American Association for Cancer Research
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Supplementary Tables 1-6 from Metformin Reduces Prostate Tumor Growth, in a Diet-Dependent Manner, by Modulating Multiple Signaling Pathways

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journal contribution
posted on 2023-04-03, 17:25 authored by André Sarmento-Cabral, Fernando L-López, Manuel D. Gahete, Justo P. Castaño, Raúl M. Luque

Supplemental Table 1. Diete composición information. Supplemental Table 2. Specific set of primers used for the amplification of human and mouse transcripts by qPCR. Supplemental Table 3. Effect of HFD on the tumors gene expression. Supplementary Table 4. Effect of metformina treatment on the tumors gene expression under a LFD. Supplementary Table 5. Effect of metformina treatment on the tumors gene expression under a HFD. Supplementary Table 6. Effect of HFD on the tumors gene expression on both metformin treated groups.



Ministerio de Economía y Competitividad

Junta de Andalucía



Prostate-cancer is strongly influenced by obesity, wherein metformin could represent a promising treatment; however, the endocrine metabolic/cellular/molecular mechanisms underlying these associations and effects are still unclear. To determine the beneficial antitumoral effects of metformin on prostate cancer progression/aggressiveness and the relative contribution of high-fat diet (HFD; independently of obesity), we used HFD-fed immunosuppressed mice inoculated with PC3 cells (which exhibited partial resistance to diet-induced obesity) compared with low-fat diet (LFD)-fed control mice. Moreover, gene expression analysis was performed on cancer-associated genes in the xenografted tumors, and the antitumorigenic role of metformin on tumoral (PC3/22Rv1/LNCaP) and normal (RWPE1) prostate cells was evaluated. The results demonstrate that HFD is associated with enhanced prostate cancer growth irrespective of body weight gain and endocrine metabolic dysregulations and that metformin can reduce prostate cancer growth under LFD but more prominently under HFD, acting through the modulation of several tumoral-associated processes (e.g., cell cycle, apoptosis, and/or necrosis). Moreover, the actions observed in vivo could be mediated by the modulation of the local expression of GH/IGF1 axis components. Finally, it was demonstrated that metformin had disparate effects on proliferation, migration, and prostate-specific antigen secretion from different cell lines. Altogether, these data reveal that metformin inhibits prostate cancer growth under LFD and, specially, under HFD conditions through multiple metabolic/tumoral signaling pathways.Implications: The current study linking dietary influence on metformin-regulated signaling pathways and antitumoral response provides new and critical insight on environment–host interactions in cancer and therapy. Mol Cancer Res; 15(7); 862–74. ©2017 AACR.

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