The ERO1L mRNA expression in pan-cancer was analyzed in the Oncomine database (www.oncomine.org) with the following thresholds: p-value of 0.001, a fold change of 1.5, and a top 10% gene ranking (11). The expression data belonging to four datasets (GSE7670, GSE31210, GSE32863, and GSE19188) were downloaded from the GEO database (https://www.ncbi.nlm.nih.gov/geo/). Expression profiles were normalized by z-scores of log₂(count+1). Using the limma package in R-4.0.3, batch normalization was also completed. Protein expression levels were analyzed using the HPA database (http://www.proteinatlas.org). Antibodies used in the HPA database included HPA026653 (Sigma-Aldrich), HPA030053 (Sigma-Aldrich) and CAB034294 (Santa Cruz Biotechnology). These three antibodies were all validated by orthogonal method (antibody staining mainly consistent with RNA expression data across 41 tissues) and by independent antibodies (protein distribution across 45 tissues similar between the independent antibodies HPA026653 and HPA030053).

TCGA LUAD data was downloaded from the UCSC Xena database (http://xena.ucsc.edu/). This data included information on: RNA-seq (HTSeq-FPKM), DNA methylation (Illumina Human Methylation 450), and clinical profiles (including both phenotype and survival data). Expression levels were normalized using the z-score of log₂(FPKM+1) to exclude potential bias. Patients were assigned into ERO1L-high and ERO1L-low groups based on the median expression value according to the RNA sequencing data. In terms of methylation analysis, we included 18 methylation sites ( Table S4 ). These sites were mapped to the ERO1L gene using the UCSC Genome Browser HG19 RefSeq database (http://genome.ucsc.edu). The methylation level of each CpG site was recorded as a β value. This value indicated the ratio of the methylated signal intensity over the sum of the methylated and unmethylated intensities at each locus. Each locus with an average β-value of less than 0.20 was considered a hypomethylation site. In addition, Kaplan-Meier survival curves were plotted to show differences in survival time. For this data, log-rank p-values reported in the survival package in R-4.0.3 were used to determine statistical significance. Path analysis was performed in the ggalluvial in R-4.0.3. Visualization was performed using the OriginPro 2019b software (version 9.6.5.169).

Mouse lung tissue was carefully dissected avoiding other tissue contamination, then minced with surgical scalpels and incubated in Trypsin (Gibco) at 37°C for 40-50 min. The digestion was terminated with 10% serum (Gibco), and digested tissues were filtered with a 70 μm cell strainer in order to filter out debris that had not been fully digested. Cells were resuspended with Matrigel (Corning) and plated in 48 well plates. Then the Matrigel was solidified in an incubator at 37°C for 15-20 min and overlaid with 150-200 μL medium. Organoid medium contains advanced DMEM/F12, FGF 100 ng/mL, EGF 10 ng/mL, B27 supplement (2 X final), N2 supplement (1 X final), Noggin 100 ng/mL, RSPO-1 (10% final), Wnt-3a (10% final), Y27632 10 μM,A83-01 10 μM, Glutamax (1 X final) and Penstrep (1 X final). Cultures were kept at 37°C, 5% CO2 in an incubator and the medium was exchanged every 4-8 days according to the number of spheres. For passaging, the Matrigel containing organoids was dissolved in 3-5 mL TrypLE at 37°C for 10 min, and pipetted vigorously (80-100 times) to dissociate organoids into single cells. Cells were filtered with 70 μm cell strainer, centrifuged at 1,500 rpm for 10 min and resuspended with Matrigel.

Organoids were dissociated into single cells as described above, resuspended with 200 μL medium ae well as 2-3 mL virus particles, and added polybrene to 1 X final. After being centrifuged at 2,000 rpm, 37°C for 1 hour, the cells were then incubated at 4°C, 5% CO₂ for 2-3 hours. Finally, an organoid culture was performed as described above.

Firstly, genes which were co-expressed were identified in the Oncomine and TCGA databases respectively. By overlapping the results from these two databases, we identified a co-expression module consisting of 17-genes. STRING (version 10.5) was used to construct a protein-protein interaction (PPI) network. The 17 genes within the module were subjected to pathway enrichment analysis using DAVID (https://david-d.ncifcrf.gov/) (12). Results were visualized using the Hmisc and ggplot2 packages in R-4.0.3. Gene set enrichment analysis (GSEA) was performed using the GSEA software (version 4.1.0) and Broad’s GSEA algorithm (13).

