Polyethylenimine-Dermatan Sulfate Complex, a Bioactive Biomaterial with Unique Toxicity to CD146-Positive Cancer Cells
- Authors
 - Kim, Bieong-Kil; Kim, Dongkyu; Kwak, Gijung; Yhee, Ji Young; Kwon, Ick-Chan; Kim, Sun Hwa; Yeo, Yoon
 
- Issue Date
 - 2017-06
 
- Publisher
 - AMER CHEMICAL SOC
 
- Citation
 - ACS BIOMATERIALS SCIENCE & ENGINEERING, v.3, no.6, pp.990 - 999
 
- Abstract
 - We report unique bioactivity of a polycation-polyanion complex with potential utility for cancer therapy. A complex of disulfide-cross-linked polyethylenimine (CLPEI), a polycation used for gene complexation, and dermatan sulfate (DS), an anionic polysaccharide to shield excessive cationic charge of the former, has toxicity to a specific group of cancer cell lines, including B16-F10 murine melanoma, A375SM human melanoma, and PC-3 human prostate cancer cells. These CLPEI-DS-sensitive cells express CD146, which binds to the complex via interaction with DS. There is a positive correlation between toxicity and intracellular level of CLPEI, indicating that the CLPEI-DS-sensitivity is attributable to the increased cellular uptake of CLPEI mediated by the DS-CD146 interactions. In vitro studies show that CLPEI-DS complex causes G(0)/G(1) phase arrest and apoptotic cell death. In syngeneic and allograft models of B16-F10 melanoma, CLPEI-DS complex administered with a subtoxic level of doxorubicin potentiates the chemotherapeutic effect of the drug by loosening tumor tissues. Given the unique toxicity, CLPEI-DS complex may be a useful carrier of gene or chemotherapeutics for the therapy of CD146-positive cancers.
 
- Keywords
 - CD146; EXPRESSION; DELIVERY; CHITOSAN; PROGRESSION; MOLECULE; ADHESION; CARRIERS; LIPIDS; DEATH; CD146; EXPRESSION; DELIVERY; CHITOSAN; PROGRESSION; MOLECULE; ADHESION; CARRIERS; LIPIDS; DEATH; bioactive biomaterials; polyethylenimine; dermatan sulfate; CD146; melanoma
 
- ISSN
 - 2373-9878
 
- URI
 - https://pubs.kist.re.kr/handle/201004/122679
 
- DOI
 - 10.1021/acsbiomaterials.7b00207
 
- Appears in Collections:
 - KIST Article > 2017
 
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