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Liposarcoma: molecular targets and therapeutic implications
Kate Lynn J Bill1,2, Lucia Casadei1,2, Bethany C Prudner1,2
1The James Comprehensive Cancer Center, The Ohio State University, Columbus, OH, USA.
Abstract:
Liposarcoma (LPS) is the most common soft tissue sarcoma and accounts for approximately 20 % of all adult sarcomas. Current treatment modalities (surgery, chemotherapy, and radiotherapy) all have limitations; therefore, molecularly driven studies are needed to improve the identification and increased understanding of genetic and epigenetic deregulations in LPS if we are to successfully target specific tumorigenic drivers. It can be anticipated that such biology-driven therapeutics will improve treatments by selectively deleting cancer cells while sparing normal tissues. This review will focus on several therapeutically actionable molecular markers identified in well-differentiated LPS and dedifferentiated LPS, highlighting their potential clinical applicability.
Insights
Liposarcoma (LPS) is a common soft tissue cancer. This review explores actionable molecular markers in LPS to develop targeted therapies that improve treatment outcomes by selectively eliminating cancer cells.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Liposarcoma (LPS) represents the most frequent soft tissue sarcoma, comprising about 20% of adult sarcomas.
- Current treatments like surgery, chemotherapy, and radiotherapy present significant limitations in efficacy and specificity.
- A deeper understanding of the genetic and epigenetic alterations in LPS is crucial for developing novel therapeutic strategies.
Purpose of the Study:
- To review therapeutically actionable molecular markers in well-differentiated and dedifferentiated liposarcoma.
- To highlight the potential clinical applicability of these molecular markers for targeted therapy development.
Main Methods:
- Literature review of studies focusing on molecular alterations in liposarcoma.
- Analysis of identified genetic and epigenetic deregulations.
- Evaluation of the clinical relevance of molecular markers for targeted therapies.
Main Results:
- Identification of several key molecular markers with therapeutic potential in LPS.
- Discussion of the biological rationale for targeting these specific pathways.
- Assessment of the potential for personalized medicine approaches in LPS treatment.
Conclusions:
- Targeting specific molecular drivers in liposarcoma offers a promising avenue for improved therapeutic outcomes.
- Biology-driven therapeutics could enhance treatment efficacy while minimizing toxicity to normal tissues.
- Further research into molecular markers is essential for advancing liposarcoma treatment strategies.
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