Article in Cancer research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
2 · The registry
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Ricardo A CordovaDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana.ORCID 0000-0003-4959-309X
May ElbannaIndiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, Indiana.ORCID 0000-0002-9745-9066
Christopher RupertDivision of Hematology and Oncology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, New York.ORCID 0000-0003-4636-1189
Sabrina A OrsiDivision of Hematology and Oncology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, New York.ORCID 0000-0001-6027-5258
Noah R SommersDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana.ORCID 0000-0002-5510-4099
Angela J KlunkDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana.ORCID 0009-0008-2224-2699
Li ShenDivision of Hematology and Oncology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, New York.ORCID 0000-0003-4182-6450
Jagannath MisraDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana.ORCID 0000-0001-9713-0298
Jocelyne N HanquierStark Neurosciences Research Institute, Indiana University School of Medicine, Indianapolis, Indiana.ORCID 0000-0001-7195-482X
Maria TsompanaDivision of Hematology and Oncology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, New York.ORCID 0000-0001-7546-3198
David W GoodrichRoswell Park Comprehensive Cancer Center, Buffalo, New York.ORCID 0000-0002-1021-1827
Ronald C WekDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana.ORCID 0000-0002-2087-5504
Luigi FontanaCharles Perkins Centre, Faculty of Medicine and Health, University of Sydney, Sydney, Australia.ORCID 0000-0001-8500-5537
Kirk A StaschkeDepartment of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana.ORCID 0000-0001-8722-9585
Roberto PiliDivision of Hematology and Oncology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, New York.ORCID 0009-0004-9993-9911
Funding
Tumor Microenvironment and Metastasis ProgramP30CA082709 · NCI · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI David W Clapp · 1999 to 2026
$59.3M
Immuno-Oncology Translation Network: Data Management and Resource-Sharing Center at RPCIU24CA232979 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI HUTSON, ALAN DAVID, LIU, SONG · 2018 to 2024
$8.9M
YAP1 and RB1 cooperate to regulate lung cancer lineage plasticity and therapeutic resistanceU24CA274159 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI DAVID W. GOODRICH, Alan David Hutson · 2022 to 2026
$8.5M
NOTCH signaling controls transformation to androgen independent neuroendocrine prostate cancerR01CA234162 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI GOODRICH, DAVID W. · 2019 to 2024
$3.0M
Regulation and Function of Integrated Stress ResponseR35GM136331 · NIGMS · INDIANA UNIVERSITY INDIANAPOLIS · PI WEK, RONALD C · 2020 to 2024
$1.9M
Immunomodulation by dietary protein restrictionR21CA221942 · NCI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI PILI, ROBERTO · 2018 to 2019
$381k
American Cancer Society (ACS) IRG-22-147-37-IRG-06Australian Youth and Health Foundation (Australian Youth Foundation)Bakewell Foundation (The Bakewell Foundation)National Health and Medical Research Council (NHMRC) APP1177797National Institutes of Health (NIH) GM136331National Institutes of Health (NIH) P30CA082709National Institutes of Health (NIH) R01CA234162National Institutes of Health (NIH) R21CA221942National Institutes of Health (NIH) U24CA274159NCI NIH HHS P30 CA082709NCI NIH HHS R01 CA234162NCI NIH HHS R21 CA221942NCI NIH HHS U24 CA232979NCI NIH HHS U24 CA274159NIGMS NIH HHS R35 GM136331Prostate Cancer Foundation (PCF) PCF22CHAL13Ralph W. and Grace M. Showalter Research Trust Fund (Showalter Foundation)U.S. Department of Defense (DOD) HT9425-24-1-0525
6 · The paper itself
Abstract
Epidemiologic studies suggest that diet can affect the incidence, progression, and response to treatment in multiple cancers, including prostate cancer. In this study, we investigated the use of dietary interventions, specifically caloric or protein restriction, in combination with antiandrogen therapy as a treatment for prostate cancer. Caloric restriction through alternate-day fasting (ADF) reduced androgen receptor (AR) expression and signaling. This reduction in AR enhanced the antitumor activity of the AR antagonist enzalutamide in multiple mouse models of prostate cancer. Mechanistic studies revealed that nutrient starvation via ADF predominantly decreased AR mRNA translation at the elongation stage due to AA limitation. Pharmacologic agents that similarly impair translation elongation and promote ribosome collisions mimicked the AR translation reduction observed with ADF. Overall, these findings suggest that AA limitation through ADF impairs translation elongation in prostate cancer, to which AR mRNA translation is susceptible, leading to a reduction in AR protein levels and enhancing AR-targeted therapy. SIGNIFICANCE: Fasting-induced caloric restriction reduces androgen receptor translation and enhances the activity of enzalutamide, suggesting that dietary intervention could be an effective strategy to enhance prostate cancer sensitivity to antiandrogen therapy. See related commentary by Anzules et al., p. 4045.
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.
Caloric Restriction Enhances the Efficacy of Antiandrogen Therapy in Prostate Cancer by Inhibiting Androgen Receptor Translation. · full record | OpenQuestion