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Gene & Protein in Disease                                        Pyroptosis-related LncRNAs in pediatric AML




            A                                                        B





















            C                                D                          E


















            Figure 11. Decision curve and nomogram. (A) A nomogram with gender, race, BM, PB, WBC, age, FAB category, and risk score. (B) 1-, 3-, and 5-year
            calibration curves. (C–E) Decision curves at 1, 3, and 5 years. BM: Bone marrow leukemic blast percentage (%); PB: Peripheral blasts (%); WB: White
            blood cell at diagnosis.


            and inhibition of NF-κB in AML CD34+cells . In a study   The low- and high-risk groups were separated according
                                                [41]
            on gastric cancer, researchers have found that NF-κB can   to the median risk score of the training set. Patients
            be stimulated by strengthening the expression of TRIM37   in the two groups showed noticeably distinct clinical
            through  ASB16-AS1 .  AC127496.5, on the other hand,   characteristics, prognosis, TME, immune checkpoint
                            [42]
            has been found to be one of the predictors of response   expressions, MSI level, and drug susceptibility. The high-
            to anti-PD-1 therapy for patients with cancer other than   risk group was characterized by poorer prognosis, lower
            AML . Unfortunately, we have not found the mechanism   immune checkpoint expressions, MSI-L/MSS, and lower
                [43]
            of the other three lncRNAs; thus, more research is needed   drug susceptibility. Interestingly, we found that one of the
            to ascertain their potential roles.                immune checkpoints, TIM-3, played a different role from
                                                               others both in the risk groups and the three clusters. In
              Seven PR-lncRNAs  were  used  to  construct  the   the previous studies, researchers have found that TIM-3
            pediatric AML prognostic signature, and the expression   may be different in AML and other leukemias; also, its
            levels of those genes were calculated using risk scores.   representations may not be the same in different FAB
            The AUC of the training set was 0.671, 0.676, and 0.665   categories. Studies have also found that TIM-3 played
            at  1,  3,  and  5  years,  respectively.  Similar  results  were   a different role in acute promyelocytic leukemia (M3)
            obtained for the testing set in validating the model. The   compared with other cases [44,45] . However, we were
            prediction model has a considerable effect on the survival   unable to find any association with M3 in our study. The
            prediction of pediatric AML patients, and the prognostic   molecular mechanisms involved in the different outcomes
            signature has a great predictive ability for these patients.   need to be further explored. As expected, the TME differed


            Volume 2 Issue 1 (2023)                         14                     https://doi.org/10.36922/gpd.v2i1.230
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