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Leaf extract of Osbeckia octandra induces apoptosis in oral squamous cell carcinoma cells

Authors
 Jue Young Kim  ;  Jin Kim  ;  B M Ratnayake Bandara  ;  Wanninayake M Tilakaratne  ;  Dokyeong Kim 
Citation
 BMC COMPLEMENTARY MEDICINE AND THERAPIES, Vol.22(1) : 20, 2022-01 
Journal Title
BMC COMPLEMENTARY MEDICINE AND THERAPIES
ISSN
 * 
Issue Date
2022-01
MeSH
Antineoplastic Agents, Phytogenic / pharmacology* ; Antineoplastic Agents, Phytogenic / therapeutic use ; Apoptosis / drug effects ; Carcinoma, Squamous Cell / drug therapy* ; Cell Line, Tumor / drug effects ; Humans ; Mouth Neoplasms / drug therapy* ; Myrtales* ; Phytotherapy ; Plant Extracts / pharmacology* ; Plant Extracts / therapeutic use ; Sri Lanka
Keywords
Apoptosis ; Cell cycle arrest ; Oral squamous cell carcinoma ; Osbeckia octandra
Abstract
Background: Osbeckia octandra is a plant endemic to Sri Lanka and is used in ethnomedicine for treating various diseases. However, the anti-cancer properties of O. octandra are yet to be fully investigated. In the present study, we evaluated the anti-cancer effects of O. octandra on oral cancer cells.

Methods: Human oral cancer cell lines (HSC2, YD10B, YD38, YD9, and YD32) were used in this study. BrdU incorporation, cell cycle and annexin-V/PI staining were all evaluated using flow cytometry to determine the extent to which O. octandra leaf extract inhibits cell proliferation and induces apoptosis. Cell viability and reactive oxygen species (ROS) were also measured in order to investigate the anti-cancer effects of O. octandra extracts. Western blotting was performed to detect cell cycle related protein such as cyclin d1 and cdk4, and to detect apoptosis-related proteins such as Bcl-2, Bcl-XL, Bax, Caspase-9, Cleaved caspase-3, Fas, Caspase-8, and Bid.

Results: Leaf extract of O. octandra reduced oral squamous cell carcinoma (OSCC) cell viability in a dose-dependent manner. Leaf extract of O. octandra has non-toxic in normal keratinocytes. Also, O. octandra extract interrupted the DNA replication via G1 phase arrests, and this effect was independent of ROS generation. In the apoptosis-related experiments, the population of annexin V-positive cells increased upon treatment with O. octandra extract. Furthermore, the expression of anti-apoptotic protein (Bcl-2 and Bcl-xL) was decreased, whereas the expression of cleaved caspase-3 protein was increased in O. octandra-treated OSCC cells.

Conclusions: The results suggest that a leaf extract of O. octandra inhibited the proliferation of OSCC cells through G1 phase arrest and interrupting DNA replication. The leaf extract of O. octandra could trigger the apoptotic response via caspase 3 activation in OSCC cells. These results suggest that O. octandra has the potential to be developed as an alternative medicine for treating OSCC.
Files in This Item:
T202204709.pdf Download
DOI
10.1186/s12906-022-03505-4
Appears in Collections:
2. College of Dentistry (치과대학) > Dept. of Oral Pathology (구강병리학교실) > 1. Journal Papers
Yonsei Authors
Kim, Ju Young(김주영)
Kim, Jin(김진)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/191212
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