re-evaluate the effect of hyperbaric oxygen therapy in cancer - a preclinical therapeutic small animal model study重新评估高压氧治疗癌症的效果,临床治疗小动物模型研究.pdfVIP

re-evaluate the effect of hyperbaric oxygen therapy in cancer - a preclinical therapeutic small animal model study重新评估高压氧治疗癌症的效果,临床治疗小动物模型研究.pdf

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re-evaluate the effect of hyperbaric oxygen therapy in cancer - a preclinical therapeutic small animal model study重新评估高压氧治疗癌症的效果,临床治疗小动物模型研究

Re-Evaluate the Effect of Hyperbaric Oxygen Therapy in Cancer - A Preclinical Therapeutic Small Animal Model Study 1 1 2 3 4 Sneha Pande , Amit Sengupta *, Anurag Srivastava , Rajiv P. Gude , Arvind Ingle 1 Bioengineering Laboratory, Advanced Centre for Treatment, Research Education in Cancer, TATA Memorial Centre, New Mumbai, Maharashtra, India, 2 Department of Cancer Surgery, All India Institute of Medical Science, New Delhi, India, 3 Gude Laboratory, Advanced Centre for Treatment, Research and Education in Cancer, TATA Memorial Centre, New Mumbai, Maharashtra, India, 4 Laboratory Animal Facilities, Advanced Centre for Treatment, Research and Education in Cancer, TATA Memorial Centre, New Mumbai, Maharashtra, India Abstract Tumor hypoxia is a known driver of angiogenesis that also facilitates tumor growth. Moreover, poorly oxygenated central tumor area remains relatively radio or chemo resistant. HBO therapy is known to elevate the levels of dissolved oxygen and eliminates tumor hypoxia. It has been one of the modalities in cancer treatment; therefore its optimization is important. In this experimental study, no cancer enhancing effect was seen during the course of HBO therapy; however, post therapy there was an accelerated growth and progression of tumor. HBO treated mice lived shorter and the response to therapy was dose tumor volume dependent. HBO therapy probably exert its effect on the cancer proliferating cells through multiple pathways such as increased DNA damage, apoptosis geno-toxicity leading to slow cancer progression while post therapy tumorigenic effect could be due to impaired DNA repair mechanism, mutagenic effect aneuploidy as well as altered blood supply nutrients. Tumor growth reached plateau with time and this finding validated theoretical model pre

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