Please use this identifier to cite or link to this item: https://doi.org/10.1186/bcr3656
Title: Combining the strength of genomics, nanoparticle technology, and direct intraductal delivery for breast cancer treatment
Authors: Teo, W.W 
Sukumar, S
Keywords: doxorubicin
nanoparticle
small interfering RNA
homeodomain protein
nanoparticle
small interfering RNA
transcription factor
article
atypical ductal hyperplasia
breast cancer
cancer model
carcinogenesis
gene silencing
gene targeting
genomics
human
immune response
immunity
intraductal drug administration
microarray analysis
nonhuman
transgenic mouse
animal
experimental mammary neoplasm
gene silencing
genetics
pathology
Animals
Gene Silencing
Homeodomain Proteins
Mammary Neoplasms, Experimental
Nanoparticles
RNA, Small Interfering
Transcription Factors
Issue Date: 2014
Citation: Teo, W.W, Sukumar, S (2014). Combining the strength of genomics, nanoparticle technology, and direct intraductal delivery for breast cancer treatment. Breast Cancer Research 16 (2) : 306. ScholarBank@NUS Repository. https://doi.org/10.1186/bcr3656
Rights: Attribution 4.0 International
Abstract: A large number of genes are altered in cancer cells. Often, reversal or inhibition of just one of these alterations leads to death of the cancer cells. Technological advances in multiple areas are necessary to potentiate clinical translation of these findings. In a recent article, Brock and colleagues reported that overexpressed HOXA1 is a critical event in tumor progression in a mouse mammary tumor model. They developed HOXA1-small interfering RNA nanoparticles and achieved effective therapeutic doses by delivering them intraductally through the nipple to the site of the tumor and at the same time circumvented the systemic immune response. This study strengthens the concept of targeting overexpressed genes by using small interfering RNA and bypassing systemic immunity through local intraductal delivery. © 2014 Teo and Sukumar; licensee BioMed Central Ltd.
Source Title: Breast Cancer Research
URI: https://scholarbank.nus.edu.sg/handle/10635/181501
ISSN: 14655411
DOI: 10.1186/bcr3656
Rights: Attribution 4.0 International
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