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组蛋白去乙酰化酶11与乳腺癌预后相关,并抑制乳腺癌细胞的侵袭和增殖。

HDAC11 is related to breast cancer prognosis and inhibits invasion and proliferation of breast cancer cells.

作者信息

Zhao Hao, Zhang Xu-Ming, Xiao Sheng, Wu Zhen-Ru, Shi Yu-Jun, Xie Ming-Jun

机构信息

Department of Thyroid Breast Surgery, Zigong Fourth People's Hospital, Southwestern Medical University Zigong 643000, Sichuan, P. R. China.

Department of Oncology, Bazhong Central Hospital Bazhong 636000, Sichuan, P. R. China.

出版信息

Int J Clin Exp Pathol. 2023 Jul 15;16(7):172-183. eCollection 2023.

Abstract

OBJECTIVE

Histone deacetylases (HDACs) not only regulate histone acetylation but also participate in many pathophysiologic processes, especially the development of cancer, including breast cancer. However, whether Histone deacetylase 11 can influence breast cancer is still unknown. This study investigated the relationship between HDAC11 expression in breast cancers and clinicopathologic parameters, and used small interference RNA (siRNA) to determine the biological behavioural changes after knockdown of HDAC11.

METHODS

Immunohistochemical (IHC) staining was employed to detect the expression of HDAC11 in a tissue microarray (TMA) of 145 patients with invasive ductal breast carcinoma. Transwell and wound healing assays were employed to analyze cell invasion and migration. The proliferation ability of cells was determined by Cell Counting Kit (CCK8).

RESULTS

The results show that the expression of HDAC11 was positively correlated with the overall survival (OS) of breast cancer patients. Specific HDAC11 knockdown enhanced MDA-MB-231 cell proliferation, migration, and invasion.

CONCLUSION

In conclusion, this study found that HDAC11 expression is positively correlated with the overall survival rate of patients. HDAC11 can inhibit the invasion and proliferation of breast cancer cells to a certain extent and can be used as a good prognosis marker.

摘要

目的

组蛋白去乙酰化酶(HDACs)不仅调节组蛋白乙酰化,还参与许多病理生理过程,尤其是癌症(包括乳腺癌)的发展。然而,组蛋白去乙酰化酶11是否会影响乳腺癌仍不清楚。本研究调查了乳腺癌中HDAC11表达与临床病理参数之间的关系,并使用小干扰RNA(siRNA)来确定HDAC11敲低后的生物学行为变化。

方法

采用免疫组织化学(IHC)染色检测145例浸润性导管癌患者组织芯片(TMA)中HDAC11的表达。采用Transwell和伤口愈合试验分析细胞侵袭和迁移。通过细胞计数试剂盒(CCK8)测定细胞增殖能力。

结果

结果显示,HDAC11的表达与乳腺癌患者的总生存期(OS)呈正相关。特异性敲低HDAC11可增强MDA-MB-231细胞的增殖、迁移和侵袭能力。

结论

总之,本研究发现HDAC11表达与患者总生存率呈正相关。HDAC11在一定程度上可抑制乳腺癌细胞的侵袭和增殖,可作为良好的预后标志物。

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