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微小RNA-129-3p抑制头颈部鳞状细胞癌的肿瘤进展和放化疗抵抗

MicroRNA-129-3p Suppresses Tumor Progression and Chemoradioresistance in Head and Neck Squamous Cell Carcinoma.

作者信息

Yoon Tae Mi, Kim Sun-Ae, Jung Eun Kyung, Kim Young-Kook, Lee Kyung-Hwa, Lim Sang Chul

机构信息

Departments of Otorhinolaryngology-Head and Neck Surgery, Chonnam National University Medical School, Hwasun Hospital, Hwasun 58128, Jeonnam, Republic of Korea.

Departments of Biochemistry, Chonnam National University Medical School, Hwasun Hospital, Hwasun 58128, Jeonnam, Republic of Korea.

出版信息

Curr Oncol. 2025 Jan 20;32(1):54. doi: 10.3390/curroncol32010054.

Abstract

(1) Background: MicroRNA-129 (miR-129) participates in tumor progression and chemoresistance in various cancer types. In this study, the role of miR-129-3p, the main mature form of miR-129, in tumor progression and chemoradiotherapy resistance in head and neck cancer was evaluated. (2) Methods: RT-PCR, western blotting, cell proliferation assays, cell apoptosis assays, and cell invasion and migration assays were used. (3) Results: In this study, the miR-129-3p overexpression suppressed the proliferation, invasion, and migration of SNU1041, SCC15, and SCC25 human HNSCC cell lines. Additionally, it induced apoptosis and enhanced radiation-/cisplatin-induced apoptosis of SNU1041, SCC15, and SCC25 cells. Therefore, miR-129-3p could suppress tumor progression and enhance chemoradiosensitivity in human HNSCC. Furthermore, miR-129-3p was downregulated in fresh tumor tissues from patients with HNSCC compared with that in the adjacent normal mucosa. In a nude mouse xenograft model with SNU15 cells, the miR-129-3p overexpression significantly decreased tumor growth, as measured by tumor weight and volume. (4) Conclusions: Our study provides evidence that miR-129-3p suppresses tumor progression and chemoradioresistance in HNSCC. This finding may serve as a basis for developing miR-129-3p-based therapeutic strategies.

摘要

(1)背景:微小RNA - 129(miR - 129)参与多种癌症类型的肿瘤进展和化疗耐药。在本研究中,评估了miR - 129的主要成熟形式miR - 129 - 3p在头颈部癌肿瘤进展和放化疗耐药中的作用。(2)方法:采用逆转录聚合酶链反应(RT - PCR)、蛋白质免疫印迹法、细胞增殖测定、细胞凋亡测定以及细胞侵袭和迁移测定。(3)结果:在本研究中,miR - 129 - 3p过表达抑制了SNU1041、SCC15和SCC25人下咽鳞状细胞癌(HNSCC)细胞系的增殖、侵袭和迁移。此外,它诱导了SNU1041、SCC15和SCC25细胞的凋亡,并增强了辐射和顺铂诱导的凋亡。因此,miR - 129 - 3p可抑制人HNSCC的肿瘤进展并增强放化疗敏感性。此外,与相邻正常黏膜相比,HNSCC患者新鲜肿瘤组织中miR - 129 - 3p表达下调。在携带SNU15细胞的裸鼠异种移植模型中,通过肿瘤重量和体积测量,miR - 129 - 3p过表达显著降低了肿瘤生长。(4)结论:我们的研究提供了证据表明miR - 129 - 3p抑制HNSCC的肿瘤进展和放化疗耐药。这一发现可能为开发基于miR - 129 - 3p的治疗策略提供依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42fd/11763343/f997807c66b2/curroncol-32-00054-g001a.jpg

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