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Upregulation of Bax, TNF-α and down-regulation of Bcl-2 in liver cancer cells treated with HL-7 and HL-10 peptides

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Abstract

Nowadays, cancer has become a pervasive disease in the world. Due to the side effects of chemotherapeutic agents, the use of peptides has been increasingly popular among scientists. The present study aimed to assess the cell toxicity and the change in the expression of Bcl-2, tumor necrosis factor-alpha (TNF-α), and Bax genes in HepG2 cancer cell line treated with peptides HL-7 (YLYELAR) and HL-10 (AFPYYGHHLG) using MTT, western blot and real-time polymerase chain reaction (PCR) analyses. The results showed that HL-7 and HL-10 peptides significantly (p < 0.05) inhibited the growth of HepG2 cancer cells; however, they did not cause any marked toxicity on human lymphocyte cells. Also, the treatment of HepG2 cancer cells with HL-7 and HL-10 led to a significant (p < 0.05) increase in the expression of TNF-α and Bax genes, as well as a substantial decrease in the expression of Bcl-2 at both protein and mRNA levels. It seems that the two peptides may contribute to increasing the expression of TNF-α, along with the ratio of Bax/Bcl-2, which may result in activating the intrinsic pathway of apoptosis in HepG2 cancer cells. Thus, these two peptides may be useful therapeutic options for the treatment of hepatocarcinoma in the future.

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Abbreviations

TNF-α:

Tumor necrosis factor-alpha

TNFR1:

tumor necrosis factor receptor 1

DMEM:

Dulbecco’s minimum essential medium

MTT:

3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide

DMSO:

dimethyl sulfoxide

FBS:

fetal bovine serum

BSA:

bovine serum albumin

PMSF:

phenylmethylsulfonyl fluoride

HEPES:

N-2-hydroxyethyl piperazine-N-ethane sulfonic acid

cDNA:

complementary DNA

PBMCs:

peripheral blood mononuclear cells

PBS:

phosphate-buffered saline

GAPDH:

glyceraldehyde 3-phosphate dehydrogenase

TBST:

Tris-buffered saline tween

HRP:

Horseradish Peroxidase

RT-PCR:

Reverse transcription-polymerase chain reaction

ROS:

reactive oxygen species

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Funding

The authors appreciate the support provided by the University of Zabol (Grant code: UOZ-GR-9718-96, 1399/07/28).

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Contributions

ZS-M; sample design and methodology, investigation and data collection, data analysis and interpretation, manuscript writing and editing; AA; research conceptualization, manuscript writing, and editing, MP; manuscript writing and editing.

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Correspondence to Zahra Setayesh-Mehr.

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The authors declare no conflict of interest.

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Setayesh-Mehr, Z., Asoodeh, A. & Poorsargol, M. Upregulation of Bax, TNF-α and down-regulation of Bcl-2 in liver cancer cells treated with HL-7 and HL-10 peptides. Biologia 76, 2735–2743 (2021). https://doi.org/10.1007/s11756-021-00800-2

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  • DOI: https://doi.org/10.1007/s11756-021-00800-2

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