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International Journal of Pharmaceutical Science Invention
ISSN (Online): 2319 – 6718, ISSN (Print): 2319 – 670X
www.ijpsi.org || Volume 4 Issue 6|| June 2015 || PP.07-10
www.ijpsi.org 7 | Page
Oral Submucous fibrosis and the role of curcumin in its
treatment: A review
Swathi.R
CRRI,Saveetha dental college and hospitals, Chennai
ABSTRACT: Oral submucous fibrosis is a chronic insidious disease which was previously designated as a
premalignant condition but presently categorized under potentially malignant disorders (WHO 2005). Oral
submucous fibrosis is highly prevalent in south Asia as people of south Asia consume large amounts of areca
nut when compared with rest of the world. Curcumin is the active component of turmeric which is a south Asian
spice commonly used for cooking. Curcumin has some important biological properties such as anti-
inflammatory, antioxidant and anti-cancer activity. Numerous studies have reported curcumin’s role in the
prevention and reduction of fibrosis caused by harmful factors. The aim of this review is to provide an update
about curcumin’s role and action in oral submucous fibrosis.
KEY WORDS – Oral submucous fibrosis, curcumin, potentially malignant disorders.
I. INTRODUCTION
Oral submucous fibrosis (OSF) is a chronic inflammatory disease, which has been categorised by
WHO as one of the potentially malignant disorders (WHO workshop, 2005). Schwartz first described it in 1952.
OSF was defined by PindborgJJ &Sirsat SM in 1966, as“An insidious chronic disease affecting any part of the
oral cavity and sometimes the pharynx.Although occasionally preceded by and/ or associated with vesicle
formation, it is always associated with a juxta-epithelial inflammatory reaction followed by a fibroelastic change
of the lamina propria, with epithelial atrophy leading to stiffness of the oral mucosa and causing trismus and
inability to eat. About 5 million people of the Indian population are reportedly affected. The main clinical
features include trismus, mucosal pain on consuming spicy foods reduced interincisal distance, stomatopyrosis,
reduced tongue movement, palpable fibrotic bands in buccal mucosa, discoloration and desquamation of oral
mucosa. In early OSF, there is dysguesia, dryness of the mouth, blisters in the palate and oral mucosa. In
advanced stages, there is blanching of the mucosa, fixation of soft palate, shortening of uvula, persistent or
recurrent glossitis/stomatitis. Malignant transformation rate of OSMF is 7.6 % over a period of 10 years has
been reported.
II. AETIOPATHOGENESIS
OSF is associated with placement of betel quid in the oral cavity. Betel quid is a substance or mixture
of substances placed in the mouth or chewed and remaining in contact with the mouth, usually containing one or
both of the two basic ingredients areca nut and slaked lime usually with tobacco and sometimes with sweeteners
and condiments wrapped in betel leaf in raw or any manufactured or processed form. Slaked lime releases
alkaloid arecadine from areca, nut that causes submucosal changes. Epithelial alterations and carcinogenesis can
be attributed to tobacco contact.An imbalance in collagen synthesis and degradation in oral mucosa is generally
believed to be the main cause of OSF. The disease is considered a type of collagen metabolism disorder as it
causes disturbance in the homeostatic equilibrium between synthesis and degradation of extra cellular
matrix.Myofibroblasts play an important role in the development of oral submucous fibrosis (OSF). The basic
mechanism is that, there is an increase in TGFβ, which stimulates the production and deposition of extracellular
matrix, and a decrease in collagenase activity causing increased crosslinking of collagen. Cytokines and growth
factors produced by activated inflammatory cells may promote fibrosis by inducing proliferation of fibroblasts,
upregulating collagen synthesis and downregulating collagenase production.
