» Articles » PMID: 14967430

Polarographic Electrode Study of Tumor Oxygenation in Clinically Localized Prostate Cancer

Overview
Specialties Oncology
Radiology
Date 2004 Feb 18
PMID 14967430
Citations 38
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: To describe the oxygenation of clinically localized prostate cancer.

Methods And Materials: Intraprostatic oxygen tension was measured using the Eppendorf electrode in 55 unanesthetized men with localized prostate cancer before radiotherapy. Measurements were made along two tracks through regions of suspected tumor in the prostate, and core needle biopsies were then obtained from the same regions.

Results: The median pO(2) ranged from 0.2 to 57.3 mm Hg, and the grand median pO(2) was 4.5 mm Hg. The percentage of oxygen readings <5 mm Hg (HP(5)) ranged from 0% to 100% (median 60%). The track 1 oxygen readings were greater than those from track 2. Statistically significant heterogeneity was found in the individual oxygen readings: the between- and within-tumor components accounted for 32% and 68% of the total variability, respectively. However, the between-tumor variability in HP(5) significantly exceeded the within-tumor variability (61% vs. 39%). No association was found between oxygen values and clinical factors, including age, T stage, Gleason score, prostate-specific antigen level, hemoglobin concentration, or prior hormonal treatment. No difference was noted in the oxygenation between regions of tumor and normal prostate tissue, as determined from the core biopsies.

Conclusion: Localized prostate cancer is characterized by marked hypoxia and significant heterogeneity in oxygenation, similar to other human tumors. The normal prostate may contain regions of low oxygen concentration. HP(5), as determined in this study, should adequately discriminate among patients with prostate cancer and allow the independent prognostic significance of oxygenation to be evaluated once the study matures.

Citing Articles

Oxygen Assessment in Tumors In Vivo Using Phosphorescence Lifetime Imaging Microscopy.

Komarova A, Shcheslavskiy V, Plekhanov A, Sirotkina M, Bochkarev L, Shirmanova M Methods Mol Biol. 2024; 2755:91-105.

PMID: 38319571 DOI: 10.1007/978-1-0716-3633-6_6.


Senescence-associated secretory phenotype constructed detrimental and beneficial subtypes and prognostic index for prostate cancer patients undergoing radical prostatectomy.

Feng D, Wang J, Li D, Wu R, Wei W, Zhang C Discov Oncol. 2023; 14(1):155.

PMID: 37624511 PMC: 10457268. DOI: 10.1007/s12672-023-00777-1.


The Prostate Stromal Transcriptome in Aggressive and Lethal Prostate Cancer.

Ma C, Zhou Y, Fanelli G, Stopsack K, Fiorentino M, Zadra G Mol Cancer Res. 2022; 21(3):253-260.

PMID: 36511902 PMC: 9991973. DOI: 10.1158/1541-7786.MCR-22-0627.


Hypoxia-mediated stabilization of HIF1A in prostatic intraepithelial neoplasia promotes cell plasticity and malignant progression.

Abu El Maaty M, Terzic J, Keime C, Rovito D, Lutzing R, Yanushko D Sci Adv. 2022; 8(29):eabo2295.

PMID: 35867798 PMC: 9307253. DOI: 10.1126/sciadv.abo2295.


Modulating Tumour Hypoxia in Prostate Cancer Through Exercise: The Impact of Redox Signalling on Radiosensitivity.

Brown M, Rebillard A, Hart N, OConnor D, Prue G, OSullivan J Sports Med Open. 2022; 8(1):48.

PMID: 35394236 PMC: 8993953. DOI: 10.1186/s40798-022-00436-9.