Please use this identifier to cite or link to this item:
https://doi.org/10.1186/bcr3656
DC Field | Value | |
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dc.title | Combining the strength of genomics, nanoparticle technology, and direct intraductal delivery for breast cancer treatment | |
dc.contributor.author | Teo, W.W | |
dc.contributor.author | Sukumar, S | |
dc.date.accessioned | 2020-10-27T11:07:37Z | |
dc.date.available | 2020-10-27T11:07:37Z | |
dc.date.issued | 2014 | |
dc.identifier.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 | |
dc.identifier.issn | 14655411 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/181501 | |
dc.description.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. | |
dc.rights | Attribution 4.0 International | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Unpaywall 20201031 | |
dc.subject | doxorubicin | |
dc.subject | nanoparticle | |
dc.subject | small interfering RNA | |
dc.subject | homeodomain protein | |
dc.subject | nanoparticle | |
dc.subject | small interfering RNA | |
dc.subject | transcription factor | |
dc.subject | article | |
dc.subject | atypical ductal hyperplasia | |
dc.subject | breast cancer | |
dc.subject | cancer model | |
dc.subject | carcinogenesis | |
dc.subject | gene silencing | |
dc.subject | gene targeting | |
dc.subject | genomics | |
dc.subject | human | |
dc.subject | immune response | |
dc.subject | immunity | |
dc.subject | intraductal drug administration | |
dc.subject | microarray analysis | |
dc.subject | nonhuman | |
dc.subject | transgenic mouse | |
dc.subject | animal | |
dc.subject | experimental mammary neoplasm | |
dc.subject | gene silencing | |
dc.subject | genetics | |
dc.subject | pathology | |
dc.subject | Animals | |
dc.subject | Gene Silencing | |
dc.subject | Homeodomain Proteins | |
dc.subject | Mammary Neoplasms, Experimental | |
dc.subject | Nanoparticles | |
dc.subject | RNA, Small Interfering | |
dc.subject | Transcription Factors | |
dc.type | Article | |
dc.contributor.department | CANCER SCIENCE INSTITUTE OF SINGAPORE | |
dc.description.doi | 10.1186/bcr3656 | |
dc.description.sourcetitle | Breast Cancer Research | |
dc.description.volume | 16 | |
dc.description.issue | 2 | |
dc.description.page | 306 | |
Appears in Collections: | Elements Staff Publications |
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