MM-129 as a Novel Inhibitor Targeting PI3K/AKT/mTOR and PD-L1 in Colorectal Cancer

被引:13
作者
Hermanowicz, Justyna Magdalena [1 ,2 ]
Pawlak, Krystyna [3 ]
Sieklucka, Beata [1 ]
Czarnomysy, Robert [4 ]
Kwiatkowska, Iwona [1 ]
Kazberuk, Adam [5 ]
Surazynski, Arkadiusz [5 ]
Mojzych, Mariusz [6 ]
Pawlak, Dariusz [1 ]
机构
[1] Med Univ Bialystok, Dept Pharmacodynam, Mickiewicza 2C, PL-15222 Bialystok, Poland
[2] Med Univ Bialystok, Dept Clin Pharm, Mickiewicza 2C, PL-15222 Bialystok, Poland
[3] Med Univ Bialystok, Dept Monitored Pharmacotherapy, Mickiewicza 2C, PL-15222 Bialystok, Poland
[4] Med Univ Bialystok, Dept Synth & Technol Drugs, Mickiewicza 2C, PL-15222 Bialystok, Poland
[5] Med Univ Bialystok, Dept Med Chem, Mickiewicza 2C, PL-15222 Bialystok, Poland
[6] Siedlce Univ Nat Sci & Humanities, Dept Chem, 3 Maja 54, PL-08110 Siedlce, Poland
关键词
1; 2; 4-triazine derivative; Akt-protein kinase B; PD-L1-programmed death ligand 1; xenograft; colon cancer; CELL-CYCLE ARREST; COLON-CANCER; IN-VITRO; 5-FLUOROURACIL; EXPRESSION; PATHWAY; GROWTH; ERYTHROPOIETIN; TRANSFORMATION; MECHANISMS;
D O I
10.3390/cancers13133203
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary MM-129 (1,2,4-triazine derivative) is a novel promising drug candidate against colon cancer. It has the ability to inhibit intracellular pathways promoting tumorigenesis with a simultaneous reduction of PD-L1 expression, a key element of the cancer immune escape axis. MM-129 may also act as a chemosensitizer, overcoming chemoresistance against 5-FU, the first-line agent in the chemother-apy of colon cancer. Our results significantly expand knowledge and help better understand the process of tumorigenesis, the intracellular pathways involved, and the mutual interactions of in-dividual proteins, and create the possibility of their pharmacological blockade. There is a real chance that the obtained results and the conclusions drawn on their basis will help in the development of a new, effective therapy, which could be an attractive alternative to the already existing methods of colon cancer treatment. Background and aims: The purpose of the present study was to examine the pharmacodynamics features of MM-129 (1,2,4-triazine derivative) as a novel promising drug candidate against colon cancer. Methods: MM-129 was assessed for antitumor activity through an in vivo study on Cby.Cg-Foxn1nu/cmdb mice. The mechanistic studies investigated cellular affinity of a new 1,2,4-triazine derivative by measuring levels of intracellular/extracellular signal molecules participating in tumorigenesis. Results: The results revealed that MM-129 significantly reduced tumor growth in mice challenged with DLD-1 and HT-29 cells. It exerted the ability to inhibit intracellular molecules promoting tumorigenesis and inducing cell cycle arrest, like Akt, mTOR, and CDK2. Simultaneously, it was able to downregulate PD-L1 expression, which involves immunological self-tolerance. Combined administration of MM-129 and 5-fluorouracil (5-FU) additionally amplified these effects, which were manifest as an increase population of cells in the G0/G1 phase. Conclusions: A novel 1,2,4-triazine derivative with a dual mechanism of antitumor activity-MM-129, may act as a chemosensitizer, overcoming chemoresistance against 5-FU, the first-line agent in the chemotherapy of colon cancer.
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页数:21
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