A decrease in the efficacy of photodynamic therapy (PDT) with phthalocyanine photosensitizers was observed for lymphoblastic murine and human cell lines as the time between the addition of the photosensitizer, aluminum phthalocyanine (AIPc), to the culture medium and exposure to light was increased from 4 h to 18 h. The total intracellular concentration of photosensitizer did not decrease significantly during this 18 h interval. For the murine cell lines, the maximum cytotoxic and mutagenic effects were observed when the time between addition of the photosensitizer and irradiation was between 1 and 4 h. The time course of the variations in efficacy did not vary greatly from one murine cell line to another, even though the cell lines differ markedly in the extent of their cytotoxic and mutagenic response. The time course of the variation was similar for cytotoxicity and mutagenicity, as well as for the induction of DNA fragmentation. The human lymphoblastic cell line, WTK1, showed less variation in survival and mutability with time than did the murine cell lines. With Pc 4 (HOSiPcOSi[CH3]2[CH2]3N[CH3]2) as the photosensitizer, the photocytotoxicity for murine L5178Y (LY)-S1 cells did not change significantly as the time between addition of Pc 4 and irradiation was increased from 2 to 18 h. However, the mutagenicity decreased by a factor of three during this interval. The mutagenicity of PDT with Pc 4 was much less in LY-S1 cells than that with AlPc. The results suggest that the variation in the efficacy observed for AlPc-induced photocytotoxicity is caused by changes in the intracellular distribution and/or the aggregation of the photosensitizer with time after its addition.
TP53 mutations have been observed in diffuse large B-cell lymphoma (DLBCL), with a mean frequency of ~20%. Studies on TP53 mutations as prognostic markers have historically been controversial, and the results have not been consistent across different studies on DLBCL. Considering the complex pathophysiological mechanisms involved in DLBCL, we wondered whether the interaction of TP53 with other genetic variants could further promote the development of DLBCL, and thus be more prognostically predictive. Moreover, whether the genetic interactions between TP53 and other oncogenic mutations could shape the discrepant immune landscape in DLBCL remains unknown, as these genetic alterations usually drive the malignant phenotype and directly or indirectly affect the tumor microenvironment (TME) and support tumor survival. In this study, we performed a comprehensive analysis of the genomic characteristics of TP53 through high-throughput sequencing in patients with de novo DLBCL. Patients' characteristics are reported in Table S1. Detailed methods are provided in the Supplementary Material. A total of 227 significantly mutated genes were identified (Table S2), of which TP53 was the second most frequently mutated gene, with a rate of 30% (53 of 176) and 62 sequence variants detected. Among these variants, 74% (n = 46/62) were missense mutations, and the remaining were inactivating frameshift indels (n = 7), nonsense mutations (n = 3), coding sequencing indels (n = 4), and splicing mutations (n = 2). Mutation patterns and distributions are shown in Figure S1 and Table S3. Importantly, most mutations (56/64, 87.5%) occurred in exons 5–8, which encoded the DNA-binding domain (DBD) region of TP53 (Figure S1C,E). Codons 175, 273, and 248 of the p53 protein had the highest mutation frequency, which are also the hot spots of TP53 mutation found in most human cancers (Figure S1D). Given that the DBD of TP53 is the functional central core domain and mutations in this region potentially have a strong impact on TP53 function, we mainly focused on mutations in this region. Patients were divided into TP53-MUT and TP53-WT groups according to TP53 mutation status in the DBD region. There were no differences in the number of small deletions/insertions and single nucleotide variants (SNVs) between the TP53-MUT and TP53-WT groups (Figure S2). Moreover, the tumor mutation burden (TMB) was similar between the two groups (Figure S2E). Clinical relevance between TP53 mutation and clinicopathological characteristics, such as age, sex, B symptoms, stage, number of extranodal sites, performance status, LDH level, and International Prognostic Index was not observed (Table S4). Note that TP53 mutations significantly enriched in the GCB subtype (p = .033, Table S4). Among the 176 patients, 155 patients having the complete follow-up data were enrolled in the survival analysis. Overall, patients with TP53-MUT tended to have inferior overall survival compared with patients with TP53-WT (median: 92.3 versus 110.8 months, respectively, p = .17, Figure 1A), but it did not reach statistical significance. A subgroup analysis showed that the potential predictive value of TP53 mutations was mainly attributed to the