III. CLINICAL FEATURES AND DIAGNOSIS
As stated earlier, the prodromal symptoms of early OSF include a burning sensation in the mouth on
consuming spicy food, appearance of blisters, ulceration and recurrent inflammation of the oral mucosa,
excessive salivation, defective gustatory sensation and dryness of the mouth. The chief complaint is, inability to
open the mouth. An interincisal distance of 20mm or less is considered severe. In advanced cases, the jays may
even be inseparable. Females are more susceptible to these changes.Vesicles, Petechiae, Melanosis, xerostomia,
Oral Submucous fibrosis and the role of curcumin in its treatment: A review
www.ijpsi.org 8 | Page
and a generalised oral burning sensation(stomatopyrosis) are usually the first signs and symptoms. The buccal
mucosa, retromolar area and soft palate are most commonly affected sites. There is a blotchy, marble like pallor
and progressive stiffness of subepithelial tissues. Betel quid chewers may exhibit a brown-red discolouration of
the mucosa with an irregular surface that tends to desquamate. This is termed betel chewer's mucosa. In
addition, some authors have reported betel quit lichenoid lesions, characterised by white parallel, wavy striae.
IV. PATHOLOGY
Structural and microstructural changes- the epithelial changes in different stages of OSF are
predominantly hyperplasia (early) and atrophy (advanced) associated with an increased tendency for
keratinising metaplasia. Subepithelial changes- on the basis of histopathological appearance, four different
stages have been defined- very early, early, moderate advanced, advanced. This grouping was based on the
amount and nature of subepithelial collagen, presence or absence of edema, physical state of mucosal collagen,
overall fibroblastic response, state of blood vessels, and predominant cell type in inflammatory exudate.
Significant hematological abnormalities have been reported in OSF, including an increased erythrocyte
sedimentation rate, anemia, eosinophilia, increased gamma globulin, decrease in serum iron and increase in total
iron binding capacity (TIBC). The percentage saturation of transferrin also decreased and a significant reduction
in total serum iron and albumin was found.
V. TREATMENT
Review of the natural history of OSF indicates that it is an insidious disorder, which progresses with
time. In clinical practice, there are a number of treatments for OSF, ranging from medical and surgical
interventions, physical therapy, and habit control (i.e. cessation of areca nut use). Often a combination of
strategies is used.People with OSF characteristically complain of two problems: inability to open their mouths
and function normally, and a burning sensation and intolerance to spicy foods that are often the mainstay of the
Asian diet, leaving an individual disadvantaged both physically and psychologically. Based on the clinical
features, the aims of treatment are to reverse these signs and symptoms, stop disease progression, and in
addition, to minimize the risk for malignant transformation. There is an array of reported medical interventions
including dietary supplementation mainly for proteins, vitamins, anti-oxidants, anti-inflammatory agents or
immunomodulatory drugs (principally corticosteroids) and proteolytic agents (such as hyaluronidase and
placental extracts), and anti-cytokines. Such agents may be administered orally, topically or via submucosal
injection.. Physical therapy may be used as a single modality or combined with other interventions.Surgical
interventions are generally reserved for more advanced cases of OSF. These treatment modalities have not been
proven completely effective in treating osmf.
VI. ROLE OF CURCUMIN IN OSMF
Curcumin, 1, 7-bis (4-hydroxy-3-methoxyphenol)-1, 6-heptadiene-3, 5-dione, is the primary active
substance isolated from Curcuma Longa L. rhizome. It is inexpensive, widely available and has almost no side
effects; it has been long used as a spice and pigment in food processing industry. Curcumin has some important
biological properties such as anti-inflammatory, antioxidant and anti-cancer acticity(Goel et al., 2008). Recently,
many studies have reported curcumin’s role in the prevention and reduction of fibrosis caused by harmful
factors (Venkatesan et al., 2007; Osawa, 2007).
Myofibroblasts, typically considered to be activated fibroblasts, play an important role in
morphogenesis, oncogenesis, inflammation, wound healing and fibrosis in most organs and tissues (Watsky et
al., 2010).
Myofibroblast persistence is a key feature of fibrotic diseases including OSF, scleroderma, and hepatic,
pancreatic, and pulmonary fibrosis(Gabbiani, 2003; Angadi et al., 2011). Myofibroblasts can be detected in the
OSF-affected tissues; this phenomenon is related to the severity of OSF (Angadi et al., 2011). Myofibroblasts
not only synthesize collagen, but also produce numerous inflammatory mediators, chemokines, and growth
factors (Powell et al., 1999), intensifying and prolonging the inflammation in OSF by activating the
inflammatory corpuscles. This self-excitation of inflammation increases the expression of fibrogenic cytokines
such as TGF-β1, and enhances fibrosis. The possibility of inhibiting proliferation and inducing apoptosis in
myofibroblasts offers a new, promising therapy line in the treatment of OSF.
