Related Experiment Video
Updated: Jul 6, 2026

Exploring the Pharmacological Action and Molecular Mechanism of Salidroside in Inhibiting MCF-7 Cell Proliferation and Migration
Published on: June 9, 2023
The potential role of Akt phosphorylation in human cancers
1Evolutionary Biology, Zoological Institute, University of Basel, Basel - Switzerland. jonas.cicenas@unibas.ch
Abstract:
Akt/protein kinase B (PKB) is a serine/threonine kinase which is implicated in mediating a variety of biological responses including cell growth, proliferation and survival. Akt is activated by phosphorylation on two critical residues, namely threonine 308 (Thr308) and serine 473 (Ser473). Several studies have found Akt2 to be amplified or overexpressed at the mRNA level in various tumor cell lines and in a number of human malignancies such as colon, pancreatic and breast cancers. Nevertheless, activation of Akt isoforms by phosphorylation appears to be more clinically significant than Akt2 amplification or overexpression. Many studies in the past 4-5 years have revealed a prognostic and/or predictive role of Akt phosphorylation in breast, prostate and non-small cell lung cancer. Several publications suggest a role of phosphorylated Akt also in endometrial, pancreatic, gastric, tongue and renal cancer. However, different types of assays were used in these studies. Before assessment of P-Akt can be incorporated into routine clinical practice, all aspects of the assay methodology will have to be standardized.
Insights
Phosphorylated Akt (protein kinase B) plays a crucial role in cancer cell survival and is a significant prognostic marker. Standardizing assays for phosphorylated Akt is essential for clinical application.
Area of Science:
- Molecular Biology
- Oncology
- Biochemistry
Background:
- Akt/protein kinase B (PKB) is a key serine/threonine kinase regulating cell growth, proliferation, and survival.
- Akt activation occurs via phosphorylation at threonine 308 (Thr308) and serine 473 (Ser473).
- Akt2 amplification/overexpression is observed in various cancers, but phosphorylated Akt (P-Akt) activation is more clinically relevant.
Purpose of the Study:
- To review the prognostic and predictive significance of Akt phosphorylation in human malignancies.
- To highlight the clinical relevance of P-Akt in cancers like breast, prostate, and lung cancer.
- To address the need for assay standardization before P-Akt assessment can be used in routine clinical practice.
Main Methods:
- Literature review of studies investigating Akt phosphorylation in cancer.
- Analysis of existing data on the role of P-Akt in various cancer types.
- Evaluation of different assay methodologies used for P-Akt detection.
Main Results:
- Akt phosphorylation demonstrates prognostic and/or predictive value in breast, prostate, and non-small cell lung cancer.
- Evidence suggests a role for P-Akt in endometrial, pancreatic, gastric, tongue, and renal cancers.
- Diverse assay methodologies have been employed, leading to variability in results.
Conclusions:
- Phosphorylated Akt is a clinically significant marker in multiple human cancers.
- Standardization of assay methodologies for P-Akt is critical for its integration into clinical practice.
- Further research is needed to establish reliable and consistent methods for P-Akt assessment.
Related Concept Videos
PI3K/mTOR/AKT Signaling Pathway
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
Protein Kinases and Phosphatases
Protein kinases
Many proteins in the cell are regulated by phosphorylation, the addition of a phosphate group. A family of enzymes called kinases...
Interactions Between Signaling Pathways
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...
Mitogens and the Cell Cycle
