Research on Correlations of lncRNA ST7-AS1 with Progression and Therapeutic Targets of Esophageal Cancer
Background/Aims: Esophageal cancer is a highly prevalent gastrointestinal tumor in China, resulting in a significant number of deaths annually. In this paper, we investigated the regulatory role and therapeutic potential of aberrant ST7-AS1 expression in esophageal cancer. Materials and Methods:...
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2025-02-01
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Series: | The Turkish Journal of Gastroenterology |
Online Access: | https://www.turkjgastroenterol.org/en/research-on-correlations-of-lncrna-st7-as1-with-progression-and-therapeutic-targets-of-esophageal-cancer-137302 |
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author | Xiao Lin Sijia Sun JiWen Zhang Yan Cai Quan Cheng |
author_facet | Xiao Lin Sijia Sun JiWen Zhang Yan Cai Quan Cheng |
author_sort | Xiao Lin |
collection | DOAJ |
description | Background/Aims: Esophageal cancer is a highly prevalent gastrointestinal tumor in China, resulting in a significant number of deaths annually. In this paper, we investigated the regulatory role and therapeutic potential of aberrant ST7-AS1 expression in esophageal cancer.
Materials and Methods: The presence of ST7-AS1 in 125 esophageal cancer tissues was identified through RT-qPCR assays. The application of Kaplan-Meier to evaluate survival rates in patients with esophageal cancer. Cell activity was assessed by both CCK-8 and Transwell assays. The luciferase activity assay verified the association of ST7-AS1 with miR-4262.
Results: ST7-AS1 expression in esophageal cancer was noticeably overexpressed compared to the control group. Patients with upregulated ST7-AS1 had shorter survival rates. Silencing ST7-AS1 reduced the proliferation level of esophageal cancer cells, as did the migration and invasion levels. Mechanistically, ST7-AS1 acted as a sponge for miR-4262, affecting the progression of esophageal cancer. This was negatively correlated with ST7-AS1. Moreover, the miR-4262 inhibitor negated the inhibitory effect of silencing ST7-AS1 on cells.
Conclusion: Knockdown of ST7-AS1 may alleviate tumor progression by targeting miR-4262, indicating that ST7-AS1 is anticipated to serve as a therapeutic biomarker for patients with esophageal cancer. |
format | Article |
id | doaj-art-cc76700ebff145ce8f347e88516e19f6 |
institution | Kabale University |
issn | 2148-5607 |
language | English |
publishDate | 2025-02-01 |
publisher | AVES |
record_format | Article |
series | The Turkish Journal of Gastroenterology |
spelling | doaj-art-cc76700ebff145ce8f347e88516e19f62025-02-10T13:13:05ZengAVESThe Turkish Journal of Gastroenterology2148-56072025-02-01362828810.5152/tjg.2024.24260Research on Correlations of lncRNA ST7-AS1 with Progression and Therapeutic Targets of Esophageal CancerXiao Lin0https://orcid.org/0009-0009-0557-5448Sijia Sun1JiWen Zhang2https://orcid.org/0009-0006-2161-1427Yan Cai3https://orcid.org/0009-0006-2161-1427Quan Cheng4https://orcid.org/0009-0008-8717-9512Department of Gastroenterology, Taizhou Integrated Chinese and Western Medicine Hospital, Wenling, ChinaDepartment of Gastroenterology, Huashan Hospital Fudan University, Shanghai, ChinaDepartment of Gastroenterology, Shanghai Baoshan Luodian Hospital, Shanghai, ChinaDepartment of Gastroenterology, Shanghai Baoshan Luodian Hospital, Shanghai, ChinaDepartment of Traditional Chinese Medicine, Affiliated Hangzhou First People’s Hospital School of Medicine, Westlake University, Hangzhou, ChinaBackground/Aims: Esophageal cancer is a highly prevalent gastrointestinal tumor in China, resulting in a significant number of deaths annually. In this paper, we investigated the regulatory role and therapeutic potential of aberrant ST7-AS1 expression in esophageal cancer. Materials and Methods: The presence of ST7-AS1 in 125 esophageal cancer tissues was identified through RT-qPCR assays. The application of Kaplan-Meier to evaluate survival rates in patients with esophageal cancer. Cell activity was assessed by both CCK-8 and Transwell assays. The luciferase activity assay verified the association of ST7-AS1 with miR-4262. Results: ST7-AS1 expression in esophageal cancer was noticeably overexpressed compared to the control group. Patients with upregulated ST7-AS1 had shorter survival rates. Silencing ST7-AS1 reduced the proliferation level of esophageal cancer cells, as did the migration and invasion levels. Mechanistically, ST7-AS1 acted as a sponge for miR-4262, affecting the progression of esophageal cancer. This was negatively correlated with ST7-AS1. Moreover, the miR-4262 inhibitor negated the inhibitory effect of silencing ST7-AS1 on cells. Conclusion: Knockdown of ST7-AS1 may alleviate tumor progression by targeting miR-4262, indicating that ST7-AS1 is anticipated to serve as a therapeutic biomarker for patients with esophageal cancer.https://www.turkjgastroenterol.org/en/research-on-correlations-of-lncrna-st7-as1-with-progression-and-therapeutic-targets-of-esophageal-cancer-137302 |
spellingShingle | Xiao Lin Sijia Sun JiWen Zhang Yan Cai Quan Cheng Research on Correlations of lncRNA ST7-AS1 with Progression and Therapeutic Targets of Esophageal Cancer The Turkish Journal of Gastroenterology |
title | Research on Correlations of lncRNA ST7-AS1 with Progression and Therapeutic Targets of Esophageal Cancer |
title_full | Research on Correlations of lncRNA ST7-AS1 with Progression and Therapeutic Targets of Esophageal Cancer |
title_fullStr | Research on Correlations of lncRNA ST7-AS1 with Progression and Therapeutic Targets of Esophageal Cancer |
title_full_unstemmed | Research on Correlations of lncRNA ST7-AS1 with Progression and Therapeutic Targets of Esophageal Cancer |
title_short | Research on Correlations of lncRNA ST7-AS1 with Progression and Therapeutic Targets of Esophageal Cancer |
title_sort | research on correlations of lncrna st7 as1 with progression and therapeutic targets of esophageal cancer |
url | https://www.turkjgastroenterol.org/en/research-on-correlations-of-lncrna-st7-as1-with-progression-and-therapeutic-targets-of-esophageal-cancer-137302 |
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