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Published on: July 17, 2020
P90 ribosomal S6 kinases: A bona fide target for novel targeted anticancer therapies?
Fani Koutsougianni1, Dimitra Alexopoulou1, Ayca Uvez2
1Department of Pharmacology, Faculty of Medicine, Health Sciences School, University of Thessaly, Larissa, Greece.
Abstract:
The 90 kDa ribosomal S6 kinase (RSK) family of proteins is a group of highly conserved Ser/Thr kinases. They are downstream effectors of the Ras/ERK/MAPK signaling cascade. ERK1/2 activation directly results in the phosphorylation of RSKs, which further, through interaction with a variety of different downstream substrates, activate various signaling events. In this context, they have been shown to mediate diverse cellular processes like cell survival, growth, proliferation, EMT, invasion, and metastasis. Interestingly, increased expression of RSKs has also been demonstrated in various cancers, such as breast, prostate, and lung cancer. This review aims to present the most recent advances in the field of RSK signaling that have occurred, such as biological insights, function, and mechanisms associated with carcinogenesis. We additionally present and discuss the recent advances but also the limitations in the development of pharmacological inhibitors of RSKs, in the context of the use of these kinases as putative, more efficient targets for novel anticancer therapeutic approaches.
Insights
Ribosomal S6 kinases (RSKs) are key regulators of cell growth and survival, and their dysregulation is linked to various cancers. This review highlights recent advances in RSK signaling and their potential as anticancer therapeutic targets.
Area of Science:
- Molecular Biology
- Cell Signaling
- Cancer Research
Background:
- Ribosomal S6 kinases (RSKs) are highly conserved Ser/Thr kinases.
- RSKs act as downstream effectors in the Ras/ERK/MAPK signaling cascade.
- RSK activation influences critical cellular processes including survival, growth, proliferation, and metastasis.
Purpose of the Study:
- To review recent advances in RSK signaling.
- To explore the role of RSKs in carcinogenesis.
- To discuss the development and limitations of RSK inhibitors for cancer therapy.
Main Methods:
- Literature review of recent scientific publications.
- Analysis of signaling pathways involving RSKs.
- Discussion of pharmacological inhibitors targeting RSKs.
Main Results:
- RSKs mediate diverse cellular functions relevant to cancer progression.
- Increased RSK expression is observed in multiple cancer types.
- RSKs represent promising targets for novel anticancer therapeutics.
Conclusions:
- RSK signaling plays a significant role in cancer development and progression.
- Targeting RSKs offers a potential strategy for novel cancer therapies.
- Further research is needed to overcome limitations in developing effective RSK inhibitors.
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