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Induction of apoptosis in response to improved gedunin by liposomal nano-encapsulation in human non-small-cell lung cancer (NCI-H292) cell line
Journal article   Open access   Peer reviewed

Induction of apoptosis in response to improved gedunin by liposomal nano-encapsulation in human non-small-cell lung cancer (NCI-H292) cell line

Chukwumaobim Daniel Uzochukwuwulu Nwokwu, Sameera Ranganath Samarakoon, Desiree Nedra Karunaratne, Nuwanthi P. Katuvawila, Geethi Kaushalya Pamunuwa, Meran Keshawa Ediriweera and Kamani Hemamala Tennekoon
Tropical journal of pharmaceutical research, Vol.16(9), pp.2079-2087
10-04-2017

Abstract

Life Sciences & Biomedicine Pharmacology & Pharmacy Science & Technology
Purpose: To investigate the anti-proliferative activity of free and nanoencapsulated gedunin against human non-small-cell lung cancer (NCI-H292) cells. Methods: Gedunin-loaded nanoliposomes (LG) were prepared using thin-film hydration method. Antiproliferative effects of free and LD were evaluated by sulforhodamine B (SRB) assay. Apoptotic effects of gedunin-loaded liposomes were assessed by evaluating expressions of p53, Bax and survivin genes, caspase 3/7 activities, DNA fragmentation and morphological changes after staining with Hoechst 33342 and acridine orange/ethidium bromide (AO/EB). Results: Cell proliferation data and microscopic visualization demonstrated a higher anti-proliferative activity for LG than the encapsulant (liposomes) alone. LG exhibited dose-and time-dependent 10-fold anti-proliferative activity compared to the free drug, while displaying tolerable belligerence towards normal human lung fibroblast (MRC-5) cells. Apoptosis detection assays and gene expression analysis revealed the transcriptional modulation of the apoptosis-related genes (p53, survivin and Bax), increased activity of caspase 3/7 and the condensation of nuclear chromatin, implying the induction of apoptosis by the nano-formulation in NCI-H292 cells. Conclusion: LG may therefore be considered as a potential nano-formulation which can target nonsmall-cell lung cancer.
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https://doi.org/10.4314/tjpr.v16i9.6View
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