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Epigenetic Regulation in Oral Squamous Cell Carcinoma Microenvironment: A Comprehensive Review.

作者信息

Mesgari Hassan, Esmaelian Samar, Nasiri Kamyar, Ghasemzadeh Shabnam, Doroudgar Parisa, Payandeh Zahra

机构信息

Oral and Maxillofacial Surgery Department, Faculty of Dentistry, Islamic Azad University Tehran Branch, Tehran 1148963537, Iran.

Faculty of Dentistry, Islamic Azad University Tehran Branch, Tehran 1148963537, Iran.

出版信息

Cancers (Basel). 2023 Nov 27;15(23):5600. doi: 10.3390/cancers15235600.


DOI:10.3390/cancers15235600
PMID:38067304
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10705512/
Abstract

Oral squamous cell carcinoma (OSCC) is a prevalent and significant type of oral cancer that has far-reaching health implications worldwide. Epigenetics, a field focused on studying heritable changes in gene expression without modifying DNA sequence, plays a pivotal role in OSCC. Epigenetic changes, encompassing DNA methylation, histone modifications, and miRNAs, exert control over gene activity and cellular characteristics. In OSCC, aberrant DNA methylation of tumor suppressor genes (TSG) leads to their inactivation, subsequently facilitating tumor growth. As a result, distinct patterns of gene methylation hold promise as valuable biomarkers for the detection of OSCC. Oral cancer treatment typically involves surgery, radiation therapy, and chemotherapy, but even with these treatments, cancer cells cannot be effectively targeted and destroyed. Researchers are therefore exploring new methods to target and eliminate cancer cells. One promising approach is the use of epigenetic modifiers, such as DNA methyltransferase (DNMT) inhibitors and histone deacetylase (HDAC) inhibitors, which have been shown to modify abnormal epigenetic patterns in OSCC cells, leading to the reactivation of TSGs and the suppression of oncogenes. As a result, epigenetic-targeted therapies have the potential to directly alter gene expression and minimize side effects. Several studies have explored the efficacy of such therapies in the treatment of OSCC. Although studies have investigated the efficacy of epigenetic therapies, challenges in identifying reliable biomarkers and developing effective combination treatments are acknowledged. Of note, epigenetic mechanisms play a significant role in drug resistance in OSCC and other cancers. Aberrant DNA methylation can silence tumor suppressor genes, while alterations in histone modifications and chromatin remodeling affect gene expression related to drug metabolism and cell survival. Thus, understanding and targeting these epigenetic processes offer potential strategies to overcome drug resistance and improve the efficacy of cancer treatments in OSCC. This comprehensive review focuses on the complex interplay between epigenetic alterations and OSCC cells. This will involve a deep dive into the mechanisms underlying epigenetic modifications and their impact on OSCC, including its initiation, progression, and metastasis. Furthermore, this review will present the role of epigenetics in the treatment and diagnosis of OSCC.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f821/10705512/3a59ffadb0be/cancers-15-05600-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f821/10705512/b18abfe49c63/cancers-15-05600-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f821/10705512/9c56dfb3d0b9/cancers-15-05600-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f821/10705512/d91de86e4163/cancers-15-05600-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f821/10705512/6ebdb65cb205/cancers-15-05600-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f821/10705512/3a59ffadb0be/cancers-15-05600-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f821/10705512/b18abfe49c63/cancers-15-05600-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f821/10705512/9c56dfb3d0b9/cancers-15-05600-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f821/10705512/d91de86e4163/cancers-15-05600-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f821/10705512/6ebdb65cb205/cancers-15-05600-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f821/10705512/3a59ffadb0be/cancers-15-05600-g005.jpg

相似文献

[1]
Epigenetic Regulation in Oral Squamous Cell Carcinoma Microenvironment: A Comprehensive Review.

Cancers (Basel). 2023-11-27

[2]
Promoter Hypermethylation of LATS2 Gene in Oral Squamous Cell Carcinoma (OSCC) Among North Indian Population.

Asian Pac J Cancer Prev. 2020-5-1

[3]
Aberrantly hypermethylated tumor suppressor genes were identified in oral squamous cell carcinoma (OSCC).

