Home About us Editorial board Ahead of print Current issue Search Archives Submit article Instructions Subscribe Contact Us Login 
An Official Publication of the Indian Association of Oral and Maxillofacial Pathologists


 
  Table of Contents    
REVIEW ARTICLE  
Year : 2022  |  Volume : 26  |  Issue : 2  |  Page : 228-235
 

Leaving no stone unturned: Role of profibrotic genes in oral submucous fibrosis – A systematic review


1 Department of Oral Pathology and Microbiology, SRM Dental College, Chennai, Tamil Nadu, India
2 Department of Oral Pathology and Microbiology, Saveetha Dental College, Chennai, Tamil Nadu, India

Date of Submission31-Mar-2021
Date of Acceptance05-Sep-2021
Date of Web Publication28-Jun-2022

Correspondence Address:
Amritha James
SRM Dental College, Ramapuram, Chennai - 600 089, Tamil Nadu
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/jomfp.jomfp_102_21

Rights and Permissions

 

   Abstract 


Introduction: Understanding the molecular pathogenesis of an entity helps in devising the mode of progression as well as mode of therapy. Even with years of research to claim the understanding of the molecular pathogenesis of oral submucous fibrosis (OSMF) is limited. More deeper knowledge of the genes responsible for this will help in understanding and managing this disease better.
Materials and Methods: The articles published during a time period of 1990–2020 were chosen in accordance with the inclusion and exclusion criteria according to the PRISMA guidelines.
Results: From a total of 80 articles obtained from both electronic search of PUBMED, EMBASE, MEDLINE and Cochrane registry as well as the manual search only 21 articles were selected and analyzed.
Conclusion: Careful analysis of the samples revealed that transforming growth factor-beta may be a potential biomarker or a candidate for targeted therapy in OSMF.


Keywords: Oral cancer, oral submucous fibrosis, profibrotic genes, SMAD, transforming growth factor-beta


How to cite this article:
James A, Jayan L, Ramadoss R, Arunachalam P. Leaving no stone unturned: Role of profibrotic genes in oral submucous fibrosis – A systematic review. J Oral Maxillofac Pathol 2022;26:228-35

How to cite this URL:
James A, Jayan L, Ramadoss R, Arunachalam P. Leaving no stone unturned: Role of profibrotic genes in oral submucous fibrosis – A systematic review. J Oral Maxillofac Pathol [serial online] 2022 [cited 2022 Aug 14];26:228-35. Available from: https://www.jomfp.in/text.asp?2022/26/2/228/348732





   Introduction Top


Genes play a vital role in determining the course of fibrosis. Numerous genes are either upregulated or downregulated during the fibrotic disease process. Pro-fibrotic genes propel the disease toward fibrosis and include growth factors such as transforming growth factor-beta (TGFβ) and fibroblast growth factor (FGF2), collagen genes like collagen type I alpha 1 (COL1A1), COL1A2, tumor necrosis factor (TNF), connective tissue growth factor (CTGF), lysyl oxidase, tissue inhibitors of matrix metalloproteinases (TIMP) and matrix metalloproteinases (MMP11, MMP12, MMP19 and MMP23).[1],[2]

Oral submucous fibrosis (OSMF) is a potentially malignant disorder with an increased prevalence in Asian countries, especially India. OSMF is a chronic, insidious disease that affects the lamina propria of the oral mucosa, and as the disease advances, it involves tissues deeper in the submucosa of the oral cavity with resulting loss of fibroelasticity. This disease is attributed to the use of areca nut and slaked lime. Earlier many factors such as chili, infections, autoimmunity were all considered but at present, arecoline is identified as the sole causative trigger in the development of OSMF. With decades of studies, still the pathogenesis of this condition is like a deep pit which refuses to be filled. Recently, many researchers have given their valuable time to try and fill this void. In this review, our aim is to analyze the literature to assess the role of profibrotic antifibrotic genes in the pathogenesis of OSMF.


   Materials and Methods Top


Criteria used for selection of studies

Types of studies

Original researches (randomized control trials, case control, cohort, etc.,) evaluating the role of profibrotic genes in the pathogenesis of OSMF were included, whereas overviews, narrative reviews, letter to editors, short communications, case reports and case series were excluded from the study.

Types of participants

Both in vitro and in vivo studies were analyzed in the existing literature for inclusion in this systematic review.

