Ketoprofen and Loxoprofen Platinum(IV) Complexes Displaying Antimetastatic Activities by Inducing DNA Damage, Inflammation Suppression, and Enhanced Immune Response.
Zuojie LiQingpeng WangLinming LiYan ChenJichun CuiMin LiuNing ZhangZhifang LiuJun HanZhengping WangPublished in: Journal of medicinal chemistry (2021)
Metastasis is a major contributor of death in cancer patients, and there is an urgent need for effective treatments of metastatic malignancies. Herein, ketoprofen (KP) and loxoprofen (LP) platinum(IV) complexes with antiproliferative and antimetastatic properties were designed and prepared by integrating chemotherapy and immunotherapy targeting cyclooxygenase-2 (COX-2), matrix metalloproteinase-9 (MMP-9), and programmed death ligand 1 (PD-L1), besides DNA. A mono-KP platinum(IV) complex with a cisplatin core is screened out as a candidate possessing potent anti-proliferative and anti-metastasis activities both in vitro and in vivo. It induces serious DNA damage and further leads to high expression of γ-H2AX and p53. Moreover, it promotes apoptosis of tumor cells through mitochondrial apoptotic pathway Bcl-2/Bax/caspase3. Then, COX-2, MMP-9, NLRP3, and caspase1 as pivotal enzymes igniting inflammation and metastasis are obviously inhibited. Notably, it significantly improves immune response through restraining the expression of PD-L1 to increase CD3+ and CD8+ T infiltrating cells in tumor tissues.
Keyphrases
- oxidative stress
- induced apoptosis
- dna damage
- immune response
- cell death
- cell cycle arrest
- poor prognosis
- endoplasmic reticulum stress
- dna repair
- squamous cell carcinoma
- binding protein
- dendritic cells
- toll like receptor
- long non coding rna
- locally advanced
- anti inflammatory
- radiation therapy
- single molecule
- nk cells
- cell free
- nitric oxide
- rectal cancer
- nitric oxide synthase
- chemotherapy induced
- nlrp inflammasome