Oral Submucous fibrosis and the role of curcumin in its treatment: A review
www.ijpsi.org 9 | Page
It has been reported in a study that Curcumin inhibits cell proliferation in fibroblasts and
myofibroblasts MTT assay revealed that curcumin treatment significantly decreases the proliferation of
fibroblasts and myofibroblasts, in a dose-dependent manner. This effect is more pronounced in myofibroblasts;
the growth inhibitory rate for myofibroblasts incubated with curcumin was double of that for the similarly
treated fibroblasts.
Curcumin induces cell cycle arrest in myofibroblasts Cell cycle analysis shows that curcumin treatment
results in a dose-dependent increase in the proportion of myofibroblast cells in G0/G1 phase.
Curcumin induces cell apoptosis in myofibroblasts. The mechanism by which Curcumin mediates is
pro-oxidant effects remain unclear. It has been suggested that mitochondria play a role in Curcumin-induced
apoptosis. It is possible that Curcumin activates mitochondrial enzymes that lead to production of reactive
oxygen species (ROS). This induction of ROS by Curcumin may occur through its interaction with thioredoxin
reductase, thus altering it's activity to NADPH oxidase, which could then lead to the production of ROS. There
have also been reports suggesting that Curcumin quenches ROS production and tugs acts as an antioxidant while
others have reported that Curcumin quenches ROS production at low concentrations and induces ROS
production at high concentrations. It also has been stated that micronutrients enhance the levels of vitamins A
and C as well as selenium, in the supplemented groups, with a concomitant regression of precancerous lesions
present on the palate. No side effects have been reported.
VII. DISCUSSION
Most of the treatment modalities for OSMF in practice are circumstantial and most of the studies that
tested various treatment regimens lacked good design and follow up. Treatment of OSMF has largely been
symptomatic. Though there are many therapeutic procedures available for OSMF, prevention is likely to be
more effective then treatment.
A study published in 2010 has suggested that mitochondria play a role in curcumin induced
apoptosis.The FDA has approved curcumin as “generally regarded as safe”; It is widely used in food industry as
a spice and coloring agent. The safety of curcumin, combined with its potential efficacy and low cost, makes it
an ideal therapeutic drug for OSF, a disease prevalent mainly in the developing countries.
H.K.E.S College of Pharmacy Gulbarga conducted a study in 2012 to determine the efficacy of
mucoadhesive gel formulation of curcumin in treating OSF. The formulation was then planned for in-vivo
studies using mice as model animal. In first phase of histopathological studies of OSMF induction in mice, a
gross change of mucosa was observed and increased significance seen with the use of gutkha gel from 1 month
application to 6 months applications. In second phase of treatment part of OSMF using prepared curcumin semi-
solid preparation the encouraging results were observed. There was a marked reduction (more than 50%) of
OSMF seen from the histopathological studies.
Recently, studies have suggested the use of curcumin in treating OSF in humans. Curcumin inhibits
proliferation, disrupts the cell cycle, induces apoptosis, and decreases the expression levels of type I and III
collagen; and it clearly demonstrates curcumin’santifibrotic potential in vitro. Further studies need to be carried
out to prove the efficiency of curcumin in treating OSMF.
VIII. CONCLUSION
Oral submucous fibrosis (OSF) is a chronic, insidious disease that is associated with significant
functional morbidity and an increased risk for malignancy. It initially affects the lamina propria of the oral
mucosa and as the disease progresses it involves the submucosa and the deeper tissues including muscles of the
oral cavity with resulting loss of fibroelasticity. The clinical manifestations include blanching and stiffening of
the oral mucosa leading to limitation in oral opening. the disease could be described as primarily as a collagen
metabolic disorder with changes observed in the extracellular matrix of the lamina propria and in the deeper
mucosal tissues of the oral cavity because of both increased collagen synthesis and/or reduced collagen
degradation. Treatment aims at reversing the signs and symptoms and stopping the disease progression. Does
not regress with habit cessation. Treatment includes Intralesional injection of corticosteroids, interferon-γand
long term followup. There is a 19 times risk than normal for cancer development. Curcumin has been proven
effective in the treatment of OSF in recent times.
