Molecular Crosstalk between the Immunological Mechanism of the Tumor Microenvironment and Epithelial-Mesenchymal Transition in Oral Cancer
- PMID: 36146567
- PMCID: PMC9504083
- DOI: 10.3390/vaccines10091490
Molecular Crosstalk between the Immunological Mechanism of the Tumor Microenvironment and Epithelial-Mesenchymal Transition in Oral Cancer
Abstract
Oral cancer is a significant non-communicable disease affecting both emergent nations and developed countries. Squamous cell carcinoma of the head and neck represent the eight major familiar cancer types worldwide, accounting for more than 350,000 established cases every year. Oral cancer is one of the most exigent tumors to control and treat. The survival rate of oral cancer is poor due to local invasion along with recurrent lymph node metastasis. The tumor microenvironment contains a different population of cells, such as fibroblasts associated with cancer, immune-infiltrating cells, and other extracellular matrix non-components. Metastasis in a primary site is mainly due to multifaceted progression known as epithelial-to-mesenchymal transition (EMT). For the period of EMT, epithelial cells acquire mesenchymal cell functional and structural characteristics, which lead to cell migration enhancement and promotion of the dissemination of tumor cells. The present review links the tumor microenvironment and the role of EMT in inflammation, transcriptional factors, receptor involvement, microRNA, and other signaling events. It would, in turn, help to better understand the mechanism behind the tumor microenvironment and EMT during oral cancer.
Keywords: epithelial-to-mesenchymal transition; immunological aspects; microenvironment; oral cancer; signaling events.
Conflict of interest statement
The authors declare no conflict of interest.
Figures
Similar articles
-
Epithelial-to-mesenchymal transition in oral squamous cell carcinoma: Challenges and opportunities.Int J Cancer. 2021 Apr 1;148(7):1548-1561. doi: 10.1002/ijc.33352. Epub 2020 Oct 29. Int J Cancer. 2021. PMID: 33091960 Review.
-
Translational Significance for Tumor Metastasis of Tumor-Associated Macrophages and Epithelial-Mesenchymal Transition.Front Immunol. 2017 Sep 13;8:1106. doi: 10.3389/fimmu.2017.01106. eCollection 2017. Front Immunol. 2017. PMID: 28955335 Free PMC article. Review.
-
Relationship between Tumor Budding and Partial Epithelial-Mesenchymal Transition in Head and Neck Cancer.Cancers (Basel). 2023 Feb 9;15(4):1111. doi: 10.3390/cancers15041111. Cancers (Basel). 2023. PMID: 36831453 Free PMC article. Review.
-
Anaplastic transition within the cancer microenvironment in early-stage oral tongue squamous cell carcinoma is associated with local recurrence.Int J Oncol. 2018 Oct;53(4):1713-1720. doi: 10.3892/ijo.2018.4515. Epub 2018 Aug 6. Int J Oncol. 2018. PMID: 30085337
-
Tumor microenvironment and noncoding RNAs as co-drivers of epithelial-mesenchymal transition and cancer metastasis.Dev Dyn. 2018 Mar;247(3):405-431. doi: 10.1002/dvdy.24548. Epub 2017 Sep 18. Dev Dyn. 2018. PMID: 28691356 Review.
Cited by
-
A nomogram with the peripheral blood neutrophil-to-lymphocyte ratio before treatment predicts the survival of patients with nasopharyngeal carcinoma.Front Oncol. 2025 May 8;15:1469191. doi: 10.3389/fonc.2025.1469191. eCollection 2025. Front Oncol. 2025. PMID: 40406251 Free PMC article.
-
[PHPS1 enhances PD-L1 serine phosphorylation by regulating ROS/SHP-2/AMPK activity to promote apoptosis of oral squamous cell carcinoma cells].Nan Fang Yi Ke Da Xue Xue Bao. 2024 Dec 20;44(12):2469-2476. doi: 10.12122/j.issn.1673-4254.2024.12.24. Nan Fang Yi Ke Da Xue Xue Bao. 2024. PMID: 39725637 Free PMC article. Chinese.
References
-
- Almangush A., Mäkitie A.A., Triantafyllou A., de Bree R., Strojan P., Rinaldo A., Hernandez-Prera J.C., Suárez C., Kowalski L.P., Ferlito A. Staging and grading of oral squamous cell carcinoma: An update. Oral Oncol. 2020;107:104799. - PubMed
-
- Ling Z., Cheng B., Tao X. Epithelial-to-mesenchymal transition in oral squamous cell carcinoma: Challenges and opportunities. Int. J. Cancer. 2021;148:1548–1561. - PubMed
Publication types
LinkOut - more resources
Full Text Sources