Breaking the niche: multidimensional nanotherapeutics for tumor microenvironment modulation

dc.contributor.authorRoy, Aniruddha
dc.date.accessioned2024-01-11T04:25:56Z
dc.date.available2024-01-11T04:25:56Z
dc.date.issued2022-06
dc.description.abstractMost of the current antitumor therapeutics were developed targeting the cancer cells only. Unfortunately, in the majority of tumors, this single-dimensional therapy is found to be ineffective. Advanced research has shown that cancer is a multicellular disorder. The tumor microenvironment (TME), which is made by a complex network of the bulk tumor cells and other supporting cells, plays a crucial role in tumor progression. Understanding the importance of the TME in tumor growth, different treatment modalities have been developed targeting these supporting cells. Recent clinical results suggest that simultaneously targeting multiple components of the tumor ecosystem with drug combinations can be highly effective. This type of “multidimensional” therapy has a high potential for cancer treatment. However, tumor-specific delivery of such multi-drug combinations remains a challenge. Nanomedicine could be utilized for the tumor-targeted delivery of such multidimensional therapeutics. In this review, we first give a brief overview of the major components of TME. We then highlight the latest developments in nanoparticle-based combination therapies, where one drug targets cancer cells and other drug targets tumor-supporting components in the TME for a synergistic effect. We include the latest preclinical and clinical studies and discuss innovative nanoparticle-mediated targeting strategies.en_US
dc.identifier.urihttps://link.springer.com/article/10.1007/s13346-022-01194-7
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/13802
dc.language.isoenen_US
dc.publisherSpringeren_US
dc.subjectPharmacyen_US
dc.subjectCancer Cellsen_US
dc.subjectTumor microenvironmenten_US
dc.titleBreaking the niche: multidimensional nanotherapeutics for tumor microenvironment modulationen_US
dc.typeArticleen_US

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