PTPRG-AS1 regulates the KITLG/KIT pathway through the ceRNA axis to promote the malignant progression of gastric cancer and the intervention effect of Compound Kushen injection on it

Gastric cancer (GC) is a common malignant tumor with high mortality, recurrence, and metastasis rates. Compound Kushen injection (CKI) combination chemotherapy has been clinically used for the treatment of GC in China for many years, but its underlying mechanisms of action remain unclear. Recent rep...

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Published inPharmacological research Vol. 215; p. 107743
Main Authors Wu, Chao, Gao, Yifei, Jin, Zhengsen, Huang, Zhihong, Wang, Haojia, Lu, Shan, Guo, Siyu, Zhang, Fanqin, Zhang, Jingyuan, Huang, Jiaqi, Tao, Xiaoyu, Liu, Xinkui, Zhang, Xiaomeng, You, Leiming, Li, Qinglin, Wu, Jiarui
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LanguageEnglish
Published Netherlands Elsevier Ltd 01.05.2025
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Abstract Gastric cancer (GC) is a common malignant tumor with high mortality, recurrence, and metastasis rates. Compound Kushen injection (CKI) combination chemotherapy has been clinically used for the treatment of GC in China for many years, but its underlying mechanisms of action remain unclear. Recent reports have highlighted the important role of the competing endogenous RNA (ceRNA) mechanism of noncoding RNA (ncRNA) and messenger RNA (mRNA) formation in GC and other tumors. This study aimed to investigate the effects of CKI on GC from the ceRNA perspective. We confirmed the inhibitory effect of CKI on GC in mouse models and cell lines. By examining the GC cell lines sensitive to CKI treatment, we developed the CNScore method to analyze the ceRNA network, revealing that the CKI-GC ceRNA network promotes GC proliferation and metastasis through the PTPRG-AS1/hsa-miR-421/KITLG axis. Finally, we constructed GC cell models with PTPRG-AS1 overexpression or knockdown and GC liver metastasis models and found that PTPRG-AS1 can sponge hsa-miR-421, releasing KITLG and promoting GC proliferation and metastasis through the KITLG/KIT pathway. Taken together, CKI can suppress these malignant phenotypes by regulating the PTPRG-AS1/hsa-miR-421/KITLG axis. [Display omitted] •Lnc RNA PTPRG-AS1 functions as a sponge for hsa-miR-421, thereby releasing KITLG and activating the KITLG/KIT pathway, which promotes the growth, proliferation, and metastasis of gastric cancer.•Compound Kushen injection inhibits the progression of gastric cancer by targeting the PTPRG-AS1/hsa-miR-421/KITLG axis through the suppression of the ceRNA network.•The ceRNA Network Score (CNScore) method was utilized to analyze and annotate the ceRNA network, thereby providing a more coherent interpretation of its biological significance.
AbstractList Gastric cancer (GC) is a common malignant tumor with high mortality, recurrence, and metastasis rates. Compound Kushen injection (CKI) combination chemotherapy has been clinically used for the treatment of GC in China for many years, but its underlying mechanisms of action remain unclear. Recent reports have highlighted the important role of the competing endogenous RNA (ceRNA) mechanism of noncoding RNA (ncRNA) and messenger RNA (mRNA) formation in GC and other tumors. This study aimed to investigate the effects of CKI on GC from the ceRNA perspective. We confirmed the inhibitory effect of CKI on GC in mouse models and cell lines. By examining the GC cell lines sensitive to CKI treatment, we developed the CNScore method to analyze the ceRNA network, revealing that the CKI-GC ceRNA network promotes GC proliferation and metastasis through the PTPRG-AS1/hsa-miR-421/KITLG axis. Finally, we constructed GC cell models with PTPRG-AS1 overexpression or knockdown and GC liver metastasis models and found that PTPRG-AS1 can sponge hsa-miR-421, releasing KITLG and promoting GC proliferation and metastasis through the KITLG/KIT pathway. Taken together, CKI can suppress these malignant phenotypes by regulating the PTPRG-AS1/hsa-miR-421/KITLG axis.
Gastric cancer (GC) is a common malignant tumor with high mortality, recurrence, and metastasis rates. Compound Kushen injection (CKI) combination chemotherapy has been clinically used for the treatment of GC in China for many years, but its underlying mechanisms of action remain unclear. Recent reports have highlighted the important role of the competing endogenous RNA (ceRNA) mechanism of noncoding RNA (ncRNA) and messenger RNA (mRNA) formation in GC and other tumors. This study aimed to investigate the effects of CKI on GC from the ceRNA perspective. We confirmed the inhibitory effect of CKI on GC in mouse models and cell lines. By examining the GC cell lines sensitive to CKI treatment, we developed the CNScore method to analyze the ceRNA network, revealing that the CKI-GC ceRNA network promotes GC proliferation and metastasis through the PTPRG-AS1/hsa-miR-421/KITLG axis. Finally, we constructed GC cell models with PTPRG-AS1 overexpression or knockdown and GC liver metastasis models and found that PTPRG-AS1 can sponge hsa-miR-421, releasing KITLG and promoting GC proliferation and metastasis through the KITLG/KIT pathway. Taken together, CKI can suppress these malignant phenotypes by regulating the PTPRG-AS1/hsa-miR-421/KITLG axis. [Display omitted] •Lnc RNA PTPRG-AS1 functions as a sponge for hsa-miR-421, thereby releasing KITLG and activating the KITLG/KIT pathway, which promotes the growth, proliferation, and metastasis of gastric cancer.•Compound Kushen injection inhibits the progression of gastric cancer by targeting the PTPRG-AS1/hsa-miR-421/KITLG axis through the suppression of the ceRNA network.•The ceRNA Network Score (CNScore) method was utilized to analyze and annotate the ceRNA network, thereby providing a more coherent interpretation of its biological significance.