Oral Submucous fibrosis and the role of curcumin in its treatment: A review
www.ijpsi.org 10 | Page
REFERENCES
[1] Antifibrotic Effect of Curcumin in TGF-β1-Induced Myofibroblasts from Human Oral Mucosa
[2] Zhang, Shan-Shan; Gong, Zhao-Jian ; Li, Wen-Hui ; Wang, Xiao ; Ling, Tian-You ; Angadi PV, Kale AD, Hallikerimath S (2011).
Evaluation of myofibroblasts in oral submucous Fibrosis: correlation with disease severity. J Oral Pathol Med, 40, 208-13.
[3] Atsumi T, Tonosaki K, Fujisawa S (2006). Induction of early apoptosis and ROS generation activity in human gingival fibroblasts
(HGF) and human submandibular gland carcinoma (HSG) cells treated with curcumin. Arch Oral Biol, 51, 913-21.
[4] Boucher BJ, Mannan N (2002). Metabolic effects of the consumption of Areca catechu. Addict Biol, 7, 103-10.
[5] Bruck R, Ashkenazi M, Weiss S, et al (2007). Prevention of liver cirrhosis in rats by curcumin. Liver Int, 27, 373-83.
[6] Chen A, Xu J (2005). Activation of PPAR{gamma} by curcumin inhibits Moser cell growth and mediates suppression of gene
expression of cyclin D1 and EGFR. Am J PhysiolGastrointest Liver Physiol, 288, G447-56.
[7] Choudhuri T, Pal S, Das T, Sa G (2005). Curcumin selectively induces apoptosis in deregulated cyclin D1-expressed cells at G2
phase of cell cycle in a p53-dependent manner. J BiolChem, 280, 20059-68.
[8] Divya CS, Pillai MR (2006). Antitumor action of curcumin in human papillomavirus associated cells involves downregulation of
viral oncogenes, prevention of NFkB and AP-1 translocation, and modulation of apoptosis. MolCarcinog, 45, 320-32.
[9] Elledge SJ (1996). Cell cycle checkpoints: preventing an identity crisis. Science, 274, 1664-72.
[10] Fedorowicz Z, Chan Shih-Yen E, Dorri M, et al (2008). Interventions for the management of oral submucous fibrosis. Cochrane
Database Syst Rev, 8, CD007156.
[11] Gabbiani G (2003). The myofibroblast in wound healing and fibrocontractive diseases. J Pathol, 200, 500-3.
[12] Goel A, Jhurani S, Aggarwal BB (2008). Multi-targeted therapy by curcumin: how spicy is it? MolNutr Food Res, 52, 1010-30.
[13] Hinz B, Phan SH, Thannickal VJ, et al (2007). The myofibroblast: one function, multiple origins. Am J Pathol, 170, 1807-16.
[14] International Agency for Research on Cancer (2005). WHO classification of tumors: pathology and genetics of head and neck
tumors. IARC Press, Lyon.
[15] Murti PR, Bhonsle RB, Pindborg JJ, Daftary DK, Gupta PC, Mehta FS. Malignant transformation rate in oral submucous fibrosis
over a 17- year period. Community Dent Oral Epidemol. 1985;13: 340-1.
[16] 1967;70(2):161-73 Subepithelial changes in oral submucous fibrosis., Sirsat SM, Pindborg JJ.

