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缺氧通过 HIF-1α-IL-8-Akt 轴促进人肝癌细胞的迁移和侵袭。

Hypoxia promotes the migration and invasion of human hepatocarcinoma cells through the HIF-1α-IL-8-Akt axis.

机构信息

Department of General Surgery, The First People's Hospital of Huzhou, No.158 Guangchanghou Road, Zhejiang Province 313000 Huzhou, People's Republic of China.

Department of Ultrasound, The First People's Hospital of Huzhou, No.158 Guangchanghou Road, Zhejiang Province 313000 Huzhou, People's Republic of China.

出版信息

Cell Mol Biol Lett. 2018 Sep 20;23:46. doi: 10.1186/s11658-018-0100-6. eCollection 2018.

Abstract

BACKGROUND

Hepatocellular carcinoma (HCC) is the fifth most common cancer and the third most common cause of cancer-related death worldwide. The 5-year survival rate remains low despite considerable research into treatments of HCC, including surgery, radiotherapy and chemotherapy. Many mechanisms within HCC still require investigation, including the influence of hypoxia, which has a crucial role in many cancers and is associated with metastasis. Hypoxia inducible factor-1α (HIF-1α) is known to regulate the expression of many chemokines, including interleukin-8 (IL-8), which is associated with tumor metastasis. Although many studies have reported that HIF-1α is associated with HCC migration and invasion, the underlying mechanisms remain unknown.

METHODS

The expression level of HIF-1α was determined in HCC cells. The correlation of IL-8 and HIF-1α expressions was assessed via knockdown of HIF-1α. HCC cells were also used to assess the influence of HIF-1α on HCC cell migration and invasion. LY294002, an inhibitor of the Akt pathway, was used to confirm the associated signaling pathways.

RESULTS

We observed a significant attenuation of cell migration and invasion after silencing of HIF-1α. Exogenously expressing IL-8 restored migration and invasion. Akt was found to be involved in this process.

CONCLUSION

Hypoxia promotes HCC cell migration and invasion through the HIF-1α-IL-8-Akt axis.

摘要

背景

肝细胞癌(HCC)是全球第五大常见癌症,也是癌症相关死亡的第三大常见原因。尽管对 HCC 的治疗方法(包括手术、放疗和化疗)进行了大量研究,但 5 年生存率仍然很低。HCC 中的许多机制仍需要研究,包括缺氧的影响,缺氧在许多癌症中起着至关重要的作用,并与转移有关。缺氧诱导因子-1α(HIF-1α)已知可调节许多趋化因子的表达,包括与肿瘤转移相关的白细胞介素-8(IL-8)。尽管许多研究报告称 HIF-1α与 HCC 的迁移和侵袭有关,但潜在机制尚不清楚。

方法

在 HCC 细胞中测定 HIF-1α 的表达水平。通过敲低 HIF-1α 评估 IL-8 和 HIF-1α 表达的相关性。还使用 HCC 细胞评估 HIF-1α 对 HCC 细胞迁移和侵袭的影响。使用 Akt 通路抑制剂 LY294002 来确认相关的信号通路。

结果

沉默 HIF-1α后,观察到细胞迁移和侵袭明显减弱。外源性表达 IL-8 恢复了迁移和侵袭。发现 Akt 参与了这一过程。

结论

缺氧通过 HIF-1α-IL-8-Akt 轴促进 HCC 细胞的迁移和侵袭。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4e8e/6149064/57feb3532140/11658_2018_100_Fig1_HTML.jpg

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