Targeting autophagy using metallic nanoparticles: a promising strategy for cancer treatment

被引:143
作者
Cordani, Marco [1 ,2 ]
Somoza, Alvaro [1 ,2 ]
机构
[1] CSIC, CNB, IMDEA Nanociencia Associated Unit Unidad Nanobiot, Inst Madrileno Estudios Avanzados Nanociencia IMD, Madrid, Spain
[2] Inst Adv Studies Nanosci IMDEA Nanociencia, Faraday 9,Off 129,Lab 137 Ciudad Univ Cantoblanco, Madrid 28049, Spain
关键词
Nanomedicine; Nanomaterials; Cancer therapy; Autophagy; ZINC-OXIDE NANOPARTICLES; MESOPOROUS SILICA NANOPARTICLES; PHOTOTHERMAL THERAPY PPTT; HYPOXIA-INDUCED AUTOPHAGY; GOLD SHELL NANOPARTICLES; APOPTOTIC CELL-DEATH; MUTANT P53 PROTEINS; 2 HUMAN HOMOLOGS; SILVER NANOPARTICLES; TITANIUM-DIOXIDE;
D O I
10.1007/s00018-018-2973-y
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Despite the extensive genetic and phenotypic variations present in the different tumors, they frequently share common metabolic alterations, such as autophagy. Autophagy is a self-degradative process in response to stresses by which damaged macromolecules and organelles are targeted by autophagic vesicles to lysosomes and then eliminated. It is known that autophagy dysfunctions can promote tumorigenesis and cancer development, but, interestingly, its overstimulation by cytotoxic drugs may also induce cell death and chemosensitivity. For this reason, the possibility to modulate autophagy may represent a valid therapeutic approach to treat different types of cancers and a variety of clinical trials, using autophagy modulators, are currently employed. On the other hand, recent progress in nanotechnology offers plenty of tools to fight cancer with innovative and efficient therapeutic agents by overcoming obstacles usually encountered with traditional drugs. Interestingly, nanomaterials can modulate autophagy and have been exploited as therapeutic agents against cancer. In this article, we summarize the most recent advances in the application of metallic nanostructures as potent modulators of autophagy process through multiple mechanisms, stressing their therapeutic implications in cancer diseases. For this reason, we believe that autophagy modulation with nanoparticle-based strategies would acquire clinical relevance in the near future, as a complementary therapy for the treatment of cancers and other diseases.
引用
收藏
页码:1215 / 1242
页数:28
相关论文
共 220 条
[1]  
Abudayyak M., 2016, Appl, V2, P157, DOI DOI 10.1089/AIVT.2016.0008
[2]   Nanomedicine: An effective tool in cancer therapy [J].
Aftab, Saima ;
Shah, Afzal ;
Nadhman, Akhtar ;
Kurbanoglu, Sevinc ;
Ozkan, Sibel Aysil ;
Dionysiou, Dionysios D. ;
Shukla, Shyam S. ;
Aminabhavi, Tejraj M. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2018, 540 (1-2) :132-149
[3]   p53 Deletion or Hotspot Mutations Enhance mTORC1 Activity by Altering Lysosomal Dynamics of TSC2 and Rheb [J].
Agarwal, Stuti ;
Bell, Catherine M. ;
Taylor, Shirley M. ;
Moran, Richard G. .
MOLECULAR CANCER RESEARCH, 2016, 14 (01) :66-77
[4]  
Albanese A, 2012, ANNU REV BIOMED ENG, V14, P1, DOI [10.1146/annurev-bioeng-071811-150124, 10.1146/annurev.bioeng-071811-150124]
[5]   Autophagy inhibition enhances therapy-induced apoptosis in a Myc-induced model of lymphoma [J].
Amaravadi, Ravi K. ;
Yu, Duonan ;
Lum, Julian J. ;
Bui, Thi ;
Christophorou, Maria A. ;
Evan, Gerard I. ;
Thomas-Tikhonenko, Andrei ;
Thompson, Craig B. .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (02) :326-336
[6]  
Andra W., 2007, Magnetism in Medicine: A Handbook, DOI [10.1002/9783527610174, DOI 10.1002/9783527610174]
[7]   Lysosomal mTORC2/PHLPP1/Akt Regulate Chaperone-Mediated Autophagy [J].
Arias, Esperanza ;
Koga, Hiroshi ;
Diaz, Antonio ;
Mocholi, Enric ;
Patel, Bindi ;
Cuervo, Ana Maria .
MOLECULAR CELL, 2015, 59 (02) :270-284
[8]   The pathways of mitophagy for quality control and clearance of mitochondria [J].
Ashrafi, G. ;
Schwarz, T. L. .
CELL DEATH AND DIFFERENTIATION, 2013, 20 (01) :31-42
[9]   The regulation and function of Class III PI3Ks: novel roles for Vps34 [J].
Backer, Jonathan M. .
BIOCHEMICAL JOURNAL, 2008, 410 (01) :1-17
[10]   Zinc oxide nanoparticles induce apoptosis and autophagy in human ovarian cancer cells [J].
Bai, Ding-Ping ;
Zhang, Xi-Feng ;
Zhang, Guo-Liang ;
Huang, Yi-Fan ;
Gurunathan, Sangiliyandi .
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2017, 12 :6521-6535