The relationship between ERO1L expression levels and immune infiltration was initially determined using the TIMER2.0 database (http://timer.comp-genomics.org). The TIMER2.0 database utilizes immunedeconv, which is an R package integrating six state-of-the-art algorithms. These algorithms include: TIMER, xCell, MCP-counter, CIBERSORT, EPIC, and quanTIseq (14). These algorithms were systematically benchmarked, and each was found to have unique properties and strengths. ERO1L expression was analyzed in the presence of seven types of immune infiltrating cells, including B cells, CD4⁺ T cells, CD8⁺ T cells, NK cells, macrophages, CAFs, and MDSCs. During immune infiltration analysis, adjustments were also made for tumor purity. The online tool CIBERSORTx (https://cibersortx.stanford.edu) was used to estimate different immune cell proportions (15).

Correlation analysis between the expression of ERO1L, immune cell markers and cytokines as well as chemokines was also performed using the TIMER2.0 database, specifically using the Gene_Corr module. The functionality of this module allows users to uncover the co-expression pattern of genes across TCGA cancer types. When provided with one initial gene of interest and up to 20 other genes, the TIMER2.0 database generates a heatmap table of Spearman’s correlation of gene expression between the gene of interest and the other input genes. After adjustment for tumor purity, a Spearman’s ρ >0 with p-value <0.05 was considered as a positive correlation and a Spearman’s ρ <0 with p-value <0.05 was considered as a positive correlation. Secondary confirmation of correlation analysis was performed using GEPIA (http://gepia.cancer-pku.cn) (16). Tertiary confirmation of correlation analysis was performed using TCGA expression data from the GEPIA database (http://gepia.cancer-pku.cn/index.html).

Processed gene expression data was download from the GEO database (GSE99254). This project consists of deep single-cell transcriptome data with complete T cell receptor information, which identified multi-dimensional characteristics of infiltrating lymphocytes (17). Single-cell transcriptome data was analyzed based on t-SNE dimension reduction using the R package Rtsne. Additionally, the Tumor Immune Single-cell Hub (TISCH) database was used to analyze the correlations between ERO1L expression and infiltrating immune cells (18). TISCH is a scRNA-seq database focusing on the tumor microenvironment. This database includes 79 datasets and 2,045,746 cells. TISCH provides detailed cell-type annotation at the single-cell level, enabling detailed exploration of the tumor microenvironment across various different cancer types.

In the first instance, in order to estimate the presence of the various immune cell populations in the LUAD tissues, the R package ESTIMATE was used. Estimation of STromal and Immune cells in MAlignant Tumor tissues using Expression data (ESTIMATE) is a tool that predicts tumor purity via the use of gene signatures. The tool calculates three scores, including stromal score, which predicts the presence of stromal cells in tumor bulk; immune score, which infers the levels of immune cells infiltration in tumor tissue; and estimate score, which estimates tumor purity. Subsequently, the R package MCPcounter was used to develop a more detailed idea of the level of immune cell infiltration. Microenvironment Cell Populations-counter (MCPcounter) is a quantification method that determines the relative abundance of an immune cell in heterogeneous tissues. This method uses marker genes optimized for interrogating microarray data (19). In order to predict the response to immune checkpoint blockade, Tumor Immune Dysfunction and Exclusion (TIDE) score was employed. TIDE is a computational method used to model two primary mechanisms of tumor immune evasion. These mechanisms are: the induction of T cell dysfunction in tumors with high infiltration of cytotoxic T lymphocytes (CTL) and the prevention of T cell infiltration in tumors with low CTL level (20, 21). Using this framework and RNA-Seq tumor expression profiles, TIDE can predict the outcomes of non-small cell lung cancer (NSCLC) patients treated with first-line anti-PD1 or anti-CTLA4 more accurately than other biomarkers such as PD-L1 levels and mutational load.

Chi-squared and Fisher’s exact tests were used to investigate the significance of the correlation of ERO1L expression with clinicopathological features in LUAD patients. Analysis was performed using SPSS (version 23.0). ANOVA was used to identify the ERO1L expression levels in different datasets (22). The correlation of gene expression was evaluated using Spearman’s correlation coefficient (23). A p value <0.05 was considered statistically significant.

