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THBS1基因敲低通过JAK2/STAT3信号通路抑制胰腺癌进展。

THBS1 knockdown suppresses pancreatic cancer progression through JAK2/STAT3 signaling pathway.

作者信息

Li Ping, Wang Kaixuan, Song Jian, Chen Zhuang, Li Yongyu, Chen Zhaowei

机构信息

Digestive Endoscopy Center, Hainan Cancer Hospital, Haikou, Hainan, 570100, China.

Department of Gastroenterology, Changhai Hospital, Naval Military Medical University, Shanghai, 200433, China.

出版信息

Mol Cell Probes. 2025 Feb;79:102003. doi: 10.1016/j.mcp.2024.102003. Epub 2024 Dec 26.

Abstract

BACKGROUND

Thrombospondin 1 (THBS1), a secreted protein, is implicated in the progression of numerous cancers, yet its specific contributions to pancreatic cancer (PC) remain underexplored.

METHODS

The association between THBS1 levels and prognosis in PC was investigated. Functional experiments in vitro were used to determine the cell functions of siTHBS1 through CCK8 assay for cell proliferation, Muse® Cell Analyzer for apoptosis, and transwell assay for invasion and migration. Colivelin was applied in recovery experiment to investigate the mechanism of THBS1 regulating the JAK2/STAT3 pathway in BXPC-3 cell. In addition, the LV-shTHBS1 lentivirus was used to construct subcutaneous tumors in nude mice to verify the function of THBS1 in vivo.

RESULTS

THBS1 expression was elevated in PC and associated with a poorer prognosis. THBS1 was highly expressed in these PC cells. siTHBS1 repressed cell growth, migration and invasiveness, while promoting apoptosis of BXPC-3 cells. THBS1 suppression also led to a decrease in the phosphorylation of JAK2 and STAT3. JAK2/STAT3 signaling activator (Colivelin) could partially reverse the biological effects. In addition, shTHBS1 can suppress the growth of implanted tumors in nude mice.

CONCLUSIONS

THBS1 knockdown suppressed cell proliferation, migration, and invasion while enhanced cell apoptosis through the JAK2/STAT3 signaling pathway.

摘要

背景

血小板反应蛋白1(THBS1)是一种分泌蛋白,与多种癌症的进展有关,但其对胰腺癌(PC)的具体作用仍未得到充分研究。

方法

研究了THBS1水平与PC预后之间的关联。体外功能实验通过CCK8法检测细胞增殖、Muse®细胞分析仪检测细胞凋亡、transwell法检测侵袭和迁移,以确定siTHBS1的细胞功能。在恢复实验中应用可立维林,研究THBS1在BXPC-3细胞中调节JAK2/STAT3信号通路的机制。此外,使用LV-shTHBS1慢病毒在裸鼠体内构建皮下肿瘤,以验证THBS1在体内的功能。

结果

THBS1在PC中表达升高,且与较差的预后相关。THBS1在这些PC细胞中高表达。siTHBS1抑制BXPC-3细胞的生长、迁移和侵袭能力,同时促进其凋亡。抑制THBS1还导致JAK2和STAT3磷酸化水平降低。JAK2/STAT3信号激活剂(可立维林)可部分逆转这些生物学效应。此外,shTHBS1可抑制裸鼠体内植入肿瘤的生长。

结论

敲低THBS1可通过JAK2/STAT3信号通路抑制细胞增殖、迁移和侵袭,同时增强细胞凋亡。

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