Investigation of the inhibitory effects of simvastatin in RPMI 2650: an in-vitro study / Jaapar K. H. ... [et al.]

Objective: The present study was carried out to investigate the antiproliferative effects of simvastatin involving Human Squamous Nasal Cell Carcinoma (RPMI 2650 cell line), which is one of the most common head and neck cancers with the highest incidence and mortality rates in Asian countries. The a...

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Main Authors: Jaapar, K.H., Rawi, A.F., Zuhairi, Z.N., Sani Gapor, N.A., Bismelah, N.A., Mohamed, N.A.H
Format: Article
Language:English
Published: Faculty of Dentistry, Universiti Teknologi MARA 2022
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Online Access:https://ir.uitm.edu.my/id/eprint/69445/1/69445.pdf
https://ir.uitm.edu.my/id/eprint/69445/
https://doi.org/10.24191/cos.v9i1.16788
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spelling my.uitm.ir.694452022-10-31T08:24:15Z https://ir.uitm.edu.my/id/eprint/69445/ Investigation of the inhibitory effects of simvastatin in RPMI 2650: an in-vitro study / Jaapar K. H. ... [et al.] Jaapar, K.H. Rawi, A.F. Zuhairi, Z.N. Sani Gapor, N.A. Bismelah, N.A. Mohamed, N.A.H RC0254 Neoplasms. Tumors. Oncology (including Cancer) Objective: The present study was carried out to investigate the antiproliferative effects of simvastatin involving Human Squamous Nasal Cell Carcinoma (RPMI 2650 cell line), which is one of the most common head and neck cancers with the highest incidence and mortality rates in Asian countries. The anti-cancer effects of simvastatin in NPC have not yet been investigated in depth, hence it will be illustrated in the present study. Materials and methods: The cells were treated with various concentrations of Simvastatin in a dose dependent (0, 0.1, 0. 4, 3.0 mg/ml) and time dependent (24, 48 and 72 hours) manner. The cancer cell viability was then assessed by using MTT assay at absorbance of 590 nm. Results: Simvastatin induced reduction in cell viability number and induced apoptosis in RPMI 2650 cell line. Simvastatin for 72 h significantly reduced cell growth as compared to 48 and 24 h pre-incubation with simvastatin treatment. After 72 h incubation with 0.1 mg/ml, 0.4 mg/ml and 3.0 mg/ml simvastatin, the cell viability decreased from 100% in treated control cells to 23%, 21% and 14% respectively. Conclusions: This finding demonstrate the potential of simvastatin and probably may have therapeutic benefit for NPC cell growth. Faculty of Dentistry, Universiti Teknologi MARA 2022 Article PeerReviewed text en https://ir.uitm.edu.my/id/eprint/69445/1/69445.pdf Investigation of the inhibitory effects of simvastatin in RPMI 2650: an in-vitro study / Jaapar K. H. ... [et al.]. (2022) Compendium of Oral Science (CORALS), 9 (1). pp. 1-7. ISSN 2489-1102; 2637-0611 https://doi.org/10.24191/cos.v9i1.16788
institution Universiti Teknologi Mara
building Tun Abdul Razak Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Teknologi Mara
content_source UiTM Institutional Repository
url_provider http://ir.uitm.edu.my/
language English
topic RC0254 Neoplasms. Tumors. Oncology (including Cancer)
spellingShingle RC0254 Neoplasms. Tumors. Oncology (including Cancer)
Jaapar, K.H.
Rawi, A.F.
Zuhairi, Z.N.
Sani Gapor, N.A.
Bismelah, N.A.
Mohamed, N.A.H
Investigation of the inhibitory effects of simvastatin in RPMI 2650: an in-vitro study / Jaapar K. H. ... [et al.]
description Objective: The present study was carried out to investigate the antiproliferative effects of simvastatin involving Human Squamous Nasal Cell Carcinoma (RPMI 2650 cell line), which is one of the most common head and neck cancers with the highest incidence and mortality rates in Asian countries. The anti-cancer effects of simvastatin in NPC have not yet been investigated in depth, hence it will be illustrated in the present study. Materials and methods: The cells were treated with various concentrations of Simvastatin in a dose dependent (0, 0.1, 0. 4, 3.0 mg/ml) and time dependent (24, 48 and 72 hours) manner. The cancer cell viability was then assessed by using MTT assay at absorbance of 590 nm. Results: Simvastatin induced reduction in cell viability number and induced apoptosis in RPMI 2650 cell line. Simvastatin for 72 h significantly reduced cell growth as compared to 48 and 24 h pre-incubation with simvastatin treatment. After 72 h incubation with 0.1 mg/ml, 0.4 mg/ml and 3.0 mg/ml simvastatin, the cell viability decreased from 100% in treated control cells to 23%, 21% and 14% respectively. Conclusions: This finding demonstrate the potential of simvastatin and probably may have therapeutic benefit for NPC cell growth.
format Article
author Jaapar, K.H.
Rawi, A.F.
Zuhairi, Z.N.
Sani Gapor, N.A.
Bismelah, N.A.
Mohamed, N.A.H
author_facet Jaapar, K.H.
Rawi, A.F.
Zuhairi, Z.N.
Sani Gapor, N.A.
Bismelah, N.A.
Mohamed, N.A.H
author_sort Jaapar, K.H.
title Investigation of the inhibitory effects of simvastatin in RPMI 2650: an in-vitro study / Jaapar K. H. ... [et al.]
title_short Investigation of the inhibitory effects of simvastatin in RPMI 2650: an in-vitro study / Jaapar K. H. ... [et al.]
title_full Investigation of the inhibitory effects of simvastatin in RPMI 2650: an in-vitro study / Jaapar K. H. ... [et al.]
title_fullStr Investigation of the inhibitory effects of simvastatin in RPMI 2650: an in-vitro study / Jaapar K. H. ... [et al.]
title_full_unstemmed Investigation of the inhibitory effects of simvastatin in RPMI 2650: an in-vitro study / Jaapar K. H. ... [et al.]
title_sort investigation of the inhibitory effects of simvastatin in rpmi 2650: an in-vitro study / jaapar k. h. ... [et al.]
publisher Faculty of Dentistry, Universiti Teknologi MARA
publishDate 2022
url https://ir.uitm.edu.my/id/eprint/69445/1/69445.pdf
https://ir.uitm.edu.my/id/eprint/69445/
https://doi.org/10.24191/cos.v9i1.16788
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score 13.211869