GCB subtype (Figure S3). We next recognized the genomic variants that co-occur or are mutually exclusive with TP53. We observed that DDX3X, MYLK2, and FUT6 mutations co-occurred with TP53 mutations, and CD58 mutations were mutually exclusive with TP53 mutations (Figure 1B and Table S5). Specifically, patients were divided into four groups based on the mutation status of these genes. No significant difference was observed in survival among the three groups according to the combination of co-occurring mutation genes with TP53 (p = .37 for DDX3X; p = .11 for MYLK2; p = .54 for FUT6; Figure S4). However, we found that the combination of TP53 and CD58 mutations could significantly distinguish the prognosis of patients with DLBCL (p = .033, Figure 1C). Patients with both wild-type TP53 and CD58 had a better prognosis than patients with either of the two mutually exclusive modes of CD58 and TP53 mutations. Unexpectedly, patients with TP53 wild-type and CD58 mutations (TP53WT&CD58MUT) had worse survival than those with TP53 mutations and CD58 wild-type (TP53MUT&CD58WT). Because TP53 and CD58 mutations were mutually exclusive, only one patient harbored both TP53 and CD58 mutations, and the patient still alive at the last follow-up. The predictive value of TP53WT&CD58MUT group was also observed in patients with GCB-DLBCL (Figure S5). Moreover, the relationship of a mutually exclusive mutant between CD58 and TP53 and the prognostic significance of this interaction were validated using publicly available data from 1001 patients with DLBCL from the Duke University's cohort1 (Figure S6). We then explored whether the cooperation of the mutually exclusive mutations between TP53 and CD58 may profoundly influence the microenvironment in DLBCL. We found that the overall TMB was significantly higher in the TP53WT&CD58MUT group than in the TP53MUT&CD58WT group (p = .0177, Figure 1D), while there was no difference in TMB when dividing patients only according to TP53 mutation status (p = .5348, Figure S2E). In addition, the ESTIMATE immune scores in the TP53WT&CD58MUT group were significantly higher than that in the TP53MUT&CD58WT groups (p = .0047) (Figure 1D). Moreover, the exhausted T cell, macrophage cell, NK cell, and Th1 cell enriched in the TP53WT&CD58MUT group (Figure 1E). The difference between the two groups was mainly due to the combined influence of the mutation pattern "TP53WT&CD58MUT," but rather only affected by the CD58 mutations, given the immune cell infiltration was similar when dividing patients just according to CD58 mutation status (Figure S7). Furthermore, the co-inhibitory receptors such as PD-1, TIM3, and LAG3 were preferentially expressed in the TP53WT&CD58MUT group (Figure 1F and Table S6). However, there was no difference in the expression of co-stimulatory molecules (Table S6). Inhibitory immunomodulators were also significantly upregulated in the TP53WT&CD58MUT group when comparing with the TP53WT&CD58WT group (Figure S8), suggesting the unique immune phenotype in the TP53WT&CD58MUT group. The findings that high immune scores and abundant infiltrating exhausted T cells in the TP53WT&CD58MUT group were validated in an independent external cohort from the REMoDL-B trail (N = 400)2 (Figure S9 and Table S7). Finally, we investigated the differentially biological pathways between the TP53WT&CD58MUT and the TP53MUT&CD58WT groups. Five hundred differentially expressed genes were identified with a false discovery rate less than 0.05 and |log2foldchange| > 1. One hundred genes were significantly upregulated and 400 genes were significantly downregulated in the TP53WT&CD58MUT group (Figure 1G). Figure S10 presented the enriched gene ontology terms in the TP53WT&CD58MUT group, including cytokine and chemokine production, binding and activity, and interferon-γ pathways. GSEA showed significantly activated interferon-α and interferon-γ responses and IL-6/JAK/STAT3 signaling in the TP53WT&CD58MUT group (Figure 1H). The immune landscape of patients with TP53WT&CD58MUT harbored was summarized and conceptualized in Figure 1I. The value of TP53 gene alterations in predicting survival in DLBCL remains controversial, even in the era of sequencing. In the L.M. Staudt' study, four prominent genetic subtypes were identified based on the molecular classifications. Notably, TP53 was not significantly enriched in one of these subtypes, although TP53 was the much frequently mutated gene (25.2%). On the basis of this classification, L.M. Staudt and colleague further distinguished ST2, A53, and mixed subtypes, and the survival of A53, characterized by inactivation of TP53, was intermediate in this model.3 The C2 molecular subtype identified in Chapuy's study corresponding to A53 also showed a tendency for a poor prognosis.4 A subsequent study demonstrated that the impact of TP53 mutations on survival was relied on the genetic context of the lymphoma, conferring