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Gene & Protein in Disease                                                 A pan-cancer analysis of HMGB1




            Table 2. Expression/mutation of HMGB1 among different tumor types and its function
             Cancer       Gene expression   Survival   Genetic variation  Protein phosphorylation  Immune infiltration
             types
            CHOL               ↑
            COAD               ↑
            ESCA               ↑
            HNSC               ↑              ↑                                                      ↑
            LIHC               ↑
            LUSC               ↑
            READ               ↑
            STAD               ↑
            BLCA               ↑
            GBM                ↑
            KIRC               --             ↓
            THCA               --
            PCPG               --
            CESC               --             ↑
            KICH               ↓
            LUAD               ↓              ↑                                 ↓
            PRAD               ↓
            DLBC               ↑
            LGG                ↑
            PAAD               ↑
            THYM               ↑              ↓                                                      ↓
            OV                 ↑
            BRCA               ↓                                                ↓                    ↑
            UCEC               ↓                             ↓                  ↓
            ACC                               ↑
            SARC                              ↑
            MESO                                                                                     ↑
            TGCT                                                                                     ↑
            ↑: Tumor-promoting effect; -- : Insignificant correlation; ↓: Tumor-suppressing effect.
            CHOL: Cholangiocarcinoma; COAD: Colon adenocarcinoma; ESCA: Esophageal carcinoma; HNSC: Head and neck squamous cell carcinoma;
            LUSC: Lung squamous cell carcinoma; STAD: Stomach adenocarcinoma; LIHC: Liver hepatocellular carcinoma; READ: Rectum adenocarcinoma;
            BLCA: Bladder urothelial carcinoma; GBM: Glioblastoma multiforme; KIRC: Kidney renal clear cell carcinoma; CESC: Cervical squamous
            cell carcinoma and endocervical adenocarcinoma; THCA: Thyroid carcinoma; PCPG: Pheochromocytoma and paraganglioma; KICH: Kidney
            chromophobe; LUAD: Lung adenocarcinoma PRAD: Prostate adenocarcinoma; DLBC: Diffuse large B-cell lymphoma; LGG: Lower grade glioma
            PAAD: Pancreatic adenocarcinoma; THYM: Thymoma; OV: Ovarian cancer; BRCA: Breast cancer; ACC: Adrenocortical carcinoma; UCEC: Uterine
            corpus endometrial carcinoma; MESO: Mesothelioma; SARC: Sarcoma; TGCT: Testicular germ cell tumors

            in different tumors may suggest different potential   and THYM. This is similar to what other studies have
            mechanisms and functions. We also found that high   found . However, Huang  et al. revealed that HMGB1
                                                                    [34]
            HMGB1 expression may predict the poor OS for patients   overexpression was significantly correlated with poor
                                                                                          [35]
            with ACC and LUAD. These results indicate that HMGB1   prognosis  of  patients  with  BLCA .  These  findings  may
            can be used as a biomarker to predict the prognosis of   suggest that HMGB1 expression is not the same across
            tumor patients.                                    various kinds of tumors. Based on the characteristics
                                                               of each tumor, high or low expression of HMGB1 may
              We discovered that the low expression of HMGB1 was   provide a useful reference for the clinical treatment of
            related to poor OS in some TCGA tumors, such as KIRC   tumor patients.


            Volume 2 Issue 1 (2023)                         10                        https://doi.org/10.36922/gpd.301
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