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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 |
Appears in Collections: | Elements Staff Publications |
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