no effect in the SOCS1/SGK1 clusters and NOTCH2 subtype and inferior prognosis in the MYD88 subtype.5 These results demonstrated that TP53 alterations have limited ability to identify a subset of patients at high risk. DLBCL is highly molecular heterogeneity and there are still a proportion of patients who could not be accurately classified according to the existing molecular classifications. In this study, we found that patients with TP53WT&CD58MUT had the worst outcomes. Interestingly, this subtype of patients harbored enhanced immune escape capacity, giving the abundant infiltration of exhausted T cells and multiple upregulated inhibitory immunomodulatory molecules. Persistent interferon signaling could augment the expression of T-cell inhibitory immune checkpoints such as PD-1, TIM-3, and LAG-3 through JAK/STAT pathway.6 We found that interferon responses and JAK/STAT pathway enriched in the TP53WT&CD58MUT group. Moreover, inhibitory immunomodulatory molecules were preferentially expressed in this group. It suggests that interferon/JAK/STAT pathway-mediated up-regulated expression of inhibitory immunomodulatory molecules could be one potential mechanism through which the inactivation of CD58 facilitated immune evasion and accelerated tumor growth in DLBCL. Despite many of such immune dysregulations had an adverse prognosis; they provided new opportunities for anti-tumor immunotherapy of the subset of DLBCL patients with TP53WT&CD58MUT. Historically, the response rate to anti-PD-1/PD-L1 therapy in unselected DLBCL patients was generally low. Consequently, patients with TP53WT&CD58MUT may be optimal candidates for novel immunotherapy in clinical trials. In conclusion, our results suggest that TP53 mutation alone is insufficient to effectively differentiate the risk of DLBCL. The mutually exclusive patterns between TP53 and CD58 mutations accurately stratified patients with DLBCL to permit the optional immunotherapy. This study was supported by Natural Science Foundation of Tianjin grants (19JCYBJC26500 and 18JCZDJC45100), National Natural Science Foundation of China grants (81770213), Clinical Oncology Research Fund of CSCO grants (Y-XD2019-162 and Y-Roche20192-0097), The Science and Technology Research Program of Tianjin Education Commission (2019KJ191), National Key New Drug Creation Special Programs grants (2018ZX09201015), and National Human Genetic Resources Sharing Service Platform/Cancer Biobank of Tianjin Medical University Cancer Institute and Hospital grant (2005DKA21300). The authors thank the Marvel Medical Laboratory, Tianjin Marvelbio Technology Co., Ltd., for providing the assistance in next-generation sequencing and bioinformatics analysis. The authors declare no conflict of interest. Xianhuo Wang conceived and designed the study; Xianhuo Wang and Huilai Zhang supervised all aspects of research project and interpreted data; Tingting Zhang, Yaxiao Lu, and Xia Liu performed the research and statistical and bioinformatics analyses; Mengmeng Zhao performed the next-generation sequencing and bioinformatics analysis; Jin He, Xia Liu, Lanfang Li, Lihua Qiu, Zhengzi Qian, and Shiyong Zhou collected samples and clinical information; Bin Meng and Qiongli Zhai reviewed the diagnosis of DLBCL; Xianhuo Wang, Huilai Zhang, and Xiubao Ren provided the clinical samples and material support; Tingting Zhang wrote the manuscript and finalized the figures; Xianhuo Wang. and Huilai Zhang reviewed the manuscript. All authors read and approved the final version of the manuscript. DNA and RNA sequencing data have been submitted to the CNGB Sequence Archive of China National GeneBank DataBase (https://db.cngb.org/cnsa/) under the accession numbers CNP0001322 and CNP0001327, respectively. The mutation data of 1001 DLBCL patients from the Duke University's cohort were downloaded from cBioPortal (http://www.cbioportal.org/). The mutation and RNA expression data of the patients from the REMoDL-B trail were downloaded from the Supplementary Material from the publication. DNA and RNA sequencing data have been submitted to the CNGB Sequence Archive of China National GeneBank DataBase (https://db.cngb.org/cnsa/) under the accession numbers CNP0001322 and CNP0001327, respectively. The mutation data of 1001 DLBCL patients from the Duke University's cohort were downloaded from cBioPortal (http://www.cbioportal.org/). The mutation and RNA expression data of the patients from the REMoDL-B trail were downloaded from the Supplementary Material from the publication. Appendix S1 Supporting Information Figure S1. Mutation profile of the TP53 gene in diffuse large B-cell lymphoma. (A) Proportions of TP53 mutations according to the effect on the protein sequence. (B) Proportions of classified point mutations. (C) Distribution of mutation numbers according to TP53 exons. (D) Codon distribution of TP53 mutations. E. Mapping of the TP53 mutation sites Figure