Cancer Research  09 AM Call for Abstracts
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online

[Cancer Research 32, 483-490, March 1, 1972]
© 1972 American Association for Cancer Research

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kallman, R. F.
Right arrow Articles by Stasch, M. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kallman, R. F.
Right arrow Articles by Stasch, M. J.

Blood Flow in Irradiated Mouse Sarcoma as Determined by the Clearance of Xenon-1331

Robert F. Kallman2, Gerald L. DeNardo3 and Mary J. Stasch

Department of Radiology, Stanford University School of Medicine, Stanford, California 94305

133Xe dissolved in 0.9% NaCl solution was injected directly into KHT sarcomas in C3H mice in order to study tumor blood flow. The rate of blood flow in ml/100 g/min was calculated from the clearance half-time and the partition coefficient. The mean rate of blood flow in the tumors of unanesthetized control mice was 21.2 ± 0.8 ml/100 g/min, which was significantly faster than the blood flow in the tumors of pentobarbital-anesthetized control mice. 133Xe was cleared exponentially in virtually all tumors, and rate of clearance decreased with increasing tumor volume in tumors larger than approximately 500 to 600 cu mm; in smaller tumors there was no conclusive evidence of dependence of clearance rate on size. Clearance rate was unaffected by multiple daily injections of 133Xe. At 3 hr after localized tumor irradiation (250 kV; half-value layer, 5.9 mm Al) with doses greater than 1,000 rads, blood flow tended to decrease with increasing radiation dose. At 3 to 4 days postirradiation, rate of blood flow was significantly increased in tumors receiving 1,000 rads; blood flow was also increased in tumors exposed to 2,000 and 4,000 rads, but not until approximately 7 days. Rate of blood flow decreased at 3 hr and 3 to 4 days in tumors irradiated with 8,000 to 16,000 rads. The postirradiation increases in blood flow were not correlated simply with gross tumor shrinkage, although tumor growth was slowed proportionally to radiation dose. Thus, irradiation brought about changes in rate of blood flow in the KHT sarcoma, and these changes were dependent on both radiation dose and postirradiation time. The observed time course of radiation-induced blood flow changes may partially account for the tumor reoxygenation shown in our previous studies and those of others.

1 This investigation was supported by USPHS Research Grant CA 03353 from the National Cancer Institute.

2 Recipient of USPHS research career program award CA K3-3576 from the National Cancer Institute.

3 Present address: Division of Nuclear Medicine, Department of Radiology, University of California School of Medicine at Davis, Davis, Calif. 95616.

Received 4/ 5/71. Accepted 11/22/71.




This article has been cited by other articles:


Home page
Cancer Res.Home page
L. Geng, J. Tan, E. Himmelfarb, A. Schueneman, K. Niermann, A. Fu, K. Cuneo, E. A. Kesicki, J. Treiberg, J. S. Hayflick, et al.
A Specific Antagonist of the p110{delta} Catalytic Component of Phosphatidylinositol 3'-Kinase, IC486068, Enhances Radiation-Induced Tumor Vascular Destruction
Cancer Res., July 15, 2004; 64(14): 4893 - 4899.
[Abstract] [Full Text] [PDF]


Home page
JNCI J Natl Cancer InstHome page
H. Choy and L. Milas
Enhancing Radiotherapy With Cyclooxygenase-2 Enzyme Inhibitors: A Rational Advance?
J Natl Cancer Inst, October 1, 2003; 95(19): 1440 - 1452.
[Abstract] [Full Text] [PDF]


Home page
Clin. Cancer Res.Home page
F. Denis, S. Colas, L. Chami, P. Louisot, O. le Floch, F. Tranquart, and P. Bougnoux
Changes in Tumor Vascularization after Irradiation, Anthracyclin, or Antiangiogenic Treatment in Nitrosomethyl Ureas-Induced Rat Mammary Tumors
Clin. Cancer Res., October 1, 2003; 9(12): 4546 - 4552.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
L. Geng, E. Donnelly, G. McMahon, P. C. Lin, E. Sierra-Rivera, H. Oshinka, and D. E. Hallahan
Inhibition of Vascular Endothelial Growth Factor Receptor Signaling Leads to Reversal of Tumor Resistance to Radiotherapy
Cancer Res., March 1, 2001; 61(6): 2413 - 2419.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1972 by the American Association for Cancer Research.