<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>61</viewCount><searchCount>0</searchCount></scores><additional><submitter>Zhu Y</submitter><funding>NIDDK NIH HHS</funding><funding>NIEHS NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>83409-83423</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5347778</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7(50)</volume><pubmed_abstract>Premenopausal breast cancer is associated with increased animal fat consumption among normal weight, but not overweight women (Farvid et al., 2014). Our previous findings in obesity-resistant BALB/c mice similarly showed promotion of carcinogen-induced mammary tumorigenesis by a diet high in saturated animal fat (HFD). This effect was specific to pubertal versus adult HFD. This study identifies the effects of HFD during puberty versus adulthood in Trp53-null transplant BALB/c mice and investigates its mechanism of enhancing tumorigenesis. Either pubertal or adult HFD is sufficient to increase incidence of Trp53-null mammary tumors. Puberty-restricted HFD exposure promoted tumor cell proliferation, increased angiogenesis, and increased recruitment of total and M2 macrophages in epithelial tumors. Adult-restricted exposure to HFD similarly increased proliferation, angiogenesis, recruitment of total and M2 macrophages, and additionally reduced apoptosis. Adult HFD also increased incidence of spindle cell carcinomas resembling claudin-low breast cancer, and thus adult HFD in the Trp53-null transplantation system may be a useful model for human claudin low breast cancer. Importantly, these results on Trp53-null and our prior studies on DMBA-induced mammary tumorigenesis demonstrate a pubertal window of susceptibility to the promotional effects of HFD, indicating the potential of early life dietary intervention to reduce breast cancer risk.</pubmed_abstract><journal>Oncotarget</journal><pubmed_title>Pubertal and adult windows of susceptibility to a high animal fat diet in Trp53-null mammary tumorigenesis.</pubmed_title><pmcid>PMC5347778</pmcid><funding_grant_id>P30 DK056350</funding_grant_id><funding_grant_id>P50 CA058223</funding_grant_id><funding_grant_id>P30 ES010126</funding_grant_id><funding_grant_id>U01 ES026119</funding_grant_id><pubmed_authors>Aupperlee MD</pubmed_authors><pubmed_authors>Zhu Y</pubmed_authors><pubmed_authors>Troester MA</pubmed_authors><pubmed_authors>Kirk EL</pubmed_authors><pubmed_authors>Tan YS</pubmed_authors><pubmed_authors>Haslam SZ</pubmed_authors><pubmed_authors>Sun X</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors><pubmed_authors>Schwartz RC</pubmed_authors><view_count>61</view_count></additional><is_claimable>false</is_claimable><name>Pubertal and adult windows of susceptibility to a high animal fat diet in Trp53-null mammary tumorigenesis.</name><description>Premenopausal breast cancer is associated with increased animal fat consumption among normal weight, but not overweight women (Farvid et al., 2014). Our previous findings in obesity-resistant BALB/c mice similarly showed promotion of carcinogen-induced mammary tumorigenesis by a diet high in saturated animal fat (HFD). This effect was specific to pubertal versus adult HFD. This study identifies the effects of HFD during puberty versus adulthood in Trp53-null transplant BALB/c mice and investigates its mechanism of enhancing tumorigenesis. Either pubertal or adult HFD is sufficient to increase incidence of Trp53-null mammary tumors. Puberty-restricted HFD exposure promoted tumor cell proliferation, increased angiogenesis, and increased recruitment of total and M2 macrophages in epithelial tumors. Adult-restricted exposure to HFD similarly increased proliferation, angiogenesis, recruitment of total and M2 macrophages, and additionally reduced apoptosis. Adult HFD also increased incidence of spindle cell carcinomas resembling claudin-low breast cancer, and thus adult HFD in the Trp53-null transplantation system may be a useful model for human claudin low breast cancer. Importantly, these results on Trp53-null and our prior studies on DMBA-induced mammary tumorigenesis demonstrate a pubertal window of susceptibility to the promotional effects of HFD, indicating the potential of early life dietary intervention to reduce breast cancer risk.</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Dec</publication><modification>2024-11-19T22:14:02.232Z</modification><creation>2019-03-27T02:38:31Z</creation></dates><accession>S-EPMC5347778</accession><cross_references><pubmed>27825136</pubmed><doi>10.18632/oncotarget.13112</doi></cross_references></HashMap>