选择性HDAC6抑制在细胞癌中具有潜在的抗癌作用

Tsutomu Anraku1, Masaki Murata1, Hiroo Kuroki1

  • 1Department of Urology, Division of Molecular Oncology, Graduate School of Medical and Dental Sciences, Niigata University, Niigata 951-8510, Japan.

概括

用选择性抑制剂向基因组脱乙酶6 (HDAC6) 显著降低细胞癌 (RCC) 细胞活力和DNA复制,诱导细胞亡,并为转移性RCC提供了有希望的治疗策略.

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