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. 2023 Dec 26;25(1):331. doi: 10.3390/ijms25010331

Table 1.

Clinicopathological role of SHP-1 in tumors.

Tumor Type Reported Findings Predicted Function Refs
Acute myeloid leukemia SHP-1 expression was negatively correlated with the overall survival of leukemia patients. Oncogenic [39]
Breast cancer SHP-1 expression is inversely correlated with pSTAT3 and positively correlated with recurrence-free survival in patients. Tumor suppressive [33]
According to the TCGA database, high expression of SHP-1 was associated with better overall survival. Tumor suppressive [34]
Higher SHP-1 expression associated with better overall survival. Tumor suppressive [35]
Colorectal cancer The survival time of patients with high SHP-1 expression is shorter than those of patients with low SHP-1 expression. Oncogenic [40]
Esophageal squamous cell carcinoma Negative correlation with the tumor-node metastasis staging system, pathological differentiation, and lymph node metastasis: The downregulation and hypermethylation of SHP-1 are associated with poor survival. Tumor suppressive [20]
Glioblastoma Upregulation of SHP-1 in GBM patients according to TCGA analysis.
High expression of SHP-1 was associated with advanced grade and poor overall survival of glioma.
Oncogenic [41]
Hepatocellular carcinoma Downregulation of SHP-1 in hepatocellular carcinoma (HCC) is negatively correlated with tumor growth and overall survival in patients with HCC and hepatitis B virus infection. Tumor suppressive [36]
Prostate cancer A decreased SHP-1 expression is associated with higher proliferation rates and increased risk of recurrence or progression-free survival after radical prostatectomy for localized prostate cancer. Tumor suppressive [37]