Skip to main content

Advertisement

Log in

Collagen deposition correlates with loss of E-cadherin and increased p63 expression in dysplastic conditions of oral submucous fibrosis

  • Original Paper
  • Published:
Medical Molecular Morphology Aims and scope Submit manuscript

Abstract

This paper focuses on the status of epithelial markers, E-cadherin, and p63 in the backdrop of an abnormal amount of collagen in the sub-mucosa of dysplastic and non-dysplastic grades of OSF. Histologically confirmed OSF and normal oral mucosa samples were procured. Samples were stained by Van Gieson’s stain (VG) and immunohistochemistry. The captured images were analyzed by ImageJ software to quantify their grayscale intensities. There was a gradual increase in the intensity of VG stain from normal to non-dysplastic and dysplastic OSF and the differences in their mean grayscale values were found to be significant (p < 0.00001). The intensity of E-cadherin was found to be the highest in non-dysplastic conditions and lowest in dysplastic conditions. The intensity difference of E-cadherin between normal and non-dysplastic OSF was found to be significant (p < 0.00001). The grayscale scale intensity values for p63 in whole epithelium depicted significant differences between normal and diseased conditions but for its intensity, in basal cells, significant differences were found between non-dysplastic and other classes of tissues. There was a positive correlation observed between VG and p63 staining intensity. The diseased oral epithelium demonstrated greater deposition of sub-epithelial collagen fibers along with subsequent loss of E-cadherin and an increased p63 expression.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  1. International Agency for Research on Cancer Lip, oral cavity: Globocan 2018 [Internet]. The Global Cancer Observatory, WHO. 2019. https://gco.iarc.fr/today/data/factsheets/cancers/1-Lip-oral-cavity-fact-sheet.pdf.

  2. International Agency for research on cancer. Lip and oral cavity cancer statistics in India: GLOBOCAN 2018 [Internet]. WHO. 2019. https://gco.iarc.fr/today/data/factsheets/populations/356-india-fact-sheets.pdf.

  3. Iocca O, Sollecito TP, Alawi F, Weinstein GS, Newman JG, De Virgilio A et al (2020) Potentially malignant disorders of the oral cavity and oral dysplasia: a systematic review and meta-analysis of malignant transformation rate by subtype. Head Neck 42(3):539–555

    Article  Google Scholar 

  4. Phookan J, Saikia KP (1998) A clinicopathological study of the pre-malignant conditions of oral cavity. Indian J Otolaryngol Head Neck Surg 50(3):246–249. https://doi.org/10.1007/BF03007000

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Yardimci G, Kutlubay Z, Engin B (2014) YTG. Precancerous lesions of oral mucosa. World J Clin Cases. 2(12):866–73.

  6. Wheelock MJ, Jensen PJ (1992) Regulation of keratinocyte intercellular junction organization and epidermal morphogenesis by E-cadherin. J Cell Biol 117(2):415–425

    Article  CAS  Google Scholar 

  7. Neville B, Damm D.D, Allen C, Chi A. Color Atlas of oral and maxillofacial diseases. 11th December 2018, 1st Edition. Elsevier, Philadelphia. ISBN: 978–0–323–55225–7.

  8. Diniz-Freitas M, García-Caballero T, Antúnez-López J, Gándara-Rey JM, García-García A (2006) Reduced E-cadherin expression is an indicator of unfavourable prognosis in oral squamous cell carcinoma. Oral Oncol 42(2):190–200

    Article  CAS  Google Scholar 

  9. Kaur G, Carnelio S, Rao N, Rao L (2009) Expression of E-cadherin in primary oral squamous cell carcinoma and metastatic lymph nodes : an immunohistochemical study. 20(1):71–6

  10. Hulmes DJ (2002) Building collagen molecules, fibrils, and suprafibrillar structures. J Struct Biol 137(1–2):2–10. https://doi.org/10.1006/jsbi.2002.4450

    Article  CAS  PubMed  Google Scholar 

  11. Kaur P, Kakar V (2012) Collagen: role in oral tissues: a review. Int J Sci Res ISSN (Online Impact Factor. 3(5):2319–7064.

