Despite advances in early detection and increased understanding of the molecular basis of breast cancer biology, approximately 30% of all patients with early-stage breast cancer have recurrent disease. In most breast cancer cases, the relapsed tumors are metastatic and refractory to subsequent treatment of the initial drug regimen. Recent evidence has implicated that acquired resistance can arise from chemotherapy-induced mutations and increase tumor cell capacity to either repair or tolerate DNA damage. Therefore, the depletion of crucial gene products involved in these pathways (e.g. Rev1 and Rev3) by RNAi therapeutics may restore the tumors chemosensitivity to treatment. Although considerable efforts have been made to explore various delivery systems for chemotherapeutics and small interfering RNA (siRNA), there remains a pressing need towards engineering nanocarriers that are clinically relevant, biocompatible, efficient, and can be tailored to specific disease targets. The objective of this proposal is to develop a versatile nanocarrier platform capable of co- delivering siRNA (anti-Rev1 and Rev3) and cisplatin for enhanced treatment of breast cancer through synergistic effects. This proposed research is based on the hypothesis that suppression of the mutagenic translesion DNA polymerases could prevent chemoresistance from arising during treatment and restore breast tumors'chemosensitivity to treatment. Thus, nanocarriers capable of simultaneously delivering gene specific siRNA (anti-Rev1 and Rev3) and cisplatin present a promising nanotherapeutic approach for breast cancer treatment. The major objective of the proposed project is to develop an innovative """"""""two-in-one"""""""" nanomedicinal approach to codeliver therapeutic siRNA (e.g., anti-Rev1 and Rev3 siRNA) and platinum-based chemotherapeutics (e.g., cisplatin) within a single polymer-lipid hybrid nanoparticle (NP) for breast cancer treatment. A library of hybrid NPs with tunable physicochemical properties will be developed using cationic lipid compounds and poly (lactide-co-glycolide)-b-poly (ethylene glycol) (PLGA-PEG). The building blocks of the PLGA-PEG copolymer (PLGA and PEG) are widely used in FDA-approved implantable and injectable drug delivery systems and have a long history as safe, biodegradable materials, which are capable of encapsulating small- and macro-molecular payloads with a wide range of physiochemical properties, and can be designed for controlled release through a combination of polymer degradation and drug diffusion. This research presents a promising therapeutic strategy through the synergy among different therapeutics with unique mechanisms. If successful, could significantly improve therapeutic outcomes for breast cancer patients that are underserved by existing therapies and so enhance their quality of life.

Public Health Relevance

Cancer drugs such as cisplatin attack cancer cells by damaging their DNA, preventing cells from copying their DNA and cause cells to commit suicide, however, cancer cells can use enzymes known as translesion DNA polymerases to copy over DNA damage, allowing them to survive. This type of DNA copying can be highly prone to error, introducing mutations into the DNA, and the newly acquired mutations make cancer cells that survive chemotherapy much more drug- resistant and aggressive. In this project, I aim to develop a versatile polymer-lipid hybrid nanoparticle (NP) platform capable of simultaneously delivering chemotherapeutics (cisplatin) and gene-specific siRNA (anti-Rev1 and Rev3), and as a promising therapeutic strategy to restore breast tumor chemosensitivity to treatment through inhibiting the activity of translesion DNA polymerases.

National Institute of Health (NIH)
National Cancer Institute (NCI)
Postdoctoral Individual National Research Service Award (F32)
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Special Emphasis Panel (ZRG1-F09-D (20))
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Jakowlew, Sonia B
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Brigham and Women's Hospital
United States
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Xue, Yuan; Xu, Xiaoyang; Zhang, Xue-Qing et al. (2016) Preventing diet-induced obesity in mice by adipose tissue transformation and angiogenesis using targeted nanoparticles. Proc Natl Acad Sci U S A 113:5552-7
Zhang, Xue-Qing; Even-Or, Orli; Xu, Xiaoyang et al. (2015) Nanoparticles containing a liver X receptor agonist inhibit inflammation and atherosclerosis. Adv Healthc Mater 4:228-36
Zhu, Xi; Xu, Yingjie; Solis, Luisa M et al. (2015) Long-circulating siRNA nanoparticles for validating Prohibitin1-targeted non-small cell lung cancer treatment. Proc Natl Acad Sci U S A 112:7779-84
Xu, Xiaoyang; Ho, William; Zhang, Xueqing et al. (2015) Cancer nanomedicine: from targeted delivery to combination therapy. Trends Mol Med 21:223-32
Bertrand, Nicolas; Wu, Jun; Xu, Xiaoyang et al. (2014) Cancer nanotechnology: the impact of passive and active targeting in the era of modern cancer biology. Adv Drug Deliv Rev 66:2-25
Wu, Jun; Kamaly, Nazila; Shi, Jinjun et al. (2014) Development of multinuclear polymeric nanoparticles as robust protein nanocarriers. Angew Chem Int Ed Engl 53:8975-9
Xu, Xiaoyang; Xie, Kun; Zhang, Xue-Qing et al. (2013) Enhancing tumor cell response to chemotherapy through nanoparticle-mediated codelivery of siRNA and cisplatin prodrug. Proc Natl Acad Sci U S A 110:18638-43
Zhang, Xue-Qing; Xu, Xiaoyang; Bertrand, Nicolas et al. (2012) Interactions of nanomaterials and biological systems: Implications to personalized nanomedicine. Adv Drug Deliv Rev 64:1363-84