Rubioncolin C targets cathepsin D to induce autophagosome accumulation and suppress gastric cancer.
10.19540/j.cnki.cjcmm.20240910.401
- Author:
Liang ZHANG
1
;
Jun-Jie CHEN
2
;
Man-Xiang GU
2
;
Yi-Fan ZHONG
2
;
Yuan SI
3
;
Ying LIU
4
Author Information
1. School of Basic Medical Sciences, Hubei University of Medicine Shiyan 442000, China Hubei Key Laboratory of Wudang Local Chinese Medicine Research, Hubei University of Medicine Shiyan 442000, China.
2. School of Basic Medical Sciences, Hubei University of Medicine Shiyan 442000, China.
3. School of Basic Medical Sciences, Hubei University of Medicine Shiyan 442000, China Hubei Key Laboratory of Embryonic Stem Cell Research, Hubei University of Medicine Shiyan 442000, China.
4. School of Basic Medical Sciences, Hubei University of Medicine Shiyan 442000, China Hubei Key Laboratory of Wudang Local Chinese Medicine Research, Hubei University of Medicine Shiyan 442000, China Hubei Key Laboratory of Embryonic Stem Cell Research, Hubei University of Medicine Shiyan 442000, China.
- Publication Type:Journal Article
- Keywords:
autophagosome;
autophagy;
cathepsin D;
gastric cancer;
rubioncolin C
- MeSH:
Humans;
Stomach Neoplasms/enzymology*;
Cathepsin D/chemistry*;
Cell Line, Tumor;
Molecular Docking Simulation;
Cell Proliferation/drug effects*;
Autophagosomes/metabolism*;
Autophagy/drug effects*
- From:
China Journal of Chinese Materia Medica
2025;50(5):1267-1275
- CountryChina
- Language:Chinese
-
Abstract:
This study aimed to explore the molecular mechanism of rubioncolin C(RuC) in inhibiting gastric cancer(GC). AGS and MGC803 cell lines were selected as cellular models. After treating the cells with RuC at different concentrations, the effects of RuC on the proliferation ability of GC cells were assessed using the CCK-8 method, real-time cellular analysis(RTCA), and colony formation assays. Transmission electron microscopy was used to observe subcellular structural changes. Immunofluorescence was applied to detect LC3 fluorescent foci. Acridine orange staining was used to evaluate the state of intracellular lysosomes. Western blot was employed to detect the expression of autophagy-related proteins LC3Ⅱ, P62, and lysosomal cathepsin D(CTSD). The SuperPred online tool was used to predict the target proteins that bound to RuC, and molecular docking analysis was conducted to identify the interaction sites between RuC and CTSD. The drug affinity responsive target stability(DARTS) assay was performed to detect the direct binding interaction between RuC and CTSD. The results showed that RuC significantly inhibited the proliferation and colony formation of GC cells at low concentrations, with 24-hour half-maximal inhibitory concentrations(IC_(50)) of 3.422 and 2.697 μmol·L~(-1) for AGS and MGC803 cells, respectively. After 24 hours of treatment with RuC at concentrations of 1, 2, and 3 μmol·L~(-1), the colony formation rates for AGS cells were 61.0%±1.5%, 28.0%±0.5%, and 18.2%±0.5%, respectively, while the rates for MGC803 cells were 56.0%±0.5%, 23.3%±1.0%, and 11.8%±1.0%, all of which were significantly reduced. Transmission electron microscopy revealed that RuC promoted an increase in autophagosome formation in GC cells. Immunofluorescence detection showed that LC3 fluorescent foci of GC cells increased with the increase in RuC dose. RuC up-regulated the expression of autophagy-related proteins LC3Ⅱ and P62 in GC cells. Acridine orange staining indicated that RuC altered the acidic environment of lysosomes. SuperPred online prediction identified CTSD as a potential target protein of RuC. Western blot analysis revealed that RuC induced the up-regulation of the inactive precursor of CTSD in GC cells. CTSD activity assays indicated that RuC reduced the activity of CTSD. Molecular docking simulations found that RuC bound to the substrate-binding region of CTSD, forming hydrogen bonds with the Tyr205 and Asp231 residues. Microscale thermophoresis and DARTS assays further confirmed that RuC directly bound to CTSD. In summary, RuC inhibits lysosomal activity by targeting and down-regulating the expression of CTSD, thereby inducing autophagosome accumulation in GC cells.
