Anoikis
Anoikis is a form of programmed cell death that occurs in anchorage-dependent cells when they detach from the surrounding extracellular matrix (ECM).[1] Usually cells stay close to the tissue to which they belong since the communication between proximal cells as well as between cells and ECM provide essential signals for growth or survival. When cells are detached from the ECM, there is a loss of normal cell–matrix interactions, and they may undergo anoikis. However, metastatic tumor cells may escape from anoikis and invade other organs.
Etymology
[edit]The word "anoikis" was coined by Frisch and Francis in a paper published in the Journal of Cell Biology in 1994.[2] "Anoikis", in their words, means "(…the state of being without a home) to describe the cells' apoptotic response to the absence of cell–matrix interactions". The word apparently is a neologism construction consisting of three Greek morphemes agglutinated together: ἀν- "without", οἰκ- "house", and the suffix -ις.
In metastasis
[edit]Using a novel high-throughput screening assay, Mawji et al. showed that anisomycin can sensitize metastatic epithelial cells to anoikis and reduce circulating tumor cell implantation in vivo.[3] Anisomycin achieved this anti-metastatic activity in part by decreasing the abundance of the death receptor inhibiting protein FLIP (c-Fas–associated death domain–like interleukin-1–converting enzyme–like inhibitory protein). In related work, Schimmer's team showed that FLIP levels are higher in metastatic cells than non-metastatic cells, and that reducing FLIP levels using RNAi (RNA Interference) or other small molecule inhibitors of FLIP can sensitize metastatic cells to anoikis.[4] Given that FLIP is an inhibitor of anoikis, and that reducing FLIP can sensitize metastatic cells to anoikis, Mawji et al. hypothesize that FLIP reduction may be a viable therapeutic strategy against cancer metastasis.
Cancer cells develop anoikis resistance by several mechanisms, including changes in integrin and matrix signaling, metabolic deregulation, and stress responses of cancer cells.[5] One key mechanism that renders cancer cells independent from tissue adherence is dysregulation of the pathway network that controls transcription factor NF-κB.
See also
[edit]References
[edit]- ^ Frisch SM, Screaton RA (October 2001). "Anoikis mechanisms". Current Opinion in Cell Biology. 13 (5): 555–62. doi:10.1016/S0955-0674(00)00251-9. PMID 11544023.
- ^ Frisch, SM.; Francis, H. (Feb 1994). "Disruption of epithelial cell-matrix interactions induces apoptosis". J Cell Biol. 124 (4): 619–26. doi:10.1083/jcb.124.4.619. PMC 2119917. PMID 8106557.
- ^ Mawji IA, Simpson CD, Gronda M, et al. (September 2007). "A chemical screen identifies anisomycin as an anoikis sensitizer that functions by decreasing FLIP protein synthesis". Cancer Research. 67 (17): 8307–15. doi:10.1158/0008-5472.CAN-07-1687. PMID 17804746.
- ^ Mawji IA, Simpson CD, Hurren R, et al. (May 2007). "Critical role for Fas-associated death domain-like interleukin-1-converting enzyme-like inhibitory protein in anoikis resistance and distant tumor formation". Journal of the National Cancer Institute. 99 (10): 811–22. doi:10.1093/jnci/djk182. PMID 17505076.
- ^ Paoli P, Giannoni E, Chiarugi P (2013). "Anoikis molecular pathways and its role in cancer progression". Biochim Biophys Acta. 1833 (12): 3481–3498. doi:10.1016/j.bbamcr.2013.06.026. PMID 23830918.
Further reading
[edit]- Liotta LA, Kohn E (August 2004). "Anoikis: cancer and the homeless cell". Nature. 430 (7003): 973–4. doi:10.1038/430973a. PMID 15329701.
- Zeng Q, Chen S, You Z, et al. (July 2002). "Hepatocyte growth factor inhibits anoikis in head and neck squamous cell carcinoma cells by activation of ERK and Akt signaling independent of NFkappa B". The Journal of Biological Chemistry. 277 (28): 25203–8. doi:10.1074/jbc.M201598200. PMID 11994287.
- Vlahopoulos, SA (August 2017). "Aberrant control of NF-κB in cancer permits transcriptional and phenotypic plasticity, to curtail dependence on host tissue: molecular mode". Cancer Biology & Medicine. 14 (3): 254–270. doi:10.20892/j.issn.2095-3941.2017.0029. PMC 5570602. PMID 28884042.
