| Literature DB >> 31368208 |
Cheng Wang1,2, Fangying Yu1, Xuerong Liu1, Shaoqing Chen1, Rui Wu1, Rui Zhao3, Fuqiang Hu1, Hong Yuan1.
Abstract
Calcium (Ca2+ ) hemeostasis is crucial for the normal function of cellular biochemistry. The abnormal frequency of Ca2+ signaling in cancer cells makes them more vulnerable to Ca2+ modulation than normal cells. Here in this study, a novel cancer-specific therapy by artificially triggering Ca2+ overload in cancer cells is proposed. The feasibility of this therapy is illustrated by successful coupling of selective extrusion (Ca2+ ) inhibition effect of Curcumin (Cur) and the effective Ca2+ generating capability of amorphous calcium carbonate (ACC) into a facilely prepared water responsive phospholipid (PL)-ACC hybrid platform (PL/ACC-Cur). The obtained results demonstrate that PL/ACC-Cur can specifically boost the intracellular Ca2+ concentration to cause Ca2+ overload and to trigger mitochondria-related apoptosis in MCF-7 cells while sparing normal hepatocyte (L02), which might be a promising approach for effective cancer therapy.Entities:
Keywords: amorphous calcium carbonate; apoptosis; calcium overload; curcumin; mitochondria
Mesh:
Substances:
Year: 2019 PMID: 31368208 DOI: 10.1002/adhm.201900501
Source DB: PubMed Journal: Adv Healthc Mater ISSN: 2192-2640 Impact factor: 9.933