» Articles » PMID: 29630640

Oxygen Microbubbles Improve Radiotherapy Tumor Control in a Rat Fibrosarcoma Model - A Preliminary Study

Overview
Journal PLoS One
Date 2018 Apr 10
PMID 29630640
Citations 26
Authors
Affiliations
Soon will be listed here.
Abstract

Cancer affects 39.6% of Americans at some point during their lifetime. Solid tumor microenvironments are characterized by a disorganized, leaky vasculature that promotes regions of low oxygenation (hypoxia). Tumor hypoxia is a key predictor of poor treatment outcome for all radiotherapy (RT), chemotherapy and surgery procedures, and is a hallmark of metastatic potential. In particular, the radiation therapy dose needed to achieve the same tumor control probability in hypoxic tissue as in normoxic tissue can be up to 3 times higher. Even very small tumors (<2-3 mm3) comprise 10-30% of hypoxic regions in the form of chronic and/or transient hypoxia fluctuating over the course of seconds to days. We investigate the potential of recently developed lipid-stabilized oxygen microbubbles (OMBs) to improve the therapeutic ratio of RT. OMBs, but not nitrogen microbubbles (NMBs), are shown to significantly increase dissolved oxygen content when added to water in vitro and increase tumor oxygen levels in vivo in a rat fibrosarcoma model. Tumor control is significantly improved with OMB but not NMB intra-tumoral injections immediately prior to RT treatment and effect size is shown to depend on initial tumor volume on RT treatment day, as expected.

Citing Articles

Progression in low-intensity ultrasound-induced tumor radiosensitization.

Xu H, Liu Z, Du M, Chen Z Cancer Med. 2024; 13(13):e7332.

PMID: 38967145 PMC: 11224918. DOI: 10.1002/cam4.7332.


Ultrasound-Mediated Antibiotic Delivery to In Vivo Biofilm Infections: A Review.

Liu J, Van Treeck K, Marston W, Papadopoulou V, Rowe S Chembiochem. 2024; 25(20):e202400181.

PMID: 38924307 PMC: 11483220. DOI: 10.1002/cbic.202400181.


Revolutionizing lymph node metastasis imaging: the role of drug delivery systems and future perspectives.

Cai Z, Li Z, Zhong N, Cao L, Xiao Y, Li J J Nanobiotechnology. 2024; 22(1):135.

PMID: 38553735 PMC: 10979629. DOI: 10.1186/s12951-024-02408-5.


Sonosensitive Cavitation Nuclei-A Customisable Platform Technology for Enhanced Therapeutic Delivery.

Lyons B, Balkaran J, Dunn-Lawless D, Lucian V, Keller S, OReilly C Molecules. 2023; 28(23).

PMID: 38067464 PMC: 10708135. DOI: 10.3390/molecules28237733.


Innate Immune System in the Context of Radiation Therapy for Cancer.

Boopathi E, Den R, Thangavel C Cancers (Basel). 2023; 15(15).

PMID: 37568788 PMC: 10417569. DOI: 10.3390/cancers15153972.


References
1.
Bradley J, Ieumwananonthachai N, Purdy J, Wasserman T, Lockett M, Graham M . Gross tumor volume, critical prognostic factor in patients treated with three-dimensional conformal radiation therapy for non-small-cell lung carcinoma. Int J Radiat Oncol Biol Phys. 2002; 52(1):49-57. DOI: 10.1016/s0360-3016(01)01772-2. View

2.
Harrison L, Shasha D, Shiaova L, White C, Ramdeen B, Portenoy R . Prevalence of anemia in cancer patients undergoing radiation therapy. Semin Oncol. 2001; 28(2 Suppl 8):54-9. DOI: 10.1016/s0093-7754(01)90214-3. View

3.
GRAY L, CONGER A, Ebert M, HORNSEY S, Scott O . The concentration of oxygen dissolved in tissues at the time of irradiation as a factor in radiotherapy. Br J Radiol. 1953; 26(312):638-48. DOI: 10.1259/0007-1285-26-312-638. View

4.
Kallman R . The phenomenon of reoxygenation and its implications for fractionated radiotherapy. Radiology. 1972; 105(1):135-42. DOI: 10.1148/105.1.135. View

5.
Chen M, Jiang G, Fu X, Wang L, Qian H, Zhao S . Prognostic factors for local control in non-small-cell lung cancer treated with definitive radiation therapy. Am J Clin Oncol. 2002; 25(1):76-80. DOI: 10.1097/00000421-200202000-00016. View