Role of GPR120 and Macrophages in Dietary Omega-3 Fatty Acid Inhibition of Prostate Cancer
Role of GPR120 and Macrophages in Dietary Omega-3 Fatty Acid Inhibition of Prostate Cancer
批准号:
10478836
负责人:
WILLIAM J ARONSON
金额:
$42.24万
依托单位国家:
美国
项目类别:
财政年份:
2018
资助国家:
美国
项目状态:
已结题
起止时间:
2018-09-17 至 2023-08-31
关键词:
AffectAllograftingBiological MarkersBiologyBiopsyBone MarrowBone Marrow CellsBone Marrow TransplantationCancer PatientCarcinomaCell Cycle ProgressionCell LineageCellsCharacteristicsClinicalClinical TrialsCollaborationsConsumptionDataDevelopmentDietDiet ModificationDietary InterventionDietary intakeEventExonsFish OilsFishesFutureG-Protein-Coupled ReceptorsGTP-Binding Protein alpha Subunits, GsGene ExpressionGenomeGoalsImmuneImmunocompetentImmunotherapyIn VitroInterventionKnock-outKnockout MiceKnowledgeLaboratoriesLeadLoxP-flanked alleleMalignant neoplasm of prostateMeasuresModelingMusMyelogenousNutritionalNutritional SupportOmega-3 Fatty AcidsOmega-6 Fatty AcidsOutcomePathway interactionsPatientsPhasePlayPolyunsaturated Fatty AcidsPrognosisProstatectomyProstatic NeoplasmsRandomizedRecording of previous eventsReportingResearch PersonnelRoleSeriesT-LymphocyteTestingTissuesTransgenic MiceTransgenic OrganismsTumor TissueTumor-DerivedTumor-associated macrophagesangiogenesisanti-canceranticancer activitybasecancer cellcell motilityclinical practiceclinical predictorsdesigndietarydietary supplementsepidemiology studyfield studyfollow-uphuman modelindexinginnovationinsightmacrophagemenmolecular markermonocytemortalitymouse modelmultidisciplinarynoveloncotypepre-clinicalprecision medicinepreclinical studypredict responsivenessprospectiveprostate biopsyprostate cancer progressionreceptortooltumor microenvironmenttumor progressionwestern diet
中文摘要
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英文摘要
PROJECT SUMMARY
Epidemiologic studies and multiple preclinical studies suggest dietary fish oil has the potential to delay prostate
cancer progression. A prospective randomized pre-prostatectomy trial conducted by our group found that
consuming a fish oil (omega-3) supplemented diet resulted in lower proliferation of prostate cancer epithelium
as measured by the Ki-67 index, and decreased Cell Cycle Progression (CCP) Score as compared to a control
Western diet. Both Ki-67 and the CCP Score are associated with prostate cancer progression and mortality,
suggesting potential benefits of consuming a fish oil supplemented diet for prostate cancer patients. In studies
with immunocompetent GPR120 knockout (KO) mice, we recently demonstrated that GPR120, a g-protein
coupled receptor important in the transport of long chain polyunsaturated fatty acids, is required in the host for
the anti-cancer activity of fish oil. Immune suppressive tumor associated macrophages with M2-like
characteristics have been associated with prostate cancer progression and poor prognosis. We also found that
fish oil inhibits the function of M2-like tumor-associated macrophages, and this effect was reversed in the
GPR120 KO mouse. Based on these findings, we hypothesize that a fish oil supplemented diet will delay the
progression of prostate cancer through GPR120 dependent effects on the tumor microenvironment. The Aims of
our proposal are: Aim 1. Determine if dietary omega-3 (ω-3) fatty acids act through GPR120 to inhibit prostate
cancer in a transgenic mouse model and study underlying mechanisms related to M2 macrophage function. Aim
2. Determine if GPR120 dependent host-derived bone marrow cells and myeloid lineage cells are essential for
the anticancer effects of dietary ω-3 FAs. Aim 3. Identify biomarkers in baseline prostate biopsy tissue that
predict responsiveness to a fish oil based dietary intervention by examining prostate biopsy tissue obtained from
an ongoing active surveillance trial in men receiving a fish oil supplemented diet (ω-6: ω-3 ratio of 3:1). We will
accomplish these aims through a series of mechanistic studies using GPR120 knockout and transgenic mouse
models fed diets varying in ω-3 and ω-6 fatty acid content, and studies on prostate biopsy tissue from a Phase
II, dietary intervention, active surveillance trial we are conducting in men with prostate cancer. Significance: Our
proposal sets a new direction for a precision medicine approach for selecting patients more likely to be
responsive to dietary modification based on GPR120 status. By studying the underlying biology of fish oil
anticancer effects through GPR120 and tumor associated macrophages/immune cells, we are establishing a
new field of study, nutritional immunotherapy, that may ultimately lead to innovative nutritional therapies for our
patients with prostate cancer. Our multidisciplinary team of investigators with a longstanding history of successful
collaborations is uniquely suited to achieve our stated goals.
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DOI:
10.1093/jncics/pkab023
发表时间:
2021-06
期刊:
JNCI cancer spectrum
影响因子:
4.4
作者:
[Kelkar S, Oyekunle T, Eisenberg A, Howard L, Aronson WJ, Kane CJ, Amling CL, Cooperberg MR, Klaassen Z, Terris MK, Freedland SJ, Csizmadi I]
通讯作者:
Csizmadi I
Monocyte counts and prostate cancer outcomes in white and black men: results from the SEARCH database.
