ORIGINAL ARTICLE
Morphology of cells undergoing epithelial mesenchymal transition in microinvasive and early invasive oral squamous cell carcinom a – a light microscopic study
 
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1
Neuron Institute of Applied Research, Amravati, India
 
2
Dental College and Hospital, Amravati, India
 
3
Sant Gadge Baba Amravati University, Amravati, India
 
4
Rajiv Gandhi Institute of IT and Bio-technology, Pune, India
 
5
Brijlal Biyani Science College, Amravati, India
 
 
Submission date: 2022-09-17
 
 
Acceptance date: 2022-11-17
 
 
Publication date: 2023-01-10
 
 
Corresponding author
Ketki Kalele
Dr. Ketki Kalele, MDS, PhD Scholar Director of Neuron Institute of Applied Research Amravati, Maharashtra, India
 
 
Pol J Pathol 2022;73(3):244-254
 
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ABSTRACT
The present study focuses on identification of cancer attributes of epithelial mesenchymal transition (EMT) at the earliest possible stage (microinvasion) under a light microscope by using hematoxylin and eosin stains, making it feasible for researchers to investigate such cases with ease without the use of extensive setups. The present study is the first in the English literature to define EMT features in micro-invasive and early invasive oral squamous cell carcinoma (OSCC) under a light microscope.
This is a retrospective study of histological sections of 43 cases of OSCC from the Department of Oral Pathology and Microbiology. The data collected were later statistically analyzed.
A total of 11 micro-invasive and 32 early invasive OSCC cases were assessed for core features of EMT.
The predominant feature defining EMT found was dense inflammatory infiltrate in both microinvasive (91%) and early invasive OSCC (88%) followed by cell individualization in 82% of microinvasive and 75% of early invasive OSCC, which was then followed by other features.
Reporting EMT in histopathological reports on a daily basis can aid in early diagnosis of OSCC as well as understanding carcinogenesis in early stages. Thereby, inclusion of EMT targeting therapeutics in early stages of OSCC can significantly alter the prognosis of cancer.
REFERENCES (25)
1.
Vigneswaran N, Williams MD. Epidemiologic trends in head and neck cancer and aids in diagnosis. Oral Maxillofac Surg Clin North Am 2014; 26: 123-141.
 
2.
JavadI S, Zhiania M, Mousavi MA, et al. Crosstalk between epidermal growth factor receptors (EGFR) and integrins in resistance to EGFR tyrosine kinase inhibitors (TKIs) in solid tumors. Eur J Cell Biol 2020; 99: 151083.
 
3.
Lawal AO, Adisa AO, Kolude B, Adeyemi BF. Immunohistochemical expression of MMP-2 and MMP-8 in oral squamous cell carcinoma. J Clin Exp Dent 2015; 7: 203-207. .
 
4.
Gloushankova NA, Rubtsova SN, Zhitnyak IY. Cadherin- mediated cell-cell interactions in normal and cancer cells. Tissue Barriers 2017; 5: e1356900.
 
5.
Pal A, Barrett TF, Paolini R, Parikh A, Puram SV. Partial EMT in head and neck cancer biology: a spectrum instead of a switch. Oncogene 2021; 40: 5049-5065.
 
6.
Ribatti D, Tamma R, Annese T. Epithelial-mesenchymal transition in cancer: a historical overview. Transl Oncol 2020; 13: 100-773. .
 
7.
Huang RY, Guilford P, Thiery JP. Early events in cell adhesion and polarity during epithelial mesenchymal transition. J Cell Sci 2012; 125: 4417-4422.
 
8.
Coradini D, Casarsa C, Oriana S. Epithelial cell polarity and tumorigenesis: new perspectives for cancer detection and treatment. Acta Pharmacol Sin 2011; 32: 552-564. .
 
9.
Yilmaz M, Christofori G. EMT, the cytoskeleton, and cancer cell invasion. Cancer Metastasis Rev 2009; 28: 15-33.
 
10.
Bax NAM, Pijnappels DA, van Oorschot AAM, et al. Epithelial- to-mesenchymal transformation alters electrical conductivity of human epicardial cells. J Cell Mol Med 2011; 15: 2675-2683.
 
11.
Vanslembrouck B, Chen J, Larabell C et al. Microscopic visualization of cell-cell adhesion complexes at micro and nanoscale. Front Cell Dev Biol 2020; 10: 819534.
 
12.
Johnston DS, Ahringer J. Cell polarity in eggs and epithelia: parallels and diversity. Cell 2010; 141: 757-774.
 
13.
Saintigy P, Bouaoud J, Farrugia G, et al. The role of apical- basal polarity in oral cancer. J Trans Sci 2019. DOI: 10.15761/JTS.1000327.
 
14.
Santoshi CK, Kumar JV, Bhagirath PV, Vinay BH, Prakash YJ. Morphometric analysis of basal cells of oral epithelium in predicting malignant transformation of oral potentially malignant disorders in patients with tobacco chewing habit. J Oral Maxillofac Pathol 2020; 24: 579.
 
15.
Dissanayaka WL, Pitiyage G, Kumarasiri PV, Liyanage RL, Dias KD, Tilakaratne WM. Clinical and histopathologic parameters in survival of oral squamous cell carcinoma. Oral Surg Oral Med Oral Pathol Oral Radiol 2012; 113: 518-525.
 
16.
Niklander SE. Inflammatory mediators in oral cancer: pathogenic mechanisms and diagnostic potential. Front Oral Health 2021; 2: 642238.
 
17.
Pesic M, Greten FR. Inflammation and cancer: tissue regeneration gone awry. Curr Opin Cell Biol 2016; 43: 55-61.
 
18.
Suarez-Carmona M, Lesage J, Cataldo D, Gilles C. EMT and inflammation: inseparable actors of cancer progression. Mol Oncol. 2017; 11: 805-823.
 
19.
Klintrup K, Mäkinen JM, Kauppila S, et al. Inflammation and prognosis in colorectal cancer. Eur J Cancer 2005; 41: 2645-2654.
 
20.
Leggett SE, Hruska AM, Guo M, et al. The epithelial-mesenchymal transition and the cytoskeleton in bioengineered systems. Cell Commun Signal 2021; 19: 32.
 
21.
Lamouille S, Xu J, Derynck R. Molecular mechanisms of epithelial-mesenchymal transition. Nat Rev Mol Cell Biol 2014; 15: 178-196.
 
22.
Mendez MG, Kojima S, Goldman RD. Vimentin induces changes in cell shape, motility, and adhesion during the epithelial to mesenchymal transition. FASEB J 2010; 24: 1838-1851.
 
23.
Friedl P, Wolf K. Plasticity of cell migration: a multiscale tuning model. J Cell Biol 2010; 188: 11-19.
 
24.
Friedl P, Locker J, Sahai E. Classifying collective cancer cell invasion. Nat Cell Biol 2012; 14: 777-783.
 
25.
Shi Y, Wu H, Zhang M, et al. Expression of the epithelial- mesenchymal transition-related proteins and their clinical significance in lung adenocarcinoma. Diagn Pathol 2013; 8: 89.
 
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ISSN:1233-9687
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