A novel small molecule inhibitor of MDM2-p53 (APG-115) enhances radiosensitivity of gastric adenocarcinoma

  • J Exp Clin Cancer Res. 2018 May 2;37(1):97. doi: 10.1186/s13046-018-0765-8.
Hanjie Yi  1  2 ,  Xianglei Yan  1 ,  Qiuyun Luo  1 ,  Luping Yuan  1 ,  Baoxia Li  1 ,  Wentao Pan  1 ,  Lin Zhang  1 ,  Haibo Chen  3 ,  Jing Wang  4 ,  Yubin Zhang  5 ,  Yifan Zhai  6 ,  Miao-Zhen Qiu  7 ,  Da-Jun Yang  8  9
Affiliations
  • 1. Department of Experimental Research, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-Sen University Cancer Center, 651 Dongfeng Road East, Guangzhou, 510060, China.
  • 2. YinZhou hospital affiliated to medical school of NingBo University, NingBo, 315000, ZheJiang Province, China.
  • 3. Peking University shenzhen hospital, Shenzhen, 518063, China.
  • 4. Guangzhou Red Cross Hospital, Guangzhou, 510060, China.
  • 5. Ascentage Pharma, Taizhou, 225300, Jiangsu, China.
  • 6. Suzhou Ascentage Pharma Inc., Jiangsu, 215123, China.
  • 7. Department of Medical Oncology, Sun Yat-Sen University Cancer Center; State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, 651 Dongfeng Road East, Guangzhou, 510060, China. [email protected].
  • 8. Department of Experimental Research, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-Sen University Cancer Center, 651 Dongfeng Road East, Guangzhou, 510060, China. [email protected].
  • 9. Suzhou Ascentage Pharma Inc., Jiangsu, 215123, China. [email protected].
PMID: 29716622 DOI: 10.1186/s13046-018-0765-8
Abstract

Background: Gastric Cancer is the leading cause of Cancer related death worldwide. Radiation alone or combined with chemotherapy plays important role in locally advanced and metastatic gastric adenocarcinoma. MDM2-p53 interaction and downstream signaling affect cellular response to DNA damage which leads to cell cycle arrest and Apoptosis. Therefore, restoring p53 function by inhibiting its interaction with MDM2 is a promising therapeutic strategy for Cancer. APG-115 is a novel small molecule inhibitor which blocks the interaction of MDM2 and p53. In this study, we investigated that the radiosensitivity of APG-115 in gastric adenocarcinoma in vitro and in vivo.

Methods: The role of APG-115 in six gastric Cancer cells viability in vitro was determined by CCK-8 assay. The expression level of MDM2, p21, PUMA and Bax in AGS and MKN45 cell lines was measured via Real-Time PCR (RT-PCR). The function of treatment groups on cell cycle and cell Apoptosis were detected through Flow Cytometry assay. Clonogenic assays were used to measure the radiosensitivity of APG-115 in p53 wild type gastric Cancer cell lines. Western blot was conducted to detect the protein expressions of mdm2-p53 signal pathway. Xenograft models in nude mice were established to explore the radiosensitivity role of APG-115 in gastric Cancer cells in vivo.

Results: We found that radiosensitization by APG-115 occurred in p53 wild-type gastric Cancer cells. Increasing Apoptosis and cell cycle arrest was observed after administration of APG-115 and radiation. Radiosensitivity of APG-115 was mainly dependent on MDM2-p53 signal pathway. In vivo, APG-115 combined with radiation decreased xenograft tumor growth much more significantly than either single treatment. Moreover, the number of proliferating cells (Ki-67) significantly decreased in combination group compared with single treatment group.

Conclusions: In summary, we found that combination of MDM2-p53 inhibitor (APG-115) and radiotherapy can enhance antitumor effect both in vitro and in vivo. This is the first report on radiosensitivity of APG-115 which shed light on clinical trial of the combination therapy of radiation with APG-115 in gastric adenocarcinoma.

Keywords
Apoptosis; Gastric cancer; MDM2; Radiation; Small molecule inhibitors; p53.
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