In order to determine the mRNA expression profile of ERO1L in pan-cancer, expression levels of ERO1L in the Oncomine database were analyzed. Comparisons of mRNA expression levels of ERO1L in pan-cancers versus normal tissue identified nine types of cancer in which ERO1L mRNA expression levels were elevated. These types of cancer included bladder, brain, central nervous system, colorectal, gastric, kidney, lung, lymphoma, ovarian, and pancreatic cancer. In addition, three types of cancer in which ERO1L mRNA expression levels were diminished were identified. These types of cancer included esophageal cancer, head and neck cancer, and leukemia ( Figure 1A ). What’s more, lung cancer was found to be associated with a significantly higher expression level of ERO1L in comparison to normal tissue. The expression levels of ERO1L were increased in seven datasets while no dataset possessed decreased levels of ERO1L.

To further investigate the mRNA expression levels of ERO1L in pan-cancers, RNA-sequencing data from The Cancer Genome Atlas (TCGA) program was analyzed. Interestingly, it was discovered that ERO1L mRNA expression levels were somewhat increased in pan-cancers in comparison to normal tissues ( Figure 1B ). This finding is consistent with our analysis of data from the Oncomine database, which revealed significantly elevated expression levels of ERO1L in lung adenocarcinoma (LUAD; p <0.001) and in lung squamous cell carcinoma (LUSC; p <0.001).

In order to study the mRNA expression levels of ERO1L in LUAD, further analysis was performed on datasets from the Gene Expression Omnibus (GEO) database. In this analysis, four datasets (GSE7670, GSE31210, GSE32863, and GSE19188) comprising a total of 526 samples were included. This included 356 tumoral and 170 paired normal biopsies ( Table S1 ). After normalizing the expression profile, it was identified that ERO1L mRNA expression levels in LUAD was significantly elevated in comparison to normal tissues. This was observed in all of the datasets analyzed. Interestingly, expression fold changes ranged from 2.8 to 4.1 times ( Figures 1C and S1A ). In addition, the mRNA expression of ERO1L in LUAD was investigated using the TCGA program. Similarly, significantly elevated expression levels of ERO1L mRNA were observed in LUAD in comparison to normal tissues. This was observed when the analysis was performed using both TCGA program and the Genotype-Tissue Expression (GTEx) program ( Figure S1B ).

These elevated ERO1L mRNA expression levels were confirmed in LUAD. As a logical next step, the protein expressions of ERO1L in LUAD were then investigated. Analysis using The Human Protein Atlas (HPA) program revealed that ERO1L was positively detected via immunohistochemistry (IHC) staining in patients with LUAD. Eleven patients with LUAD were identified in the HPA database, all of these patients possessed positive ERO1L protein expression ( Figures 1D–G ). Out of these patients, the intensity of IHC staining is as follows: three patients were associated with strong intensity, six with moderate, and two with weak intensities of IHC staining ( Table S2 ).

In order to study the correlation between ERO1L expression and prognosis in LUAD patients, six cohorts of patients were obtained from the PrognoScan database ( Table S3 ). Via the analysis of hazard ratios (HR) and 95% confidence intervals (CI), four cohorts of LUAD patients (HLM, Nagoya, UM, and NCCRI) with high expression of ERO1L were identified. This high expression of ERO1L was associated with worsened prognoses in these patients as measured by overall survival (OS) and recurrent-free survival (RFS). Similarly, analysis was performed on survival data from the Kaplan-Meier plotter database. This is based on the Affymetrix microarrays with probe ID 218498_s_at for the ERO1L gene. These results showed consistently that overexpression of ERO1L was associated with worse prognoses in patients with LUAD in terms of OS (HR: 1.52, 95% CI: 1.27-1.82; Figure 2A ) and RFS (HR: 1.93, 95% CI: 1.47-2.53; Figure 2B ).

