MiR-183-5p inhibitor promotes mitoxantrone-induced immunogenic death of hepatoma cells by targeting STC1

This study aimed to unravel the regulatory mechanism of the microRNA (miR)-183-5p/STC1 axis in regulating mitoxantrone (MIT)-induced immunogenic cell death (ICD) within hepatocellular carcinoma (HCC) cells and assess its therapeutic potential. Dual-luciferase reporter assays were employed to validate that miR-183-5p directly interacts with the 3'-untranslated region (3'-UTR) of STC1 mRNA. HepG2 cells were subjected to treatment with MIT, either in the presence of miR-183-5p inhibitors or STC1 knockout. The expression levels of ICD markers, namely adenosine triphosphate (ATP), high mobility group box 1 (HMGB1), calreticulin (CALR), along with cellular proliferation and apoptosis, were subsequently evaluated. The dual-luciferase assays confirmed that miR-183-5p specifically binds to a defined sequence (5'-GUGCCAU-3') within the 3'-UTR of STC1 mRNA. In MIT-treated HepG2 cells, inhibition of miR-183-5p resulted in a significant upregulation of both STC1 mRNA (+0.78-fold) and protein levels (+0.21-fold). This was accompanied by an enhanced the expression of ICD markers, including a 0.26-fold increase in CALR membrane exposure, a 0.27-fold rise in ATP secretion, and a 0.44-fold elevation in HMGB1 release. Notably, the effects induced by miR-183-5p inhibition were partially mitigated by STC1 gene knockout. Further investigations demonstrated that combination of miR-183-5p inhibitors with MIT synergistically boosted STC1 expression by 5.08-fold. Conversely, STC1 knockout triggered a 184.1% surge in miR-183-5p expression, indicating a negative feedback loop between them. Functional cellular assays revealed that miR-183-5p inhibition significantly augmented MIT's anti-proliferative efficacy, increasing the inhibition rate from 41.9% to 68.0%, and enhanced its pro-apoptotic effects, elevating the apoptosis rate from 30.57% to 36.08%. However, STC1 knockout attenuated these effects. Collectively, our finding indicate that the miR-183-5p/STC1 axis modulates MIT's cytotoxicity through targeted regulation and a negative feedback mechanisms, thereby influencing HCC cell proliferation, apoptosis, and ICD. These insights offer noval strategies for synergistic therapy that integrate epigenetics and the immune microenvironment in HCC treatment.

Authors

Institutions

Publication Details

Journal
International Journal of Clinical and Experimental Pathology
Published
2025-01-01
DOI
https://doi.org/10.62347/zpfv7918
Citations
1
Primary Topic
MicroRNA in disease regulation
Type
article
Field-Weighted Citation Impact
0.94

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

MiR-183-5p inhibitor promotes mitoxantrone-induced immunogenic death of hepatoma cells by targeting STC1

Yang Song
1 citations
International Journal of Clinical and Experimental Pathology
MicroRNA in disease regulation
0.94
article

MiR-183-5p inhibitor promotes mitoxantrone-induced immunogenic death of hepatoma cells by targeting STC1

Yang Song
article en
1 citations

Abstract

This study aimed to unravel the regulatory mechanism of the microRNA (miR)-183-5p/STC1 axis in regulating mitoxantrone (MIT)-induced immunogenic cell death (ICD) within hepatocellular carcinoma (HCC) cells and assess its therapeutic potential. Dual-luciferase reporter assays were employed to validate that miR-183-5p directly interacts with the 3'-untranslated region (3'-UTR) of STC1 mRNA. HepG2 cells were subjected to treatment with MIT, either in the presence of miR-183-5p inhibitors or STC1 knockout. The expression levels of ICD markers, namely adenosine triphosphate (ATP), high mobility group box 1 (HMGB1), calreticulin (CALR), along with cellular proliferation and apoptosis, were subsequently evaluated. The dual-luciferase assays confirmed that miR-183-5p specifically binds to a defined sequence (5'-GUGCCAU-3') within the 3'-UTR of STC1 mRNA. In MIT-treated HepG2 cells, inhibition of miR-183-5p resulted in a significant upregulation of both STC1 mRNA (+0.78-fold) and protein levels (+0.21-fold). This was accompanied by an enhanced the expression of ICD markers, including a 0.26-fold increase in CALR membrane exposure, a 0.27-fold rise in ATP secretion, and a 0.44-fold elevation in HMGB1 release. Notably, the effects induced by miR-183-5p inhibition were partially mitigated by STC1 gene knockout. Further investigations demonstrated that combination of miR-183-5p inhibitors with MIT synergistically boosted STC1 expression by 5.08-fold. Conversely, STC1 knockout triggered a 184.1% surge in miR-183-5p expression, indicating a negative feedback loop between them. Functional cellular assays revealed that miR-183-5p inhibition significantly augmented MIT's anti-proliferative efficacy, increasing the inhibition rate from 41.9% to 68.0%, and enhanced its pro-apoptotic effects, elevating the apoptosis rate from 30.57% to 36.08%. However, STC1 knockout attenuated these effects. Collectively, our finding indicate that the miR-183-5p/STC1 axis modulates MIT's cytotoxicity through targeted regulation and a negative feedback mechanisms, thereby influencing HCC cell proliferation, apoptosis, and ICD. These insights offer noval strategies for synergistic therapy that integrate epigenetics and the immune microenvironment in HCC treatment.

International Journal of Clinical and Experimental PathologyVol. 18(7)
Karamay Central Hospital of Xinjiang (CN)
Natural Science Foundation of Xinjiang
Good health and well-being
Openalex Percentile: Top 22%
MicroRNA in disease regulation
0.94
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.