» Articles » PMID: 29478262

Roles of Protein Kinase R in Cancer: Potential As a Therapeutic Target

Overview
Journal Cancer Sci
Specialty Oncology
Date 2018 Feb 26
PMID 29478262
Citations 27
Authors
Affiliations
Soon will be listed here.
Abstract

Double-stranded (ds) RNA-dependent protein kinase (PKR) is a ubiquitously expressed serine/threonine protein kinase. It was initially identified as an innate immune antiviral protein induced by interferon (IFN) and activated by dsRNA. PKR is recognized as a key executor of antiviral host defense. Moreover, it contributes to inflammation and immune regulation through several signaling pathways. In addition to IFN and dsRNA, PKR is activated by multiple stimuli and regulates various signaling pathways including the mitogen-activated protein kinase (MAPK) and nuclear factor kappa-light-chain-enhancer of activated B cells pathways. PKR was initially thought to be a tumor suppressor as a result of its ability to suppress cell growth and interact with major tumor suppressor genes. However, in several types of malignant disease, such as colon and breast cancers, its role remains controversial. In hepatocellular carcinoma, hepatitis C virus (HCV) is the main cause of liver cancer, and PKR inhibits HCV replication, indicating its role as a tumor suppressor. However, PKR is overexpressed in cirrhotic patients, and acts as a tumor promoter through enhancement of cancer cell growth by mediating MAPK or signal transducer and activator of transcription pathways. Moreover, PKR is reportedly required for the activation of inflammasomes and influences metabolic disorders. In the present review, we introduce the multifaceted roles of PKR such as antiviral function, tumor cell growth, regulation of inflammatory immune responses, and maintaining metabolic homeostasis; and discuss future perspectives on PKR biology including its potential as a therapeutic target for liver cancer.

Citing Articles

PKR associates with 4.1R to promote anchorage-independent growth of hepatocellular carcinoma and lead to poor prognosis.

Okujima Y, Watanabe T, Ito T, Inoue Y, Kasai Y, Imai Y Sci Rep. 2024; 14(1):27768.

PMID: 39532917 PMC: 11557841. DOI: 10.1038/s41598-024-75142-5.


The Versatile Roles of nc886, a Fascinating and Peculiar Regulatory Non-Coding RNA, in Cancer.

Jang J, Kang D, Lee Y, Lee Y Int J Mol Sci. 2024; 25(19).

PMID: 39409154 PMC: 11476670. DOI: 10.3390/ijms251910825.


Sterile activation of RNA-sensing pathways in autoimmunity.

Li J, Zhu J, Yang H, Hou F J Mol Cell Biol. 2024; 16(7).

PMID: 39143032 PMC: 11659683. DOI: 10.1093/jmcb/mjae029.


Activation of protein kinase receptor (PKR) plays a pro-viral role in mammarenavirus-infected cells.

Witwit H, Khafaji R, Salaniwal A, Kim A, Cubitt B, Jackson N J Virol. 2024; 98(3):e0188323.

PMID: 38376197 PMC: 10949842. DOI: 10.1128/jvi.01883-23.


Eukaryotic translation initiation factor 2α kinase 2 in pancreatic cancer: An approach towards managing clinical prognosis and molecular immunological characterization.

Du H, Wang H, Ma X, Chen H, Dai A, Zhu K Oncol Lett. 2023; 26(5):478.

PMID: 37818134 PMC: 10561166. DOI: 10.3892/ol.2023.14066.


References
1.
Blalock W, Grimaldi C, Fala F, Follo M, Horn S, Basecke J . PKR activity is required for acute leukemic cell maintenance and growth: a role for PKR-mediated phosphatase activity to regulate GSK-3 phosphorylation. J Cell Physiol. 2009; 221(1):232-41. DOI: 10.1002/jcp.21848. View

2.
Wong A, Tam N, Yang Y, Cuddihy A, Li S, Kirchhoff S . Physical association between STAT1 and the interferon-inducible protein kinase PKR and implications for interferon and double-stranded RNA signaling pathways. EMBO J. 1997; 16(6):1291-304. PMC: 1169727. DOI: 10.1093/emboj/16.6.1291. View

3.
Kim S, Forman A, Mathews M, Gunnery S . Human breast cancer cells contain elevated levels and activity of the protein kinase, PKR. Oncogene. 2000; 19(27):3086-94. DOI: 10.1038/sj.onc.1203632. View

4.
Goh K, deVeer M, Williams B . The protein kinase PKR is required for p38 MAPK activation and the innate immune response to bacterial endotoxin. EMBO J. 2000; 19(16):4292-7. PMC: 302024. DOI: 10.1093/emboj/19.16.4292. View

5.
Lu B, Nakamura T, Inouye K, Li J, Tang Y, Lundback P . Novel role of PKR in inflammasome activation and HMGB1 release. Nature. 2012; 488(7413):670-4. PMC: 4163918. DOI: 10.1038/nature11290. View