Tumor microenvironment-responsive nanoparticles for cancer theragnostic applications
Background Cancer is one of the deadliest threats to human health. Abnormal physiochemical conditions and dysregulated biosynthetic intermediates in the tumor microenvironment (TME) play a significant role in modulating cancer cells to evade or defend conventional anti-cancer therapy such as surgery...
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Published in | Biomaterials research Vol. 22; no. 1; pp. 22 - 11 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
London
BioMed Central
23.08.2018
BioMed Central Ltd American Association for the Advancement of Science (AAAS) 한국생체재료학회 |
Subjects | |
Online Access | Get full text |
ISSN | 2055-7124 1226-4601 2055-7124 |
DOI | 10.1186/s40824-018-0132-z |
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Summary: | Background
Cancer is one of the deadliest threats to human health. Abnormal physiochemical conditions and dysregulated biosynthetic intermediates in the tumor microenvironment (TME) play a significant role in modulating cancer cells to evade or defend conventional anti-cancer therapy such as surgery, chemotherapy and radiotherapy. One of the most important challenges in the development of anti-tumor therapy is the successful delivery of therapeutic and imaging agents specifically to solid tumors.
Main body
The recent progresses in development of TME responsive nanoparticles offers promising strategies for combating cancer by making use of the common attributes of tumor such as acidic and hypoxic microenvironments. In this review, we discussed the prominent strategies utilized in the development of tumor microenvironment-responsive nanoparticles and mode of release of therapeutic cargo.
Conclusion
Tumor microenvironment-responsive nanoparticles offers a universal approach for anti-cancer therapy. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Review-3 content type line 23 https://biomaterialsres.biomedcentral.com/track/pdf/10.1186/s40824-018-0132-z |
ISSN: | 2055-7124 1226-4601 2055-7124 |
DOI: | 10.1186/s40824-018-0132-z |