Necroptosis in cancer: An angel or a demon?
- PMID: 28651499
- DOI: 10.1177/1010428317711539
Necroptosis in cancer: An angel or a demon?
Abstract
In the past few decades, apoptosis has been regarded as the only form of programmed cell death. However, the traditional view has been challenged by the identification of several forms of regulated necrosis, including necroptosis. Necroptosis is typified by a necrotic cell death morphology and is controlled by RIP1, RIP3, and mixed lineage kinase domain-like protein. The physiological role of necroptosis is to serve as a "fail-safe" form of cell death for cells that fail to undergo apoptosis during embryonic development and disease defense. Currently, established studies have indicated that necroptosis is involved in cancer initiation and progression. Although elevated necroptosis contributes to cancer cell death, extensive cell death also increases the risk of proliferation and metastasis of the surviving cells by inducing the generation reactive oxygen species, activation of inflammation, and suppression of the immune response. Thus, questions regarding the overall impact of necroptosis on cancer remain open. In this review, we introduce the basic knowledge regarding necroptosis, summarize its dual effects on cancer progression, and analyze its advantages and disadvantages in clinical applications.
Keywords: Cancer progression; chemotherapy; metastasis; proliferation.
Similar articles
-
Necroptosis: an emerging form of programmed cell death.Crit Rev Oncol Hematol. 2012 Jun;82(3):249-58. doi: 10.1016/j.critrevonc.2011.08.004. Epub 2011 Oct 1. Crit Rev Oncol Hematol. 2012. PMID: 21962882 Review.
-
Cytosolic calcium mediates RIP1/RIP3 complex-dependent necroptosis through JNK activation and mitochondrial ROS production in human colon cancer cells.Free Radic Biol Med. 2017 Jul;108:433-444. doi: 10.1016/j.freeradbiomed.2017.04.010. Epub 2017 Apr 14. Free Radic Biol Med. 2017. PMID: 28414098
-
RIP1/RIP3-regulated necroptosis as a target for multifaceted disease therapy (Review).Int J Mol Med. 2019 Sep;44(3):771-786. doi: 10.3892/ijmm.2019.4244. Epub 2019 Jun 14. Int J Mol Med. 2019. PMID: 31198981 Free PMC article. Review.
-
Assays for necroptosis and activity of RIP kinases.Methods Enzymol. 2014;545:1-33. doi: 10.1016/B978-0-12-801430-1.00001-9. Methods Enzymol. 2014. PMID: 25065884 Review.
-
Extracts derived from a traditional Chinese herbal formula triggers necroptosis in ectocervical Ect1/E6E7 cells through activation of RIP1 kinase.J Ethnopharmacol. 2019 Jul 15;239:111922. doi: 10.1016/j.jep.2019.111922. Epub 2019 Apr 26. J Ethnopharmacol. 2019. PMID: 31034957
Cited by
-
PARP1 and Poly(ADP-ribosyl)ation Signaling during Autophagy in Response to Nutrient Deprivation.Oxid Med Cell Longev. 2019 Jun 9;2019:2641712. doi: 10.1155/2019/2641712. eCollection 2019. Oxid Med Cell Longev. 2019. PMID: 31281570 Free PMC article. Review.
-
The dietary flavonoid isoliquiritigenin is a potent cytotoxin for human neuroblastoma cells.Neuronal Signal. 2019 Mar;3(1):NS20180201. doi: 10.1042/NS20180201. Epub 2019 Jan 30. Neuronal Signal. 2019. PMID: 32269833 Free PMC article.
-
A new approach: Evaluation of necroptosis and immune status enables prediction of the tumor microenvironment and treatment targets in pancreatic cancer.Comput Struct Biotechnol J. 2023 Mar 23;21:2419-2433. doi: 10.1016/j.csbj.2023.03.037. eCollection 2023. Comput Struct Biotechnol J. 2023. PMID: 37090434 Free PMC article.
-
Erythronecroptosis: an overview of necroptosis or programmed necrosis in red blood cells.Mol Cell Biochem. 2024 Dec;479(12):3273-3291. doi: 10.1007/s11010-024-04948-8. Epub 2024 Mar 1. Mol Cell Biochem. 2024. PMID: 38427167 Review.
-
A Necroptosis-Related Prognostic Model of Uveal Melanoma Was Constructed by Single-Cell Sequencing Analysis and Weighted Co-Expression Network Analysis Based on Public Databases.Front Immunol. 2022 Feb 15;13:847624. doi: 10.3389/fimmu.2022.847624. eCollection 2022. Front Immunol. 2022. PMID: 35242144 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Miscellaneous