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Histone Deacetylases and their Inhibitors in Colorectal Cancer Therapy: Current Evidence and Future Considerations.
Current Medicinal Chemistry ( IF 3.5 ) Pub Date : 2022-01-01 , DOI: 10.2174/0929867328666210915105929
Nikolaos Garmpis 1, 2 , Christos Damaskos 2, 3 , Anna Garmpi 4 , Afroditi Nonni 5 , Vasiliki E Georgakopoulou 6 , Efstathios Antoniou 1, 2 , Dimitrios Schizas 7 , Panagiotis Sarantis 8 , Alexandros Patsouras 2 , Athanasios Syllaios 7 , Christos Vallilas 8 , Evangelos Koustas 8 , Konstantinos Kontzoglou 1, 2 , Nikolaos Trakas 9 , Dimitrios Dimitroulis 1
Affiliation  

Colorectal cancer (CRC) comprises a heterogeneous group of gastrointestinal tract tumors. It is a multifactorial disease, and a plethora of distinct factors are involved in its pathogenesis and pathophysiology. The development of CRC is not limited to genetic changes, but epigenetic and environmental factors are also involved. Among the epigenetic factors, histone deacetylases (HDACs), a group of epigenetic enzymes that regulate gene expression, have been reported to be over-expressed in CRC. HDACs and their inhibitors seem to play an important role in the molecular pathophysiology of CRC. The aim of this review was to define the role of HDAC inhibitors as potential anticancer agents against CRC.

中文翻译:

结直肠癌治疗中的组蛋白脱乙酰酶及其抑制剂:当前证据和未来考虑。

结直肠癌 (CRC) 包括一组异质的胃肠道肿瘤。它是一种多因素疾病,其发病机制和病理生理学涉及许多不同的因素。结直肠癌的发展不仅限于遗传变化,还涉及表观遗传和环境因素。在表观遗传因素中,组蛋白去乙酰化酶 (HDACs) 是一组调节基因表达的表观遗传酶,据报道在 CRC 中过度表达。HDACs 及其抑制剂似乎在 CRC 的分子病理生理学中起重要作用。本综述的目的是确定 HDAC 抑制剂作为潜在抗 CRC 药物的作用。
更新日期:2021-09-14
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