The following hypothesis was proposed: ERO1L is a potential biomarker in patients with LUAD. To investigate this hypothesis, survival analysis was applied to the RNA-sequencing data obtained from the TCGA program. This analysis revealed that there was a significant correlation between ERO1L overexpression, shorter overall survival (HR: 2.20, 95% CI: 1.71-2.56; Figure 2C ) and disease-free survival (HR: 1.43, 95% CI: 1.10-1.79; Figure 2D ). Interestingly, via correlation and multiple linear regression analysis, it was found that the expression level of ERO1L correlated with specific clinicopathological characteristics in LUAD patients ( Figure 2E ). As shown in Table 1 , ERO1L overexpression was significantly correlated with tumor recurrence, pathologic N stage, primary treatment outcome, tumor histology, and tumor stage.

Furthermore, we applied an organoid model to study the biological function of ERO1L. We designed a protocol for organoid infection through dissociating organoid spheres into single cells and then co-culturing with virus particles. By introducing cDNA encoding ERO1L (labeled with mCherry) into organoids (labeled with eGFP), we obtained ERO1L-overexpressed organoids labeled in different colors. Organoids would turn red when transduced with cDNA, indicating the overexpression of ERO1L ( Figure 2F ). Using this, we detected infected organoids and calculated the ratios of chimeric organoids from passage 1 to 4. The initial percentage of chimeric organoids was about 16%, and it gradually increased to 75% after passaging three times ( Figure 2F ). Besides, the doubling time of organoid cells decreased from five to six days at passage 1 to two to two and a half days at passage 4. Transduction of cDNA of ERO1L in organoids was also performed. One thousand cells in each group were seeded and cultured for fourteen days (passage 2). Sphere formation was enhanced from cells overexpressing ERO1L compared with the control ( Figure 2G ). Hence, we concluded that organoids with ERO1L overexpression gradually gained an advantage in development, which could be extended over time.

In order to elucidate the mechanism underlying ERO1L expression, promoter methylation levels of ERO1L were investigated in 503 samples. This was performed via analysis of methylation profiles (Illumina Human Methylation 450) from the TCGA program ( Table S4 ). A significant decrease in the methylation level of the ERO1L was identified in the promoter region in LUAD tissues in comparison to normal tissues ( Figure 3A ). Tumor stage subgroup analysis revealed that levels of ERO1L promoter methylation were most significantly decreased in stage IV patients ( Figure 3B ). In addition, correlation analysis revealed a significant negative correlation between mRNA levels and methylation levels of ERO1L (Spearman’s ρ: -0.25, p <0.001). This confirmed that ERO1L mRNA expression was regulated by promoter methylation in LUAD patients ( Figure S1C ).

In order to analyze the clinical outcomes associated with methylation and expression of ERO1L, datasets of 468 patients in the TCGA database were analyzed. These datasets all contained data corresponding to methylation, expression, and survival profiles. Path analysis via a Sankey diagram was performed. This quantified and visualized the transitions with various lines and widths, and described paths and patterns across tumor stages, promoter methylation levels, ERO1L mRNA expression, and survival status ( Figure 3C ). As a result, it was determined that hypomethylation of the ERO1L promoter potentially induced overexpression of ERO1L mRNA and finally led to poor prognoses in individuals with LUAD. This pattern was observed more significantly in patients with advanced stages of cancer ( Figure S2A ). This data is consistent with the survival analysis based on ERO1L expression. This provides compelling evidence that ERO1L is associated with poor prognoses in patients with LUAD.

In order to investigate proteins that were in close relationship to ERO1L, a co-expression analysis of expression data from the TCGA program and Oncomine database was conducted. Via overlapping co-expression results and module mining, 29 proteins were found to be closely related to ERO1L ( Figure S2B ). This included ERO1LB, GPX7, GPX8, P4HB, INS, PDIA3, PDIA4, PDIA6, TXNDC5, and ERP44 among others. ( Table S5 ). Based on these results, the protein-protein interaction (PPI) network of the ERO1L co-expression module was created ( Figure 3D , Table S6 ). Furthermore, the biological functions of the module were investigated by Gene Otology (GO) analysis ( Figure 3E ) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis ( Figure 3F ). Interestingly, it was found that these genes showed strong associations with significant processes such as response to endoplasmic reticulum stress, response to reactive oxygen species, oxidation-reduction process, and glycolytic process. Integrally, this module was shown to be closely related to hypoxia responses as well as the HIF-1 signaling pathway. These might also play a role in shaping the TIME.