Outcomes of the study

Primary outcome

Effect of profibrotic genes in the pathogenesis of OSMF.

Secondary outcome

  1. Evaluation of the role of these genes in malignant transformation of OSMF
  2. Evaluation of the ability of these genes to act as potential targets in the management of OSMF.


Search strategy

Systematic review is the gold standard for answering any medicine-related question, for assessing association between a disease and cause or intervention or outcome. Detailed search strategies were developed for inclusion of studies for this review in accordance with the PRISMA checklist for systematic review as well as the Cochrane Highly Sensitive Search Strategy. The databases PUBMED, MEDLINE, Embase, LILAC and Cochrane Library were searched from 1990 to September 2020. The computer search strategy included two components where the first component focused on identifying the disease (OSMF) and the second component for the pathogenic factor (profibrotic genes). The search strategy was modified in accordance with the database that is searched to account for the difference in the vocabulary as well as the syntax rules. The first strategy utilizes the keywords fibrosis, OSMF, oral fibrosis or combination of the above for identifying the studies done on these conditions. The second strategy identified studies utilizing the profibrotic genes using the keywords profibrotic genes, CTGF, TGF-beta, SMAD, hypoxia-inducible factor 1 (HIF)-alpha, MMP, TIMP TNF, etc., either alone or in various combinations. Broad search pathway was ensured by not including any keywords related to outcomes as well as study design. Manual search for researches was also performed for identifying relevant researches.

Databases searched for the samples

The electronic databases reviewed for the selection of the studies were the Cochrane Oral Health Group Trials Register, the Cochrane Central Register of Controlled Trials, MEDLINE through OVID, EMBASE through OVID, PUBMED CENTRAL, LILAC and Cochrane Library. In addition, manual search of articles was also conducted. Only articles published in English languages were considered. All articles published from 1990 to September 2020 were included in this review.

Exclusion criteria

Articles published in languages other than English were excluded. Articles that evaluated other pathogenic factors of fibrosis were excluded. Articles that included studies on other pathological conditions using these gene molecules were excluded.

Collection and analysis of data from the study samples

Two individual reviewers evaluated the title and abstract of each of the articles obtained from the electronic search engines to assess the eligibility. A third reviewer was included in case of disagreement in the eligibility of a study by the two reviewers. Full-text copies of all the eligible as well as potentially eligible studies were further evaluated next by all the reviewers. From this, the studies which did not meet the inclusion criteria were excluded. Any disagreement was resolved by discussion among all the authors.

Data extraction and management

The data were independently extracted by the two review authors. The reviewers were not blinded to the details of the study and its authors. All the data were extracted in accordance with the guidelines provided by the Cochrane Handbook for Systematic Reviews of Interventions (Higgins 2011). For clarification or requirement of additional details, the authors of the studies were contacted through E-mail.

Assessment of risk of bias in included studies

Four main categories of bias are commonly encountered in a systematic review

  1. Selection bias
  2. Performance bias
  3. Attrition bias
  4. Reporting bias.


Risk was then categorized as high, low and unclear.


   Results Top


The search strategy using the combination of keywords yielded a total of 80 articles, from this, 59 articles were excluded in accordance with the PRISMA guidelines which included a series of systematic screening of the articles [identification, screening, eligibility and inclusion] giving a final sample size of 21 articles which satisfied all the inclusion and exclusion criterion. The search strategy of inclusion and exclusion of articles is illustrated in [Figure 1]. The specific study characteristics are recorded in [Table 1] which depicts the evidence level of the studies included in the review. The profibrotic genes included in the current study are illustrated in the form of a pie chart [Figure 2].
Table 1: Overview of the studies included in the review

Click here to view
Figure 1: Diagrammatic representation of selection of articles for the systematic review using PRISMA checklist

Click here to view
Figure 2: Profibrotic genes included in this systematic review

Click here to view



   Discussion Top


OSMF is one of the most researched potentially malignant disorders as it has high malignant potential and even with years of research, there are still many stones left unturned which has impeded the understanding of this entity. Many esteemed researchers have made many enlightening breakthroughs in the molecular pathogenesis of OSMF. At present, profibrotic and antifibrotic genes have gained a lot of attention in the pathogenesis of OSMF. In our study, we have cumulated the literature for researches that have analyzed the role of profibrotic genes in OSMF. Out of the 21 studies included in our systematic review, 10 studies were conducted using TGF-beta, 4 on MMP and TIMPs, 2 on SMAD including one study conducted in our institution and one each on TGF-alpha, TNF-alpha, HIF-1 alpha, FGF.

