The role of the globular heads of the C1q receptor in HPV-16 E2-induced human cervical squamous carcinoma cell apoptosis via a mitochondria-dependent pathway

被引:10
|
作者
Chen, Zheng-lin [1 ]
Su, Ya-Juan [2 ]
Zhang, Hui-lin [3 ]
Gu, Ping-qing [3 ,4 ]
Gao, Ling-juan [3 ,4 ]
机构
[1] Jiangsu Prov Official Hosp, Clin Lab, Nanjing 210024, Peoples R China
[2] Harbin Med Univ, Clin Lab, Canc Hosp, Harbin 150080, Peoples R China
[3] Nanjing Med Univ, State Key Lab Reprod Med, Dept Clin Lab, Nanjing Matern & Child Hlth Care Hosp, Nanjing 210004, Peoples R China
[4] Nanjing Matern & Child Hlth Care Hosp, Clin Lab, Nanjing 210004, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Human papillomavirus type 16 (HPV-16) E2; Receptor for the globular heads of the human C1q (gC1qR); Mitochondrial dysfunction; Apoptosis; Human cervical squamous carcinoma cells; CANCER CELLS; HPV16; E2; E6; EXPRESSION; HABP1/P32/GC1QR; INVOLVEMENT; LESIONS;
D O I
10.1186/s12967-014-0286-y
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Human papillomavirus type-16 (HPV-16) E2 protein acts as a transcriptional modulator and plays a key role in regulating many biological responses. The purpose of this study was to investigate the relationship between HPV-16 E2, the receptor for the globular heads of human C1q (gC1qR) gene expression, mitochondrial dysfunction and apoptosis regulation in human cervical squamous carcinoma cells (C33a and SiHa). Methods: HPV-16 E2 and gC1qR expression was examined using real-time PCR and western blot analysis. Apoptosis in C33a and SiHa cells was assessed by flow cytometry. Mitochondrial function was detected via ROS generation, the amount of cytosolic Ca2+, and changes in the mitochondrial membrane potential (Delta psi m). Results: The expression of the HPV-16 E2 and gC1qR gene significantly decreased in human cervical squamous carcinoma samples relative to the non-cancerous cervix samples. C33a and SiHa cells that were transfected with a vector encoding HPV-16 E2 displayed significantly increased gC1qR gene expression and mitochondrial dysfunction as well as an up-regulation of cellular apoptosis, which was abrogated by the addition of gC1qR small-interfering RNA (siRNA). Conclusions: These data support a mechanism whereby gC1qR plays an important role in HPV-16 E2-induced human cervical squamous carcinoma cell apoptosis via a mitochondria-dependent pathway.
引用
收藏
页数:9
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