{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,16]],"date-time":"2026-09-16T02:01:01Z","timestamp":1789524061274,"version":"build-2803163510"},"reference-count":202,"publisher":"Bioscientifica","issue":"11","content-domain":{"domain":["erc.bioscientifica.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2024,8,21]]},"abstract":"<jats:p>Cancer is the second leading cause of death in the United States and among the most prevalent diseases globally, with an incidence expected to grow because of smoking, pollution, poor dietary habits, obesity, and the rise in the older population. Given their ability to reduce risk factors, albeit with varying efficacy, nutrition and fasting could help prevent cancer and other age-related disorders. Calorie restriction (CR), various forms of intermittent fasting (IF) or periodic fasting (PF), and fasting-mimicking diets (FMDs) have been shown to improve health span, increase lifespan, and prevent or postpone cancer in rodents. The effects of specific diets and fasting regimens on aging and cancer appear to be mediated in part by the reduction in the activity of the growth hormone (GH)\/insulin-like-growth-factor-I (IGF-1) axis. Nevertheless, recent data indicate that the alternation of low and normal levels of these hormones and factors may be ideal for optimizing longevity and function. Here, we review the role of nutrition, CR, and fasting\/FMD on cancer, focusing on the hypothesis that the modulation of GH, IGF-1, and insulin signaling partly mediates the effect of these dietary interventions on cancer prevention.<\/jats:p>","DOI":"10.1530\/erc-23-0048","type":"journal-article","created":{"date-parts":[[2024,8,28]],"date-time":"2024-08-28T07:18:26Z","timestamp":1724829506000},"update-policy":"https:\/\/doi.org\/10.1530\/crossmarkpolicy-8","source":"Crossref","is-referenced-by-count":24,"title":["Nutrition, GH\/IGF-1 signaling, and cancer"],"prefix":"10.1530","volume":"31","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-8627-666X","authenticated-orcid":true,"given":"Maura","family":"Fanti","sequence":"first","affiliation":[{"name":"Longevity Institute, Leonard Davis School of Gerontology and Department of Biological Sciences, University of Southern California, Los Angeles, California, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-0946-7534","authenticated-orcid":true,"given":"Valter D","family":"Longo","sequence":"additional","affiliation":[{"name":"Longevity Institute, Leonard Davis School of Gerontology and Department of Biological Sciences, University of Southern California, Los Angeles, California, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"416","reference":[{"key":"bib1","series-title":"Clinical Endocrinology","first-page":"771","article-title":"The study of spontaneous GH secretion after 36-h fasting distinguishes between GH-deficient and normal adults","volume":"51","author":"Aimaretti","year":"1999","unstructured":"Aimaretti GColao ACorneli GPivonello RMaccario MMorrison KPflaum CDStrasburger CJLombardi G & Ghigo E1999The study of spontaneous GH secretion after 36-h fasting distinguishes between GH-deficient and normal adults. 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