Annemarie J.F. Westheim , Ludwig J Dubois , Elia Prades-Sagarra , Jella G.M. van de Laak , Hester van Mourik , Lesley Schuitmaker , Lara M. Stoffels , Ala Yaromina , Miriam van Dijk , Jeroen van Bergenhenegouwen , Ardy van Helvoort , Ramon C.J. Langen , Ronit Shiri-Sverdlov , Jan Theys
{"title":"Dietary enrichment with n-3 lc-PUFA-rich fish oil improves preclinical outcome of radiotherapy and anti-PD-L1 combination treatment","authors":"Annemarie J.F. Westheim , Ludwig J Dubois , Elia Prades-Sagarra , Jella G.M. van de Laak , Hester van Mourik , Lesley Schuitmaker , Lara M. Stoffels , Ala Yaromina , Miriam van Dijk , Jeroen van Bergenhenegouwen , Ardy van Helvoort , Ramon C.J. Langen , Ronit Shiri-Sverdlov , Jan Theys","doi":"10.1016/j.ctarc.2025.100943","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Emerging evidence suggests a positive impact of long-chain polyunsaturated fatty acids (lc-PUFAs) on radiotherapy and anti-PD-L1 efficacy, however whether this translates into better outcomes in multimodality combination treatments remains unclear. We hypothesized that dietary lc-PUFAs can improve the outcome of RT/IT combination treatment.</div></div><div><h3>Methods</h3><div>Effects of different lc-PUFAs on CT26 surface PDL-1 expression were measured <em>in vitro</em> in absence or presence of radiotherapy using flow cytometry. Immunocompetent BALB/cOlaHsd mice, inoculated with CT26 cells, were randomized across different isocaloric AIN93M-based diets enriched with either eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) rich fish oil, arachidonic acid (ARA) rich ARASCO oil or combination of both. When tumors reached ±200 mm<sup>3</sup>, irradiation (2.33 Gy, QD5) was started. anti-PD-L1 (10 mg/kg, i.p., Q2Dx5) treatment started 1 day later. Study endpoint was defined as time to reach four times starting volume. Effects on splenic cytotoxic CD8+ <em>T</em>-cell number and activity was measured by flow cytometry.</div></div><div><h3>Results</h3><div>All lc-PUFAs tested and irradiation, upregulated PD-L1 expression <em>in vitro</em> with a stronger increase when combined. n-3 lc-PUFA-rich fish oil administration may support responsiveness to combined RT/anti-PD-L1 therapy, compared to control diet based on soybean oil, although borderline significant (hazard ratio 0.35 [0.11–1.02], <em>p</em> = 0.053). No effects of the oil blends were observed on tumor take, body weight, food intake or activation of splenic cytotoxic CD8+ <em>T</em>-cells.</div></div><div><h3>Conclusion</h3><div>A modest reduction in the risk of local tumor failure was observed upon n-3 lc-PUFA-rich fish oil administration, highlighting a need for further research.</div></div>","PeriodicalId":9507,"journal":{"name":"Cancer treatment and research communications","volume":"44 ","pages":"Article 100943"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cancer treatment and research communications","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2468294225000796","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
Background
Emerging evidence suggests a positive impact of long-chain polyunsaturated fatty acids (lc-PUFAs) on radiotherapy and anti-PD-L1 efficacy, however whether this translates into better outcomes in multimodality combination treatments remains unclear. We hypothesized that dietary lc-PUFAs can improve the outcome of RT/IT combination treatment.
Methods
Effects of different lc-PUFAs on CT26 surface PDL-1 expression were measured in vitro in absence or presence of radiotherapy using flow cytometry. Immunocompetent BALB/cOlaHsd mice, inoculated with CT26 cells, were randomized across different isocaloric AIN93M-based diets enriched with either eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) rich fish oil, arachidonic acid (ARA) rich ARASCO oil or combination of both. When tumors reached ±200 mm3, irradiation (2.33 Gy, QD5) was started. anti-PD-L1 (10 mg/kg, i.p., Q2Dx5) treatment started 1 day later. Study endpoint was defined as time to reach four times starting volume. Effects on splenic cytotoxic CD8+ T-cell number and activity was measured by flow cytometry.
Results
All lc-PUFAs tested and irradiation, upregulated PD-L1 expression in vitro with a stronger increase when combined. n-3 lc-PUFA-rich fish oil administration may support responsiveness to combined RT/anti-PD-L1 therapy, compared to control diet based on soybean oil, although borderline significant (hazard ratio 0.35 [0.11–1.02], p = 0.053). No effects of the oil blends were observed on tumor take, body weight, food intake or activation of splenic cytotoxic CD8+ T-cells.
Conclusion
A modest reduction in the risk of local tumor failure was observed upon n-3 lc-PUFA-rich fish oil administration, highlighting a need for further research.
期刊介绍:
Cancer Treatment and Research Communications is an international peer-reviewed publication dedicated to providing comprehensive basic, translational, and clinical oncology research. The journal is devoted to articles on detection, diagnosis, prevention, policy, and treatment of cancer and provides a global forum for the nurturing and development of future generations of oncology scientists. Cancer Treatment and Research Communications publishes comprehensive reviews and original studies describing various aspects of basic through clinical research of all tumor types. The journal also accepts clinical studies in oncology, with an emphasis on prospective early phase clinical trials. Specific areas of interest include basic, translational, and clinical research and mechanistic approaches; cancer biology; molecular carcinogenesis; genetics and genomics; stem cell and developmental biology; immunology; molecular and cellular oncology; systems biology; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; cancer policy; and integration of various approaches. Our mission is to be the premier source of relevant information through promoting excellence in research and facilitating the timely translation of that science to health care and clinical practice.