Difference between revisions of "Chidamide (Epidaza)"

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''Not FDA approved, but is approved for use in China.''
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==Mechanism of action==
 
==Mechanism of action==
 
From the [https://www.cancer.gov/publications/dictionaries/cancer-drug/def/tucidinostat NCI Drug Dictionary]: An orally bioavailable benzamide type inhibitor of histone deacetylase (HDAC) isoenzymes 1, 2, 3 and 10, with potential antineoplastic activity. Tucidinostat selectively binds to and inhibits HDAC leading to an increase of acetylation levels of histone protein H3. This agent also inhibits the expression of signaling kinases in the PI3K/Akt and MAPK/Ras signaling pathways and may result in cell cycle arrest and the induction of tumor cell apoptosis. This may inhibit tumor cell proliferation in susceptible tumor cells.
 
From the [https://www.cancer.gov/publications/dictionaries/cancer-drug/def/tucidinostat NCI Drug Dictionary]: An orally bioavailable benzamide type inhibitor of histone deacetylase (HDAC) isoenzymes 1, 2, 3 and 10, with potential antineoplastic activity. Tucidinostat selectively binds to and inhibits HDAC leading to an increase of acetylation levels of histone protein H3. This agent also inhibits the expression of signaling kinases in the PI3K/Akt and MAPK/Ras signaling pathways and may result in cell cycle arrest and the induction of tumor cell apoptosis. This may inhibit tumor cell proliferation in susceptible tumor cells.
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*[[Breast cancer]]
 
*[[Breast cancer]]
 
*[[Peripheral T-cell lymphoma]]
 
*[[Peripheral T-cell lymphoma]]
 
==History of changes in FDA indication==
 
''Not FDA approved, but is approved for use in China.''
 
  
 
==Also known as==
 
==Also known as==

Revision as of 13:04, 8 May 2021

Not FDA approved, but is approved for use in China.

Mechanism of action

From the NCI Drug Dictionary: An orally bioavailable benzamide type inhibitor of histone deacetylase (HDAC) isoenzymes 1, 2, 3 and 10, with potential antineoplastic activity. Tucidinostat selectively binds to and inhibits HDAC leading to an increase of acetylation levels of histone protein H3. This agent also inhibits the expression of signaling kinases in the PI3K/Akt and MAPK/Ras signaling pathways and may result in cell cycle arrest and the induction of tumor cell apoptosis. This may inhibit tumor cell proliferation in susceptible tumor cells.

Diseases for which it is used

Also known as

  • Code names: CS055, HBI-8000
  • Generic name: tucidinostat
  • Brand name: Epidaza