S2. TP53 mutation status and genomic instability at the individual nucleotide level. (A) The distribution of small deletion, small insertion, single nucleotide variant (SNV), and tumor mutation burden (TMB) in patients with TP53-MUT and TP53-WT. (B–E) Comparison of the number of small deletions, small insertions, SNVs, and TMB in patients with TP53-MUT and TP53-WT, respectively. Significance threshold was set at p < .05 Figure S3. Survival analysis by TP53 mutations in the molecular subtypes of diffuse large B-cell lymphoma (DLBCL). (A) Overall survival of patients with GCB-DLBCL with TP53 mutations. (B) Overall survival of patients with non-GCB-DLBCL with TP53 mutations Figure S4. Survival analysis by genomic alterations correlated with TP53 mutations in diffuse large B-cell lymphoma (DLBCL) patients. (A) Overall survival of DLBCL patients based on the mutation status of TP53 and DDX3X, MYLK2 (B) and FUT6 (C) Figure S5. Survival analysis by TP53 combined with CD58 in the molecular subtypes of diffuse large B-cell lymphoma (DLBCL). (A) Overall survival of DLBCL patients based on the mutation status of CD58 and TP53 in GCB subtype. (B) Overall survival of DLBCL patients based on the mutation status of CD58 and TP53 in non-GCB subtype Figure S6. Validation of mutually exclusive mutational patterns of TP53 and CD58 using a public data set from 1001 diffuse large B-cell lymphoma (DLBCL) patients. (A) CD58 mutations were mutually exclusive with TP53 mutations according to Fisher's exact test. (B) Overall survival in DLBCL patients according to the different mutational patterns of TP53 and CD58. (C) Overall survival in DLBCL patients, excluding the TP53MUT&CD58MUT mutational pattern due to the lower occurrence of co-mutations between TP53 and CD58 Figure S7. Comparison of immune infiltrating cells between the CD58 mutation group and CD58 wild-type group. *p < .05; NS, p > .05 Figure S8. Comparison of immunomodulatory molecule expression between the TP53WT&CD58MUT group and the TP53WT&CD58WT group Figure S9. Enhanced immune escape in the TP53WT&CD58MUT group in the external validation cohort from the REMoDL-B trail. (A) Comparison of ESTIMATE immune scores, tumor purity, and stromal scores between the TP53MUT&CD58WT and the TP53WT&CD58MUT groups. (B) Comparison of the exhausted CD8+ T cell abundance between the TP53MUT&CD58WT and the TP53WT&CD58MUT groups. (C) Comparison of the inhibitory immunomodulatory molecule expression between the TP53MUT&CD58WT and the TP53WT&CD58MUT groups. The adjusted p values were .076 for PDCD1, 0.009 for LAG3, 0.009 for HAVCR2, and 0.023 for IDO1, respectively Figure S10. Gene ontology analysis based on the significantly upregulated genes in the TP53WT&CD58MUT group. Selected and significantly enriched (FDR-adjusted p-value < .05) gene ontology annotations for biological processes and molecular functions are represented as dots Table S1. Clinicopathologic features of the 176 diffuse large B cell lymphoma patients enrolled in the study Table S2. List of the significantly mutated genes identified in our study Table S3. List of identified somatic non-silent mutations of TP53 in 53 DLBCL cases Table S4. Association of TP53 mutation statues and clinicopathologic parameters Table S5. Genes that are significantly co-mutated or mutually exclusive with TP53 mutations Table S6. Comparison of immunomodulatory molecule expression in the TP53WT&CD58MUT group versus the TP53MUT&CD58WT group Table S7. Comparison of immunomodulatory molecule expression in the TP53WT&CD58MUT group versus the TP53MUT&CD58WT group in the external cohort from the REMoDL-B trail Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
Photodynamic therapy, a novel cancer treatment using a photosensitive dye and visible light, produces an oxidative stress in cells, often leading to apoptotic cell death. Because ceramide is a second messenger that has been associated with stress-induced apoptosis, we investigated a possible link between photodynamic treatment (PDT), ceramide, and apoptosis in L5178Y-R (LY-R) cells. The cells undergo rapid apoptosis, initiating within 30 min of PDT. After a dose of PDT producing a 99.9% loss of clonogenicity, LY-R cells responded by an increased production of ceramide, which reached a maximum level in 60 min. For a constant light fluence and varying concentrations of the phthalocyanine photosensitizer Pc 4 [HOSiPcOSi(CH3)2(CH2)3N(CH3)2], the ED50 for ceramide generation (46 nM) was similar to the LD50 for clonogenic cell death (40 nM). We suggest that the PDT-stimulated increase in synthesis of ceramide in LY-R cells may be coupled to PDT-induced apoptosis. When the cells were exposed to exogenous N-acetyl-sphingosine (10 microM), apoptotic changes were observed only after 12-24 h. The delayed apoptotic response to the synthetic ceramide may be due to an induction of apoptosis by a different route than the one used by PDT.
