Abstract:Objective: To investigate the in vitro effect of atrial natriuretic peptide (ANP) on human gastric cancer cell line MGC-803 and the combined effect of PI3K/Akt signaling pathway inhibitor (LY294002) on human gastric cancer cell line MGC-803 and the possible mechanism. Methods: The gastric cancer MGC-803 cells were treated with different concentrations of ANP and different concentrations of LY294002 .The cell proliferation inhibition rate was detected by MTT assay. MGC-803 cells were randomly divided into four groups: control group, ANP group , LY294002 group and ANP combined LY294002 group. CCK8 was used to detect cell proliferation, scratch test was used to detect cell migration, cell morphology was observed under an inverted microscope and Western blot was used to detect the expression of key signal molecules total Akt (t-Akt) and p-Akt protein of PI3K/Akt signaling pathway. Results: CCK8 results showed that compared with control group, ANP group and LY294002 group, the combination of ANP and LY294002 can inhibit the proliferation of MGC-803 cells, with statistically significant differences(P<0.05); the inhibition of ANP alone and LY294002 alone on the proliferation of MGC-803 cells was time-dependent and dose-dependent. The 24-hour scratch area repair rate of the control group, ANP group, LY294002 group and ANP combined LY294002 group were (50.99±1.80)%, (43.33±2.22)%,(35.81±4.09)%,(26.67±1.69)% and the difference was statistically significant (P<0.05). Four groups of MGC-803 cells showed different cell morphology changes. Both ANP and LY294002 decreased the expression level of p-Akt protein in MGC-803 cells, and ANP combined with LY294002 had a more significant inhibitory effect on the expression of p-Akt protein than they were used alone (P<0.05). The expression level of t-Akt had no significant change in the four groups of cells (P>0.05). Conclusion: ANP can inhibit the proliferation and migration of human gastric cancer cell MGC-803. The combination of ANP and LY294002 can increase the inhibitory effect on gastric cancer cell MGC-803. The mechanism may be related to the inhibition of PI3K/Akt signaling pathway.
朱亚清, 李春辉, 何涛, 刘宁宁. ANP对胃癌MGC-803细胞增殖迁移的影响及机制的研究[J]. 河北医学, 2020, 26(12): 1943-1946.
ZHU Yaqing, LI Chunhui, et al. Study on the Effect of ANP on the Proliferation and Migration of Gastric Cancer MGC-803 Cells and Its Mechanism. HeBei Med, 2020, 26(12): 1943-1946.
[1] Bray F, Ferlay J, Soerjomataram I, et al. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries[J]. CA Cancer J Clin, 2018, 68(6): 394~424. [2] 作婷婷,郑荣寿,曾红梅,等.中国胃癌流行病学现状[J].中国肿瘤临床,2017,44(1):52~58. [3] 王振宁,朱志,孙景旭.胃癌的转化医学研究[J].中华消化外科杂志,2018,17(4):338~342. [4] Nojiri T, Hosoda H, Tokudome T, et al .Atrial natriuretic peptide prevents cancer metastasis through vascular endothelial cells[J].Proc Natl Acad Sci, 2015, 112(13):4086~4091. [5] 张佳,李强,闫妍,等.ANP对人胃癌细胞AGS增殖的影响及其机制[J].中国现代普通外科进展,2015,18(6):425~429. [6] Nishizawa N, Nakamura G,Noguchi Y, et al. A potent and selective natriuretic peptide receptor-3 blocker 11-mer peptide created by hybridization of musclin and atrial natriuretic peptide[J]. Bioorg Med Chem Lett, 2017, 27(15): 3542~3545. [7] Xu T,Zhang R,Dong M, et al. Osteoglycin (OGN) inhibits cell proliferation and invasiveness in breast cancer via PI3K/Akt/mTOR signaling pathway.[J]. Onco Targets and Therapy,2019,4(12). 10639~10650. [8] Shu F, Zou XQ, Tuo H, et al.Stathmin gene silencing suppresses proliferation, migration and invasion of gastric cancer cells via AKT/sCLU and STAT3 signaling[J]. International Journal of Oncology, 2019, 54(3): 1086~1098.