Please use this identifier to cite or link to this item: https://doi.org/10.1186/bcr3656
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dc.titleCombining the strength of genomics, nanoparticle technology, and direct intraductal delivery for breast cancer treatment
dc.contributor.authorTeo, W.W
dc.contributor.authorSukumar, S
dc.date.accessioned2020-10-27T11:07:37Z
dc.date.available2020-10-27T11:07:37Z
dc.date.issued2014
dc.identifier.citationTeo, 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
dc.identifier.issn14655411
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/181501
dc.description.abstractA 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.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectdoxorubicin
dc.subjectnanoparticle
dc.subjectsmall interfering RNA
dc.subjecthomeodomain protein
dc.subjectnanoparticle
dc.subjectsmall interfering RNA
dc.subjecttranscription factor
dc.subjectarticle
dc.subjectatypical ductal hyperplasia
dc.subjectbreast cancer
dc.subjectcancer model
dc.subjectcarcinogenesis
dc.subjectgene silencing
dc.subjectgene targeting
dc.subjectgenomics
dc.subjecthuman
dc.subjectimmune response
dc.subjectimmunity
dc.subjectintraductal drug administration
dc.subjectmicroarray analysis
dc.subjectnonhuman
dc.subjecttransgenic mouse
dc.subjectanimal
dc.subjectexperimental mammary neoplasm
dc.subjectgene silencing
dc.subjectgenetics
dc.subjectpathology
dc.subjectAnimals
dc.subjectGene Silencing
dc.subjectHomeodomain Proteins
dc.subjectMammary Neoplasms, Experimental
dc.subjectNanoparticles
dc.subjectRNA, Small Interfering
dc.subjectTranscription Factors
dc.typeArticle
dc.contributor.departmentCANCER SCIENCE INSTITUTE OF SINGAPORE
dc.description.doi10.1186/bcr3656
dc.description.sourcetitleBreast Cancer Research
dc.description.volume16
dc.description.issue2
dc.description.page306
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