Tert‐Butylcarbamate‐Containing Histone Deacetylase Inhibitors: Apoptosis Induction, Cytodifferentiation, and Antiproliferative Activities in Cancer Cells. Issue 5 (25th March 2013)
- Record Type:
- Journal Article
- Title:
- Tert‐Butylcarbamate‐Containing Histone Deacetylase Inhibitors: Apoptosis Induction, Cytodifferentiation, and Antiproliferative Activities in Cancer Cells. Issue 5 (25th March 2013)
- Main Title:
- Tert‐Butylcarbamate‐Containing Histone Deacetylase Inhibitors: Apoptosis Induction, Cytodifferentiation, and Antiproliferative Activities in Cancer Cells
- Authors:
- Valente, Sergio
Trisciuoglio, Daniela
Tardugno, Maria
Benedetti, Rosaria
Labella, Donatella
Secci, Daniela
Mercurio, Ciro
Boggio, Roberto
Tomassi, Stefano
Di Maro, Salvatore
Novellino, Ettore
Altucci, Lucia
Del Bufalo, Donatella
Mai, Antonello
Cosconati, Sandro - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Herein we report novel pyrrole‐ and benzene‐based hydroxamates (<bold>8</bold>, <bold>10</bold>) and 2′‐aminoanilides (<bold>9</bold>, <bold>11</bold>) bearing the <italic>tert</italic>‐butylcarbamate group at the CAP moiety as histone deacetylase (HDAC) inhibitors. Compounds <bold>8 b</bold> and <bold>10 c</bold> selectively inhibited HDAC6 at the nanomolar level, whereas the other hydroxamates effected an increase in acetyl‐α‐tubulin levels in human acute myeloid leukemia U937 cells. In the same cell line, compounds <bold>8 b</bold> and <bold>10 c</bold> elicited 18.4 and 21.4 % apoptosis, respectively (SAHA: 16.9 %), and the pyrrole anilide <bold>9 c</bold> displayed the highest cytodifferentiating effect (90.9 %). In tests against a wide range of various cancer cell lines to determine its antiproliferative effects, compound <bold>10 c</bold> exhibited growth inhibition from sub‐micromolar (neuroblastoma LAN‐5 and SH‐SY5Y cells, chronic myeloid leukemia K562 cells) to low‐micromolar (lung H1299 and A549, colon HCT116 and HT29 cancer cells) concentrations. In HT29 cells, <bold>10 c</bold> increased histone H3 acetylation, and decreased the colony‐forming potential of the cancer cells by up to 60 %.</p> </abstract>
- Is Part Of:
- ChemMedChem. Volume 8:Issue 5(2013:May)
- Journal:
- ChemMedChem
- Issue:
- Volume 8:Issue 5(2013:May)
- Issue Display:
- Volume 8, Issue 5 (2013)
- Year:
- 2013
- Volume:
- 8
- Issue:
- 5
- Issue Sort Value:
- 2013-0008-0005-0000
- Page Start:
- 800
- Page End:
- 811
- Publication Date:
- 2013-03-25
- Subjects:
- Pharmaceutical chemistry -- Periodicals
615.19005 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1860-7187 ↗
http://www3.interscience.wiley.com/cgi-bin/jhome/110485305 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cmdc.201300005 ↗
- Languages:
- English
- ISSNs:
- 1860-7179
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3172.254000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3077.xml