The role of SRGN in the survival and immune infiltrates of skin cutaneous melanoma (SKCM) and SKCM-metastasis patients

BMC Cancer. 2020 May 5;20(1):378. doi: 10.1186/s12885-020-06849-7.

Abstract

Background: Skin cutaneous melanoma (SKCM) is one of most aggressive type of cancers worldwide. Serglycin (SRGN) is an intracellular proteoglycan that playing an important role in various tumors. However, its effect on immune infiltrates and whether it associates with survival of SKCM and SKCM-metastasis patients has not been explored.

Methods: We evaluated SRGN expression via the databases of Oncomine, Tumor Immune Estimation Resource (TIMER) and Gene Expression Profiling Interactive Analysis (GEPIA). The influence of SRGN expression on survival of SKCM and SKCM-metastasis patients was analyzed using TIMER database. Furthermore, the correlations between SRGN expression and immune infiltrates or gene marker sets of immune infiltrates were also analyzed via TIMER database.

Results: We found that the expression of SRGN in SKCM and SKCM-metastasis tissues was significantly increased compared to the normal skin tissues (P < 0.001). Interestingly, it was showed that lower level of SRGN expression and lower immune infiltrates of B cell, CD8+ T cell, Neutrophil, and Dendritic cell were correlated with poor survival rate of SKCM and SKCM-metastasis patients (P < 0.001) but not SKCM primary patients. We also demonstrated that SRGN expression was positively associated with the immune infiltrates and diverse immune marker sets in SKCM and SKCM-metastasis.

Conclusions: Our findings indicated that SRGN was associated with the survival of SKCM and SKCM-metastasis patients. SRGN may be a new immune therapy target for treating SKCM and SKCM-metastasis.

Keywords: Immune infiltrates; SKCM; SKCM-metastasis; SRGN; Survival.

MeSH terms

  • B-Lymphocytes / immunology
  • Biomarkers, Tumor / immunology
  • Biomarkers, Tumor / metabolism*
  • CD8-Positive T-Lymphocytes / immunology
  • Databases, Genetic / statistics & numerical data
  • Epithelial-Mesenchymal Transition*
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Melanoma / immunology
  • Melanoma / metabolism
  • Melanoma / mortality*
  • Melanoma / pathology
  • Melanoma, Cutaneous Malignant
  • Neoplasm Metastasis
  • Prognosis
  • Proteoglycans / genetics
  • Proteoglycans / metabolism*
  • Skin Neoplasms / immunology
  • Skin Neoplasms / metabolism
  • Skin Neoplasms / mortality*
  • Skin Neoplasms / pathology
  • Skin Neoplasms / secondary
  • Survival Rate
  • Tumor Microenvironment / immunology
  • Vesicular Transport Proteins / genetics
  • Vesicular Transport Proteins / metabolism*

Substances

  • Biomarkers, Tumor
  • Proteoglycans
  • Vesicular Transport Proteins
  • serglycin