PEGylated lipid bilayer-supported mesoporous silica nanoparticle composite for synergistic co-delivery of axitinib and celastrol in multi-targeted cancer therapy

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• 作者：Ju Yeon Choi^a ; Thiruganesh Ramasamy^a ; Sung Yub Kim^a ; Jeonghwan Kim^a ; Sae Kwang Ku^b ; Yu Seok Youn^c ; Jae-Ryong Kim^d ; Jee-Heon Jeong^a ; Han-Gon Choi^e ; ^{hangon@hanyang.ac.kr" class="auth_mail" title="E-mail the corresponding author} ; Chul Soon Yong^a ; ^{csyong@ynu.ac.kr" class="auth_mail" title="E-mail the corresponding author} ; Jong Oh Kim^a ; ^{jongohkim@yu.ac.kr" class="auth_mail" title="E-mail the corresponding author}
• 关键词：Axitinib ; Celastrol ; Mitochondria ; Mesoporous silica nanoparticle ; Lipid
• 刊名：Acta Biomaterialia
• 出版年：2016
• 出版时间：15 July 2016
• 年：2016
• 卷：39
• 期：Complete
• 页码：94-105
• 全文大小：2853 K

文摘

Small-molecule drug combination therapies are an attractive approach to enhancing cancer chemotherapeutic responses. Therefore, this study aimed to investigate the potential of axitinib (AXT) and celastrol (CST) in targeting angiogenesis and mitochondrial-based apoptosis in cancer. Therefore, we prepared AXT/CST-loaded combination nanoparticles (ACML) with CST loaded in the mesoporous silica nanoparticles (MSN) and AXT in PEGylated lipidic bilayers. We showed that ACML effectively inhibited angiogenesis and mitochondrial function and was efficiently internalized in SCC-7, BT-474, and SH-SY5Y cells. Furthermore, hypoxia-inducible factor (HIF)-1α expression, which increased under hypoxic conditions in all cell lines exposed to ACML, markedly decreased, which may be critical for tumor inhibition. Western blotting showed the superior anticancer effect of combination nanoparticles in different cancer cells. Compared to the cocktail (AXT/CST), ACML induced synergistic cancer cell apoptosis. The AXT/CST-based combination nanoparticle synergism might be mediated by AXT, which controls vascular endothelial growth factor receptors while CST acts on target cell mitochondria. Importantly, ACML-treated mice showed remarkably higher tumor inhibition (64%) than other groups did in tumor xenograft models. Tumor xenograft immunohistochemistry revealed elevated caspase-3 and poly (ADP-ribose) polymerase and reduced CD31 and Ki-67 expression, clearly suggesting tumor apoptosis through mitochondrial and antiangiogenic effects. Overall, our results indicate that ACML potentially inhibited cell proliferation and induced apoptosis by blocking mitochondrial function, leading to enhanced antitumor efficacy.

Statement of Significance

In this research, we formulated an anticancer drug combination nanoparticle loaded with axitinib (AXT) in the lipidic bilayer of PEGylated liposomes and celastrol (CST) in mesoporous silica nanoparticles. The anticancer effects of the AXT/CST-loaded combination nanoparticle (ACML) were synergistic and superior to the other formulations and involved more efficient drug delivery to the tumor site with enhanced effects on angiogenesis and mitochondrial function. Therefore, our study demonstrated that the inhibition of cell proliferation and induction of apoptosis by ACML, which was mediated by blockade of mitochondrial function and anti-angiogenesis, led to enhanced antitumor efficacy, which may be potentially useful in the clinical treatment of cancer.