Transforming growth factor-beta

TGF-beta is a multifunctional cytokine of the TGF superfamily which includes three isoforms 1, 2, 3. It is produced by all white blood cells. It is the most important cytokine implicated in the pathogenesis of OSMF. Research has shown that it is produced by the epithelium in the early stages of the disease and later, the stroma begins to produce with disease progression, possibly by the epithelial-mesenchymal interactions mediated by the signaling molecules seen in normal as well as the lesional mucosa. In our review, 10 studies were conducted to evaluate either the role of TGF-beta in the pathogenesis or as a potential biomarker in the detection of the condition.

Sukumaran et al. from their study to analyze the TGF-beta polymorphisms in OSMF inferred that polymorphism of 5′UTR C-T in TGF-beta has a significant association in OSMF. They also suggested that although the exact role of this region in the progression or presentation of the disease is uncertain, at the same time is an area with potential for further research.[8] Khan et al. used tissue microarray to identify and validate the genes expressed in OSMF. They also attempted to show the regulation of some of these genes by TGF-b and arecoline in keratinocytes and fibroblast cells. They showed that there is upregulation of TGF-b1, TGFBIp, THBS1, SPP1 and TIG1 and downregulation of BMP7. According to them, upregulation of profibrotic genes or cytokines and downregulation of antifibrotic molecules by TGF-beta may be the possible mechanism by which OSMF develops.[9] The same authors published another paper in 2012, studying the gene expression profile in epithelial cells and fibroblasts following treatment with areca nut extract. They concluded that the expression of the profibrotic genes, especially TGF-beta induced by the polyphenols and alkaloids in areca nut, had little influence on the profibrotic molecule expression from fibroblast but induced increase expression in the epithelium. They proposed that the areca nut has a causative role in triggering profibrotic genes in the epithelial cells which further influence the underlying stroma to elicit the fibrotic response.[10] Kale et al. evaluated the expression of TGF-beta in OSMF and its role in reduction of adipose tissue seen in this condition. They showed that the TGF-beta promotes lipodystrophy and inhibits angiogenesis. It is suggested that the reduction of adipose tissue may also contribute to the stiffness of mucosa and sunken appearance of the cheeks.[11] Kamath et al. on correlating the levels of TGF-beta with different stages and grades of OSMF using IHC found a progressive increase TGF-beta with advancing grades of OSMF and also noted a substantial increase in scar tissue. This suggested that the fibrotic change in OSMF may be a reparative process in response to the injury by the noxious agents in areca nut, and thus, targeting this molecule may help in controlling the progression of the disease.[13] Pant et al. showed in their study that Maria et al. injected Sprague-Dawley mice with extracts of pan masala and areca nut, producing OSMF like lesions with similar clinical and histopathological features. The levels of TGF-beta were analyzed using quantitative real-time PCR which showed a significant increase in the levels, confirming that areca nut and pan masala induce the production of TGF-beta which induces the fibrotic change in OSMF.[18],[24] Iyengar et al. aimed at evaluating the role of TGF-beta and COX-2 in the pathogenesis of OSMF to analyze potential targeted therapeutic applications. The levels of COX-2 were found to be higher in the early and moderate stages and grades of the disease progression whereas the levels of TGF-beta showed that progressive increase is noted with the progression of the disease.[19]

Rai et al. conducted a case–control study evaluating the expression of TGF-beta in OSMF to understand its role in the molecular pathogenesis of OSMF by RT-PCR which was confirmed with IHC evaluation. They inferred that TGF-beta 1 was most expressed isoform of the molecule and that the receptors 1, 2 were also elevated. Increase in the mRNA for all three isoforms was also noticed, confirming that it plays a major role in the molecular pathogenesis of OSMF.[21]

Connective tissue growth factor

CTGF or CCN2 is a matricellular associated heparin-binding protein. It plays important role in cell adhesion, migration, proliferation, angiogenesis, wound healing and skeletal development. Studies conducted on various fibrotic lesions revealed active participation of this gene, but this gene is not expressed in oral cavity under normal conditions. OSMF is the only condition where this gene is expressed and this may be a potential target for therapy. In this current review, only one study was included. Patil et al. estimated the serum levels of CTGF in OSMF, correlating the level of this gene with the different grades of the condition. It was inferred that the levels of CTGF levels were increased progressively from Grade 1 to Grade 3.[15] Blocking the activation of this profibrotic gene may pave a way in managing this condition better.

