The Synergistic Anti-colon Cancer Effect of Aurora A Inhibitors and AKT Inhibitors Through PI3K/AKT Pathway

被引:6
作者
Sun, Cheng [1 ]
Qu, Zhen [2 ]
Liu, Weilin [3 ]
Qiu, Zhigang [4 ]
Lu, Yanfeng [5 ]
Sun, Zhenqing [4 ]
机构
[1] Qingdao Chengyang Peoples Hosp, Med Oncol Div, Qingdao 266109, Shandong, Peoples R China
[2] Joint Logist Support Force Chinese Peoples Libera, 970 Hosp, Dept Oncol, Yantai 264002, Shandong, Peoples R China
[3] Chengyang Dist Ctr Dis Control & Prevent, Qingdao 266109, Shandong, Peoples R China
[4] Affiliated Hosp Qingdao Univ, Dept Gastrointestinal Surg, Qingdao 266000, Shandong, Peoples R China
[5] Shandong Univ, Hosp 2, Cheeloo Coll Med, Dept Colorectal & Anal Surg, Jinan 250033, Shandong, Peoples R China
关键词
Aurora kinase A; colon cancer; PI3K; Akt; P53; proliferation; apoptosis; CELL-PROLIFERATION; A KINASE; ALISERTIB; APOPTOSIS; AUTOPHAGY; ARREST; TARGET;
D O I
10.2174/1871520622666220422133537
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Both AKT and Aurora inhibitors are a potential therapeutic agent for the treatment of malignant tumors. However, the role of combined inhibition of AKT and Aurora in colon cancer and its underlying mechanism have yet to be fully investigated. Objective To investigate the role of combined AKT and Aurora inhibitors in colon cancer and its underlying mechanisms. Methods CCK8 assay, colony formation assay, and flow cytometry were performed to analyze the proliferation and apoptosis of colon cancer cell line SW480 treated with combined AKT inhibitor MK2206 and Aurora inhibitor Alisertib, respectively. And tumor formation and growth were measured in tumor allograft model mice administered with the combined inhibitors. Western blot analysis was used to examine the expression levels of apoptosis-related proteins and signal transduction pathway components. The PI3K agonist 740Y-P and Overexpression of AKT are used to verify whether the PI3K/AKT pathway plays an anti-tumor effect when combined with inhibitory administration. Results Aurora A inhibitor Alisertib and AKT inhibitor MK2206 displayed consistent and synergistic antiproliferation and proapoptotic effects. Combined inhibition of Aurora A and AKT down-regulated the expression of Bcl-2/Bax and up-regulated the expression of cleaved-caspase-3 and cleaved-PARP. While single-drug treatment can significantly inhibit the expression of P-PI3K and P-AKT as well as increase the expression of P53 and H2A.X, the combined drugs had a more significant inhibitory effect than the single drug. Moreover, administration of PI3K agonist 740Y-P and AKT1 overexpression in experiments proved that the combined drugs exert an anticancer effect by inhibiting the PI3K/AKT pathway. Meanwhile, we showed that the combined administration had an anti-colon cancer effect on tumor allograft mice, and the underlying mechanism involved inhibition of the PI3K/AKT pathway. Conclusion Combined administration of Aurora A inhibitor Alisertib and AKT inhibitor MK2206 can inhibit the proliferation of colon cancer cells and induce apoptosis, while inhibiting tumor growth in vivo. The underlying mechanism may involve the PI3K/AKT pathway and DNA damage pathway.
引用
收藏
页码:87 / 93
页数:7
相关论文
共 25 条
[1]   MicroRNA-340-5p inhibits colon cancer cell migration via targeting of RhoA [J].
Algaber, Anwar ;
Al-Haidari, Amr ;
Madhi, Raed ;
Rahman, Milladur ;
Syk, Ingvar ;
Thorlacius, Henrik .
SCIENTIFIC REPORTS, 2020, 10 (01)
[2]   IDO1 and Kynurenine Pathway Metabolites Activate PI3K-Akt Signaling in the Neoplastic Colon Epithelium to Promote Cancer Cell Proliferation and Inhibit Apoptosis [J].
Bishnupuri, Kumar S. ;
Alvarado, David M. ;
Khouri, Alexander N. ;
Shabsovich, Mark ;
Chen, Baosheng ;
Dieckgraefe, Brian K. ;
Ciorba, Matthew A. .
CANCER RESEARCH, 2019, 79 (06) :1138-1150
[3]   A comprehensive review on Aurora kinase: Small molecule inhibitors and clinical trial studies [J].
Borisa, Ankit C. ;
Bhatt, Hardik G. .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2017, 140 :1-19
[4]   Aurora-A Is Essential for the Tumorigenic Capacity and Chemoresistance of Colorectal Cancer Stem Cells [J].
Cammareri, Patrizia ;
Scopelliti, Alessandro ;
Todaro, Matilde ;
Eterno, Vincenzo ;
Francescangeli, Federica ;
Moyer, Mary Pat ;
Agrusa, Antonino ;
Dieli, Francesco ;
Zeuner, Ann ;
Stassi, Giorgio .
CANCER RESEARCH, 2010, 70 (11) :4655-4665
[5]   Coordination of care in colon cancer [J].
Chang, George J. ;
Kopetz, Scott .
CANCER, 2015, 121 (18) :3201-3202
[6]   Therapeutically actionable signaling node to rescue AURKA driven loss of primary cilia in VHL-deficient cells [J].
Chowdhury, Pratim ;
Perera, Dimuthu ;
Powell, Reid T. ;
Talley, Tia ;
Tripathi, Durga Nand ;
Park, Yong Sung ;
Mancini, Michael A. ;
Davies, Peter ;
Stephan, Clifford ;
Corfa, Cristian ;
Dere, Ruhee .
SCIENTIFIC REPORTS, 2021, 11 (01)
[7]   DNA double-strand breaks induce H2Ax phosphorylation domains in a contact-dependent manner [J].
Collins, Patrick L. ;
Purman, Caitlin ;
Porter, Sofia, I ;
Nganga, Vincent ;
Saini, Ankita ;
Hayer, Katharina E. ;
Gurewitz, Greer L. ;
Sleckman, Barry P. ;
Bednarski, Jeffrey J. ;
Bassing, Craig H. ;
Oltz, Eugene M. .
NATURE COMMUNICATIONS, 2020, 11 (01)
[8]   Aurora A Kinase Is a Priority Pharmaceutical Target for the Treatment of Cancers [J].
Damodaran, Arun Prasath ;
Vaufrey, Lucie ;
Gavard, Olivia ;
Prigent, Claude .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2017, 38 (08) :687-700
[9]   Combined inhibition of Aurora A and p21-activated kinase 1 as a new treatment strategy in breast cancer [J].
Korobeynikov, Vladislav ;
Borakove, Michelle ;
Feng, Yayi ;
Wuest, William M. ;
Koval, Alex B. ;
Nikonova, Anna S. ;
Serebriiskii, Ilya ;
Chernoff, Jonathan ;
Borges, Virginia F. ;
Golemis, Erica A. ;
Shagisultanova, Elena .
BREAST CANCER RESEARCH AND TREATMENT, 2019, 177 (02) :369-382
[10]  
Laszlo Landherr, 2010, Magy Onkol, V54, P383, DOI 10.1556/MOnkol.54.2010.4.13