  12. Kamath V, Rajkumar K, Kumar A (2015) Expression of type I and type III collagens in oral submucous fibrosis: an immunohistochemical study. J Dent Res Rev 2(4):161

    Article  Google Scholar 

  13. Dellavalle RP, Walsh P, Marchbank A, Grayson TE, Su LJ, Parker ER et al (2002) CUSP/p63 expression in basal cell carcinoma. Exp Dermatol 11(3):203–208

    Article  CAS  Google Scholar 

  14. Gatti V, Bongiorno-Borbone L, Fierro C, Annicchiarico-Petruzzelli M, Melino G, Peschiaroli A. p63 at the Crossroads between Stemness and Metastasis in Breast Cancer. Int J Mol Sci. 2019;20(11):2683. Published 2019 May 31. https://doi.org/10.3390/ijms20112683.

  15. Sharma M, Fonseca FP, Hunter KD et al (2020) Loss of oral mucosal stem cell markers in oral submucous fibrosis and their reactivation in malignant transformation. Int J Oral Sci 12:23. https://doi.org/10.1038/s41368-020-00090-5

    Article  PubMed  PubMed Central  Google Scholar 

  16. Yang A, Schweitzer R, Sun D, Kaghad M, Walker N, Bronson RT et al (1999) P63 is essential for regenerative proliferation in limb. Craniofacial Epithelial Dev Nat 398(6729):714–718

    CAS  Google Scholar 

  17. Cho HJ, Lee HK, Kim DS, Na JI, Shin JW, Youn SW et al (2008) C-terminal peptide of IGFBP-3, KGRKR, prolongs the proliferative potential of basal keratinocytes. J Dermatol Sci 50(1):61–64

    Article  CAS  Google Scholar 

  18. Hosoya A, Lee JM, Cho SW, Kim JY, Shinozaki N, Shibahara T et al (2008) Morphological evidence of basal keratinocyte migration during the re-epithelialization process. Histochem Cell Biol 130(6):1165–1175

    Article  CAS  Google Scholar 

  19. Haniffa AM, Saitoh M, Abiko Y, Takeshima M, Nishimura M, Yamazaki M et al (2007) Expression pattern of p63 in oral epithelial lesions and submucous fibrosis associated with betel-quid chewing in Sri Lanka. Med Mol Morphol 40(4):203–207

    Article  CAS  Google Scholar 

  20. Xavier FCA, Takiya CM, Reis SRA, Ramalho LMP (2009) P63 Immunoexpression in lip carcinogenesis. J Mol Histol 40(2):131–137

    Article  CAS  Google Scholar 

  21. Saravanan C. Color image to grayscale image conversion. 2010 2nd Int Conf Comput Eng Appl ICCEA 2010. 2010;2(April 2010):196–9.

  22. Kiernan JA (2008) Histological and Histochemical Methods: Theory and Practice, fourth ed. Bloxham, UK

  23. Varghese F, Bukhari AB, Malhotra R, De A (2014) IHC Profiler: an open source plugin for the quantitative evaluation and automated scoring of immunohistochemistry images of human tissue samples. PLoS One. 9(5):e96801. Published 2014 May 6. https://doi.org/10.1371/journal.pone.0096801

  24. Takiyama W, Moriwaki S, Mandai K, Takashima S (1996) Relationship of esophageal dysplasia to associated head and neck cancer in patients with esophageal carcinoma. Jpn J Clin Oncol 26(1):12–17

    Article  CAS  Google Scholar 

  25. Kobayashi M, Kawachi H, Takizawa T, Uchida K, Sekine M, Kumagai J et al (2007) P53 mutation analysis of low-grade dysplasia and high-grade dysplasia/carcinoma in situ of the esophagus using laser capture microdissection. Oncology 71(3–4):237–245

    Google Scholar 

  26. Perez-Ordoñez B, Beauchemin M, Jordan RCK (2006) Molecular biology of squamous cell carcinoma of the head and neck. J Clin Pathol 59(5):445–453

    Article  Google Scholar 

  27. Bedi R, Butterworth M CG et al. Opportunistic Oral Cancer Screening. British Dental Association. Occasional Paper. April 2000; Issue no. 6.

  28. Pindborg JJ, Reichart PA, Smith CJ, van der Waal I. Berlin: Springer-Verlag; 1997. World Health Organization: Histological Typing of Cancer and Pre-cancer of the Oral Mucosa.