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Oral Submucous fibrosis and the role of curcumin in its treatment: A review

  • 1. International Journal of Pharmaceutical Science Invention ISSN (Online): 2319 – 6718, ISSN (Print): 2319 – 670X www.ijpsi.org || Volume 4 Issue 6|| June 2015 || PP.07-10 www.ijpsi.org 7 | Page Oral Submucous fibrosis and the role of curcumin in its treatment: A review Swathi.R CRRI,Saveetha dental college and hospitals, Chennai ABSTRACT: Oral submucous fibrosis is a chronic insidious disease which was previously designated as a premalignant condition but presently categorized under potentially malignant disorders (WHO 2005). Oral submucous fibrosis is highly prevalent in south Asia as people of south Asia consume large amounts of areca nut when compared with rest of the world. Curcumin is the active component of turmeric which is a south Asian spice commonly used for cooking. Curcumin has some important biological properties such as anti- inflammatory, antioxidant and anti-cancer activity. Numerous studies have reported curcumin’s role in the prevention and reduction of fibrosis caused by harmful factors. The aim of this review is to provide an update about curcumin’s role and action in oral submucous fibrosis. KEY WORDS – Oral submucous fibrosis, curcumin, potentially malignant disorders. I. INTRODUCTION Oral submucous fibrosis (OSF) is a chronic inflammatory disease, which has been categorised by WHO as one of the potentially malignant disorders (WHO workshop, 2005). Schwartz first described it in 1952. OSF was defined by PindborgJJ &Sirsat SM in 1966, as“An insidious chronic disease affecting any part of the oral cavity and sometimes the pharynx.Although occasionally preceded by and/ or associated with vesicle formation, it is always associated with a juxta-epithelial inflammatory reaction followed by a fibroelastic change of the lamina propria, with epithelial atrophy leading to stiffness of the oral mucosa and causing trismus and inability to eat. About 5 million people of the Indian population are reportedly affected. The main clinical features include trismus, mucosal pain on consuming spicy foods reduced interincisal distance, stomatopyrosis, reduced tongue movement, palpable fibrotic bands in buccal mucosa, discoloration and desquamation of oral mucosa. In early OSF, there is dysguesia, dryness of the mouth, blisters in the palate and oral mucosa. In advanced stages, there is blanching of the mucosa, fixation of soft palate, shortening of uvula, persistent or recurrent glossitis/stomatitis. Malignant transformation rate of OSMF is 7.6 % over a period of 10 years has been reported. II. AETIOPATHOGENESIS OSF is associated with placement of betel quid in the oral cavity. Betel quid is a substance or mixture of substances placed in the mouth or chewed and remaining in contact with the mouth, usually containing one or both of the two basic ingredients areca nut and slaked lime usually with tobacco and sometimes with sweeteners and condiments wrapped in betel leaf in raw or any manufactured or processed form. Slaked lime releases alkaloid arecadine from areca, nut that causes submucosal changes. Epithelial alterations and carcinogenesis can be attributed to tobacco contact.An imbalance in collagen synthesis and degradation in oral mucosa is generally believed to be the main cause of OSF. The disease is considered a type of collagen metabolism disorder as it causes disturbance in the homeostatic equilibrium between synthesis and degradation of extra cellular matrix.Myofibroblasts play an important role in the development of oral submucous fibrosis (OSF). The basic mechanism is that, there is an increase in TGFβ, which stimulates the production and deposition of extracellular matrix, and a decrease in collagenase activity causing increased crosslinking of collagen. Cytokines and growth factors produced by activated inflammatory cells may promote fibrosis by inducing proliferation of fibroblasts, upregulating collagen synthesis and downregulating collagenase production. III. CLINICAL FEATURES AND DIAGNOSIS As stated earlier, the prodromal symptoms of early OSF include a burning sensation in the mouth on consuming spicy food, appearance of blisters, ulceration and recurrent inflammation of the oral mucosa, excessive salivation, defective gustatory sensation and dryness of the mouth. The chief complaint is, inability to open the mouth. An interincisal distance of 20mm or less is considered severe. In advanced cases, the jays may even be inseparable. Females are more susceptible to these changes.Vesicles, Petechiae, Melanosis, xerostomia,
