Combined Anti-Angiogenic Therapy Targeting PDGF and VEGF Receptors Lowers the Interstitial Fluid Pressure in a Murine Experimental Carcinoma

被引:40
作者
Klosowska-Wardega, Agnieszka [1 ]
Hasumi, Yoko [1 ]
Burmakin, Mikhail [1 ]
Ahgren, Aive [1 ]
Stuhr, Linda [2 ]
Moen, Ingrid [2 ]
Reed, Rolf K. [2 ]
Rubin, Kristofer [3 ]
Hellberg, Carina [1 ]
Heldin, Carl-Henrik [1 ]
机构
[1] Uppsala Univ, Ludwig Inst Canc Res, Biomed Ctr, Uppsala, Sweden
[2] Univ Bergen, Dept Biomed, Bergen, Norway
[3] Uppsala Univ, Dept Med Biochem & Microbiol, Biomed Ctr, Uppsala, Sweden
关键词
GROWTH-FACTOR-BB; INHIBITION; CANCER; CHEMOTHERAPY; TUMORS; TRANSPORT; PERICYTES; EFFICACY; IMATINIB; VESSELS;
D O I
10.1371/journal.pone.0008149
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Elevation of the interstitial fluid pressure (IFP) of carcinoma is an obstacle in treatment of tumors by chemotherapy and correlates with poor drug uptake. Previous studies have shown that treatment with inhibitors of platelet-derived growth factor ( PDGF) or vascular endothelial growth factor ( VEGF) signaling lowers the IFP of tumors and improve chemotherapy. In this study, we investigated whether the combination of PDGFR and VEGFR inhibitors could further reduce the IFP of KAT-4 human carcinoma tumors. The tumor IFP was measured using the wick-in-needle technique. The combination of STI571 and PTK/ZK gave an additive effect on the lowering of the IFP of KAT-4 tumors, but the timing of the treatment was crucial. The lowering of IFP following combination therapy was accompanied by vascular remodeling and decreased vascular leakiness. The effects of the inhibitors on the therapeutic efficiency of Taxol were investigated. Whereas the anti-PDGF and anti-VEGF treatment did not significantly inhibit tumor growth, the inhibitors enhanced the effect of chemotherapy. Despite having an additive effect in decreasing tumor IFP, the combination therapy did not further enhance the effect of chemotherapy. Simultaneous targeting of VEGFR and PDGFR kinase activity may be a useful strategy to decrease tumor IFP, but the timing of the inhibitors should be carefully determined.
引用
收藏
页数:7
相关论文
共 28 条
[11]   Taming vessels to treat cancer [J].
Jain, Rakesh K. .
SCIENTIFIC AMERICAN, 2008, 298 (01) :56-63
[12]   HEMODYNAMIC AND TRANSPORT BARRIERS TO THE TREATMENT OF SOLID TUMORS [J].
JAIN, RK .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1991, 60 (1-2) :85-100
[13]  
Lee CG, 2000, CANCER RES, V60, P5565
[14]   FLOW THROUGH INTERSTITIUM AND OTHER FIBROUS MATRICES [J].
LEVICK, JR .
QUARTERLY JOURNAL OF EXPERIMENTAL PHYSIOLOGY AND COGNATE MEDICAL SCIENCES, 1987, 72 (04) :409-438
[15]   Platelet-derived growth factor BB-mediated normalization of dermal interstitial fluid pressure after mast cell degranulation depends on β3 but not β1 integrins [J].
Lidén, Å ;
Berg, A ;
Nedrebo, T ;
Reed, RK ;
Rubin, K .
CIRCULATION RESEARCH, 2006, 98 (05) :635-641
[16]   Abnormalities in pericytes on blood vessels and endothelial sprouts in tumors [J].
Morikawa, S ;
Baluk, P ;
Kaidoh, T ;
Haskell, A ;
Jain, RK ;
McDonald, DM .
AMERICAN JOURNAL OF PATHOLOGY, 2002, 160 (03) :985-1000
[17]   Collagen-binding proteoglycan fibromodulin can determine stroma matrix structure and fluid balance in experimental carcinoma [J].
Oldberg, Ake ;
Kalamajski, Sebastian ;
Sainikov, Alexei V. ;
Stuhr, Linda ;
Morgelin, Matthias ;
Reed, Rolf K. ;
Heldin, Nils-Erik ;
Rubin, Kristofer .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (35) :13966-13971
[18]  
Pietras K, 2003, CLIN CANCER RES, V9, P3779
[19]  
Pietras K, 2002, CANCER RES, V62, P5476
[20]  
Pietras K, 2001, CANCER RES, V61, P2929