To first understand the relationship between ERO1L and infiltrating immune cells, a correlation analysis across ERO1L and markers for immune cells was performed. These biomarkers are widely used for the purpose of immune cell characterization ( Table 2 ). ERO1L expression showed strong correlations with markers for infiltrating lymphocytes including regulatory T cells (T_regs), exhausted T cells, macrophages, tumor-associated macrophages (TAMs), myeloid-derived suppressor cells (MDSCs), and cancer-associated fibroblasts (CAFs), thus indicating infiltrations of immune-suppressive cells are mediated by ERO1L signaling ( Figure 4A ). Interestingly, ERO1L expression was shown to be positively correlated with the phenotype of M2-type macrophages while negatively correlated with the phenotype of M1-type macrophages. This implies that overexpression of ERO1L could indicate the polarization of M1-type to M2-type macrophage ( Figure 4B ).

To confirm whether ERO1L expression impacts the TIME, the coefficients of ERO1L expression and TIME infiltrations were calculated in the Tumor IMune Estimation Resource 2.0 (TIMER 2.0) database. In relation to tumor-infiltrating lymphocytes, it was found that immune-active cells including B cells (Spearman’s ρ=-0.250, p <0.001), CD8⁺ T cells (Spearman’s ρ=-0.299, p <0.001), and NK cells (Spearman’s ρ=-0.258, p <0.001) correlated negatively with ERO1L expression. After adjustments to account for tumor purity, immune-suppressive cells CAFs (Spearman’s ρ=0.286, p <0.001) and MDSCs (Spearman’s ρ=0.423, p <0.001) were shown to be positively correlated with ERO1L expression ( Figure 4C ).

As a positive correlation was observed between ERO1L and CD4⁺ T cells (Spearman’s ρ=0.199, p <0.001), intrinsic CD4⁺ T cell heterogeneity was further investigated via analysis of single-cell sequencing data from dataset GSE99254. Dimensional reduction analysis (t-SNE) applied to the expression data showed that ERO1L was highly expressed in most CD4⁺ T cell clusters. This was consistent with our previous findings ( Figure 4D ). The clusters of CD4-CTLA4 (cluster C9) and CD4-CXCL13 (cluster C7), representing suppressive T_regs and exhausted T cells respectively, showed the highest ERO1L expression levels. To further confirm ERO1L expression across infiltrating cells in TIME, single-cell sequencing data from four projects (GSE7670, GSE31210, GSE32863, and GSE19188) was analyzed. Results showed that ERO1L expression closely correlated with infiltrating cell levels including B cells, T cells, NK cells, endothelial cells, macrophages, monocytes, MDSCs, and CAFs ( Figure 4E , Figure S2C ). ERO1L was more closely associated with the phenotype of a M2 macrophage than a M1 macrophage, which was consistent with our previous findings.

Of note, MDSCs are known to play a key role in immunosuppression in various cancer types. In recent years, increasing evidence has highlighted MDSCs as a major driver behind the immunosuppressive tumor microenvironment. As C/EBPβ and c-Rel have been implicated in MDSC expansion, C/EBPβ and c-Rel expressions were examined. Consistent with previous findings, it was identified that both C/EBPβ and c-Rel were significantly positively correlated with ERO1L expression (C/EBPβ: Spearman’s ρ=0.144, p <0.001; c-Rel: Spearman’s ρ=0.201, p <0.001). This supports the notion that ERO1L signaling potentially results in the accumulation of functional MDSCs ( Figure S2D ). Based on the strong correlation observed between ERO1L and MDSCs, a survival analysis was performed by constructing a Cox proportional hazards model according to expression profiles of ERO1L and MDSC ( Figure 4F ). Results revealed that patients exhibiting low levels of both ERO1L and MDSCs experienced a significantly better OS in comparison to those with simultaneously high levels of ERO1L and MDSCs (HR:1.55, 95% CI: 1.12-1.84, log-rank p <0.001). This indicates that the combination of high levels of ERO1L and MDSC expression can predict poor prognoses in patients with LUAD. In tumors where the high expression level of ERO1L was a result of copy number variations including gain and amplification compared with deletion or normal diploid, significant differences were also noted. In specific cases there a decrease in CD8⁺ T cells and an increase of CAFs and macrophages ( Figures S2E, F ). Taken together, these results indicate that ERO1L overexpression is closely related to infiltration of immune-suppressive cells and the deficiency of immune-active cells, thus shaping an immunosuppressive TIME.

