Deletion of arylamine N ‐acetyltransferase 1 in MDA‐MB‐231 human breast cancer cells reduces primary and secondary tumor growth in vivo with no significant effects on metastasis
Author:
Affiliation:
1. Department of Pharmacology and Toxicology University of Louisville Louisville Kentucky USA
2. Department of Medicine University of Louisville Louisville Kentucky USA
3. Brown Cancer Center University of Louisville Louisville Kentucky USA
Funder
National Institute of Environmental Health Sciences
National Institute of Diabetes and Digestive and Kidney Diseases
Publisher
Wiley
Subject
Cancer Research,Molecular Biology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/mc.23392
Reference39 articles.
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3. Molecular genetics and epidemiology of the NAT1 and NAT2 acetylation polymorphisms;Hein DW;Cancer Epidemiol Biomarkers Prev,2000
4. Congenic rats with higher arylamine N-acetyltransferase 2 activity exhibit greater carcinogen-induced mammary tumor susceptibility independent of carcinogen metabolism
5. Differences between murine arylamine N-acetyltransferase type 1 and human arylamine N-acetyltransferase type 2 defined by substrate specificity and inhibitor binding
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1. Arylamine N-Acetyltransferases;Reference Module in Biomedical Sciences;2024
2. Stable Isotope Tracing Reveals an Altered Fate of Glucose in N-Acetyltransferase 1 Knockout Breast Cancer Cells;Genes;2023-03-31
3. Upregulation of cytidine deaminase in NAT1 knockout breast cancer cells;Journal of Cancer Research and Clinical Oncology;2022-11-03
4. Proteomic analysis of arylamine N-acetyltransferase 1 knockout breast cancer cells: Implications in immune evasion and mitochondrial biogenesis;Toxicology Reports;2022
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