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               ·1228 ·                           南 京    医 科 大 学 学         报                        2025年9月


               A            Control    PARP1⁃WT   PARP1⁃K192A       B           **       D    2.5
                                                                       (A.U.)  0.8
                  p⁃ERK1/2                                  42 kDa      1.0   ***  ***       (A.U.)  2.0
                   GAPDH                                    37 kDa                           level  1.5
                                                                       level  0.6
               C                                                        0.4                   1.0
                                                                       p⁃ERK1/2               0.5
                            Control    PARP1⁃WT   PARP1⁃K192A                                ERK1/2
                   ERK1/2                                   42 kDa      0.2
                                                                         0                     0
                                                                                                    PARP1⁃K192A
                   GAPDH                                    37 kDa                              Control
                                                                          Control PARP1⁃K192A     PARP1⁃WT
                                                                            PARP1⁃WT
                 A,B:Western blotting and quantification showed that PARP1 over expression significantly decreased p⁃ERK1/2. C,D:Western blotting showed
                                                                                             **
              the protein levels of ERK1/2 in Control,PARP1⁃WT,and PARP1⁃K192A were identical,with GAPDH as an internal control. P < 0.01 and  *** P < 0.001
             (n=3).
                                               图9 PARP1过表达降低p⁃ERK1/2水平
                                         Figure 9 PARP1 overexpression decreased p⁃ERK1/2


                  Author’s Contributions:                            cer:Mechanisms in tumour biology and therapeutic poten⁃
                  SU Ning was the primary charger in most of the experi⁃  tials[J]. Clin Transl Med,2024,14(11):e70070
              ments,data collection and analysis,CAO Ying did many funda⁃  [8] ZHANG D,TANG Z Y,HUANG H,et al. Metabolic regu⁃
              mental jobs(clinical sample collection,pan⁃PTM screen,etc);  lation of gene expression by histone lactylation[J]. Na⁃
              ZHANG Shuping made substantial contribution;YING Xiaoyan,  ture,2019,574(7779):575-580
              YANG Lili,and ZHANG Dong designed the research;All others  [9] JIANG J,HUANG D L,JIANG Y,et al. Lactate modu⁃
              assisted in some of the experiments. ZHANG Dong wrote the  lates cellular metabolism through histone lactylation⁃me⁃
              manuscript with the assistance of SU Ning. YING Xiaoyan and  diated gene expression in non⁃small cell lung cancer[J].
              YANG Lili proofread and gave advice. All authors read and ap⁃  Front Oncol,2021,11:647559
              proved the final manuscript.                      [10]LI F,ZHANG H H,HUANG Y,et al. Single⁃cell transcrip⁃
                                                                     tome analysis reveals the association between histone lac⁃
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