volume 32 issue 3 pages 194-205

Anti-Cancer Bioactive Peptide Induces Apoptosis in Gastric Cancer Cells through TP53 Signaling Cascade

Publication typeJournal Article
Publication date2025-03-01
scimago Q3
wos Q4
SJR0.338
CiteScore2.4
Impact factor1.1
ISSN09298665, 18755305
Abstract
Introduction:

Gastric cancer has emerged as one of the major diseases threatening human health. Our previous studies indicated that the anti-cancer bioactive peptide (ACBP) inhibits the initiation and progression of gastric cancer through apoptosis and cell cycle arrest, yet the mechanisms remain unclear. To elucidate the relationships between the effects of ACBP and the levels of cell differentiation, as well as the functional mechanisms of ACBP, we conducted a study using three human gastric cancer cell lines: NCI-N87, MGC-803, and another unspecified line.

Method:

We investigated the impact of ACBP on the survival and morphology of these cancer cell lines, examined apoptosis and cell cycle progression, and detected the expression of TP53, TP63, and TP73 in cancer cells, as well as the expression of Bax, PUMA, and Mcl-1 in a xenograft mouse model. ACBP inhibited the proliferation of all three cancer cell lines in a dose-dependent manner, similar to the positive control and 5-fluorouracil (5-FU). The effect of ACBP correlated with the degree of differentiation of the cancer cells; the lower the differentiation degree, the stronger the inhibitory effect.

Result:

After ACBP treatment, the expression of TP53, TP63, and TP73 increased in all cell lines. In the xenograft mouse model, ACBP inhibited the growth of MGC-803 cells in vivo. The apoptotic- related genes Bax and PUMA were upregulated, while Mcl-1 was downregulated. ACBP inhibited tumor cell growth by inducing apoptosis through the TP53 signaling cascade, upregulating TP53, TP63, and TP73 and their downstream apoptosis-promoting genes Bax and PUMA while downregulating the anti-apoptotic gene Mcl-1.

Conclusion:

Notably, after ACBP treatment, Mcl-1 expression was significantly reduced in the tumor tissue of the xenograft model, indicating that ACBP induced apoptosis through the TP53 signaling cascade. This project provides a scientific basis for exploring the antitumor mechanism of ACBP in gastric cancer therapy.

other:

This project provides a scientific basis for exploring the antitumor mechanism of ACBP in gastric cancer therapy.

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Suyila Q. et al. Anti-Cancer Bioactive Peptide Induces Apoptosis in Gastric Cancer Cells through TP53 Signaling Cascade // Protein and Peptide Letters. 2025. Vol. 32. No. 3. pp. 194-205.
GOST all authors (up to 50) Copy
Suyila Q., Li X., Su X. Anti-Cancer Bioactive Peptide Induces Apoptosis in Gastric Cancer Cells through TP53 Signaling Cascade // Protein and Peptide Letters. 2025. Vol. 32. No. 3. pp. 194-205.
RIS |
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RIS Copy
TY - JOUR
DO - 10.2174/0109298665350654250111144722
UR - https://www.eurekaselect.com/239295/article
TI - Anti-Cancer Bioactive Peptide Induces Apoptosis in Gastric Cancer Cells through TP53 Signaling Cascade
T2 - Protein and Peptide Letters
AU - Suyila, Qimuge
AU - Li, Xian
AU - Su, Xiulan
PY - 2025
DA - 2025/03/01
PB - Bentham Science Publishers Ltd.
SP - 194-205
IS - 3
VL - 32
SN - 0929-8665
SN - 1875-5305
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2025_Suyila,
author = {Qimuge Suyila and Xian Li and Xiulan Su},
title = {Anti-Cancer Bioactive Peptide Induces Apoptosis in Gastric Cancer Cells through TP53 Signaling Cascade},
journal = {Protein and Peptide Letters},
year = {2025},
volume = {32},
publisher = {Bentham Science Publishers Ltd.},
month = {mar},
url = {https://www.eurekaselect.com/239295/article},
number = {3},
pages = {194--205},
doi = {10.2174/0109298665350654250111144722}
}
MLA
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MLA Copy
Suyila, Qimuge, et al. “Anti-Cancer Bioactive Peptide Induces Apoptosis in Gastric Cancer Cells through TP53 Signaling Cascade.” Protein and Peptide Letters, vol. 32, no. 3, Mar. 2025, pp. 194-205. https://www.eurekaselect.com/239295/article.