Guggulsterone Promotes Nasopharyngeal Carcinoma Cells Exosomal Circfip1L1 to Mediate miR-125a-5p/VEGFA Affecting Tumor Angiogenesis.

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ting Zhou, Shunli Zhao, Sanyuan Tang, Yongli Wang, Ruoxia Wu, Xiaoyan Zeng, Ping Yang, Xi Zhang, Xuefei Tian
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引用次数: 0

Abstract

Background: Nasopharyngeal carcinoma (NPC) is a usual head and neck malignancy. Guggulsterone (GS) has potential in cancer chemoprophylaxis and treatment, but its therapeutic effect on NPC is unknown. We aimed to explore whether GS could promote the secretion of exosomal circFIP1L1 from NPC cells and its regulatory mechanism.

Methods: NPC tissues and adjacent tissues were collected from NPC patients. Human nasopharyngeal epithelial cell lines (NP69) and NPC lines (5-8F, CNE1, and HNE1) were used for in vitro experiments. HNE1 cells were treated with GS (20, 40, 60 μmol/L). The expressions of miR-125a-5p and circFIP1L1 were evaluated by qRT-PCR. Cell proliferation and apoptosis abilities were measured by CCK-8 and flow cytometry. HNE1 cell exosomes were extracted and identified, and the levels of VEGFA and VEGFR2 were detected by ELISA. Then miR-125a-5p was knocked down and overexpressed. HUVECs angiogenesis was determined by the tube formation assay. qRT-PCR and Western blot were utilized to evaluate the expressions of VEGFA, MMP-2, MMP-9, and ICAM-1 in HUVECs.

Results: miR-125a-5p was highly expressed in NPC tissues and cells. GS promoted the secretion of exosomal circFIP1L1 from HNE1 cells to affect HUVECs proliferation and angiogenesis. Overexpression of miR-125a-5p accelerated HUVECs proliferation and angiogenesis. Knocking down miR-125a- 5p inhibited VEGFA expression. In addition, exosomal circFIP1L1 sponged miR-125a-5p, inhibiting the VEGFA pathway to repress HUVECs angiogenesis.

Conclusions: GS promoted exosomal circFIP1L1 in NPC cells to mediate miR-125a-5p/VEGFA axis affecting tumor angiogenesis.

Guggulsterone促进鼻咽癌细胞外泌体cirfip1l1介导miR-125a-5p/VEGFA影响肿瘤血管生成
背景:鼻咽癌是一种常见的头颈部恶性肿瘤。谷固酮(Guggulsterone, GS)在癌症化学预防和治疗方面具有潜力,但其对鼻咽癌的治疗效果尚不清楚。我们旨在探讨GS是否能促进鼻咽癌细胞外泌体cirfip1l1的分泌及其调控机制。方法:收集鼻咽癌患者的鼻咽癌组织及邻近组织。体外实验采用人鼻咽上皮细胞系NP69和鼻咽癌细胞系5-8F、CNE1和HNE1。分别用20、40、60 μmol/L的GS处理HNE1细胞。采用qRT-PCR检测miR-125a-5p和circirfip1l1的表达。采用CCK-8和流式细胞术检测细胞增殖和凋亡能力。提取并鉴定HNE1细胞外泌体,ELISA检测VEGFA和VEGFR2水平。然后敲低miR-125a-5p并过表达。用成管法测定HUVECs血管生成情况。采用qRT-PCR和Western blot检测huvec中VEGFA、MMP-2、MMP-9、ICAM-1的表达。结果:miR-125a-5p在鼻咽癌组织和细胞中高表达。GS促进HNE1细胞外泌体cirfip1l1的分泌,影响HUVECs增殖和血管生成。过表达miR-125a-5p可加速huvec的增殖和血管生成。下调miR-125a- 5p可抑制VEGFA的表达。此外,外泌体cirfip1l1海绵化miR-125a-5p,抑制VEGFA通路抑制HUVECs血管生成。结论:GS促进鼻咽癌细胞外泌体cirfip1l1介导miR-125a-5p/VEGFA轴影响肿瘤血管生成。
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来源期刊
Current molecular pharmacology
Current molecular pharmacology Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
CiteScore
4.90
自引率
3.70%
发文量
112
期刊介绍: Current Molecular Pharmacology aims to publish the latest developments in cellular and molecular pharmacology with a major emphasis on the mechanism of action of novel drugs under development, innovative pharmacological technologies, cell signaling, transduction pathway analysis, genomics, proteomics, and metabonomics applications to drug action. An additional focus will be the way in which normal biological function is illuminated by knowledge of the action of drugs at the cellular and molecular level. The journal publishes full-length/mini reviews, original research articles and thematic issues on molecular pharmacology. Current Molecular Pharmacology is an essential journal for every scientist who is involved in drug design and discovery, target identification, target validation, preclinical and clinical development of drugs therapeutically useful in human disease.
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