How stiff the tissue is affects cancer cell growth through a specific signaling pathway (Hippo) that controls whether cells multiply, which is important for tumor development.
Scientific Claim
Matrix stiffness influences tumor cell proliferation via integrin-mediated Hippo pathway and YAP/TAZ signaling.
Original Statement
“On a hard surface, the Hippo pathway is involved in the proliferation of tumor cells, consisting of three main components: large tumor suppressor 1/2 (LATS1/2), yes-associated transcriptional regulator/tafazzin (YAP/TAZ) and mammalian Ste20-like kinases 1/2 (MST1/2). In detail, on the stiffer matrix, the ILK-integrin signal inhibits the activity of myosin phosphatase target subunit 1 and suppresses the signaling cascade of Merlin, MST1/2, and LATS1/2, which results in the YAP/TAZ translocation to the nucleus from the cytoplasm and initiated cell proliferation gene (such as cyclin D1 and forkhead box M1) transcription, where they initiate the transcription of genes involved in tumor cell proliferation.”
Evidence Quality Assessment
Claim Status
appropriately stated
Study Design Support
Design supports claim
Appropriate Language Strength
definitive
Can make definitive causal claims
Assessment Explanation
The mechanistic link between matrix stiffness and tumor proliferation is experimentally validated, supporting definitive language.
Evidence from Studies
Supporting (1)
The Molecular Interaction of Collagen with Cell Receptors for Biological Function