of prediction models based on individual and combined features using logistic regression (A, D, G, and J) Receiver operating characteristic (ROC) and (B, E, H, and K) precision-recall curve (PRC) analysis comparing diagnostic performance among AFP, DCP, miRNA, and their combinations of miRNA with these proteins. (C, F, I, and L) Upset plots showing positive detection of hepatocellular carcinoma (HCC) samples by models with different feature combinations. Numbers in the upper panel bars indicate sample counts identified by multiple models, while numbers in left panel bars denote detection by models with individual and combined features. Results are presented for combined cohorts and individual cohorts 1, 2, and 3. The miRNA model exhibits superior diagnostic performance across various clinical indicators While the model’s performance was previously evaluated across three distinct cohorts, we have conducted a more extensive investigation to better comprehend its clinical applicability. This involved considering additional clinical parameters and performing statistical analyses to evaluate the model’s effectiveness across various indicators. In all RT-qPCR cohorts, comprising healthy controls, patients with benign hepatic diseases, and those with HCC, we systematically ranked the model’s prediction probability scores in ascending order, as illustrated in [137]Figure 6A. Notably, HCC samples with prediction scores below the threshold of 0.5 often exhibited DCP negativity and small tumor sizes, demonstrating low tumor burdens. The miRNA model accurately predicted all cases of benign hepatic tumors, 99.5% of healthy individuals, 85.2% of cirrhosis cases, and 86.3% of hepatitis cases ([138]Figure 6B). For a more detailed analysis of diagnostic accuracy in cirrhosis, we examined the recall rates across different Child-Pugh stages. The model accurately predicted all patients classified under Child-Pugh stage C, 89.7% of those in stage A, and 73.3% of those in stage B ([139]Figure 6C). This demonstrates the model’s high accuracy in predicting cirrhosis in various stages. We also assessed the diagnostic accuracy of HCC patients, stratifying them according to AFP and DCP. The model showed a sensitivity of 88.1% among AFP-negative HCC patients (AFP <7) and 86.5% for DCP-negative patients (DCP <40) ([140]Figures 6D and 6E). In comparison, the diagnostic performance of AFP and DCP alone in HCC patients across various disease stages, tumor sizes, and dimensions was consistently inferior to that of the miRNA classifier model ([141]Figures 6F–6H). Notably, the miRNA model exhibited a positive detection rate of 85.7% in early-stage HCC patients classified under Barcelona Clinic Liver Cancer (BCLC) staging system, while both AFP and DCP showed positive detection rates of only 14.3%. These compelling results underscore the significant clinical value of the EV-miRNA ratio signature, demonstrating sustained efficacy even in early-stage HCC cases. Figure 6. [142]Figure 6 [143]Open in a new tab Performance evaluation of the miRNA model under various clinical factors (A) Logistic regression model prediction probability scores for a cohort of 606 individuals, showing scores for various clinical factors and miRNA expression ratios. (B) Predictions for benign liver tumors, cirrhosis, hepatitis, and health populations. (C) Predictions for cirrhosis patients categorized by Child-Pugh class A, B, and C. (D) Predictions for HCC patients categorized by AFP levels (<7 μg/L, 7–400 μg/L, and >400 μg/L). (E) Predictions for HCC patients categorized by DCP levels (<40 μg/L, ≥40 μg/L). (F) Predictions for HCC patients categorized by BCLC stages (0, A, B, C, and D) using miRNA, AFP, and DCP model, respectively. (G) Predictions for HCC patients categorized by tumor count (1, 2, and ≥3) using miRNA, AFP, and DCP model, respectively. (H) Predictions for HCC patients categorized by tumor size (<3 cm, 3–5 cm, 5–10 cm, and ≥10 cm) using miRNA, AFP, and DCP model, respectively. Each model’s performance is based on multiple biological replicates. Discussion In this study, we developed an approach for efficiently extracting and enriching Fu-EVs, characterized by high throughput, rapidity, and user-friendly operation, rendering it suitable for clinical biomarker detection. Using this extraction methodology, we isolated Fu-EVs from the serum of 276 individuals and analyzed their miRNA expression profiles using NGS. This extensive dataset enabled comparative analysis of Fu-EVs miRNA expression patterns across diverse groups, including patients diagnosed with HCC, cirrhosis, hepatitis, benign hepatic tumor, and healthy individuals. Moreover, we developed a highly accurate logistic regression model based on a three-miRNA ratio signature, enabling precise differentiation between HCC patients and non-HCC controls. The model underwent rigorous validation through RT-qPCR over multiple cohorts, comprising 779 individuals. Despite the varied strategies developed for profiling EV composition,[144]^36 the development of efficient and high-throughput isolation methods remains a persistent technical challenge. In clinical practice, altered glycosylation patterns within glycoproteins and glycoconjugates are valuable serological biomarkers for cancer diagnosis.