Exploring the Influence of miR-597-5p on the Tumor Stem Cell Characteristics of Gastric Cancer Cells Through the STAT3/NF-κB Signaling Pathway

IF 0.9 4区 材料科学
Yuchao Zhang, Guangyu Zhong, Kaihu Fan, Jialun He, Ying Sun, Linping Li
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引用次数: 1

Abstract

In this study, we investigated the impact of miR-597-5p on the tumor stem cell characteristics of gastric cancer cells and the underlying mechanisms. Gastric cancer cell lines were transfected with miR-597-5p mimics to elevate miR-597-5p expression, confirmed by qRT-PCR. Overexpression of miR-597-5p led to reduced cell viability, proliferation, migration, invasion, and sphere-forming ability, while increasing apoptosis. Additionally, the expression of stem cell markers OCT4 and SOX2, as well as the phosphorylation of STAT3 and NF- κ B, decreased with miR-597-5p overexpression. Co-treatment with a STAT3 activator reversed these effects, promoting cell proliferation, invasion, migration, sphere formation, and increasing p-STAT3, p-NF- κ B, SOX2, and OCT4 expression. Importantly, miR-597-5p inhibited the STAT3/NF- κ B signaling pathway, preventing gastric cancer cells from exhibiting stem-like characteristics. These findings suggest that miR-597-5p may have therapeutic potential in suppressing the stem cell properties of gastric cancer cells through STAT3/NF- κ B pathway regulation.
通过STAT3/NF-κB信号通路探讨miR-597-5p对胃癌细胞肿瘤干细胞特性的影响
在本研究中,我们研究了miR-597-5p对胃癌细胞肿瘤干细胞特性的影响及其潜在机制。通过qRT-PCR证实,转染miR-597-5p模拟物可提高miR-597-5p的表达。过表达miR-597-5p导致细胞活力、增殖、迁移、侵袭和成球能力降低,同时增加细胞凋亡。此外,干细胞标志物OCT4和SOX2的表达,以及STAT3和NF- κ B的磷酸化,随着miR-597-5p的过表达而降低。与STAT3激活剂共同处理可逆转这些作用,促进细胞增殖、侵袭、迁移、球形形成,并增加p-STAT3、p-NF- κ B、SOX2和OCT4的表达。重要的是,miR-597-5p抑制STAT3/NF- κ B信号通路,阻止胃癌细胞表现出干细胞样特征。这些发现提示miR-597-5p可能通过STAT3/NF- κ B通路调控抑制胃癌细胞干细胞特性,具有治疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Science of Advanced Materials
Science of Advanced Materials NANOSCIENCE & NANOTECHNOLOGY-MATERIALS SCIENCE, MULTIDISCIPLINARY
自引率
11.10%
发文量
98
审稿时长
4.4 months
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