Epigenetic Abnormalities in Chondrosarcoma.
Michał BerezaMateusz DembińskiAgnieszka E ZającJakub PiątkowskiMonika Dudzisz-ŚledźPiotr Lukasz RutkowskiAnna Małgorzata CzarneckaPublished in: International journal of molecular sciences (2023)
In recent years, our understanding of the epigenetic mechanisms involved in tumor pathology has improved greatly. DNA and histone modifications, such as methylation, demethylation, acetylation, and deacetylation, can lead to the up-regulation of oncogenic genes, as well as the suppression of tumor suppressor genes. Gene expression can also be modified on a post-transcriptional level by microRNAs that contribute to carcinogenesis. The role of these modifications has been already described in many tumors, e.g., colorectal, breast, and prostate cancers. These mechanisms have also begun to be investigated in less common tumors, such as sarcomas. Chondrosarcoma (CS) is a rare type of tumor that belongs to sarcomas and is the second most common malignant bone tumor after osteosarcoma. Due to unknown pathogenesis and resistance to chemo- and radiotherapies of these tumors, there is a need to develop new potential therapies against CS. In this review, we summarize current knowledge on the influence of epigenetic alterations in the pathogenesis of CS by discussing potential candidates for future therapies. We also emphasize ongoing clinical trials that use drugs targeting epigenetic modifications in CS treatment.
Keyphrases
- dna methylation
- gene expression
- genome wide
- clinical trial
- prostate cancer
- healthcare
- transcription factor
- randomized controlled trial
- high grade
- radiation therapy
- bone mineral density
- oxidative stress
- single molecule
- genome wide identification
- high resolution
- circulating tumor
- mass spectrometry
- locally advanced
- cell free
- climate change
- young adults
- drug delivery
- genome wide analysis
- smoking cessation
- soft tissue
- heat shock
- bioinformatics analysis
- postmenopausal women