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Updated: May 8, 2026

Testing Targeted Therapies in Cancer using Structural DNA Alteration Analysis and Patient-Derived Xenografts
Published on: July 25, 2020
Expression proteomics predicts loss of RXR-γ during progression of epithelial ovarian cancer
Rajkumar S Kalra1, Sharmila A Bapat
1National Centre for Cell Science, NCCS Complex, Pune University Campus, Ganeshkhind, Pune, Maharashtra, India.
Abstract:
The process of cellular transformation involves cascades of molecular changes that are modulated through altered epigenetic, transcription, post-translational and protein regulatory networks. Thus, identification of transformation-associated protein alterations can provide an insight into major regulatory pathways activated during disease progression. In the present protein expression profiling approach, we identified differential sets of proteins in a two-dimensional gel electrophoresis screen of a serous ovarian adenocarcinoma progression model. Function-based categorization of the proteins exclusively associated with pre-transformed cells identified four cellular processes of which RXR-γ is known to modulate cellular differentiation and apoptosis. We thus probed the functional relevance of RXR-γ expression and signaling in these two pathways during tumor progression. RXR-γ expression was observed to modulate cellular differentiation and apoptosis in steady-state pre-transformed cells. Interestingly, retinoid treatment was found to enhance RXR-γ expression in transformed cells and sensitize them towards apoptosis in vitro, and also reduce growth of xenografts derived from transformed cells. Our findings emphasize that loss of RXR-γ levels appears to provide mechanistic benefits to transformed cells towards the acquisition of resistance to apoptosis hallmark of cancer, while effective retinoid treatment may present a viable approach towards sensitization of tumor cells to apoptosis through induction of RXR-γ expression.
Insights
This study reveals that reduced Retinoid X Receptor gamma (RXR-γ) levels aid cancer cells in resisting apoptosis. Retinoid treatment boosts RXR-γ, sensitizing tumor cells to apoptosis and inhibiting growth.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Cellular transformation involves complex molecular regulatory network alterations.
- Identifying protein changes during transformation offers insights into disease progression pathways.
Purpose of the Study:
- To investigate the role of Retinoid X Receptor gamma (RXR-γ) in ovarian cancer progression.
- To explore the functional relevance of RXR-γ in cellular differentiation and apoptosis during tumor development.
Main Methods:
- Utilized two-dimensional gel electrophoresis for protein expression profiling in an ovarian adenocarcinoma model.
- Analyzed differential protein sets to identify key cellular processes and pathways.
- Investigated RXR-γ expression and signaling in pre-transformed and transformed cells.
- Assessed the effect of retinoid treatment on RXR-γ levels, apoptosis, and xenograft growth.
Main Results:
- Identified RXR-γ as a key protein modulating cellular differentiation and apoptosis in pre-transformed cells.
- Observed enhanced RXR-γ expression in transformed cells upon retinoid treatment.
- Demonstrated that retinoid treatment sensitizes transformed cells to apoptosis in vitro and reduces xenograft growth.
Conclusions:
- Loss of RXR-γ contributes to apoptosis resistance in transformed cancer cells.
- Retinoid treatment represents a potential therapeutic strategy to induce RXR-γ expression and sensitize tumor cells to apoptosis.
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