<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE324nnn/GSE324100/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE324100</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Exercise Training Prior To and During Cancer in Mice Preserves Muscle Mass, Reduces Tumor Weight, and Suppresses Molecular Mediators of Cachexia</name><description>We investigated the prophylactic effects of exercise before and during cancer cachexia (CC) using a model designed to mimic endurance and resistance (i.e., concurrent) adaptations. Male and female Balb/c mice were randomly assigned to exercise or control groups whereby exercise groups were subjected to an 8-week voluntary progressive weighted wheel running (PoWeR) program of habitual loading-mediated physical activity beginning at 8 weeks of age. At 16 weeks of age, mice were injected bilaterally with colon-26 adenocarcinoma (C26) cells or PBS, and exercise training was maintained throughout disease progression. Twenty-five days post-tumor induction, we assessed whole-body and muscle phenotype, muscle protein synthesis, a priori targeted gene expression, and transcriptomic adaptations via RNA sequencing. PoWeR training preserved skeletal muscle mass across nearly all muscle groups and maintained tumor-free body and cardiac mass. Muscle mass adaptations related to running volume; and running distance relative to controls was not appreciably reduced by tumor status. Tumor burden was reduced after ~11.5 weeks of PoWeR compared to sedentary, but this was not explanatory for muscle adaptations. PoWeR induced a faster-to-slower muscle fiber type transition in the gastrocnemius and suppressed key protein turnover markers (Redd1, Murf1, Atrogin, Ubc, Gadd45a) as well as the mitophagy-related marker Bnip3 in tumor-bearing muscle; 24h muscle protein synthesis remained stable. PoWeR counteracted tumor-induced impairments in the muscle mitochondrial- and metabolic-related transcriptome. Collectively, physical activity prior to and during cancer preserves muscle mass, reduces tumor growth, and mitigates molecular drivers of CC, underscoring its preventive and therapeutic potential as a lifestyle intervention.</description><dates><publication>2026/06/10</publication></dates><accession>GSE324100</accession><cross_references><GSM>GSM9568252</GSM><GSM>GSM9568241</GSM><GSM>GSM9568253</GSM><GSM>GSM9568242</GSM><GSM>GSM9568254</GSM><GSM>GSM9568243</GSM><GSM>GSM9568255</GSM><GSM>GSM9568244</GSM><GSM>GSM9568256</GSM><GSM>GSM9568245</GSM><GSM>GSM9568257</GSM><GSM>GSM9568246</GSM><GSM>GSM9568258</GSM><GSM>GSM9568247</GSM><GSM>GSM9568259</GSM><GSM>GSM9568248</GSM><GSM>GSM9568249</GSM><GSM>GSM9568260</GSM><GSM>GSM9568261</GSM><GSM>GSM9568250</GSM><GSM>GSM9568251</GSM><GSM>GSM9568240</GSM><GPL>24247</GPL><GSE>324100</GSE><taxon>Mus musculus</taxon><PMID>[42241015]</PMID></cross_references></HashMap>