白人和黑人的单核细胞计数和前列腺癌的结果:搜索数据库的结果。
DOI:
10.1007/s10552-020-01373-2
发表时间:
2021-03
期刊:
Cancer causes & control : CCC
影响因子:
--
作者:
[Yirga A, Oyekunle T, Howard LE, De Hoedt AM, Cooperberg MR, Kane CJ, Aronson WJ, Terris MK, Amling CL, Taioli E, Fowke JH, Klaanssen Z, Freedland SJ, Vidal AC]
通讯作者:
Vidal AC
Safety of concomitant therapy with radium-223 and abiraterone or enzalutamide in a real-world population.
在现实世界人群中,镭 223 和阿比特龙或恩杂鲁胺联合治疗的安全性。
DOI:
10.1002/pros.24115
发表时间:
2021
期刊:
The Prostate
影响因子:
--
作者:
[Zhao,Hanson, Howard,LaurenE, DeHoedt,AmandaM, Terris,MarthaK, Amling,ChristopherL, Kane,ChristopherJ, Cooperberg,MatthewR, Aronson,WilliamJ, Klaassen,Zachary, Polascik,ThomasJ, Vidal,AdrianaC, Freedland,StephenJ]
通讯作者:
Freedland,StephenJ
Is time to castration resistant prostate cancer a potential intermediate end-point for time to metastasis among men initiating androgen deprivation therapy for non-metastatic prostate cancer with rapid PSA doubling time (<9 months)?
对于针对 PSA 快速倍增时间(<9 个月)的非转移性前列腺癌开始雄激素剥夺治疗的男性,去势抵抗性前列腺癌的时间是否是转移时间的潜在中间终点?
DOI:
10.1038/s41391-022-00585-8
发表时间:
2023
期刊:
Prostate cancer and prostatic diseases
影响因子:
4.8
作者:
[Klaassen,Zachary, Howard,Lauren, Wallis,ChristopherJD, Janes,JessicaL, DeHoedt,Amanda, Aronson,WilliamJ, Polascik,ThomasJ, Amling,ChristopherJ, Kane,ChristopherJ, Cooperberg,MatthewR, Terris,MarthaK, Wu,Yuan, Freedland,StephenJ]
通讯作者:
Freedland,StephenJ
Role of GPR120 and Macrophages in Dietary Omega-3 Fatty Acid Inhibition of Prostate Cancer
-
批准号:10229545
-
项目类别:
-
资助金额:$43.1万
-
财政年份:2018
-
负责人:WILLIAM J ARONSON
-
依托单位:
LOW-FAT DIET AND OMEGA-FATTY ACIDS FOR PROSTATE CANCER PREVENTION
-
批准号:7951526
-
项目类别:
-
资助金额:$2.28万
-
财政年份:2009
-
负责人:WILLIAM J ARONSON
-
依托单位:
LOW-FAT DIET AND OMEGA-FATTY ACIDS FOR PROSTATE CANCER PREVENTION
-
批准号:8167067
-
项目类别:
-
资助金额:$0.07万
-
财政年份:2009
-
负责人:WILLIAM J ARONSON
-
依托单位:
Dietary Fat Modulation and Targeted Therapies for Prostate Cancer Prevention
-
批准号:7315072
-
项目类别:
-
资助金额:$19.22万
-
财政年份:2007
-
负责人:WILLIAM J ARONSON
-
依托单位:
LOW-FAT DIET AND OMEGA-FATTY ACIDS FOR PROSTATE CANCER PREVENTION
-
批准号:7606748
-
项目类别:
-
资助金额:$2.13万
-
财政年份:2007
-
负责人:WILLIAM J ARONSON
-
依托单位:
LOW-FAT DIET AND OMEGA-FATTY ACIDS FOR PROSTATE CANCER PREVENTION
-
批准号:7717963
-
项目类别:
-
资助金额:$1.85万
-
财政年份:2007
-
负责人:WILLIAM J ARONSON
-
依托单位:
Effects of Low Fat Diet on Serum Factors /Prostate Cance
-
批准号:7043081
-
项目类别:
-
资助金额:$0.46万
-
财政年份:2003
-
负责人:WILLIAM J ARONSON
-
依托单位:
Low-Fat/Fish Oil Diet and prostate Cancer Outcomes in Human Cohorts and Mouse Mo
-
批准号:8760361
-
项目类别:
-
资助金额:$24.64万
-
财政年份:2002
-
负责人:WILLIAM J ARONSON
-
依托单位:
Dietary Fat Modulation and Targeted Therapies for Prostate Cancer Prevention
-
批准号:8291329
-
项目类别:
-
资助金额:$19.62万
-
财政年份:2002
-
负责人:WILLIAM J ARONSON
-
依托单位:
Dietary Fat Modulation and Targeted Therapies for Prostate Cancer Prevention
-
批准号:8094358
-
项目类别:
-
资助金额:$20.65万
-
财政年份:2002
-
负责人:WILLIAM J ARONSON
-
依托单位:
Low-Fat/Fish Oil Diet and prostate Cancer Outcomes in Human Cohorts and Mouse Mo
-
批准号:8555089
-
项目类别:
-
资助金额:$24.53万
-
财政年份:2002
-
负责人:WILLIAM J ARONSON
-
依托单位:
Dietary Fat Modulation and Targeted Therapies for Prostate Cancer Prevention
-
批准号:7879466
-
项目类别:
-
资助金额:$20.65万
-
财政年份:2002
-
负责人:WILLIAM J ARONSON
-
依托单位:
Dietary Fat Modulation and Targeted Therapies for Prostate Cancer Prevention
-
批准号:7679546
-
项目类别:
-
资助金额:$20.64万
-
财政年份:2002
-
负责人:WILLIAM J ARONSON
-
依托单位:
海外基金