A Rationale for the Use of Proton Pump Inhibitors as Antineoplastic Agents

被引:44
作者
De Milito, Angelo [1 ,2 ]
Marino, Maria Lucia [2 ]
Fais, Stefano [2 ]
机构
[1] Karolinska Inst, Canc Ctr Karolinska, Dep Oncol Pathol, Stockholm, Sweden
[2] Ist Super Sanita, Unit Antitumor Drugs, Dept Therapeut Res & Med Evaluat, I-00161 Rome, Italy
关键词
Proton pump inhibitors; omeprazole; cancer therapy; tumor pH; V-ATPase; HUMAN-MELANOMA CELLS; VACUOLAR H+-ATPASE; EXTRACELLULAR PH; COLORECTAL-CANCER; INTRACELLULAR PH; TUMOR-CELLS; NA+/H+ EXCHANGER; DRUG-RESISTANCE; ACIDIC PH; IN-VIVO;
D O I
10.2174/138161212799504911
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
It is becoming increasingly acknowledged that tumorigenesis is not simply characterized by the accumulation of rapidly proliferating, genetically mutated cells. Microenvironmental biophysical factors like hypoxia and acidity dramatically condition cancer cells and act as selective forces for malignant cells, adapting through metabolic reprogramming towards aerobic glycolysis. Avoiding intracellular accumulation of lactic acid and protons, otherwise detrimental to cell survival is crucial for malignant cells to maintain cellular pH homeostasis. As a consequence of the upregulated expression and/or function of several pH-regulating systems, cancer cells display an alkaline intracellular pH (pHi) and an acidic extracellular pH (pHe). Among the pH-regulating proteins, proton pumps play an important role in both drug-resistance and metastatic spread, thus representing a suitable therapeutic target. Proton pump inhibitors (PPI) have been reported as cytotoxic drugs active against several human tumor cells and preclinical data have prompted the investigation of PPI as anticancer agents in humans. This review will update the current knowledge on the antitumor activities of PPI and their potential applications.
引用
收藏
页码:1395 / 1406
页数:12
相关论文
共 164 条
[1]  
Äbelö A, 2000, DRUG METAB DISPOS, V28, P966
[2]  
Adams David J., 2005, Current Medicinal Chemistry - Anti-Cancer Agents, V5, P1, DOI 10.2174/1568011053352596
[3]   Microvesicles Messengers and mediators of tumor progression [J].
Al-Nedawi, Khalid ;
Meehan, Brian ;
Rak, Janusz .
CELL CYCLE, 2009, 8 (13) :2014-2018
[4]   Long-term Safety Concerns with Proton Pump Inhibitors [J].
Ali, Tauseef ;
Roberts, David Neil ;
Tierney, William M. .
AMERICAN JOURNAL OF MEDICINE, 2009, 122 (10) :896-903
[5]   Defective acidification in human breast tumor cells and implications for chemotherapy [J].
Altan, N ;
Chen, Y ;
Schindler, M ;
Simon, SM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (10) :1583-1598
[6]   Autophagy inhibition enhances therapy-induced apoptosis in a Myc-induced model of lymphoma [J].
Amaravadi, Ravi K. ;
Yu, Duonan ;
Lum, Julian J. ;
Bui, Thi ;
Christophorou, Maria A. ;
Evan, Gerard I. ;
Thomas-Tikhonenko, Andrei ;
Thompson, Craig B. .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (02) :326-336
[7]   Pharmacokinetics and pharmacodynamics of esomeprazole, the S-isomer of omeprazole [J].
Andersson, T ;
Röhss, K ;
Bredberg, E ;
Hassan-Alin, M .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2001, 15 (10) :1563-1569
[8]   Pharmacokinetic studies with esomeprazole, the (S)-isomer of omeprazole [J].
Andersson, T ;
Hassan-Alin, M ;
Hasselgren, G ;
Röhss, K ;
Weidolf, L .
CLINICAL PHARMACOKINETICS, 2001, 40 (06) :411-426
[9]   Stereoselective disposition of proton pump inhibitors [J].
Andersson, Tommy ;
Weidolf, Lars .
CLINICAL DRUG INVESTIGATION, 2008, 28 (05) :263-279
[10]  
Aplin AE, 2011, J INVEST DERMAT 0519