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Updated: Jul 1, 2025

Experimental Metastasis and CTL Adoptive Transfer Immunotherapy Mouse Model
Published on: November 26, 2010
SPINK5 inhibits esophageal squamous cell carcinoma metastasis via immune activity
Jie Chen1, Juncheng Lu2, Zhiqiang Chen3
1Department of Oncology, Jiangyin People's Hospital, Jiangyin Clinical College of Xuzhou Medical University, Jiangyin Hospital Affiliated to Nantong University, Jiangyin, Jiangsu, China.
Background:
Esophageal squamous cell carcinoma (ESCC) is a predominant subtype of esophageal cancer with relatively high mortality worldwide. Serine peptidase inhibitor Kazal-type 5 (SPINK5) is reported to be downregulated in ESCC. However, its explicit role in ESCC remains further investigation.
Methods:
The tumor tissues and adjacent non-cancerous tissues were obtained from 196 patients with ESCC for the determination of SPINK5 mRNA levels. Additionally, the relationship between SPINK5 mRNA levels and clinicopathological features of ESCC patients was explored. The effects of SPINK5 on the invasion and migration of ESCC cells were assessed using Transwell assays. Furthermore, SPINK5 mRNA and LEKTI protein were measured in ESCC cell lines after treatment with poly (I:C), lipopolysaccharide (LPS) or unmethylated CpG DNA. Moreover, the correlation between expression of SPINK5 and nuclear factor-kappa B (NF-κB) signaling pathway-related genes was analyzed in the TCGA-ESCC cohort, and the effects of SPINK5 on NF-κB transcription was analyzed using a luciferase reporter gene assay. Finally, the correlations between SPINK5 and infiltration of immune cells, immune scores, stromal scores and ESTIMATE (i.e., Estimation of STromal and Immune cells in MAlignant Tumor tissues using Expression data) scores were explored.
Results:
SPINK5 mRNA levels were downregulated in tumor tissues, which was significantly correlated with higher lymph node metastases. Overexpressed SPINK5 inhibited cell invasion and migration in ESCC cell lines. Mechanistically, LPS-induced activation of Toll-like receptor 4 (TLR4) decreased SPINK5 mRNA and LEKTI in KYSE150 and KYSE70 cells. Spearman correlation analysis revealed that SPINK5 mRNA was significantly negatively correlated with a total of seven NF-κB signaling pathway-related genes in TCGA-ESCC patients. Moreover, downregulation of SPINK5 increased and upregulation of SPINK5 decreased the activity of the NF-κB promoter in HEK293T cells. Finally, immune cells infiltration analysis revealed that SPINK5 was significantly correlated with the infiltration of various immune cells, stromal scores, immune scores and ESTIMATE scores.
Conclusions:
SPINK5 plays critical roles in the TLR4/NF-κB pathway and immune cells infiltration, which might contribute to the ESCC metastasis. The findings of the present study may provide a promising biomarker for the diagnosis and treatment of esophageal squamous cell carcinoma.
Insights
Serine peptidase inhibitor Kazal-type 5 (SPINK5) is downregulated in esophageal squamous cell carcinoma (ESCC), inhibiting metastasis. SPINK5 influences the TLR4/NF-κB pathway and immune cell infiltration, offering potential diagnostic and therapeutic insights for ESCC.
Area of Science:
- Oncology
- Molecular Biology
- Immunology
Background:
- Esophageal squamous cell carcinoma (ESCC) is a significant cause of cancer mortality.
- Serine peptidase inhibitor Kazal-type 5 (SPINK5) is observed to be downregulated in ESCC.
- The precise function of SPINK5 in ESCC requires further elucidation.
Purpose of the Study:
- To investigate the role of SPINK5 in ESCC.
- To explore the relationship between SPINK5 expression and clinicopathological features.
- To determine the impact of SPINK5 on ESCC cell invasion, migration, and the underlying molecular pathways.
Main Methods:
- SPINK5 mRNA levels were quantified in tumor and adjacent non-cancerous tissues from 196 ESCC patients.
- Transwell assays assessed the effects of SPINK5 on ESCC cell invasion and migration.
- Mechanisms involving Toll-like receptor 4 (TLR4), nuclear factor-kappa B (NF-κB) signaling, and immune cell infiltration were analyzed.
Main Results:
- SPINK5 mRNA was downregulated in ESCC tissues and correlated with increased lymph node metastasis.
- Overexpression of SPINK5 suppressed ESCC cell invasion and migration.
- SPINK5 negatively correlated with NF-κB pathway genes and modulated NF-κB promoter activity, while influencing immune cell infiltration and ESTIMATE scores.
Conclusions:
- SPINK5 plays a crucial role in the TLR4/NF-κB pathway and immune cell infiltration in ESCC.
- These functions of SPINK5 may contribute to ESCC metastasis.
- SPINK5 presents potential as a biomarker for ESCC diagnosis and treatment.
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