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Onosma bracteata Wall. induces G0/G1 arrest and apoptosis in MG-63 human osteosarcoma cells via ROS generation and AKT/GSK3β/cyclin E pathway

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Abstract

Onosma bracteata Wall. (Boraginaceae), commonly known as “gaozaban” is a highly valuable medicinal herb, useful in the treatment of body swellings, abdominal pain, eye-related problems, fever, and urinary calculi. The present study was performed to investigate the antioxidant properties of extract/fractions, viz. ethanol (Obeth) extract, hexane (Obhex) fraction, chloroform (Obcl) fraction, ethyl acetate (Obea) fraction, butanol (Obbu) fraction, and aqueous (Obaq) fraction isolated from O. bracteata. Obea fraction showed stronger free radical quenching ability in various antioxidant assays, as compared to the other fractions. Obea fraction with effective free radical-scavenging properties was further evaluated for the antiproliferative activity against human osteosarcoma MG-63, human neuroblastoma IMR-32, and human lung cancer A549 cell lines using MTT assay. Obea fraction showed strong cytotoxicity with GI50 value of 88.56, 101.61, and 112.7 μg/ml towards MG-63, IMR-32, and A549 cells respectively. Mechanistic studies revealed that Obea fraction in osteosarcoma MG-63 cells increased reactive oxygen species (ROS) level and reduced mitochondrial membrane potential. In the presence of Obea, the cells were found to be arrested in the G0/G1 phase in a dose-dependent manner which is also confirmed by the enhancement in the early apoptotic cell population in flow cytometer analysis. Western blotting demonstrated the decrease in expression of p-NFκB, COX-2, p-Akt, and Bcl-xL, whereas upregulation was observed in the expression of GSK-3β, p53, caspase-3, and caspase-9 proteins. RT-qPCR studies revealed downregulation of Bcl-2, cyclin E, CDK2, and mortalin gene expression and upregulation in the expression of p53 genes. The antioxidant and cytotoxic potential of Obea was attributed to the presence of catechin, kaempferol, onosmin A, and epicatechin, as revealed by HPLC analysis. This is the first report regarding the antiproliferative potential of O. bracteata against osteosarcoma.

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The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation, to any qualified researcher.

Abbreviations

Apaf-1:

Apoptotic protease activating factor 1

AO/EtBr:

Acridine orange/ethidium bromide

Bcl-2:

B cell lymphoma 2

CHO:

Chinese hamster ovary

COX-2:

Cyclooxygenase-2

CO2 :

Carbon dioxide

EA:

Early apoptosis

EDTA:

Ethylenediaminetetraacetic acid

GSK:

Glycogen synthase kinase

LA:

Late apoptosis

L:

Live

MG-63:

Human osteosarcoma cells

MMP:

Mitochondria membrane potential

N:

Necrotic

NFκB:

Nuclear factor kappa B

p-Akt:

Phosphorylated-Akt

PVDF:

Polyvinylidene fluoride

PAGE:

Polyacrylamide gel electrophoresis

PBS:

Phosphate-buffered saline

RT-qPCR:

Quantitative real-time polymerase chain reaction

ROS:

Reactive oxygen species

Rh123:

Rhodamine123

rpm:

Revolutions per minute

SDS:

Sodium dodecyl sulfate

SEM:

Scanning electron microscopy

WB:

Western blotting

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Acknowledgments

The authors thankful to University Grants Commission (UGC) - Basic Scientific Research (BSR), DST-FIST (Grant No. SR/FST/LSI-691/2016 (C)) program for providing financial assistance. The authors also acknowledge UGC, New Delhi, for the instrumentation facility under UGC-DRS V (Grant No. F4-13/2015/DRS-II), CPEPA, RUSA 2.0 scheme, UPE program, and the Centre of Emerging Life Sciences, Guru Nanak Dev University, Amritsar (India), for providing the required support and facilities.

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Authors and Affiliations

Authors

Contributions

Ajay Kumar: conceptualization, methodology, validation, writing—original draft, investigation, software. Sandeep Kaur: conceptualization, investigation. Kritika Pandit: investigation, formal analysis. Varinder Kaur: investigation, formal analysis. Sharad Thakur: investigation, Satwinderjeet Kaur: supervision, validation, methodology, conceptualization, validation, writing—original draft. All authors have read and agreed to the published version of the manuscript.

Corresponding author

Correspondence to Satwinderjeet Kaur.

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This manuscript is original, has not been published before, and is not currently being considered for publication elsewhere. Accepted principles of ethical and professional conduct have been followed while executing this research work. No experiment was carried out on human or animal to accomplish this research work.

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The authors declare that they have no competing interests.

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No human participants were required/used to carry out the reported research work. As there are no participants, so consent to participate is not required.

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We the undersigned declare that this manuscript is original, has not been published before, and is not currently being considered for publication elsewhere. We confirm that the manuscript has been read and approved by all named authors and that there are no other persons who satisfied the criteria for authorship but are not listed. We further confirm that the order of authors listed in the manuscript has been approved by all of us. We understand that the corresponding author is the sole contact for the editorial process. He/she is responsible for communicating with the other authors about progress, submissions of revisions, and final approval of proofs.

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Responsible Editor: Mohamed M. Abdel-Daim

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Kumar, A., Kaur, S., Pandit, K. et al. Onosma bracteata Wall. induces G0/G1 arrest and apoptosis in MG-63 human osteosarcoma cells via ROS generation and AKT/GSK3β/cyclin E pathway. Environ Sci Pollut Res 28, 14983–15004 (2021). https://doi.org/10.1007/s11356-020-11466-9

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  • DOI: https://doi.org/10.1007/s11356-020-11466-9

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