High-mobility group protein B1 (HMGB1) and its potential in diagnosis and treatment of ovarian cancer

Yingchun Li, Jing Tian, Hairong Yao, Wenqi Zhang, Q. Hao
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引用次数: 3

Abstract

Objective: The objective of this research is to study the serum level of the high-mobility group protein B1 (HMGB1) in human ovarian tumor (OvCa) and in a healthy control. This study also aims to identify different HMGB1 levels before and after surgery and to explore the inhibitory effect of HMGB1 gene silencing in the proliferation and invasion ability of OvCa. Methods: Enzyme-linked immunosorbent assay was used to measure the serum level of HMGB1 in OvCa patients and healthy subjects. Lentivirus vector with HMGB1 shRNA was constructed and used to infect OvCa cells. The expressions of HMGB1 mRNA and protein were tested by real-time PCR and Western blot. Cell proliferation was detected using the Cell Counting Kit-8 assay, whereas cell invasion and migration were detected by Transwell assay. Results: The serum level of HMGB1 was more elevated in patients with malignant diseases compared with individuals with benign diseases and the control groups. In the malignant group, the serum level of HMGB1 decreased noticeably after therapy. Down-regulation of HMGB1 expression resulted in the inhibition of the biological behavior and metastasis of ovarian cancer cells. Conclusion: HMGB1 is closely associated with clinicopathologic features of OvCa. Knockdown of HMGB1 expression can significantly inhibit cell proliferation, cell migration, and cell invasion of OvCa. These findings indicate that HMGB1 can function as a therapeutic target for ovarian neoplasm in the future.
高迁移率蛋白B1 (HMGB1)及其在卵巢癌诊断和治疗中的潜力
目的:研究卵巢肿瘤(OvCa)患者及健康对照者血清中高迁移率组蛋白B1 (HMGB1)的水平。本研究还旨在鉴定手术前后不同的HMGB1水平,探讨HMGB1基因沉默对OvCa增殖和侵袭能力的抑制作用。方法:采用酶联免疫吸附法检测OvCa患者和健康人血清HMGB1水平。构建了带HMGB1 shRNA的慢病毒载体,并将其用于感染OvCa细胞。采用实时荧光定量PCR和Western blot检测HMGB1 mRNA和蛋白的表达。采用细胞计数试剂盒-8法检测细胞增殖,Transwell法检测细胞侵袭和迁移。结果:恶性疾病患者血清HMGB1水平高于良性疾病患者及对照组。恶性组治疗后血清HMGB1水平明显降低。下调HMGB1表达可抑制卵巢癌细胞的生物学行为和转移。结论:HMGB1与OvCa的临床病理特征密切相关。下调HMGB1表达可显著抑制OvCa的细胞增殖、细胞迁移和细胞侵袭。这些发现提示HMGB1在未来可作为卵巢肿瘤的治疗靶点。
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