// Peng Xu 1, * , Jie Yao 1, * , Jin He 1 , Long Zhao 1 , Xiaodong Wang 1 , Zhennan Li 1 , Jianjun Qian 1 1 Department of Hepatobiliary and Pancreatic Surgery, Northern Jiangsu People’s Hospital, Clinical medical college of Yangzhou University, Yangzhou city, Jiangsu Provence of P. R. China, 225001 * These authors have contributed equally to this work Correspondence to: Jie Yao, e-mail: docyao@126.com Keywords: CIP2A, pancreatic ductal adenocarcinoma, gemcitabine, prognosis, overall survival Received: November 03, 2015 Accepted: January 29, 2016 Published: February 17, 2016 ABSTRACT Cancerous inhibitor of protein phosphatase 2A (CIP2A) is an oncoprotein which participates in inhibiting tumor apoptosis in pancreatic cancer cells. Using immunohistochemical staining, we investigated the expression of CIP2A protein in 72 cases of human pancreatic ductal adenocarcinoma (PDAC) tissue and 27 cases of adjacent normal pancreatic tissue. The positive rate of CIP2A protein expression in pancreatic cancer tissue was70.83 %, which was significantly higher than that in adjacent non- cancerous pancreatic tissue (11.11%). The expression of CIP2A was found to be correlated with TNM stage, but not correlated with age, gender, tumor location, smoking status, alcohol consumption, diabetes, high blood pressure, BMI, tumor size, lymph node metastasis or distant metastases. Kaplan- Meier survival analysis showed that patients with positive CIP2A protein expression had a lower overall survival rate than patients without CIP2A expression. COX regression analysis indicated that expression of CIP2A was an independent prognostic factor for pancreatic ductal adenocarcinoma. In addition, down-regulation of CIP2A inhibited cell proliferation and increased sensitivity to gemcitabine in pancreatic cancer cells by decreasing AKT signaling pathway. Our results indicated that down-regulation of CIP2A could be a novel therapeutic strategy for pancreatic cancer
Mouse lymphoma L5178Y-R cells respond to photodynamic therapy (PDT) by undergoing rapid apoptosis, which is induced by PDT-activated signal transduction initiating in the damaged cellular membranes. To relate the level of PDT damage and photosensitizer to the mechanism of cell death, apoptosis has been detected by agarose gel electrophoresis of fragmented DNA and quantified by flow cytometry of cells after staining with Hoechst33342 and propidium iodide, a technique which can distinguish between live, apoptotic, and necrotic cells. When the silicon phthalocyanine Pc 4 or Pc 12 served as photosensitizer, lethal doses (as defined by clonogenic assay) of PDT induced apoptosis in essentially all cells, whereas supralethal doses prevented the characteristic degradation of DNA into oligonucleosomal fragments. In contrast with aluminum phthalocyanine (AlPc) cells died by apoptosis after all doses studied. It appears that high PDT doses with Pc 4 or Pc 12 damage enzymes needed to carry out the program of apoptosis; the absence of this effect with AlPc suggests either a different intracellular location or different photocytotoxic mechanism for the two photosensitizers.
