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Modeling Oral-Esophageal Squamous Cell Carcinoma in 3D Organoids
Published on: December 23, 2022
Targeting Aberrant Histone Posttranscription Modification Machinery in Esophageal Squamous Cell Carcinoma: Current
Gang Ma1, Tongyang Gong2, Zhihua Liu2
1Department of Gastric Surgery, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, Tianjin's Clinical Research Center for Cancer, Tianjin 300060, China.
Abstract:
Esophageal squamous cell carcinoma (ESCC) is an aggressive malignancy, but the survival rates of patients with ESCC have not improved as yet largely because the available targeted therapies are limited. Histone posttranscription modification (PTM) is a critical epigenetic regulation. Several deregulations in histone PTM machinery have been identified to promote malignant phenotypes of ESCC, providing druggable targets in treating ESCC. Hereby, we briefly describe current progress and challenges ahead in this field.
Insights
Targeted therapies for esophageal squamous cell carcinoma (ESCC) are limited. Histone posttranscription modifications (PTM) offer potential druggable targets for treating this aggressive cancer, with ongoing research into their role.
Area of Science:
- Oncology
- Epigenetics
- Molecular Biology
Background:
- Esophageal squamous cell carcinoma (ESCC) is an aggressive cancer with limited effective targeted therapies.
- Survival rates for ESCC have remained stagnant due to a lack of treatment options.
- Histone posttranscription modifications (PTMs) are crucial epigenetic regulators implicated in cancer development.
Purpose of the Study:
- To review the current understanding of histone PTMs in ESCC.
- To identify deregulations in histone PTM machinery that drive ESCC.
- To highlight potential druggable targets within histone PTM pathways for ESCC treatment.
Main Methods:
- Literature review of recent studies on histone PTMs in ESCC.
- Analysis of epigenetic alterations in ESCC.
- Identification of therapeutic targets based on PTM dysregulation.
Main Results:
- Deregulations in histone PTM machinery are identified as drivers of malignant phenotypes in ESCC.
- Specific histone PTMs are implicated in the progression of esophageal squamous cell carcinoma.
- These epigenetic alterations present novel therapeutic avenues.
Conclusions:
- Histone PTMs represent a promising area for developing targeted therapies for ESCC.
- Further research is needed to overcome challenges and translate findings into clinical practice.
- Targeting epigenetic modifications could improve outcomes for patients with esophageal squamous cell carcinoma.
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