SMAD

It comprises a family of structurally similar proteins which act as signal transducers for receptors of the TGF-beta, regulating cell development and growth. Two researches were included in our current review. Hu et al. investigate the expression and function of SMAD7 in the progression of OSMF and OSCC. The SMAD7 levels were consistently upregulated in OSMF and OSCC, and the subsequent bioinformatics evaluation revealed that there was no mutation in the SMAD7 protein encountered in HNSCC and was elevated in OSCC.[22] Another study conduction in our instituition by Zagabathina et al. in 2020 revealed that the levels of SMAD2 were more in OSMF than in reactive lesions or normal tissues. As mentioned before, SMAD2 being the initiator of transcription of TGF-beta further emphasizes the role of this cytokine if fibrogenesis in OSMF.[23]

Matrix metalloproteinases and tissue inhibitors of matrix metalloproteinases

Matrix metalloproteinase or collagenase is a group of enzymes produced by fibroblasts for degrading the extracellular matrix, and TIMPs are the enzymes responsible for inhibiting the action of MMPs. Chaudhary et al. analyzed the role of functional polymorphism of MMP-2 and 9 promoters in OSMF and HNSCC. The results concluded that SNPs in MMP-2 (-1306 C/T) and MMP-9 (-1562 C/T) promoter region may be associated with susceptibility to HNSCC, and addiction habits such as areca nut chewing and tobacco smoking may enhance the polymorphic association of C/T allele of the MMP-2 and MMP-9 gene polymorphisms in an Indian population. This polymorphism could be a prognostic maker in head-and-neck cancer.[25] Katarkar et al. concluded that a definitive role of MMP-9 coding SNPs has predictive and prognostic value in determining OSMF and can promote to the basement membrane degradation and epithelial atrophy.[20] Mishra et al. evaluated the role of collagenase 1 in OSMF. The intensity of MMP1 expression was decreased as the grade of the disease progressed.[7]

Fibroblast growth factor

FGF belongs to a family of cell signaling proteins necessary for normal development. One study conducted by Bishen et al. in 2008 was included in this review. The study evaluated the role of bFGF in the progression of OSMF and to study the changes in the stroma with increase in the severity of OSMF. The increase in bFGF expression in early stages of OSMF is parallel to the stage of injury caused by areca nut consumption.[5] This might be a contributory event or element in the molecular alteration at a cellular event in OSMF.

Tumor necrosis factor-alpha

TNF alpha is a cytokine which plays an important role in mediating inflammatory reactions in the body. Sodhi et al. evaluated the levels of TNF alpha with increase in disease severity. They found that the levels of TNF alpha increased with the severity of the disease.[12]

Hypoxia inducible factor 1 alpha

This gene is located on chromosome14 and codes for a transcription factor that controls cellular responses to reduced oxygen concentrations within tissues. HIF-1α regulates numerous profibrotic mediators and contributes to fibrosis. TGF-β1 induces HIF1A stabilization in fibroblasts even without prominent hypoxic conditions. Tilkaratne et al. tested the role of hypoxia in the progression as well as malignant transformation of OSMF. They found that as the grade of dysplasia increased, the mRNA as well as the protein levels of HIF-1 alpha also increased. It may act as a potential marker for malignant transformation in OSMF.[6]

In our study, we focused on the literature which has been done to evaluate the role of profibrotic genes in OSMF. We had collected 21 articles including one conducted in our institution and reviewed all of the samples. Out of these 21 articles, 10 were conducted using TGF-beta, all of the studies evaluated showed an increase in the molecule as the disease progresses. All the studies conducted had shown a positive response with each of these molecules showing elevation with progression of the disease. Since the research obtained for the other genes was scanty, the available literature supports the statement that TGF-beta as plays an important role in the promotion of the disease. The role of these profibrotic genes has potential as both a promoter and a potential biomarker in OSMF. The expression of the genes when closely monitored may also be useful in analyzing the progression to a malignancy. The exact inference was difficult to obtain as there is no standardized procedure used, and many studies used IHC to study the molecules whereas others utilized PCR for the quantification of these genes. In addition to all this, if the exact function of these genes can be blocked, it may help in stopping the progression of the disease. Thus, profibrotic genes may be the future of research in OSMF as it may provide answer to the dilemma of the management of OSMF.


