Ultrasound‐mediated mechanical forces activate selective tumor cell apoptosis

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Argitaratua izan da:Bioengineering & Translational Medicine vol. 10, no. 2 (Mar 1, 2025)
Egile nagusia: Tijore, Ajay
Beste egile batzuk: Margadant, Felix, Dwivedi, Nehal, Morgan, Leslie, Yao, Mingxi, Hariharan, Anushya, Chew, Claire Alexandra Zhen, Powell, Simon, Bonney, Glenn Kunnath, Sheetz, Michael
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John Wiley & Sons, Inc.
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022 |a 2380-6761 
024 7 |a 10.1002/btm2.10737  |2 doi 
035 |a 3174223231 
045 0 |b d20250301 
100 1 |a Tijore, Ajay  |u Mechanobiology Institute, National University of Singapore, Singapore 
245 1 |a Ultrasound‐mediated mechanical forces activate selective tumor cell apoptosis 
260 |b John Wiley & Sons, Inc.  |c Mar 1, 2025 
513 |a Journal Article 
520 3 |a Recent studies show that tumor cells undergo apoptosis after mechanical stretching, which promotes normal cell growth. Since ultrasound can produce similar sub‐cellular mechanical stresses on the nanoscale, here we test the effect of ultrasound‐mediated mechanical forces on tumors and normal cell survival. Surprisingly, tumor cells undergo apoptosis through a calpain‐dependent mitochondrial pathway that relies upon calcium entry through the mechanosensitive Piezo1 channels. This is a general property of all tumor cell lines tested irrespective of tissue origin, but normal cells are unaffected. In vivo, ultrasound treatment promotes tumor cell killing in a mouse model with invasive CT26 cancer cell subcutaneous tumors and in the chick chorioallantoic membrane (CAM) model with relatively minor damage to chick embryos. Further, patient‐derived pancreatic tumor organoids are killed by ultrasound treatment. Because ultrasound‐mediated mechanical forces cause apoptosis of tumor cells from many different tissues in different microenvironments, it may offer a safe, non‐invasive approach to augment tumor treatments. 
653 |a Apoptosis 
653 |a Cells 
653 |a Tumors 
653 |a In vivo methods and tests 
653 |a Cancer therapies 
653 |a Ultrasonic processing 
653 |a Ultrasonic imaging 
700 1 |a Margadant, Felix  |u Mechanobiology Institute, National University of Singapore, Singapore 
700 1 |a Dwivedi, Nehal  |u Biochemistry and Molecular Biology Department, University of Texas Medical Branch, Galveston, Texas, USA 
700 1 |a Morgan, Leslie  |u Biochemistry and Molecular Biology Department, University of Texas Medical Branch, Galveston, Texas, USA 
700 1 |a Yao, Mingxi  |u Mechanobiology Institute, National University of Singapore, Singapore 
700 1 |a Hariharan, Anushya  |u Mechanobiology Institute, National University of Singapore, Singapore 
700 1 |a Chew, Claire Alexandra Zhen  |u Division of Hepatobiliary & Pancreatic Surgery, Department of Surgery, National University Hospital, Singapore 
700 1 |a Powell, Simon  |u Biochemistry and Molecular Biology Department, University of Texas Medical Branch, Galveston, Texas, USA 
700 1 |a Bonney, Glenn Kunnath  |u Division of Hepatobiliary & Pancreatic Surgery, Department of Surgery, National University Hospital, Singapore 
700 1 |a Sheetz, Michael  |u Mechanobiology Institute, National University of Singapore, Singapore 
773 0 |t Bioengineering & Translational Medicine  |g vol. 10, no. 2 (Mar 1, 2025) 
786 0 |d ProQuest  |t Engineering Database 
856 4 1 |3 Citation/Abstract  |u https://www.proquest.com/docview/3174223231/abstract/embedded/7BTGNMKEMPT1V9Z2?source=fedsrch 
856 4 0 |3 Full Text  |u https://www.proquest.com/docview/3174223231/fulltext/embedded/7BTGNMKEMPT1V9Z2?source=fedsrch 
856 4 0 |3 Full Text - PDF  |u https://www.proquest.com/docview/3174223231/fulltextPDF/embedded/7BTGNMKEMPT1V9Z2?source=fedsrch