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Advancing the role of gamma-tocotrienol as proteasomes inhibitor:: A quantitative proteomic analysis of MDA-MB-231 human breast cancer cells

Advancing the role of gamma-tocotrienol as proteasomes inhibitor:: A quantitative proteomic analysis of MDA-MB-231 human breast cancer cells
Advancing the role of gamma-tocotrienol as proteasomes inhibitor:: A quantitative proteomic analysis of MDA-MB-231 human breast cancer cells
Tocotrienol, an analogue of vitamin E has been known for its numerous health benefits and anti-cancer effects. Of the four isoforms of tocotrienols, gamma-tocotrienol (γT3) has been frequently reported for their superior anti-tumorigenic activity in both in vitro and in vivo studies, when compared to its counterparts. In this study, the effect of γT3 treatment in the cytoplasmic and nuclear fraction of MDA-MB-231 human breast cancer cells were assessed using the label-free quantitative proteomics analysis. The cytoplasmic proteome results revealed the ability of γT3 to inhibit a group of proteasome proteins such as PSMA, PSMB, PSMD, and PSME. The inhibition of proteasome proteins is known to induce apoptosis in cancer cells. As such, the findings from this study suggest γT3 as a potential proteasome inhibitor that can overcome deficiencies in growth-inhibitory or pro-apoptotic molecules in breast cancer cells. The nuclear proteome results revealed the involvement of important nuclear protein complexes which hardwire the anti-tumorigenesis mechanism in breast cancer following γT3 treatment. In conclusion, this study uncovered the advancing roles of γT3 as potential proteasomes inhibitor that can be used for the treatment of breast cancer.
Ramdas, Premdass
4a86e6c9-a322-4749-8724-0e1aacbab46d
Radhakrishnan, Ammu Kutty
d12cd909-ae1c-4024-832e-4199b23b8790
Abdu Sani, Asmahani Azira
b01b7428-1b71-477f-89a5-435cbe9cee17
Kumari, Mangala
b1c1e6ab-59b0-41dd-8990-1e43508f7cc8
Anandha Rao, Jeya Seela
4ca17027-67b7-4931-8467-7dab4d22b2f7
Abdul-Rahman, Puteri Shafinaz
f59efde5-7086-4dcc-b231-28003afcb713
Ramdas, Premdass
4a86e6c9-a322-4749-8724-0e1aacbab46d
Radhakrishnan, Ammu Kutty
d12cd909-ae1c-4024-832e-4199b23b8790
Abdu Sani, Asmahani Azira
b01b7428-1b71-477f-89a5-435cbe9cee17
Kumari, Mangala
b1c1e6ab-59b0-41dd-8990-1e43508f7cc8
Anandha Rao, Jeya Seela
4ca17027-67b7-4931-8467-7dab4d22b2f7
Abdul-Rahman, Puteri Shafinaz
f59efde5-7086-4dcc-b231-28003afcb713

Ramdas, Premdass, Radhakrishnan, Ammu Kutty, Abdu Sani, Asmahani Azira, Kumari, Mangala, Anandha Rao, Jeya Seela and Abdul-Rahman, Puteri Shafinaz (2020) Advancing the role of gamma-tocotrienol as proteasomes inhibitor:: A quantitative proteomic analysis of MDA-MB-231 human breast cancer cells. Biomolecules, 10 (1). (doi:10.3390/biom10010019).

Record type: Article

Abstract

Tocotrienol, an analogue of vitamin E has been known for its numerous health benefits and anti-cancer effects. Of the four isoforms of tocotrienols, gamma-tocotrienol (γT3) has been frequently reported for their superior anti-tumorigenic activity in both in vitro and in vivo studies, when compared to its counterparts. In this study, the effect of γT3 treatment in the cytoplasmic and nuclear fraction of MDA-MB-231 human breast cancer cells were assessed using the label-free quantitative proteomics analysis. The cytoplasmic proteome results revealed the ability of γT3 to inhibit a group of proteasome proteins such as PSMA, PSMB, PSMD, and PSME. The inhibition of proteasome proteins is known to induce apoptosis in cancer cells. As such, the findings from this study suggest γT3 as a potential proteasome inhibitor that can overcome deficiencies in growth-inhibitory or pro-apoptotic molecules in breast cancer cells. The nuclear proteome results revealed the involvement of important nuclear protein complexes which hardwire the anti-tumorigenesis mechanism in breast cancer following γT3 treatment. In conclusion, this study uncovered the advancing roles of γT3 as potential proteasomes inhibitor that can be used for the treatment of breast cancer.

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More information

e-pub ahead of print date: 21 December 2019
Published date: 1 January 2020
Additional Information: © 2019 by the authors

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Local EPrints ID: 469915
URI: http://eprints.soton.ac.uk/id/eprint/469915
PURE UUID: ad5884a7-bf29-4284-b975-bf6b37b8aba4

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Date deposited: 28 Sep 2022 17:01
Last modified: 16 Mar 2024 21:22

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Contributors

Author: Premdass Ramdas
Author: Ammu Kutty Radhakrishnan
Author: Asmahani Azira Abdu Sani
Author: Mangala Kumari
Author: Jeya Seela Anandha Rao
Author: Puteri Shafinaz Abdul-Rahman

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