   Conclusion Top


TGF-beta is a key mediator of the fibrotic cascade in OSMF. Careful analysis of the samples revealed that TGF-beta may be used as a potential biomarker or a candidate for targeted therapy and could aid in early diagnosis as well as predict the malignant transformation in OSMF.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
   References Top

1.
Fagone P, Mangano K, Mammana S, Pesce A, Pesce A, Caltabiano R, et al. Identification of novel targets for the diagnosis and treatment of liver fibrosis. Int J Mol Med 2015;36:747-52.  Back to cited text no. 1
    
2.
Karsdal MA, Nielsen SH, Leeming DJ, Langholm LL, Nielsen MJ, Manon-Jensen T, et al. The good and the bad collagens of fibrosis – Their role in signaling and organ function. Adv Drug Deliv Rev 2017;121:43-56.  Back to cited text no. 2
    
3.
Srinivasan M, Jewell SD. Quantitative estimation of PCNA, c-myc, EGFR and TGF-alpha in oral submucous fibrosis--an immunohistochemical study. Oral Oncol 2001;37:461-7.  Back to cited text no. 3
    
4.
Tu HF, Liu CJ, Chang CS, Lui MT, Kao SY, Chang CP, et al. The functional (-1171 5A-->6A) polymorphisms of matrix metalloproteinase 3 gene as a risk factor for oral submucous fibrosis among male areca users. J Oral Pathol Med 2006;35:99-103.  Back to cited text no. 4
    
5.
Bishen KA, Radhakrishnan R, Satyamoorthy K. The role of basic fibroblast growth factor in oral submucous fibrosis pathogenesis. J Oral Pathol Med 2008;37:402-11.  Back to cited text no. 5
    
6.
Tilakaratne WM, Iqbal Z, Teh MT, Ariyawardana A, Pitiyage G, Cruchley A, et al. Upregulation of HIF-1alpha in malignant transformation of oral submucous fibrosis. J Oral Pathol Med 2008;37:372-7.  Back to cited text no. 6
    
7.
Mishra G, Ranganathan K. Matrix metalloproteinase-1 expression in oral submucous fibrosis: An immunohistochemical study. Indian J Dent Res 2010;21:320-5.  Back to cited text no. 7
[PUBMED]  [Full text]  
8.
Sukumaran A, Vidyadharan R, Banerjee M, Rajendran R, Harish R. Transforming growth factor-β-1 polymorphisms are infrequent but exist at selected loci in oral submucous fibrosis. Indian J Dent Res 2010;21:413.  Back to cited text no. 8
    
9.
Khan I, Agarwal P, Thangjam GS, Radhesh R, Rao SG, Kondaiah P. Role of TGF-β and BMP7 in the pathogenesis of oral submucous fibrosis. Growth Factors 2011;29:119-27.  Back to cited text no. 9
    
10.
Khan I, Kumar N, Pant I, Narra S, Kondaiah P. Activation of TGF-β pathway by areca nut constituents: A possible cause of oral submucous fibrosis. PLoS One 2012;7:e51806.  Back to cited text no. 10
    
11.
Kale AD, Mane DR, Shukla D. Expression of transforming growth factor β and its correlation with lipodystrophy in oral submucous fibrosis: An immunohistochemical study. Med Oral Patol Oral Cir Bucal 2013;18:e12-8.  Back to cited text no. 11
    
12.
Sodhi S, Sodhi JS, Khambete N, Kumar R, Marthala M, Sodhi NK. Expression of tumor necrosis factor α and its correlation with severity of oral submucous fibrosis: A case-control study. Oral Surg Oral Med Oral Pathol Oral Radiol 2014;117:704-8.  Back to cited text no. 12
    
13.
Kamath VV, Satelur KP, Rajkumar K, Krishnamurthy S. Transforming growth factor beta 1 in oral submucous fibrosis: An immunohistochemical study – Understanding the pathogenesis. J Dent Res Rev 2014;1:75.  Back to cited text no. 13
    