Based on the notion that ERO1L overexpression shaped an immune-suppressive TIME, it was hypothesized that high levels of ERO1L might also lead to immunotherapy resistance. Given that the MC-38 cell line was sensitive to ICI treatment while the LLC and A549 cell lines were relatively insensitive to ICI treatment, we first performed Western blotting to examine the expression levels of ERO1L protein across these cell lines. Results showed that ERO1L protein was overexpressed in the LLC and A549 cell lines while downregulated in the MC-38 cell line ( Figure S3A ), which was consistent with our hypothesis that overexpression of ERO1L might be associated with resistance to ICI treatment.

To further investigate this hypothesis, the stromal and immune cell infiltration levels were analyzed within ERO1L ^low and ERO1L ^high samples using ESTIMATE software. Low expression of ERO1L was accompanied with a higher abundance of stromal cells and immune cells in comparison to overexpression of ERO1L, which was associated with a significantly higher Estimate score. This suggested that an immune-inflamed TIME that may well be susceptible to immunotherapy ( Figure 5A ). To explore this issue in more detail, the Tumor Immune Dysfunction and Exclusion (TIDE) score was used. This score is a computational framework designed to evaluate the potential of tumor immune escape and is a surrogate biomarker to predict response to immunotherapy. TIDE scores showed that the ERO1L ^low group had a significantly higher response rate (86.0%) in comparison to the ERO1L ^high group (31.0%) ( Figures 5B, C ). It was also observed that the ERO1L ^high group scored high in MDSCs (p <0.001) and immune dysfunction (p <0.001), while scored low in CD8⁺ T cells (p <0.001) in comparison with the ERO1L ^low group ( Figure 5D ). To validate these results, the MCP counter was applied to quantify the different immune cell populations within the two groups. In agreement with our results, ERO1L overexpression scored low in NK cells (p <0.001), myeloid dendritic cells (p <0.001), neutrophils (p <0.001), and endothelial cells (p <0.001). ERO1L overexpression scored high in B lineage (p =0.004), monocyte lineage (p =0.020), and fibroblast (p <0.001; Figure S3B ). These results suggest that ERO1L is in fact a biomarker with potential applications in the prediction of immunotherapy response in patients with LUAD.

Gene set enrichment analysis (GSEA) was performed in order determine whether the transcriptional signature produced by ERO1L overexpression was significantly related to other previously studied conditions. By using hallmark gene sets and all curated gene sets as references, GSEA was performed between the ERO1L ^low group and ERO1L ^high group in patients from the TCGA cohort. The global expression changes produced in LUAD patients were positively correlated with the signatures of hypoxia (NES =2.02; FDR q-value =0.0) and VEGF (NES =2.27; FDR q-value =0.0; Figure 6A ). Moreover, GSEA also revealed that the gene signatures of the JAK-STAT (NES =1.65, FDR q-value =0.0) and NF-κB (NES =2.03, FDR q-value =0.0; Figure 6B ) signaling pathways were commonly enriched when ERO1L signaling was upregulated. The expression levels of the components involved in the two pathways were examined, including JAK1, JAK2, STAT1, STAT2, STAT3, NF-κB1, NF-κB2, RelA, RelB, and c-Rel. Consistent with previous findings, there were significant correlations observed between ERO1L overexpression and the aforementioned components ( Figure 6C ).

As the JAK-STAT and NF-κB pathways have previously been reported to play a role in increasing the secretion of immune-suppressive factors, we further explored whether ERO1L expression could affect the pattern of cytokines and chemokines secreted by tumor cells and infiltrating immune cells, which play a role in shaping TIME. Via TCGA expression profiling analysis, it was identified that cytokines and chemokines secreted by tumors (such as CSF-1, IL-1β, and IL-6), which have been reported to recruit immune-suppressive cells including MDSCs, TAMs, and CAFs, were positively correlated with overexpression of ERO1L ( Figure 6D ). Moreover, it was also identified that immune-suppressive cytokines and chemokines (including IL-10, TGF-β, MMP2, MMP9, and VEGF), which are known to be mostly secreted by immune-suppressive cells, were simultaneously in a positive correlation with overexpression of ERO1L. Taken together, these data suggest a potential mechanism for ERO1L-associated immune-suppressive TIME ( Figure 6E ).