Screening and Identification of ESR1 as a Target of Icaritin in Hepatocellular Carcinoma : Evidence from Bibliometrics and Bioinformatic Analysis
Copyright© Bentham Science Publishers; For any queries, please email at epubbenthamscience.net..
BACKGROUND: In 2022, icaritin a Traditional Chinese Medicine with estrogen-like activities was recommended by the CSCO guidelines as a systematic treatment for patients with advanced HCC due to its clinical safety and efficacy. However the mechanism and targets of icaritin are unclear. In this study we aimed to reveal the target of icaritin in HCC.
METHODS: First literature related to icaritin was downloaded from the Web of Science. The software programs "Rstudio" "VOSviewer" and "Mendeley Desktop" were used to analyze the distribution of icaritin publications and research hotspots. Meanwhile icaritin-related genes were obtained by combining them with the PubChem database. Second transcriptome data of HCC patients were obtained from the TCGA database. The proteinprotein interaction (PPI) analysis of icaritin-related genes was performed using the String data platform and the visualization and network topology analysis were performed using Cytoscape. Cox regression analyses were combined to screen the hub target and verified it through cell experiments.
RESULTS: A total of 239 icaritin-related articles were obtained HCC is a new hotspot in the icaritin field. 292 icaritin-related genes were obtained and a core module containing 34 genes was obtained by module division. Among them ESR1 was an independent prognostic factor. Molecular docking showed that ESR1 and icaritin had a high affinity. Functional studies revealed that ESR1 inhibits HCC cell malignant proliferation and improves the sensitivity of HCC cells to icaritin.
CONCLUSION: We propose that ESR1 as a target of icaritin may be conducive to improving icaritin therapy.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2023 |
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| Erschienen: |
2023 |
| Enthalten in: |
Zur Gesamtaufnahme - year:2023 |
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| Enthalten in: |
Current molecular pharmacology - (2023) vom: 19. Okt. |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Zhou, Yinghui [VerfasserIn] |
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| Links: |
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| Themen: |
Bibliometrics |
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| Anmerkungen: |
Date Revised 19.01.2024 published: Print-Electronic Citation Status Publisher |
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| doi: |
10.2174/0118761429260902230925044009 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM367295644 |
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| 100 | 1 | |a Zhou, Yinghui |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Screening and Identification of ESR1 as a Target of Icaritin in Hepatocellular Carcinoma |b Evidence from Bibliometrics and Bioinformatic Analysis |
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| 500 | |a Date Revised 19.01.2024 | ||
| 500 | |a published: Print-Electronic | ||
| 500 | |a Citation Status Publisher | ||
| 520 | |a Copyright© Bentham Science Publishers; For any queries, please email at epubbenthamscience.net. | ||
| 520 | |a BACKGROUND: In 2022, icaritin a Traditional Chinese Medicine with estrogen-like activities was recommended by the CSCO guidelines as a systematic treatment for patients with advanced HCC due to its clinical safety and efficacy. However the mechanism and targets of icaritin are unclear. In this study we aimed to reveal the target of icaritin in HCC | ||
| 520 | |a METHODS: First literature related to icaritin was downloaded from the Web of Science. The software programs "Rstudio" "VOSviewer" and "Mendeley Desktop" were used to analyze the distribution of icaritin publications and research hotspots. Meanwhile icaritin-related genes were obtained by combining them with the PubChem database. Second transcriptome data of HCC patients were obtained from the TCGA database. The proteinprotein interaction (PPI) analysis of icaritin-related genes was performed using the String data platform and the visualization and network topology analysis were performed using Cytoscape. Cox regression analyses were combined to screen the hub target and verified it through cell experiments | ||
| 520 | |a RESULTS: A total of 239 icaritin-related articles were obtained HCC is a new hotspot in the icaritin field. 292 icaritin-related genes were obtained and a core module containing 34 genes was obtained by module division. Among them ESR1 was an independent prognostic factor. Molecular docking showed that ESR1 and icaritin had a high affinity. Functional studies revealed that ESR1 inhibits HCC cell malignant proliferation and improves the sensitivity of HCC cells to icaritin | ||
| 520 | |a CONCLUSION: We propose that ESR1 as a target of icaritin may be conducive to improving icaritin therapy | ||
| 650 | 4 | |a Journal Article | |
| 650 | 4 | |a Bibliometrics | |
| 650 | 4 | |a Bioinformatics | |
| 650 | 4 | |a Cell experiment. | |
| 650 | 4 | |a ESR1 | |
| 650 | 4 | |a Hepatocellular carcinoma (HCC) | |
| 650 | 4 | |a Icaritin | |
| 650 | 4 | |a Molecular docking | |
| 700 | 1 | |a Gu, Jia |e verfasserin |4 aut | |
| 700 | 1 | |a Yu, Huiying |e verfasserin |4 aut | |
| 700 | 1 | |a Chen, Fengyang |e verfasserin |4 aut | |
| 700 | 1 | |a Long, Chao |e verfasserin |4 aut | |
| 700 | 1 | |a Maihemuti, Maiweilan |e verfasserin |4 aut | |
| 700 | 1 | |a Chen, Tingsong |e verfasserin |4 aut | |
| 700 | 1 | |a Zhang, Wei |e verfasserin |4 aut | |
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