The mantle cell lymphoma (MCL) International Prognostic Index (MIPI) and combined MIPI (MIPI-c) are commonly used for risk classification of MCL patients. However, these indexes lack immune-related parameters. The purpose of this study was to develop a novel prognostic model that integrated clinical and immune parameters. A total of 189 patients with newly diagnosed MCL from January 2010 to June 2020 were enrolled in our study. A nomogram and immune-related prognostic index (IRPI) were established to predict the overall survival (OS) of patients according to univariate and multivariate analyses. Discrimination and calibration were used to compare the prognostic performance of the IRPI, MIPI, and MIPI-c. External validation was performed based on validation dataset (n = 150) from two other centers. The results for the training dataset indicated that B symptoms, platelet count, B2M level, CD4+ T-cell count<26.7% and CD8+ T-cell count>44.2% were predictors for OS. All the prognostic factors were integrated into the nomogram. For the overlap of confidence intervals of each variable, we assigned one point for each factor. The IRPI categorized patients into three risk categories: a score of zero indicated low risk, a score of one or two indicated intermediate risk, and a score of ≥3 indicated high risk. The IRPI showed better discrimination and calibration power than the MIPI and MIPI-c in the training dataset and validation dataset. The novel IRPI is a refined risk stratification index and reflects the strong complementary prognostic effects between clinical and immune parameters in MCL.
Follicular lymphoma (FL), the most common indolent lymphoma, is a clinically and genetically heterogeneous disease. However, the prognostic value of driver gene mutations and copy number alterations has not been systematically assessed. Here, we analysed the clinical-biological features of 415 FL patients to identify variables associated with disease progression within 24 months of first-line therapy (POD24). Patients with B symptoms, elevated lactate dehydrogenase and β2-microglobulin levels, unfavourable baseline haemoglobin levels, advanced stage, and high-risk FL International Prognostic Index (FLIPI) scores had an increased risk of POD24, with FLIPI being the most important factor in logistic regression. HIST1H1D, identified as a driver mutation, was correlated with POD24. Gains of 6p22.2 (HIST1H1D) and 18q21.33 (BCL2) and loss of 1p36.13 (NBPF1) predicted POD24 independent of FLIPI. Gene expression profiling of FL samples showed that the POD24 cohort was significantly enriched in the inflammatory response (mediated by interferon and tumour necrosis factor), cell cycle regulation (transcription, replication and proliferation) sets and PI3K-AKT-mTOR signalling. This result was further validated with transcriptome-wide information provided by RNA-seq at single-cell resolution. Our study, performed on a large cohort of FL patients, highlights the importance of distinctive genetic alterations and gene expression relevant to disease diagnosis and early progression.
Abstract Early diagnosis of liver fibrosis is critical for early intervention and prognosis of various chronic liver diseases. Conventional repeated histological assessment is impractical due to the associated invasiveness. In the current study, we evaluated circulating miR-185 as a potential biomarker to predict initiation and progression of liver fibrosis. We found that miR-185 was significantly up-regulated in blood specimens from patients with HBV-liver fibrosis and rats with liver fibrosis, the miR-185 levels were correlated with liver fibrosis progression, but not with the different viral loads in HBV-infected patients. miR-185 was observed in collagen deposition regions during advanced liver fibrosis. We found that differences in miR-185 levels facilitated the discrimination between early-staged or advanced-staged liver fibrosis and the healthy controls with high specificity, sensitivity, and likelihood ratio using receiver-operator characteristic analysis. miR-185 targeted SREBF1, and increased expression of COL1A1 and a-SMA genes that are hallmarks of liver fibrosis. Our data supported that circulating miR-185 levels could be used as potential biomarkers for the early diagnosis of liver fibrosis.
Psoriasis is a complex chronic inflammatory skin disease. The aim of this study was to analyze potential risk genes and molecular mechanisms associated with psoriasis.GSE54456, GSE114286, and GSE121212 were collected from gene expression omnibus (GEO) database. Differentially expressed genes (DEGs) between psoriasis and controls were screened respectively in three datasets and common DEGs were obtained. The biological role of common DEGs were identified by enrichment analysis. Hub genes were identified using protein-protein interaction (PPI) networks and their risk for psoriasis was evaluated through logistic regression analysis. Moreover, differentially methylated positions (DMPs) between psoriasis and controls were obtained in the GSE115797 dataset. Methylation markers were identified after comparison with the common genes.A total of 118 common DEGs were identified, which were mainly involved in keratinocyte differentiation and IL-17 signaling pathway. Through PPI network, we identified top 10 degrees as hub genes. Among them, high expression of CXCL9 and SPRR1B may be risk factors for psoriasis. In addition, we selected 10 methylation-modified genes with the higher area under receiver operating characteristic curve (AUC) value as methylation markers. Nomogram showed that TGM6 and S100A9 may be associated with an increased risk of psoriasis.This suggests that immune and inflammatory responses are active in keratinocytes of psoriatic skin. CXCL9, SPRR1B, TGM6 and S100A9 may be potential targets for the diagnosis and treatment of psoriasis.
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