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Tumor Discovery                                                    Prognostic biomarkers in pancreatic cancer



            demonstrated the accuracy of the prognostic model. PAAD   have not been fully elucidated. In the future, the accuracy of
            patients were divided into a low-risk group and a high-risk   this model will be verified with more experiments to explore
            group according to the median prognostic risk level. It was   the role of lncRNA and its interaction with m6A.
            found that the high-risk group had poorer survival than
            the low-risk group. The model validation results of clinical   5. Conclusion
            grouping showed that the model we constructed was   Understanding the mechanism of m6A-related lncRNA in
            more suitable for patients who are 65 years old and below,   the development of PAAD may provide new ideas for the
            female patients, and PAAD patients with tumor stage I and   prognosis and treatment of pancreatic cancer patients. Our
            II. Multivariate Cox regression analysis showed that the   study provides new clues and ways for survival prediction
            m6A-related lncRNAs prognostic model was an own risk   in PAAD patients and may help to elucidate the process
            factor for survival. ROC analysis showed that the model   and mechanism of regulation between m6A and lncRNA.
            outperformed traditional clinical features in predicting
            survival in PAAD patients. In addition, a nomogram was   Acknowledgments
            constructed  showing  the  agreement  between  the  1-,  3-,
            and 5-year prognostic model prediction rates for PAAD   We would like acknowledge TCGA for the dataset we
            patients. In terms of the accuracy of the prognostic model   extracted.
            based on m6A-related lncRNAs in predicting patient   Funding
            survival, the prediction model can provide a certain basis
            for subsequent research to identify new biomarkers.  No external funding was received for this work.
              TMB is the total number of somatically encoded mutations   Conflict of interest
            associated with the emergence of neoantigens that trigger
            antitumor immunity [23,24] . Studies have reported that patients   The authors declare that the research was conducted in the
            with low-risk endometrial cancer have higher TMB and are   absence of any commercial or financial relationships that
            more sensitive to chemotherapy than patients with high-risk   could be construed as a potential conflicts of interest. The
            scores . Here, we found that TMB in the low-risk group was   authors declare that they have no conflicts of interest.
                [25]
            lower than that in the high-risk group and then performed a
            survival analysis of TMB, finding that the low – TMB group   Author contributions
            had better survival than the high TMB group. Risk scores   Conceptualization: Yiyang Chen, Xi Ou
            were used for survival analysis and found that patients with   Formal analysis: Yiyang Chen, Yiju Gong
            low TMB and low-risk scores had better survival. However,   Writing – original draft: Yiyang Chen, Wanbang Zhou
            our prognostic model showed that there was no significant   Writing – review & editing: Yiyang Chen, Yiju Gong
            difference between high- and low-risk groups when receiving
            immunotherapy in the analysis of immune escape and   All authors contributed to the article and approved the
            immunotherapy, which is probably due to limited samples.   submitted version.
            More samples can be used in future studies. The tumor   Ethics approval and consent to participate
            microenvironment can regulate the biological properties
            of tumor cells such as chemotherapy resistance through   Not applicable.
            metabolism and other means. Six drugs with significantly
            different estimated IC50s were screened out between the   Consent for publication
            high-  and low-risk groups. The low-risk group was found   Not applicable.
            to be more sensitive to most potential drugs, the discovery
            of which may provide new insights into the subsequent   Availability of data
            treatment of patients with PAAD ideas. Pathological   The datasets presented, in this study, can be found in online
            stage is a decisive factor for the diagnosis and prognosis of
            PAAD . The current staging is not precise in providing   repositories. The names of the repository/repositories and
                 [26]
            reliable predictions and reflecting the heterogeneity of PAAD.   accession number(s) can be found in the article.
            Therefore, it  is critical to  explore new  potential  predictive   References
            markers and immunotherapeutic agents. The m6A-related
            lncRNA prognostic model established in this paper provides   1.   Yan Q, Ni C, Lin Y, et al., 2021, ELK1 enhances pancreatic
            a  new  idea  for  predicting  the  survival  of  PAAD  patients.   cancer progression via LGMN and correlates with poor
            However, there are some shortcomings and limitations in this   prognosis. Front Mol Biosci, 8: 764900.
            study, the biological mechanisms of m6A-related lncRNAs      https://doi.org/10.3389/fmolb.2021.764900


            Volume 1 Issue 2 (2022)                         13                      https://doi.org/10.36922/td.v1i2.165
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