14.
Shrestha A, Carnelio S. Evaluation of matrix metalloproteinases-2 (MMP-2) and tissue inhibitors of metalloproteinases-2 (TIMP-2) in oral submucous fibrosis and their correlation with disease severity. Kathmandu Univ Med J (KUMJ) 2013;11:274-81.  Back to cited text no. 14
    
15.
Patil AA, Bhavthankar JD, Barpande SR, Mandale MS. Estimation of serum connective tissue growth factor in oral submucous fibrosis patients and its clinico-pathologic correlation. Journal of International Oral Health 2015;7:84-90.  Back to cited text no. 15
    
16.
Kamath V, Krishnamurthy S, Satelur K, Rajkumar K. Transforming growth factor-β1 and TGF-β2 act synergistically in the fibrotic pathway in oral submucous fibrosis: An immunohistochemical observation. Indian J Med Paediatr Oncol 2015;36:111.  Back to cited text no. 16
[PUBMED]  [Full text]  
17.
Maria S, Kamath VV, Satelur K, Rajkumar K. Evaluation of transforming growth factor beta1 gene in oral submucous fibrosis induced in Sprague-Dawley rats by injections of areca nut and pan masala (commercial areca nut product) extracts. J Cancer Res Ther 2016;12:379-85.  Back to cited text no. 17
    
18.
Pant I, Rao SG, Kondaiah P. Role of areca nut induced JNK/ATF2/Jun axis in the activation of TGF-β pathway in precancerous Oral Submucous Fibrosis. Sci Rep 2016;6:34314.  Back to cited text no. 18
    
19.
Iyengar AR, Kumar V, Karnam S, Patil S, Simon SD, Zainab S, et al. The expression of cox-2 and TGF β in oral submucous fibrosis. International Journal of Development Research 2017;7.  Back to cited text no. 19
    
20.
Katarkar A, Prodhan C, Mukherjee S, Ray JG, Chaudhuri K. Role of matrix metalloproteinase-9 polymorphisms in basement membrane degradation and pathogenesis of oral submucous fibrosis. Meta Gene 2018;16:255-63.  Back to cited text no. 20
    
21.
Rai A, Ahmad T, Parveen S, Parveen S, Faizan MI, Ali S. Expression of transforming growth factor beta in oral submucous fibrosis. J Oral Biol Craniofac Res 2020;10:166-70.  Back to cited text no. 21
    
22.
Hu X, Xiong H, Wang W, Huang L, Mao T, Yang L, et al. Study on the expression and function of smad family member 7 in oral submucous fibrosis and oral squamous cell carcinoma. Arch Oral Biol 2020;112:104687.  Back to cited text no. 22
    
23.
Zagabathina S, Ramadoss R, Ah HP, Krishnan R. Comparative evaluation of SMAD-2 expression in oral submucous fibrosis and reactive oral lesions. Asian Pac J Cancer Prev 2020;21:399-403.  Back to cited text no. 23
    
24.
Brembilla NC, Dufour AM, Alvarez M, Hugues S, Montanari E, Truchetet ME, et al. IL-22 capacitates dermal fibroblast responses to TNF in scleroderma. Ann Rheum Dis 2016;75:1697-705.  Back to cited text no. 24
    
25.
Chaudhary AK, Pandya S, Mehrotra R, Singh M, Singh M. Role of functional polymorphism of matrix metalloproteinase-2 (-1306 C/T and -168 G/T) and MMP-9 (-1562 C/T) promoter in oral submucous fibrosis and head and neck squamous cell carcinoma in an Indian population. Biomarkers 2011;16:577-86.  Back to cited text no. 25
    


    Figures

  [Figure 1], [Figure 2]
 
 
    Tables

  [Table 1]



 

Top
Print this article  Email this article
            

    

 
   Search
 
  
    Similar in PUBMED
  Related articles
    Article in PDF (1,409 KB)
    Citation Manager
    Access Statistics
    Reader Comments
    Email Alert *
    Add to My List *
* Registration required (free)  


    Abstract
   Introduction
    Materials and Me...
   Results
   Discussion
   Conclusion
    References
    Article Figures
    Article Tables

 Article Access Statistics
    Viewed172    
    Printed6    
    Emailed0    
    PDF Downloaded37    
    Comments [Add]    

Recommend this journal

Journal of Oral and Maxillofacial Pathology | Published by Wolters Kluwer - Medknow
Online since 15th Aug, 2007