TY - JOUR
T1 - Mechanical regulation of mitochondrial morphodynamics in cancer cells by extracellular microenvironment
AU - Lunova, Mariia
AU - Jirsa, Milan
AU - Dejneka, Alexandr
AU - Sullivan, Gareth John
AU - Lunov, Oleg
N1 - Funding: The authors would like to thank the Czech Science Foundation
(GACR) (Grant number: 22-18634S). The authors acknowledge the MH
CZ - DRO Institute for Clinical and Experimental Medicine – IKEM, IN
00023001. The work was partially supported by the Strategy AV21
"Breakthrough technologies for the future – sensing, digitization, artificial intelligence, and quantum technologies". GJS the financial support from UiO:Life Science (Project MORGI-20493) is gratefully acknowledged.
PY - 2024/6
Y1 - 2024/6
N2 - Recently, it has been recognized that physical abnormalities (e.g. elevated solid stress, elevated interstitial fluid pressure, increased stiffness) are associated with tumor progression and development. Additionally, these mechanical forces originating from tumor cell environment through mechanotransduction pathways can affect metabolism. On the other hand, mitochondria are well-known as bioenergetic, biosynthetic, and signaling organelles crucial for sensing stress and facilitating cellular adaptation to the environment and physical stimuli. Disruptions in mitochondrial dynamics and function have been found to play a role in the initiation and advancement of cancer. Consequently, it is logical to hypothesize that mitochondria dynamics subjected to physical cues may play a pivotal role in mediating tumorigenesis. Recently mitochondrial biogenesis and turnover, fission and fusion dynamics was linked to mechanotransduction in cancer. However, how cancer cell mechanics and mitochondria functions are connected, still remain poorly understood. Here, we discuss recent studies that link mechanical stimuli exerted by the tumor cell environment and mitochondria dynamics and functions. This interplay between mechanics and mitochondria functions may shed light on how mitochondria regulate tumorigenesis.
AB - Recently, it has been recognized that physical abnormalities (e.g. elevated solid stress, elevated interstitial fluid pressure, increased stiffness) are associated with tumor progression and development. Additionally, these mechanical forces originating from tumor cell environment through mechanotransduction pathways can affect metabolism. On the other hand, mitochondria are well-known as bioenergetic, biosynthetic, and signaling organelles crucial for sensing stress and facilitating cellular adaptation to the environment and physical stimuli. Disruptions in mitochondrial dynamics and function have been found to play a role in the initiation and advancement of cancer. Consequently, it is logical to hypothesize that mitochondria dynamics subjected to physical cues may play a pivotal role in mediating tumorigenesis. Recently mitochondrial biogenesis and turnover, fission and fusion dynamics was linked to mechanotransduction in cancer. However, how cancer cell mechanics and mitochondria functions are connected, still remain poorly understood. Here, we discuss recent studies that link mechanical stimuli exerted by the tumor cell environment and mitochondria dynamics and functions. This interplay between mechanics and mitochondria functions may shed light on how mitochondria regulate tumorigenesis.
KW - Cancer
KW - Tumour metabolism
KW - Mechanotransduction
KW - Mitochondria
KW - Mitochondrial dynamics
U2 - 10.1016/j.bbiosy.2024.100093
DO - 10.1016/j.bbiosy.2024.100093
M3 - Article
C2 - 38585282
SN - 2666-5344
VL - 14
SP - 1
EP - 9
JO - Biomaterials and Biosystems
JF - Biomaterials and Biosystems
M1 - 100093
ER -