[145]^37^,[146]^38 EVs secreted by cancer cells are enriched with diverse aberrant glyco-signatures, including mannose, complex type N-glycans, polylactosamine, and sialylated glycans,[147]^36 making them promising targets for affinity purification. Therefore, we introduced a method for isolating Fu-EVs from serum samples using a fucose-specific lectin. Compared to UC, our GlyExo-Capture method preserves EV morphology, offers a broader size distribution, and enhances purity. Moreover, its rapid processing time and high throughput represent a significant advance in EV isolation, facilitating its potential streamlined clinical application. Our investigation reveals a heightened prevalence of glycosylated EVs in liver cancer cells relative to their healthy counterparts ([148]Figure 1F). Furthermore, tumor cells exhibit a significantly increased uptake rate of glycosylated EVs relative to non-glycosylated EVs ([149]Figures 1 and [150]S2). These findings highlight the pronounced inclination of liver cancer cells toward both the secretion and uptake of glycosylated EVs. Prior research has uncovered the role of surface proteins on both EVs and recipient cells in facilitating EV uptake.[151]^39 Therefore, we postulate that glycosylated EVs exert a more profound influence on the initiation and progression of liver cancer. This is supported by the promising diagnostic outcomes achieved using miRNA derived from Fu-EVs as biomarkers for HCC diagnosis in our study. miRNAs play a pivotal role in maintaining biological processes essential for homeostasis, significantly contributing to the balance necessary for liver function.[152]^40 Consequently, miRNAs, particularly those within EVs well-preserved by bilayer membranes, emerge as promising candidates for the early-stage diagnostic of various malignancies.[153]^12^,[154]^41 In this study, we developed classifier models integrating an Fu-EVs-derived three-miRNA ratio signature with AFP and/or DCP, employing logistic regression, random forest, support vector classification (SVC), and multilayer perceptron (MLP) algorithms ([155]Figures 5 and [156]S9–S11; [157]Tables S3–S6). Among these models, logistic regression demonstrated the highest performance, followed by random forest, while MLP and SVC showed relatively poorer performance, particularly in the cohort from the First Medical Center of Chinese PLA General Hospital. The area under the precision-recall curve for SVC models was notably lower by approximately 10 percentage points compared to logistic regression and random forest. Our results showed superior performance of the miRNA-based model compared to models using AFP/DCP features alone ([158]Figures 5 and [159]S9; [160]Tables S3–S6). While integrating miRNAs with AFP or DCP marginally improved performance, simultaneous integration did not produce additional enhancement. Notably, the miRNA model effectively identified a substantial proportion of AFP-negative HCC patients, complementing AFP’s detection and reducing false negatives. Our comprehensive analysis, encompassing diverse clinical parameters, exhibited robust predictive capabilities across different cohorts, with particular efficacy observed in early-stage HCC diagnosis according to the BCLC staging criteria ([161]Figure 6F). Lower prediction scores in HCC samples were related to DCP-negative statuses and smaller tumor burdens. Notably, the favorable predictive performance of the miRNA model in tumors outside of HCC suggests a robust specificity of the three-miRNA ratio signature for HCC. These findings underscore the clinical significance and robustness of our miRNA-based diagnostic model, especially for early-stage HCC detection. In conclusion, our study presents Fu-EVs-derived miRNA signatures developed using our innovative EV capture method tailored for identifying HCC patients. The validated three-miRNA ratio signatures underwent rigorous validation across multiple independent cohorts, including HCC patients and non-HCC controls. When combined with AFP expression levels, our classifier model exhibited enhanced diagnostic performance compared to routine clinical assessment relying solely on AFP. Notably, our miRNA biomarkers demonstrated clinical relevance by accurately characterizing AFP-negative HCC patients, highlighting their potential as reliable and non-invasive biomarkers for early detection of HCC. Limitations of the study Although our HCC diagnosis model has been validated in three distinct cohorts, prospective cohort studies are also crucial for confirming the utility of these biomarkers in early diagnosis within real-world clinical settings. Such studies will enhance the credibility and clinical feasibility of our findings. Additionally, a comparative analysis of the miRNA-based model with established clinical biomarkers and imaging techniques in prospective cohorts is essential. This approach will provide a comprehensive evaluation of the model’s diagnostic accuracy and clinical relevance, facilitating its potential integration into routine clinical practice and improving patient management. Resource availability Lead contact Further information and requests for resources and reagents should be directed to and will be fulfilled by the lead contact, Qi Gao (gaoqi@youngen.net.cn). Materials availability Serum or RNA generated in this study are available from the [162]lead contact with a completed Materials Transfer Agreement (some samples are depleted). Glycosylated Exosome Extraction Kits are available for purchase from Hotgen Biotech. Data and code availability Messager RNAseq data generated during the current study are available from the NCBI’s Gene Expression Omnibus database (GEO: [163]GSE266634 ). The scripts used for machine learning modeling are available on Zendo ([164]https://doi.org/10.5281/zenodo.13182532). Any additional information required to reanalyze the data reported in this work is available from the [165]lead contact upon request. Acknowledgments