收藏切换
A novel chalcone derivative C13 inhibits the growth of human gastric cancer cells through suppressing ErbB4/PI3K/AKT signaling pathway
收藏切换
PDF
Peng TAN, Yun-feng ZHANG, Long-yan WANG, Hui-ming HUANG, Fei WANG, Xue-jiao WEI, Zhu-guo WANG, Jun LI*, Zhong-dong HU*
Acta Pharmaceutica Sinica | 2024, 59(4) : 957 - 964
Less
收藏切换
Acta Pharmaceutica Sinica | 2024, 59(4): 957-964
Original Articles
A novel chalcone derivative C13 inhibits the growth of human gastric cancer cells through suppressing ErbB4/PI3K/AKT signaling pathway
Full
Peng TAN, Yun-feng ZHANG, Long-yan WANG, Hui-ming HUANG, Fei WANG, Xue-jiao WEI, Zhu-guo WANG, Jun LI*, Zhong-dong HU*
Affiliations
  • Modern Research Center for Traditional Chinese Medicine, Beijing Institute of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing 100029, China
Published: 2024-04-12 doi: 10.16438/j.0513-4870.2023-1262
Outline
收藏切换

3ʹ-Hydroxy-4ʹ-methoxy-2-hydroxy-5-bromochalcone (hereinafter referred to as C13) is a novel chalcone derivative obtained in the process of structural modification of DHMMF, the antitumor active compound of Resina Draconis, in our laboratory. In this study, we investigated the effects of C13 on the proliferation and apoptosis of human gastric cancer HGC-27 and AGS cells and its potential mechanism of action. Firstly, through methyl thiazolyl tetrazolium (MTT), colony formation assay, and 5-ethynyl-2'-deoxyuridine (EdU) staining, we found that C13 inhibited the proliferation ability of human gastric cancer HGC-27 and AGS cells. Using flow cytometry and Western blot, it was found that C13 induced apoptosis in human gastric cancer HGC-27 and AGS cells, and up-regulated the protein level of cleaved poly ADP-ribose polymerase (cleaved-PARP). The results of RNA sequencing analysis showed that the Erb-b2 receptor tyrosine kinase 4/phosphoinositide 3-kinases/AKT (ErbB4/PI3K/AKT) signaling pathway may be involved in anti-gastric cancer activity of C13. Finally, the results of immunoblotting assay showed that C13 treatment down-regulated the protein levels of ErbB4 and phospho-ErbB4, as well as down-regulated the phosphorylation levels of PI3K and AKT in human gastric cancer HGC-27 and AGS cells, which verified the results from RNA-seq analysis. In conclusion, C13 inhibited the proliferation and induced apoptosis of human gastric cancer cells, which may be related to the down-regulation of ErbB4/PI3K/AKT signaling pathway. This study may provide a candidate drug for the treatment of gastric cancer.

chalcone derivative C13  /  human gastric cancer cell  /  proliferation  /  apoptosis  /  ErbB4/PI3K/AKT signaling pathway
Peng TAN, Yun-feng ZHANG, Long-yan WANG, Hui-ming HUANG, Fei WANG, Xue-jiao WEI, Zhu-guo WANG, Jun LI, Zhong-dong HU. A novel chalcone derivative C13 inhibits the growth of human gastric cancer cells through suppressing ErbB4/PI3K/AKT signaling pathway[J]. Acta Pharmaceutica Sinica, 2024 , 59 (4) : 957 -964 . DOI: 10.16438/j.0513-4870.2023-1262
Year 2024 volume 59 Issue 4
PDF
161
62
Cite this Article
BibTeX
Article Info
doi: 10.16438/j.0513-4870.2023-1262
  • Receive Date:2023-11-08
  • Online Date:2025-11-28
  • Published:2024-04-12
Article Data
Affiliations
History
  • Received:2023-11-08
  • Revised:2024-01-12
Funding
Affiliations
    Modern Research Center for Traditional Chinese Medicine, Beijing Institute of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing 100029, China
References
Share
https://castjournals.cast.org.cn/joweb/yxxb/EN/10.16438/j.0513-4870.2023-1262
Share to
QR

Scan QR to access full text

Cite this article
BibTeX
Citations
表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
关闭全屏
  • BibTeX
  • EndNote
  • RefWorks
  • TxT