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Updated: May 5, 2026

An In Vitro Model for Studying Cellular Transformation by Kaposi Sarcoma Herpesvirus
Published on: August 25, 2017
Akt pathway protein expression in gastrointestinal Kaposi sarcomas: relevance for tumor biology
Alina Badescu1, Anne Couvelard, Adriana Handra-Luca
1APHP GHU Avicenne, Universite Paris Nord Sorbonne Cite, Bobigny, Romania; Universitatea de Medicina, Craiova, Romania.
Abstract:
Gastrointestinal Kaposi sarcoma (KS) is classical, but rare. The AKT signaling pathway plays a central role in G protein-coupled receptor, key protein of KS histogenesis, encoded by KSHV/HHV8. There is increasing evidence that rapamycin, acting on AKT pathway, may be useful in the treatment of KS, including in HIV patients. We aimed to study the expression pattern of AKT pathway proteins in gastrointestinal KS. Expression of AKT, 4EBP1, PTEN, mTOR was assessed in 19 gastrointestinal KS biopsies by immunohistochemistry (17 patients). Protein expression in tumor spindle cells and in intratumor stromal vascular endothelial cells was analyzed with regard to clinicomorphological features. Tumor AKT related to lack of marked extravasated erythrocytes, tumor PTEN to presence of intratumor hemosiderin (p = 0.04 for both comparisons). Presence of both extravasated erythrocytes and hemosiderin related directly to endothelial stromal vascular nuclear PTEN and to low endothelial mTOR (p = 0.4 and 0.03, respectively). High tumor 4EBP1 related to a high slit-type abnormal vascular component (p = 0.04). The results of our study suggest pro-permeability or pro-angiogenic roles for 4EBP1 and PTEN and, opposite roles for AKT and mTOR in KS. Our hypotheses warrant further studies to obtain more generally applicable results.
Insights
This study investigated the AKT signaling pathway in gastrointestinal Kaposi sarcoma (KS). Researchers found that specific proteins in this pathway correlate with disease characteristics, suggesting potential therapeutic targets for KS treatment.
Area of Science:
- Oncology
- Molecular Biology
- Virology
Background:
- Gastrointestinal Kaposi sarcoma (KS) is a rare manifestation of KS.
- The AKT signaling pathway is implicated in KS pathogenesis, involving G protein-coupled receptors and KSHV/HHV8.
- Rapamycin's potential in KS treatment, particularly in HIV patients, is under investigation due to its action on the AKT pathway.
Purpose of the Study:
- To investigate the expression patterns of AKT pathway proteins in gastrointestinal KS.
- To correlate protein expression with clinicomorphological features of the disease.
Main Methods:
- Immunohistochemistry was used to assess the expression of AKT, 4EBP1, PTEN, and mTOR.
- Expression levels were analyzed in tumor spindle cells and intratumor stromal vascular endothelial cells from 19 gastrointestinal KS biopsies.
- Correlations with clinicomorphological features such as extravasated erythrocytes and hemosiderin were examined.
Main Results:
- Tumor AKT expression correlated with a lack of extravasated erythrocytes.
- Tumor PTEN expression correlated with the presence of intratumor hemosiderin.
- Endothelial PTEN and low endothelial mTOR were associated with extravasated erythrocytes and hemosiderin.
- High tumor 4EBP1 expression was linked to a high slit-type abnormal vascular component.
Conclusions:
- The study suggests potential pro-permeability or pro-angiogenic roles for 4EBP1 and PTEN in KS.
- Conversely, AKT and mTOR may have opposing roles in KS development.
- These findings provide hypotheses for further research into KS pathogenesis and treatment.
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