Epigenetic Features in Uterine Leiomyosarcoma and Endometrial Stromal Sarcomas: An Overview of the Literature.
Bruna Cristine de AlmeidaLaura Gonzalez Dos AnjosAndrey Senos DobroffEdmund Chada BaracatQiwei YangAyman Al-HendyKatia Candido CarvalhoPublished in: Biomedicines (2022)
There is a consensus that epigenetic alterations play a key role in cancer initiation and its biology. Studies evaluating the modification in the DNA methylation and chromatin remodeling patterns, as well as gene regulation profile by non-coding RNAs (ncRNAs) have led to the development of novel therapeutic approaches to treat several tumor types. Indeed, despite clinical and translational challenges, combinatorial therapies employing agents targeting epigenetic modifications with conventional approaches have shown encouraging results. However, for rare neoplasia such as uterine leiomyosarcomas (LMS) and endometrial stromal sarcomas (ESS), treatment options are still limited. LMS has high chromosomal instability and molecular derangements, while ESS can present a specific gene fusion signature. Although they are the most frequent types of "pure" uterine sarcomas, these tumors are difficult to diagnose, have high rates of recurrence, and frequently develop resistance to current treatment options. The challenges involving the management of these tumors arise from the fact that the molecular mechanisms governing their progression have not been entirely elucidated. Hence, to fill this gap and highlight the importance of ongoing and future studies, we have cross-referenced the literature on uterine LMS and ESS and compiled the most relevant epigenetic studies, published between 2009 and 2022.
Keyphrases
- dna methylation
- genome wide
- gene expression
- high grade
- copy number
- case control
- systematic review
- bone marrow
- papillary thyroid
- dna damage
- endometrial cancer
- transcription factor
- randomized controlled trial
- squamous cell carcinoma
- clinical practice
- oxidative stress
- cancer therapy
- young adults
- meta analyses
- lymph node metastasis
- genome wide identification