Literature DB >> 14517345

Arylamine N-acetyltransferase-1 is highly expressed in breast cancers and conveys enhanced growth and resistance to etoposide in vitro.

Paul J Adam1, Joanne Berry, Julie A Loader, Kerry L Tyson, Graham Craggs, Paul Smith, Jackie De Belin, Graham Steers, Francesco Pezzella, Kris F Sachsenmeir, Alasdair C Stamps, Athula Herath, Edith Sim, Michael J O'Hare, Adrian L Harris, Jonathan A Terrett.   

Abstract

Comparative two-dimensional proteome analysis was used to identify proteins differentially expressed in multiple clinical normal and breast cancer tissues. One protein, the expression of which was elevated in invasive ductal and lobular breast carcinomas when compared with normal breast tissue, was arylamine N-acetyltransferase-1 (NAT-1), a Phase II drug-metabolizing enzyme. NAT-1 overexpression in clinical breast cancers was confirmed at the mRNA level and immunohistochemical analysis of NAT-1 in 108 breast cancer donors demonstrated a strong association of NAT-1 staining with estrogen receptor-positive tumors. Analysis of the effect of active NAT-1 overexpression in a normal luminal epithelial-derived cell line demonstrated enhanced growth properties and etoposide resistance relative to control cells. Thus, NAT-1 may not only play a role in the development of cancers through enhanced mutagenesis but may also contribute to the resistance of some cancers to cytotoxic drugs.

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Year:  2003        PMID: 14517345

Source DB:  PubMed          Journal:  Mol Cancer Res        ISSN: 1541-7786            Impact factor:   5.852


  39 in total

1.  NATb/NAT1*4 promotes greater arylamine N-acetyltransferase 1 mediated DNA adducts and mutations than NATa/NAT1*4 following exposure to 4-aminobiphenyl.

Authors:  Lori M Millner; Mark A Doll; Jian Cai; J Christopher States; David W Hein
Journal:  Mol Carcinog       Date:  2011-08-11       Impact factor: 4.784

2.  Glucocorticoid receptor-mediated transcriptional regulation of N-acetyltransferase 1 gene through distal promoter.

Authors:  Barbara Bonamassa; Yongjie Ma; Dexi Liu
Journal:  AAPS J       Date:  2012-05-30       Impact factor: 4.009

3.  Genetic and small molecule inhibition of arylamine N-acetyltransferase 1 reduces anchorage-independent growth in human breast cancer cell line MDA-MB-231.

Authors:  Marcus W Stepp; Mark A Doll; Samantha M Carlisle; J Christopher States; David W Hein
Journal:  Mol Carcinog       Date:  2018-02-03       Impact factor: 4.784

4.  Phenotype of the most common "slow acetylator" arylamine N-acetyltransferase 1 genetic variant (NAT1*14B) is substrate-dependent.

Authors:  Lori M Millner; Mark A Doll; Jian Cai; J Christopher States; David W Hein
Journal:  Drug Metab Dispos       Date:  2011-10-18       Impact factor: 3.922

5.  Genetic polymorphisms in the metabolic pathway and non-Hodgkin lymphoma survival.

Authors:  Xuesong Han; Tongzhang Zheng; Francine M Foss; Qing Lan; Theodore R Holford; Nathaniel Rothman; Shuangge Ma; Yawei Zhang
Journal:  Am J Hematol       Date:  2010-01       Impact factor: 10.047

6.  Methylation patterns of genes coding for drug-metabolizing enzymes in tamoxifen-resistant breast cancer tissues.

Authors:  Sun Jung Kim; Han-Sung Kang; So-Youn Jung; Sun Young Min; Seeyoun Lee; Seok Won Kim; Youngmee Kwon; Keun Seok Lee; Kyung Hwan Shin; Jungsil Ro
Journal:  J Mol Med (Berl)       Date:  2010-07-14       Impact factor: 4.599

Review 7.  Arylamine N-acetyltransferases: a structural perspective.

Authors:  Xiaotong Zhou; Zhiguo Ma; Dong Dong; Baojian Wu
Journal:  Br J Pharmacol       Date:  2013-06       Impact factor: 8.739

8.  Over-expression, purification, and characterization of recombinant human arylamine N-acetyltransferase 1.

Authors:  Haiqing Wang; Gregory M Vath; Akane Kawamura; Caleb A Bates; Edith Sim; Patrick E Hanna; Carston R Wagner
Journal:  Protein J       Date:  2005-02       Impact factor: 2.371

9.  Untargeted polar metabolomics of transformed MDA-MB-231 breast cancer cells expressing varying levels of human arylamine N-acetyltransferase 1.

Authors:  Samantha M Carlisle; Patrick J Trainor; Xinmin Yin; Mark A Doll; Marcus W Stepp; J Christopher States; Xiang Zhang; David W Hein
Journal:  Metabolomics       Date:  2016-06-21       Impact factor: 4.290

10.  Identification of differentially expressed sense and antisense transcript pairs in breast epithelial tissues.

Authors:  Anita Grigoriadis; Gavin R Oliver; Austin Tanney; Howard Kendrick; Matt J Smalley; Parmjit Jat; A Munro Neville
Journal:  BMC Genomics       Date:  2009-07-17       Impact factor: 3.969

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