
Cancer Letters, Journal Year: 2024, Volume and Issue: unknown, P. 217278 - 217278
Published: Sept. 1, 2024
Language: Английский
Cancer Letters, Journal Year: 2024, Volume and Issue: unknown, P. 217278 - 217278
Published: Sept. 1, 2024
Language: Английский
Digestive and Liver Disease, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 1, 2025
Language: Английский
Citations
1Heliyon, Journal Year: 2025, Volume and Issue: unknown, P. e42237 - e42237
Published: Jan. 1, 2025
Language: Английский
Citations
0OncoTargets and Therapy, Journal Year: 2025, Volume and Issue: Volume 18, P. 161 - 177
Published: Feb. 1, 2025
Background: Cancer remains a major global health challenge, with early detection and prompt treatment being crucial for reducing mortality rates. The SPINK4 has been linked to the development of several tumors, there is growing evidence its involvement. However, specific functions effects in different cancer types remain unclear. Methods: association between expression levels tumor progression was investigated confirmed using TCGA dataset. Kaplan-Meier curves were utilized examine correlation survival outcomes pan-cancer patients. Pearson method employed investigate microenvironment, stemness score, immunoinfiltrating subtype, chemotherapy sensitivity human types. Wound healing Transwell assays performed confirm roles model gene colon adenocarcinoma cells. Results: shows heterogeneity across tissues, closely associated poor prognosis, immune cell invasion, resistance, metastasis various cancer. Mutation hold significant predictive value prognosis In addition, significantly correlated microenvironment (stromal cells cells) score (DNAss RNAss) particularly BLCA COAD. Single-cell sequencing analysis showed that mainly expressed endothelial malignant Drug resistance drugs. Importantly, overexpression promoted lines (HCT116 RKO), whereas knockout markedly inhibited their metastasis. Conclusion: These findings reveal role process may have implications diagnosis future. Keywords: analysis, infiltration, genetic alteration, single-cell sequencing, drug
Language: Английский
Citations
0Current Tissue Microenvironment Reports, Journal Year: 2025, Volume and Issue: unknown
Published: April 12, 2025
Language: Английский
Citations
0Frontiers in Immunology, Journal Year: 2025, Volume and Issue: 16
Published: May 5, 2025
TNFRSF12A is abnormally expressed in various malignancies, especially stomach adenocarcinoma (STAD), which related to tumor invasiveness and prognosis of patients. This study examined the expression pattern STAD predicted immunotherapy response. Data were derived from The Cancer Gene Atlas (TCGA), Expression Omnibus (GEO), Profiling Interactive Analysis (GEPIA) analyze pan-cancer STAD, as well its correlation with clinical features. Biological pathways involved analyzed by "clusterProfiler" package. Immune cell infiltration was evaluated "GSVA" "CIBERSORT" packages. Immunotherapy response assessed TIDE score mutation burden (TMB) level. level single scRNA-seq. Finally, vitro test detected mRNA cells, Wound healing Transwell assays performed measure capabilities migrate invade. highly STAD. However, did not shown significant difference relation exhibited notably positive many carcinogenic signaling immune cells such T macrophages. High group showed a higher score, Exclusion TMB than low group, indicated that patients high responded more poorly immunotherapy. most checkpoint genes. By scRNA-seq analysis, chiefly Fibroblasts Mast Further, verified migration invasion suppressed silencing (p<0.05). present only reveals potential therapeutic target for but also explores great finding opens up new way thinking personalized treatment
Language: Английский
Citations
0Cancer Letters, Journal Year: 2024, Volume and Issue: unknown, P. 217278 - 217278
Published: Sept. 1, 2024
Language: Английский
Citations
2