Gastric cancer (GC) is a common malignant tumor with high mortality, recurrence, and metastasis rates. Compound Kushen injection (CKI) combination chemotherapy has been clinically used for the treatment of GC in China for many years, but its underlying mechanisms of action remain unclear. Recent reports have highlighted the important role of the competing endogenous RNA (ceRNA) mechanism of noncoding RNA (ncRNA) and messenger RNA (mRNA) formation in GC and other tumors. This study aimed to investigate the effects of CKI on GC from the ceRNA perspective. We confirmed the inhibitory effect of CKI on GC in mouse models and cell lines. By examining the GC cell lines sensitive to CKI treatment, we developed the CNScore method to analyze the ceRNA network, revealing that the CKI-GC ceRNA network promotes GC proliferation and metastasis through the PTPRG-AS1/hsa-miR-421/KITLG axis. Finally, we constructed GC cell models with PTPRG-AS1 overexpression or knockdown and GC liver metastasis models and found that PTPRG-AS1 can sponge hsa-miR-421, releasing KITLG and promoting GC proliferation and metastasis through the KITLG/KIT pathway. Taken together, CKI can suppress these malignant phenotypes by regulating the PTPRG-AS1/hsa-miR-421/KITLG axis.Gastric cancer (GC) is a common malignant tumor with high mortality, recurrence, and metastasis rates. Compound Kushen injection (CKI) combination chemotherapy has been clinically used for the treatment of GC in China for many years, but its underlying mechanisms of action remain unclear. Recent reports have highlighted the important role of the competing endogenous RNA (ceRNA) mechanism of noncoding RNA (ncRNA) and messenger RNA (mRNA) formation in GC and other tumors. This study aimed to investigate the effects of CKI on GC from the ceRNA perspective. We confirmed the inhibitory effect of CKI on GC in mouse models and cell lines. By examining the GC cell lines sensitive to CKI treatment, we developed the CNScore method to analyze the ceRNA network, revealing that the CKI-GC ceRNA network promotes GC proliferation and metastasis through the PTPRG-AS1/hsa-miR-421/KITLG axis. Finally, we constructed GC cell models with PTPRG-AS1 overexpression or knockdown and GC liver metastasis models and found that PTPRG-AS1 can sponge hsa-miR-421, releasing KITLG and promoting GC proliferation and metastasis through the KITLG/KIT pathway. Taken together, CKI can suppress these malignant phenotypes by regulating the PTPRG-AS1/hsa-miR-421/KITLG axis.
ArticleNumber 107743
Author You, Leiming
Gao, Yifei
Wang, Haojia
Liu, Xinkui
Zhang, Xiaomeng
Wu, Jiarui
Zhang, Jingyuan
Lu, Shan
Guo, Siyu
Zhang, Fanqin
Wu, Chao
Tao, Xiaoyu
Jin, Zhengsen
Huang, Zhihong
Huang, Jiaqi
Li, Qinglin
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Keywords IHC
PFA
Compound Kushen injection
SsGSEA
BSA
PFI
RBC
TUNEL
DEmRNAs
IC50
MREs
CCK-8
KEGG
MF
MiRNAs
UPLC-Q/TOF-MSE
CeRNA
RT-qPCR
Gastric cancer
HGB
NSG
DSS
DEmiRNAs
LncRNAs
GMP
EMT
TCA
NC
HCT
Hsa-miR-421
MRNA
MET
ELISA
TCM
DElncRNAs
PCT
SRB
MRI
PPI
BP
PTPRG-AS1
DEGs
NMPA
OD
CD117
PLT
WBC
ESI
GC
WT
CC
CKI
OS
GO
QPCR
NcRNA
KITLG
EdU
SCF
TMT
DEPs
CNScore
HER2
NEU
Language English
License This is an open access article under the CC BY-NC-ND license.
Copyright © 2025 The Authors. Published by Elsevier Ltd.. All rights reserved.
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Snippet Gastric cancer (GC) is a common malignant tumor with high mortality, recurrence, and metastasis rates. Compound Kushen injection (CKI) combination chemotherapy...
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SubjectTerms Animals
Antineoplastic Agents - pharmacology
Antineoplastic Agents - therapeutic use
Cell Line, Tumor
Cell Proliferation - drug effects
Compound Kushen injection
Disease Progression
Drugs, Chinese Herbal - pharmacology
Drugs, Chinese Herbal - therapeutic use
Gastric cancer
Gene Expression Regulation, Neoplastic - drug effects
Hsa-miR-421
Humans
KITLG
Male
Mice
Mice, Inbred BALB C
Mice, Nude
MicroRNAs - genetics
MicroRNAs - metabolism
Proto-Oncogene Proteins c-kit - genetics
Proto-Oncogene Proteins c-kit - metabolism
PTPRG-AS1
RNA, Competitive Endogenous
RNA, Long Noncoding - genetics
RNA, Long Noncoding - metabolism
Signal Transduction - drug effects
Stem Cell Factor - genetics
Stem Cell Factor - metabolism
Stomach Neoplasms - drug therapy
Stomach Neoplasms - genetics
Stomach Neoplasms - metabolism
Stomach Neoplasms - pathology
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Title PTPRG-AS1 regulates the KITLG/KIT pathway through the ceRNA axis to promote the malignant progression of gastric cancer and the intervention effect of Compound Kushen injection on it
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