Clin Epigenetics. 2019-8-12

[4]
Impact of Epigenetic Alterations in the Development of Oral Diseases.

Curr Med Chem. 2021

[5]
Epigenetics in oral squamous cell carcinoma.

J Oral Maxillofac Pathol. 2017

[6]
Histone lysine methyltransferase SMYD3 promotes oral squamous cell carcinoma tumorigenesis via H3K4me3-mediated HMGA2 transcription.

Clin Epigenetics. 2023-5-26

[7]
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Med Oncol. 2023-3-20

[8]
PTEN and p16 genes as epigenetic biomarkers in oral squamous cell carcinoma (OSCC): a study on south Indian population.

Tumour Biol. 2016-6

[9]
The expanding role of epigenetics in the development, diagnosis and treatment of prostate cancer and benign prostatic hyperplasia.

J Urol. 2007-3

[10]
Epigenetic disregulation in oral cancer.

Int J Mol Sci. 2012

引用本文的文献

[1]
Unravelling molecular mechanism of oral squamous cell carcinoma and genetic landscape: an insight into disease complexity, available therapies, and future considerations.

Front Immunol. 2025-8-13

[2]
CD44-targeted therapy using mP6/Rg3 micelles inhibits oral cancer stem cell proliferation and migration.

Cell Biol Toxicol. 2025-8-1

[3]
Dysregulated PI3K/AKT signaling in oral squamous cell carcinoma: The tumor microenvironment and epigenetic modifiers as key drivers.

Oncol Res. 2025-7-18

[4]
Molecular and Genetic Pathogenesis of Oral Cancer: A Basis for Customized Diagnosis and Treatment.

Biology (Basel). 2025-7-10

[5]
Cell-Free DNA as a Prognostic Biomarker in Oral Carcinogenesis and Oral Squamous Cell Carcinoma: A Translational Perspective.

Cancers (Basel). 2025-7-16

[6]
Oral squamous cell carcinoma: Insights into cellular heterogeneity, drug resistance, and evolutionary trajectories.

Cell Biol Toxicol. 2025-6-12

[7]
Porphyromonas gingivalis outer membrane vesicles augments proliferation and metastasis of oral squamous cell carcinoma cells.

BMC Oral Health. 2025-5-10

[8]
Pathogenomic fingerprinting to identify associations between tumor morphology and epigenetic states.

Eur J Cancer. 2025-5-15

[9]
Field Cancerisation in Oral Squamous Cell Carcinoma Patients: A Systematic Review.

J Maxillofac Oral Surg. 2025-4

[10]
Immunohistochemical Expression of DAPK-1 in Oral Leukoplakia And Oral Squamous Cell Carcinoma: A Preliminary Study.

Cureus. 2025-2-16

本文引用的文献

[1]
High expression of HSP60 and survivin predicts poor prognosis for oral squamous cell carcinoma patients.

BMC Oral Health. 2023-9-3

[2]
CEACAM1 as a molecular target in oral cancer.

Aging (Albany NY). 2023-8-16

[3]
Macrophage IL-1β contributes to tumorigenesis through paracrine AIM2 inflammasome activation in the tumor microenvironment.

Front Immunol. 2023

[4]
Current Treatment Strategies and Risk Stratification for Oral Carcinoma.

Am Soc Clin Oncol Educ Book. 2023-5

[5]
Effect of CDH1 and CDH2 genes polymorphisms in oral squamous cell carcinoma susceptibility in a sample of Iranian population: A case-control study.

Health Sci Rep. 2023-4-19

[6]
Targeting p53 pathways: mechanisms, structures, and advances in therapy.

Signal Transduct Target Ther. 2023-3-1

[7]
NAD Homeostasis and NAD-Consuming Enzymes: Implications for Vascular Health.

Antioxidants (Basel). 2023-2-4

[8]
NNMT Is an Immune-Related Prognostic Biomarker That Modulates the Tumor Microenvironment in Pan-Cancer.

Dis Markers. 2023

[9]
Role of tumor microenvironment in cancer progression and therapeutic strategy.

Cancer Med. 2023-5

[10]
Targeting epigenetic regulators to overcome drug resistance in cancers.

Signal Transduct Target Ther. 2023-2-17

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