Mammary fat pad transcriptomics of calorie restriction applied breast cancer-prone transgenic mice

Age-related dysfunction in neuroendocrine signaling, which influences adipose tissue homeostasis, has been implicated in numerous diseases, including breast cancer. Caloric restriction has been shown to improve metabolic health and prolong lifespan, yet the molecular mechanisms underlying its long-term effects remain largely unclear. In this study, we investigated the impact of long-term chronic (CCR) and intermittent caloric restriction (ICR) on the whole transcriptome of mammary fat pad tissue (MFP) in a breast cancer mouse model. Transgenic female Mouse Mammary Tumor Virus-Transforming Growth Factor-Alpha C57BL6 mice were randomized into ad libitum (AL), CCR, and ICR groups. Total RNA was isolated from the samples collected at weeks 10 (baseline), 49/50 (adult), and 81/82 (old), then subjected to RNA sequencing.