  29. Lamouille S, Xu J, Derynck R (2014) Molecular mechanisms of epithelial-mesenchymal transition. Nat Rev Mol Cell Biol 15(3):178–196. https://doi.org/10.1038/nrm3758

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Jang M, Koh I, Lee JE, Lim JY, Cheong JH, Kim P (2018) Increased extracellular matrix density disrupts E-cadherin/beta-catenin complex in gastric cancer cells. Biomater Sci 6(10):2704–2713

    Article  CAS  Google Scholar 

  31. Choi HR, Batsakis JG, Zhan F, Sturgis E, Luna MA, El-Naggar AK (2002) Differential expression of p53 gene family members p63 and p73 in head and neck squamous tumorigenesis. Hum Pathol 33(2):158–164. https://doi.org/10.1053/hupa.2002.30722

    Article  CAS  PubMed  Google Scholar 

  32. Takeda T, Sugihara K, Hirayama Y, Hirano M, Tanuma JI, Semba I (2006) Immunohistological evaluation of Ki-67, p63, CK19 and p53 expression in oral epithelial dysplasias. J Oral Pathol Med 35(6):369–375. https://doi.org/10.1111/j.1600-0714.2006.00444.x

    Article  CAS  PubMed  Google Scholar 

  33. Chen Y-K, Hsue S-S (2005) Lin L-M Expression of p63 protein and mRNA in oral epithelial dysplasia. J Oral Pathol Med 34:232–239

    Article  CAS  Google Scholar 

  34. Signoretti S, Waltregny D, Dilks J et al (2000) p63 is a prostate basal cell marker and is required for prostate development. Am J Pathol 157(6):1769–1775. https://doi.org/10.1016/S0002-9440(10)64814-6

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Moll UM, Slade N (2004) p63 and p73: roles in development and tumor formation. Mol Cancer Res 2(7):371–386

    CAS  PubMed  Google Scholar 

  36. Lindsay J, McDade SS, Pickard A, McCloskey KD, McCance DJ (2011) Role of DeltaNp63gamma in epithelial to mesenchymal transition. J Biol Chem 286(5):3915–3924. https://doi.org/10.1074/jbc.M110.162511

    Article  CAS  PubMed  Google Scholar 

  37. Das RK, Anura A, Pal M et al (2013) Epithelio-mesenchymal transitional attributes in oral sub-mucous fibrosis. Exp Mol Pathol 95(3):259–269. https://doi.org/10.1016/j.yexmp.2013.08.006

    Article  CAS  PubMed  Google Scholar 

  38. Das RK, Pal M, Barui A et al (2010) Assessment of malignant potential of oral submucous fibrosis through evaluation of p63, E-cadherin and CD105 expression. J Clin Pathol 63(10):894–899. https://doi.org/10.1136/jcp.2010.078964

    Article  PubMed  Google Scholar 

  39. Cherukuri P, DeCastro AJ, Balboni AL et al (2012) Phosphorylation of ΔNp63α via a novel TGFβ/ALK5 signaling mechanism mediates the anti-clonogenic effects of TGFβ. PLoS ONE 7(11):e50066. https://doi.org/10.1371/journal.pone.0050066

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

The authors would like to thank Guru Nanak Institute of Dental Science and Research, Kolkata; School of Medical Science and Technology, Indian Institute of Technology, Kharagpur and Centre for Biomaterial, Cellular and Molecular Theranostics, Vellore Institute of Technology, Vellore for providing support to carry out the research. We especially thank Vellore Institute of Technology (VIT), Vellore for providing institutional internal research funding (seed 2578).

Funding

No external funding was received for this work.

Author information

Authors and Affiliations

Authors

Contributions

SC: data acquisition, data analysis and interpretation, statistical analysis, manuscript preparation, and editing. RRP: study concept and study design. MP: study concept and study design. JC: study concept and study design. RKD: data acquisition, manuscript review and editing, study design, and study concept.

Corresponding author

Correspondence to Raunak Kumar Das.

Ethics declarations

Conflict of interest

The authors would like to declare that there is no conflict of interest.

Ethical clearance

Samples were collected under informed consent of patients and ethical clearance from GNIDSR (GNIDSR/IEC/07/16).

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Chakraborti, S., Paul, R.R., Pal, M. et al. Collagen deposition correlates with loss of E-cadherin and increased p63 expression in dysplastic conditions of oral submucous fibrosis. Med Mol Morphol 55, 20–26 (2022). https://doi.org/10.1007/s00795-021-00304-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00795-021-00304-7

Keywords

Navigation