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Panax notoginseng saponins radiosensitize colorectal cancer cells by regulating the SNHG6/miR-137 axis
Caihui Xu1, Teng Liu2, Haiyan Liu1
1Department of Oncology, Shangqiu First People's Hospital No. 292, South Kaixuan Road, Suiyang District Shangqiu 476100 Henan China guoym18917@163.com +86-0370-3255630.
Abstract:
Panax notoginseng saponins (PNS) have recently attracted great attention for their anti-cancer activity in colorectal cancer (CRC). The aim of this study was to explore the functional role and underlying mechanisms of PNS on CRC radiosensitivity. Cell viability was assessed by a Cell Counting kit-8 assay. Cell survival and apoptosis were determined using colony formation assay and flow cytometry, respectively. Quantitative real-time PCR was used to quantify the levels of SNHG6 and miR-137. The targeted correlation between SNHG6 and miR-137 was validated by dual-luciferase reporter and RNA immunoprecipitation assays. Our data supported that PNS weakened the viability of CRC cells. Moreover, PNS promoted the radiosensitivity of CRC cells. Mechanistically, PNS enhanced CRC cell radiosensitivity by upregulating SNHG6. SNHG6 directly targeted miR-137 and inhibited miR-137 expression. MiR-137 was involved in the regulatory effect of SNHG6 on CRC cell radiosensitivity. Furthermore, PNS increased miR-137 expression through SNHG6 in CRC cells. Our study suggested that PNS promoted radiosensitivity in CRC cells at least partly through regulating the SNHG6/miR-137 axis, providing a novel understanding of the anti-cancer mechanism of PNS in CRC.
Insights
Panax notoginseng saponins (PNS) enhance colorectal cancer (CRC) cell radiosensitivity. PNS promotes radiosensitivity by upregulating SNHG6, which targets miR-137, offering a new therapeutic strategy for CRC.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Colorectal cancer (CRC) remains a significant global health challenge.
- Panax notoginseng saponins (PNS) show potential anti-cancer properties.
- The role of PNS in CRC radiosensitivity requires further elucidation.
Purpose of the Study:
- To investigate the functional role of PNS in colorectal cancer radiosensitivity.
- To explore the underlying molecular mechanisms of PNS action in CRC.
- To determine the involvement of the SNHG6/miR-137 axis in PNS-mediated radiosensitization.
Main Methods:
- Cell viability assays (Cell Counting kit-8).
- Colony formation and flow cytometry for cell survival and apoptosis.
- Quantitative real-time PCR for SNHG6 and miR-137 expression.
- Dual-luciferase reporter and RNA immunoprecipitation assays for target validation.
Main Results:
- PNS significantly reduced colorectal cancer cell viability.
- PNS treatment enhanced the radiosensitivity of CRC cells.
- PNS upregulated SNHG6 expression, which directly targeted and inhibited miR-137.
- PNS promoted CRC cell radiosensitivity via the SNHG6/miR-137 pathway.
Conclusions:
- PNS exhibits radiosensitizing effects in colorectal cancer.
- The SNHG6/miR-137 axis is a key mediator of PNS's radiosensitizing activity in CRC.
- PNS represents a potential therapeutic agent for enhancing CRC radiosensitivity.
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