Effects of hyperbaric oxygen exposure on experimental head and neck tumor growth, oxygenation, and vasculature

Background. Hyperbaric oxygen (HBO2) is used to promote healing in irradiated tissues, but concern persists about the possibility that it may promote residual tumor growth. Methods. The tumor growth of SQ20B and Detroit 562 head and neck squamous cell carcinoma xenografts were studied after single‐d...

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Veröffentlicht in:Head & neck 2005-05, Vol.27 (5), p.362-369
Hauptverfasser: Shi, Yuquan, Lee, Caroline S., Wu, Junmin, Koch, Cameron J., Thom, Stephen R., Maity, Amit, Bernhard, Eric J.
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container_end_page 369
container_issue 5
container_start_page 362
container_title Head & neck
container_volume 27
creator Shi, Yuquan
Lee, Caroline S.
Wu, Junmin
Koch, Cameron J.
Thom, Stephen R.
Maity, Amit
Bernhard, Eric J.
description Background. Hyperbaric oxygen (HBO2) is used to promote healing in irradiated tissues, but concern persists about the possibility that it may promote residual tumor growth. Methods. The tumor growth of SQ20B and Detroit 562 head and neck squamous cell carcinoma xenografts were studied after single‐dose irradiation and 5×/week HBO2 treatment at 2.4 atm absolute for 90 minutes. The effect of HBO2 treatment on tumor hypoxia and vasculature was also examined by immunohistochemical analysis. Results. HBO2 treatment increased tumor oxygenation during the treatment interval but did not promote the growth of either irradiated or unirradiated tumors. No increase in tumor vascular endothelial growth factor expression or vascularization was detected. Conclusions. This study found no evidence for persistent changes in tumor microenvironment or tumor growth promotion caused by hyperbaric oxygen exposure. © 2005 Wiley Periodicals, Inc. Head Neck 27: XXX–XXX, 2005
doi_str_mv 10.1002/hed.20169
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Hyperbaric oxygen (HBO2) is used to promote healing in irradiated tissues, but concern persists about the possibility that it may promote residual tumor growth. Methods. The tumor growth of SQ20B and Detroit 562 head and neck squamous cell carcinoma xenografts were studied after single‐dose irradiation and 5×/week HBO2 treatment at 2.4 atm absolute for 90 minutes. The effect of HBO2 treatment on tumor hypoxia and vasculature was also examined by immunohistochemical analysis. Results. HBO2 treatment increased tumor oxygenation during the treatment interval but did not promote the growth of either irradiated or unirradiated tumors. No increase in tumor vascular endothelial growth factor expression or vascularization was detected. Conclusions. This study found no evidence for persistent changes in tumor microenvironment or tumor growth promotion caused by hyperbaric oxygen exposure. © 2005 Wiley Periodicals, Inc. 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Hyperbaric oxygen (HBO2) is used to promote healing in irradiated tissues, but concern persists about the possibility that it may promote residual tumor growth. Methods. The tumor growth of SQ20B and Detroit 562 head and neck squamous cell carcinoma xenografts were studied after single‐dose irradiation and 5×/week HBO2 treatment at 2.4 atm absolute for 90 minutes. The effect of HBO2 treatment on tumor hypoxia and vasculature was also examined by immunohistochemical analysis. Results. HBO2 treatment increased tumor oxygenation during the treatment interval but did not promote the growth of either irradiated or unirradiated tumors. No increase in tumor vascular endothelial growth factor expression or vascularization was detected. Conclusions. This study found no evidence for persistent changes in tumor microenvironment or tumor growth promotion caused by hyperbaric oxygen exposure. © 2005 Wiley Periodicals, Inc. Head Neck 27: XXX–XXX, 2005</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Carcinoma, Squamous Cell - blood supply</subject><subject>Carcinoma, Squamous Cell - metabolism</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Cell Hypoxia</subject><subject>Dose-Response Relationship, Radiation</subject><subject>EF-5</subject><subject>Head and Neck Neoplasms - blood supply</subject><subject>Head and Neck Neoplasms - metabolism</subject><subject>Head and Neck Neoplasms - pathology</subject><subject>hyperbaric oxygen</subject><subject>Hyperbaric Oxygenation</subject><subject>hypoxia</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Nude</subject><subject>Neoplasms, Experimental</subject><subject>Neovascularization, Pathologic</subject><subject>Otorhinolaryngology. 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subjects Animals
Biological and medical sciences
Carcinoma, Squamous Cell - blood supply
Carcinoma, Squamous Cell - metabolism
Carcinoma, Squamous Cell - pathology
Cell Hypoxia
Dose-Response Relationship, Radiation
EF-5
Head and Neck Neoplasms - blood supply
Head and Neck Neoplasms - metabolism
Head and Neck Neoplasms - pathology
hyperbaric oxygen
Hyperbaric Oxygenation
hypoxia
Immunohistochemistry
Male
Medical sciences
Mice
Mice, Nude
Neoplasms, Experimental
Neovascularization, Pathologic
Otorhinolaryngology. Stomatology
radiation
squamous cell carcinoma
Transplantation, Heterologous
Vascular Endothelial Growth Factor A - metabolism
title Effects of hyperbaric oxygen exposure on experimental head and neck tumor growth, oxygenation, and vasculature
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