Apoptotic caspases in promoting cancer: Implications from their roles in development and tissue homeostasis

27Citations
Citations of this article
27Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Apoptosis, a major form of programmed cell death, is an important mechanism to remove extra or unwanted cells during development. In tissue homeostasis apoptosis also acts as a monitoring machinery to eliminate damaged cells in response to environmental stresses. During these processes, caspases, a group of proteases, have been well defined as key drivers of cell death. However, a wealth of evidence is emerging which supports the existence of many other non-apoptotic functions of these caspases, which are essential not only in proper organism development but also in tissue homeostasis and post-injury recovery. In particular, apoptotic caspases in stressinduced dying cells can activate mitogenic signals leading to proliferation of neighbouring cells, a phenomenon termed apoptosis-induced proliferation. Apparently, such non-apoptotic functions of caspases need to be controlled and restrained in a contextdependent manner during development to prevent their detrimental effects. Intriguingly, accumulating studies suggest that cancer cells are able to utilise these functions of caspases to their advantage to enable their survival, proliferation and metastasis in order to grow and progress. This book chapter will review non-apoptotic functions of the caspases in development and tissue homeostasis with focus on how these cellular processes can be hijacked by cancer cells and contribute to tumourigenesis.

Cite

CITATION STYLE

APA

Dabrowska, C., Li, M., & Fan, Y. (2016). Apoptotic caspases in promoting cancer: Implications from their roles in development and tissue homeostasis. In Advances in Experimental Medicine and Biology (Vol. 930, pp. 89–112). Springer New York LLC. https://doi.org/10.1007/978-3-319-39406-0_4

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free