Migrasome-related prognostic signature TSPAN4 correlates with immune infiltrates and metabolic disturbances in hepatocellular carcinoma
- PMID: 39799524
- DOI: 10.1007/s00535-025-02212-4
Migrasome-related prognostic signature TSPAN4 correlates with immune infiltrates and metabolic disturbances in hepatocellular carcinoma
Abstract
Background: We aim to comprehensively analyze and validate the prognostic efficacy of tetraspanin 4 (TSPAN4) and several other migrasome-related markers in hepatocellular carcinoma (HCC).
Methods: The expression, diagnostic, and prognostic efficacy of five migrasome-related genes in HCC were analyzed using several databases. Five pairs of adjacent non-tumor tissues and HCC tissues were used to validate the expression. The prognostic efficacy of TSPAN4 was validated in a HCC cohort. TSPAN4 was knocked down in Huh-7 cells, EdU, and CCK-8, and wound healing assays were conducted to analyze its effects on cell proliferation and migration. In addition, transcriptomic sequencing was used to identify differentially expressed genes.
Results: Compared with those in normal tissues, four genes (TSPAN4, PIGK, NDST1, and CPQ) were elevated in liver hepatocellular carcinoma (LIHC), but not TSPAN7. Of these, only elevated TSPAN4 predicted unfavorable prognosis of HCC patients. The expression and prognostic efficacy of TSPAN4 were further confirmed in a HCC cohort (97 patients); and patients in the TSPAN4high group showed unfavorable overall survival (log-rank P = 0.0055). Functional analysis showed that TSPAN4 knockdown significantly suppressed cell migration, but not cell proliferation. Moreover, TSPAN4 knockdown induced disturbances of the metabolic pathways, mainly pentose and glucuronate interconversions.
Conclusions: TPSAN4 is a promising prognostic and therapeutic target for HCC treatment and may be involved in the metabolic pathways that affect disease progression.
Keywords: Hepatocellular carcinoma; Metabolic; Migrasome; Prognosis; Tetraspanin 4.
© 2025. Japanese Society of Gastroenterology.
Conflict of interest statement
Declarations. Conflict of interest: None.
Similar articles
-
TSPAN4+ fibroblasts coordinate metastatic niche assembly through migrasome-driven metabolic reprogramming and stromal-immune crosstalk in pancreatic adenocarcinoma.Front Immunol. 2025 May 15;16:1594879. doi: 10.3389/fimmu.2025.1594879. eCollection 2025. Front Immunol. 2025. PMID: 40443671 Free PMC article.
-
Migrasome-related ITGA5 for predicting prognosis, immune infiltration and drug sensitivity of hepatocellular carcinoma.Apoptosis. 2025 Jun;30(5-6):1424-1439. doi: 10.1007/s10495-025-02103-2. Epub 2025 Mar 27. Apoptosis. 2025. PMID: 40146484
-
CD151-enriched migrasomes mediate hepatocellular carcinoma invasion by conditioning cancer cells and promoting angiogenesis.J Exp Clin Cancer Res. 2024 Jun 6;43(1):160. doi: 10.1186/s13046-024-03082-z. J Exp Clin Cancer Res. 2024. PMID: 38840183 Free PMC article.
-
Integrated analysis and experimental validation reveal the prognostic and immunological features associated with coagulation in hepatocellular carcinoma.Sci Rep. 2025 Mar 13;15(1):8626. doi: 10.1038/s41598-025-85491-4. Sci Rep. 2025. PMID: 40074769 Free PMC article.
-
Migrasome regulator TSPAN4 shapes the suppressive tumor immune microenvironment in pan-cancer.Front Immunol. 2024 Dec 11;15:1419420. doi: 10.3389/fimmu.2024.1419420. eCollection 2024. Front Immunol. 2024. PMID: 39723210 Free PMC article.
Cited by
-
TSPAN4+ fibroblasts coordinate metastatic niche assembly through migrasome-driven metabolic reprogramming and stromal-immune crosstalk in pancreatic adenocarcinoma.Front Immunol. 2025 May 15;16:1594879. doi: 10.3389/fimmu.2025.1594879. eCollection 2025. Front Immunol. 2025. PMID: 40443671 Free PMC article.
References
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous