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Tumor Discovery                                                    Prognostic biomarkers in pancreatic cancer




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            Figure 3. (A) Risk score distribution based on m6A-related lncRNAs prognostic model. (B) Different survival status and survival time of high-risk and
            low-risk groups. (C) Cluster analysis heatmap showing the expression criteria of 5 prognosis-related lncRNAs for each patient. (D) Kaplan–Meier survival
            curves of patients in high-risk and low-risk groups.

            package in the R studio software was used to assess the   when receiving immunotherapy. The half maximal inhibitory
            mutation frequencies of the high-risk and low-risk groups   concentration (IC50) of compounds obtained from the
            in the model. Principal component analysis (PCA) which   GDSC website Genomics of Drug Sensitivity in Cancer
            is used for efficient dimensionality reduction, model   (https://www.cancerrxgene.org/) in the TCGA project of
            identification, and grouping of high-dimensional data of   the PAAD dataset were calculated to obtain potential drugs
            whole gene expression profiles, m6A genes, m6A-related   for clinical use in PAAD treatment. IC50s of compounds
            lncRNAs,  and  risk  models  based  on  gene  expression   obtained from the GDSC website were predicted in PAAD
            patterns visualization was performed. Kaplan–Meier   patients using the pRRophetic package in R studio software.
            survival analysis was then used to assess the diversity of   2.7. Construction and validation of the nomogram
            survival between high- and low-risk groups. The R packages
            survminer and survival are the tools used for this research.  The predictive power of nomogram and other predictors (age,
                                                               gender, risk score, TNM stage, T stage, N stage, and M stage)
            2.6. Analysis of prognostic models and screening of   for 1-, 3-, and 5-year survival was set. A calibration curve based
            potential drugs                                    on the Nomogram-predicted test was applied to illustrate the
                                                               agreement between actual and model-predicted results.
            Multivariate  and  univariate  Cox  regression  analyses
            were performed to test whether the prognostic model   3. Results
            was an independent variable considering other clinical
            characteristics  of  PAAD  patients  (sex,  age,  tumor  grade,   3.1. Identification of m6A-associated lncRNAs in
            and tumor stage). Analyses of immune evasion and   PAAD patients
            immunotherapy were also performed to find out whether   The matrix expression of 23 m6A genes and 14,056 lncRNAs
            there were differences between high- and low-risk groups   was extracted from the TCGA database. Two hundred and


            Volume 1 Issue 2 (2022)                         5                       https://doi.org/10.36922/td.v1i2.165
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