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 in | Pharmacological research Vol. 215; p. 107743 |
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Main Authors | , , , , , , , , , , , , , , , |
Format | Journal Article |
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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.
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•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. |
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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 |
Author_xml | – sequence: 1 givenname: Chao surname: Wu fullname: Wu, Chao organization: School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China – sequence: 2 givenname: Yifei surname: Gao fullname: Gao, Yifei organization: School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China – sequence: 3 givenname: Zhengsen surname: Jin fullname: Jin, Zhengsen organization: School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China – sequence: 4 givenname: Zhihong surname: Huang fullname: Huang, Zhihong organization: School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China – sequence: 5 givenname: Haojia surname: Wang fullname: Wang, Haojia organization: School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China – sequence: 6 givenname: Shan surname: Lu fullname: Lu, Shan organization: School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China – sequence: 7 givenname: Siyu surname: Guo fullname: Guo, Siyu organization: School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China – sequence: 8 givenname: Fanqin surname: Zhang fullname: Zhang, Fanqin organization: School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China – sequence: 9 givenname: Jingyuan surname: Zhang fullname: Zhang, Jingyuan organization: School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China – sequence: 10 givenname: Jiaqi surname: Huang fullname: Huang, Jiaqi organization: School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China – sequence: 11 givenname: Xiaoyu surname: Tao fullname: Tao, Xiaoyu organization: School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China – sequence: 12 givenname: Xinkui surname: Liu fullname: Liu, Xinkui organization: School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China – sequence: 13 givenname: Xiaomeng surname: Zhang fullname: Zhang, Xiaomeng organization: School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China – sequence: 14 givenname: Leiming surname: You fullname: You, Leiming email: youleiming@bucm.edu.cn organization: School of Life Science, Beijing University of Chinese Medicine, Beijing 102488, China – sequence: 15 givenname: Qinglin surname: Li fullname: Li, Qinglin email: qinglin200886@126.com organization: Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences, Hangzhou, Zhejiang Province 310022, China – sequence: 16 givenname: Jiarui orcidid: 0000-0002-1617-6110 surname: Wu fullname: Wu, Jiarui email: exogamy@163.com organization: School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/40250508$$D View this record in MEDLINE/PubMed |
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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 |
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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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StartPage | 107743 |
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 |
URI | https://dx.doi.org/10.1016/j.phrs.2025.107743 https://www.ncbi.nlm.nih.gov/pubmed/40250508 https://www.proquest.com/docview/3191616692 https://doaj.org/article/7f73d09be6344d50b8998b4a881d7fdc |
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