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Influence of a single bout of endurance exercise on epigenetic modifications, effector function and tumorinfiltration of natural killer cells

Influence of a single bout of endurance exercise on epigenetic modifications, effector function and tumorinfiltration of natural killer cells

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00010442
Enrollment
28
Registered
2016-05-17
Start date
2016-11-18
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate cancer C61

Interventions

Group 1: Intervention group - Approximately 12 hours before patients surgery for removal of tumor tissue, the patients performe a singel bout of exercise on a bycicle ergometer for 30 minutes at 75% o

Sponsors

Deutsche Sporthochschule Köln Institut für Kreislaufforschung ung Sportmedizin, Abteilung für molekulare und zelluläre Sportmedizin
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with diagnosed high-risc prostate cancer (PSA > 20ng/ml or biopsie gleason score 8-10 or clinical cT3 stadium); imminent resection of tumor tissue; age > 18 years

Exclusion criteria

Exclusion criteria: Neoadjuvant chemotherapy or radiation; prior chemotherapy because of prior cancer disease; thrombocytopenia < 20.000/µl; cardivascular diseases

Design outcomes

Primary

MeasureTime frame
Primary Endpoint is the change of epigenetic modifications (promoter methylation) of the NKG2D gene due to the intervention. Before, after and 12 h after the single bout of exercise (IG) or rest (CG) blood samples will be drawn. Lymphocytes are attained by centrifugation with a separation medium and are used for a magnetbead isolation of NK cells (natural killer cells). DNA is extracted from NK cells and the promoter methylation of the NKG2D gene is analyzed by bisulfite treatment and real time PCR.

Secondary

MeasureTime frame
Besides the primary endpoint also (1) changes of global histone acetylation in NK cells will be investigated. Therefore the cells will be stained by immunocytochemistry for histone acetylation at H4K5 and H3K9. Further (2) the NK cell cytotoxicity will be analyzed by performing cytotoxicity assays with fresh isolated NK cells and the tumor cell line K652. For this purpose the NK cells will also be characterized for their subgroups (CD56bright and CD56dim) by flow cytometry. In addition the resected tumor tissue will be under investigation for (3) the number of intratumoral NK cells and (4) the expression of NKG2D ligands on tumor cells. Both parameters will be analyzed by immunohistochemistry and evaluated microscopically.

Countries

Germany

Contacts

Public ContactAlexander Schenk

Deutsche Sporthochschule Köln Institut für Kreislaufforschung und Sportmedizin Abteilung für molekulare und zelluläre Sportmedizin

a.schenk@dshs-koeln.de+49221 4982 5450

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026