Guo Pingping, Chen Wenqi, Li Huiyu, Li Meiying, Li Lisha
The Key Laboratory of Pathobiology, Ministry of Education, Norman Bethune Medical College, Jilin University, Changchun, 130021, China.
Pathol Oncol Res. 2018 Oct;24(4):807-813. doi: 10.1007/s12253-018-0433-5. Epub 2018 Jun 11.
The histone acetylation modifications (HAMs) influence a large number of cellular functions. They are mediated through histone acetyltransferase (HAT) and histone deacetylase (HDAC). Nowadays, people have realized that HAMs are crucial for development and prognosis of breast cancer. Investigations about abnormal HAMs in breast cancer focus on initiating molecular mechanisms in breast cancer development, identification of new biomarkers to predict breast cancer aggressiveness and the therapeutic potential. As HAMs are reversible, breast cancer may be treated by restoring HAMs to normal levels. Indeed, some HDAC inhibitors have been approved by the US Food and Drug Administration to treat certain cancers. Furthermore, HAT inhibitors, HAT activators and HDAC activators may also be used as drugs to treat breast cancer.
组蛋白乙酰化修饰(HAMs)影响大量细胞功能。它们由组蛋白乙酰转移酶(HAT)和组蛋白去乙酰化酶(HDAC)介导。如今,人们已经认识到HAMs对乳腺癌的发展和预后至关重要。关于乳腺癌中异常HAMs的研究集中在乳腺癌发展的起始分子机制、预测乳腺癌侵袭性的新生物标志物的鉴定以及治疗潜力方面。由于HAMs是可逆的,乳腺癌可以通过将HAMs恢复到正常水平来治疗。事实上,一些HDAC抑制剂已被美国食品药品监督管理局批准用于治疗某些癌症。此外,HAT抑制剂、HAT激活剂和HDAC激活剂也可能用作治疗乳腺癌的药物。