{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Zhang X"],"funding":["the opening project of State Key Laboratory of Explosion Science and Technology","the Shenzhen Science and Technology Program","the National Nature Science Foundation of China"],"pagination":["9769"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11928545"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["15(1)"],"pubmed_abstract":["Shock waves are widely used to treat various diseases and have numerous medical applications. In particular, extracorporeal shock waves (ESV) can substantially inhibit tumour growth. However, the therapeutic efficacy of ESV in colorectal cancer and its underlying mechanisms are not well understood. To address this gap in our knowledge, colorectal cancer cell lines HT29 and SW620 were used to generate xenograft mouse models and examined the therapeutic effects of a stepwise increase in ESV energy on tumour growth. In vivo, 60 mJ ESV significantly delayed xenograft growth compared with 120 and 240 mJ ESV, with no impact on body weight or hepatic and renal function. Transcriptome analysis revealed that 60 mJ ESV suppressed colorectal cancer cell proliferation and induced apoptosis and ferropt"],"journal":["Scientific reports"],"pubmed_title":["Extracorporeal shock waves effectively suppress colorectal cancer proliferation and growth."],"pmcid":["PMC11928545"],"funding_grant_id":["KFJJ22-16M","82203229","JCYJ20220531094005012"],"pubmed_authors":["Ran C","Lv G","Zhang X","Song Q"],"additional_accession":[]},"is_claimable":false,"name":"Extracorporeal shock waves effectively suppress colorectal cancer proliferation and growth.","description":"Shock waves are widely used to treat various diseases and have numerous medical applications. In particular, extracorporeal shock waves (ESV) can substantially inhibit tumour growth. However, the therapeutic efficacy of ESV in colorectal cancer and its underlying mechanisms are not well understood. To address this gap in our knowledge, colorectal cancer cell lines HT29 and SW620 were used to generate xenograft mouse models and examined the therapeutic effects of a stepwise increase in ESV energy on tumour growth. In vivo, 60 mJ ESV significantly delayed xenograft growth compared with 120 and 240 mJ ESV, with no impact on body weight or hepatic and renal function. Transcriptome analysis revealed that 60 mJ ESV suppressed colorectal cancer cell proliferation and induced apoptosis and ferropt","dates":{"release":"2025-01-01T00:00:00Z","publication":"2025 Mar","modification":"2025-07-04T03:05:50.41Z","creation":"2025-07-04T03:05:50.41Z"},"accession":"S-EPMC11928545","cross_references":{"pubmed":["40119128"],"doi":["10.1038/s41598-025-94386-3"]}}