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NF-κB Affects Proliferation and Invasiveness of Breast Cancer Cells by Regulating CD44 Expression

Overview of attention for article published in PLOS ONE, September 2014
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Title
NF-κB Affects Proliferation and Invasiveness of Breast Cancer Cells by Regulating CD44 Expression
Published in
PLOS ONE, September 2014
DOI 10.1371/journal.pone.0106966
Pubmed ID
Authors

Shannon M. Smith, Yi Lisa Lyu, Li Cai

Abstract

NF-κB plays an important role in cancer initiation and progression. CD44, a cell surface glycoprotein, is involved in many cellular processes including cell adhesion, migration and proliferation. However, whether and how the two molecules interact in breast cancer is not clear. In recent years, the up-regulation of CD44 has served as a marker for tumor initiating cells in breast cancer and other cancer types. Despite the important role of CD44 in cellular processes and cancer, the mechanism underlying CD44 up-regulation in cancers remains poorly understood. Previously, we have identified a novel cis-element, CR1, located upstream of the CD44 promoter. We demonstrated that NF-κB and AP-1 are key trans-acting factors that interact with CR1. Here, we further analyzed the role of NF-κB in regulating CD44 expression in triple negative breast cancer cells, MDA-MB-231 and SUM159. Inhibition of NF-κB by Bay-11-7082 resulted in a reduction in CD44 expression. CD44 repression via NF-κB inhibition consequently decreased proliferation and invasiveness of breast cancer cells. These findings provide not only new insight into the molecular mechanism underlying CD44 regulation but also potential therapeutic targets that may help eliminate chemo- and radiation-resistant cancer cells.

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The data shown below were compiled from readership statistics for 115 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
India 1 <1%
Austria 1 <1%
Unknown 113 98%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 25 22%
Student > Master 19 17%
Student > Bachelor 17 15%
Researcher 9 8%
Professor > Associate Professor 7 6%
Other 10 9%
Unknown 28 24%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 26 23%
Medicine and Dentistry 21 18%
Agricultural and Biological Sciences 19 17%
Pharmacology, Toxicology and Pharmaceutical Science 10 9%
Chemistry 3 3%
Other 4 3%
Unknown 32 28%