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dc.contributor.authorChowdhury, Rajdeep-
dc.contributor.authorChowdhury, Shibasish-
dc.contributor.authorMukherjee, Sudeshna-
dc.date.accessioned2024-08-23T04:20:47Z-
dc.date.available2024-08-23T04:20:47Z-
dc.date.issued2022-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S221475002200213X?via%3Dihub-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15368-
dc.description.abstractBreast cancer is one of the most frequent forms of cancer. Although different treatment modalities are available, none has proved to be a game-changer. In this context, nanomedicine is one of the hot research areas, with different nano-formulations being explored as a therapeutic strategy against breast cancer. Herein, silver nanoparticles (AgNPs) have shown prospects with their anti-tumor properties and are currently being explored aggressively; however, the underlying molecular mechanisms of AgNP action remain to be unearthed. As part of this study, human breast cancer cells- MCF7 were exposed to AgNPs (∼9 nm), and the effect of the same was explored on mitochondrial and endoplasmic reticulum (ER) dynamicity. We observed that the AgNPs co-localize with mitochondria and cause mitochondrial membrane depolarization, ROS generation, and destabilized mitochondrial homeostasis. Also, the NPs were found to enhance ER stress. We further found that increased ER stress is linked to the disruption of mitochondrial dynamics. Overall, our study shows that the AgNPs can effectively cause apoptosis of MCF-7 cells by regulating the mitochondrial-ER dynamicity. The results provide an insight into the mechanisms via which AgNPs act and can be used in developing a potential chemotherapeutic agent.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectBiologyen_US
dc.subjectSilver nanoparticlesen_US
dc.subjectMitochondriaen_US
dc.subjectEndoplasmic reticulumen_US
dc.titleSilver nanoparticle-induced alteration of mitochondrial and ER homeostasis affects human breast cancer cell fateen_US
dc.typeArticleen_US
Appears in Collections:Department of Biological Sciences

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