KIF20A promotes the development of fibrosarcoma via PI3K-Akt signaling pathway

被引:15
|
作者
Jin, Zheng [1 ]
Tao, Shuang [2 ]
Zhang, Chao [3 ]
Xu, Damo [1 ,4 ]
Zhu, Zhenhua [5 ]
机构
[1] Shenzhen Univ, Dept Respirol & Allergy, Affiliated Hosp 3, Shenzhen, Guangdong, Peoples R China
[2] Guangzhou Univ Chinese Med, Longgang Cent Hosp Shenzhen, Dept Otorhinolaryngol Head & Neck Surg, Guangzhou, Guangdong, Peoples R China
[3] Guangzhou Med Univ, Guangzhou Women & Childrens Med Ctr, Guangdong Prov Clin Res Ctr Child Hlth, Guangzhou, Guangdong, Peoples R China
[4] Shenzhen Univ, State Key Lab Resp Dis Allergy Shenzhen Univ, Shenzhen Key Lab Allergy & Immunol, Sch Med, Shenzhen, Guangdong, Peoples R China
[5] Southern Med Univ, Dept Orthopaed Trauma, Affiliated Hosp 3, Guangzhou, Guangdong, Peoples R China
关键词
KIF20A; Fibrosarcoma; PI3K-Akt; CELL-CYCLE ARREST; NF-KAPPA-B; HEPATOCELLULAR-CARCINOMA; THERAPEUTIC TARGETS; CANCER; EXPRESSION; SENESCENCE; INVASION; ASPM; MIGRATION;
D O I
10.1016/j.yexcr.2022.113322
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Adult fibrosarcoma is an aggressive subtype of soft tissue sarcoma (STS), in which high expression of KIF20A indicates a poor prognosis. However, the precise role of KIF20A in fibrosarcoma progression remains unknown. In this study, we initially examined KIF20A expression and function in the human fibrosarcoma cell line HT -1080. The results showed that KIF20A was highly expressed in HT-1080, knockdown of KIF20A impaired cell proliferation, migration, invasion and induced G2/M arrest and cell apoptosis. Transcriptome study suggested that PI3K-Akt signal pathway was involved in these biological changes. We confirmed that PI3K-Akt and NF-kappa B signaling pathways were impaired after the down-regulation of KIF20A, which can be reversed by the Akt activator SC79 in HT-1080 in vitro. In a xenograft mouse model, knockdown of KIF20A inhibited tumor growth, Ki67 expression and liver metastasis. Taken together, our results suggested that KIF20A promoted fibrosarcoma progression via PI3K-Akt signaling pathway and might be a potential therapeutic target for fibrosarcoma.
引用
收藏
页数:11
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