Literature DB >> 19513533

Suberoylanilide hydroxamic acid (SAHA) changes microRNA expression profiles in A549 human non-small cell lung cancer cells.

Eun-Mee Lee1, Sangsu Shin, Hwa Jun Cha, Youngmin Yoon, Seunghee Bae, Jin Hyuk Jung, Sun-Mi Lee, Su-Jae Lee, In-Chul Park, Young-Woo Jin, Sungkwan An.   

Abstract

Suberoylanilide hydroxamic acid (SAHA) is a histone deacetylase inhibitor (HDACI) with antitumor effects that is being explored as a therapeutic drug. However, it has been reported that non-small cell lung cancer (NSCLC) is resistant to HDACIs. MicroRNAs (miRNAs) are a key class of small, non-coding RNA molecules that modulate post-transcriptional regulation of gene expression in multi-cellular organisms. miRNA expression patterns are involved in deregulation of gene expression in human lung cancer. Here we identified miRNA expression profile changes in response to SAHA treatment in the human lung carcinoma cell line A549. We also examined potential mRNA targets of SAHA-responsive miRNAs by using a target prediction program. Using microarray analysis, we found 64 miRNAs with >2-fold expression changes in SAHA-treated A549 cells. Among them, two unique miRNAs were altered in 2.5 microM SAHA-treated cells, 31 unique miRNAs were altered in 5.0 microM SAHA-treated cells and 31 miRNAs were altered with both doses. These miRNAs are predicted to have several target genes related to angiogenesis, apoptosis, chromatin modification, cell proliferation and differentiation. In conclusion, we have identified a unique set of miRNAs and their expression profiles that are influenced significantly by SAHA in the A549 NSCLC cell line model, which might provide useful information for understanding the anticancer mechanism of SAHA.

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Year:  2009        PMID: 19513533     DOI: 10.3892/ijmm_00000204

Source DB:  PubMed          Journal:  Int J Mol Med        ISSN: 1107-3756            Impact factor:   4.101


  32 in total

1.  Myc represses miR-15a/miR-16-1 expression through recruitment of HDAC3 in mantle cell and other non-Hodgkin B-cell lymphomas.

Authors:  X Zhang; X Chen; J Lin; T Lwin; G Wright; L C Moscinski; W S Dalton; E Seto; K Wright; E Sotomayor; J Tao
Journal:  Oncogene       Date:  2011-10-17       Impact factor: 9.867

Review 2.  Histone deacetylase inhibitors: a chemical genetics approach to understanding cellular functions.

Authors:  Paul A Marks
Journal:  Biochim Biophys Acta       Date:  2010-06-08

3.  Suberoylanilide hydroxamic acid inhibits growth of head and neck cancer cell lines by reactivation of tumor suppressor microRNAs.

Authors:  Jharna Datta; Mozaffarul Islam; Samidha Dutta; Sounak Roy; Quintin Pan; Theodoros N Teknos
Journal:  Oral Oncol       Date:  2016-03-19       Impact factor: 5.337

Review 4.  The clinical development of histone deacetylase inhibitors as targeted anticancer drugs.

Authors:  Paul A Marks
Journal:  Expert Opin Investig Drugs       Date:  2010-09       Impact factor: 6.206

5.  Endoplasmic reticulum stress plays a pivotal role in cell death mediated by the pan-deacetylase inhibitor panobinostat in human hepatocellular cancer cells.

Authors:  Roberta Montalbano; Petra Waldegger; Karl Quint; Samir Jabari; Daniel Neureiter; Romana Illig; Matthias Ocker; Pietro Di Fazio
Journal:  Transl Oncol       Date:  2013-04-01       Impact factor: 4.243

Review 6.  MicroRNAs as targets for dietary and pharmacological inhibitors of mutagenesis and carcinogenesis.

Authors:  Alberto Izzotti; Cristina Cartiglia; Vernon E Steele; Silvio De Flora
Journal:  Mutat Res       Date:  2012-06-07       Impact factor: 2.433

7.  Global miRNA/proteomic analyses identify miRNAs at 14q32 and 3p21, which contribute to features of chronic iron-exposed fallopian tube epithelial cells.

Authors:  Ravneet Chhabra; Stephanie Rockfield; Jennifer Guergues; Owen W Nadeau; Robert Hill; Stanley M Stevens; Meera Nanjundan
Journal:  Sci Rep       Date:  2021-03-18       Impact factor: 4.379

8.  The histone deacetylase inhibitor, vorinostat, reduces tumor growth at the metastatic bone site and associated osteolysis, but promotes normal bone loss.

Authors:  Jitesh Pratap; Jacqueline Akech; John J Wixted; Gabriela Szabo; Sadiq Hussain; Meghan E McGee-Lawrence; Xiaodong Li; Krystin Bedard; Robinder J Dhillon; Andre J van Wijnen; Janet L Stein; Gary S Stein; Jennifer J Westendorf; Jane B Lian
Journal:  Mol Cancer Ther       Date:  2010-12       Impact factor: 6.261

9.  Histone deacetylases inhibitor trichostatin A increases the expression of Dleu2/miR-15a/16-1 via HDAC3 in non-small cell lung cancer.

Authors:  Chi-Qi Chen; Cheng-Shui Chen; Jun-Jie Chen; Lian-Ping Zhou; Hong-Lei Xu; Wei-Wei Jin; Jian-Bo Wu; Shen-Meng Gao
Journal:  Mol Cell Biochem       Date:  2013-07-19       Impact factor: 3.396

10.  Cancer Epigenetics: Mechanisms and Crosstalk of a HDAC Inhibitor, Vorinostat.

Authors:  Jean Lee; Stephanie Huang R
Journal:  Chemotherapy (Los Angel)       Date:  2013-06-05
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