  • 2. Oral Submucous fibrosis and the role of curcumin in its treatment: A review www.ijpsi.org 8 | Page and a generalised oral burning sensation(stomatopyrosis) are usually the first signs and symptoms. The buccal mucosa, retromolar area and soft palate are most commonly affected sites. There is a blotchy, marble like pallor and progressive stiffness of subepithelial tissues. Betel quid chewers may exhibit a brown-red discolouration of the mucosa with an irregular surface that tends to desquamate. This is termed betel chewer's mucosa. In addition, some authors have reported betel quit lichenoid lesions, characterised by white parallel, wavy striae. IV. PATHOLOGY Structural and microstructural changes- the epithelial changes in different stages of OSF are predominantly hyperplasia (early) and atrophy (advanced) associated with an increased tendency for keratinising metaplasia. Subepithelial changes- on the basis of histopathological appearance, four different stages have been defined- very early, early, moderate advanced, advanced. This grouping was based on the amount and nature of subepithelial collagen, presence or absence of edema, physical state of mucosal collagen, overall fibroblastic response, state of blood vessels, and predominant cell type in inflammatory exudate. Significant hematological abnormalities have been reported in OSF, including an increased erythrocyte sedimentation rate, anemia, eosinophilia, increased gamma globulin, decrease in serum iron and increase in total iron binding capacity (TIBC). The percentage saturation of transferrin also decreased and a significant reduction in total serum iron and albumin was found. V. TREATMENT Review of the natural history of OSF indicates that it is an insidious disorder, which progresses with time. In clinical practice, there are a number of treatments for OSF, ranging from medical and surgical interventions, physical therapy, and habit control (i.e. cessation of areca nut use). Often a combination of strategies is used.People with OSF characteristically complain of two problems: inability to open their mouths and function normally, and a burning sensation and intolerance to spicy foods that are often the mainstay of the Asian diet, leaving an individual disadvantaged both physically and psychologically. Based on the clinical features, the aims of treatment are to reverse these signs and symptoms, stop disease progression, and in addition, to minimize the risk for malignant transformation. There is an array of reported medical interventions including dietary supplementation mainly for proteins, vitamins, anti-oxidants, anti-inflammatory agents or immunomodulatory drugs (principally corticosteroids) and proteolytic agents (such as hyaluronidase and placental extracts), and anti-cytokines. Such agents may be administered orally, topically or via submucosal injection.. Physical therapy may be used as a single modality or combined with other interventions.Surgical interventions are generally reserved for more advanced cases of OSF. These treatment modalities have not been proven completely effective in treating osmf. VI. ROLE OF CURCUMIN IN OSMF Curcumin, 1, 7-bis (4-hydroxy-3-methoxyphenol)-1, 6-heptadiene-3, 5-dione, is the primary active substance isolated from Curcuma Longa L. rhizome. It is inexpensive, widely available and has almost no side effects; it has been long used as a spice and pigment in food processing industry. Curcumin has some important biological properties such as anti-inflammatory, antioxidant and anti-cancer acticity(Goel et al., 2008). Recently, many studies have reported curcumin’s role in the prevention and reduction of fibrosis caused by harmful factors (Venkatesan et al., 2007; Osawa, 2007). Myofibroblasts, typically considered to be activated fibroblasts, play an important role in morphogenesis, oncogenesis, inflammation, wound healing and fibrosis in most organs and tissues (Watsky et al., 2010). Myofibroblast persistence is a key feature of fibrotic diseases including OSF, scleroderma, and hepatic, pancreatic, and pulmonary fibrosis(Gabbiani, 2003; Angadi et al., 2011). Myofibroblasts can be detected in the OSF-affected tissues; this phenomenon is related to the severity of OSF (Angadi et al., 2011). Myofibroblasts not only synthesize collagen, but also produce numerous inflammatory mediators, chemokines, and growth factors (Powell et al., 1999), intensifying and prolonging the inflammation in OSF by activating the inflammatory corpuscles. This self-excitation of inflammation increases the expression of fibrogenic cytokines such as TGF-β1, and enhances fibrosis. The possibility of inhibiting proliferation and inducing apoptosis in myofibroblasts offers a new, promising therapy line in the treatment of OSF.
  • 3. Oral Submucous fibrosis and the role of curcumin in its treatment: A review www.ijpsi.org 9 | Page It has been reported in a study that Curcumin inhibits cell proliferation in fibroblasts and myofibroblasts MTT assay revealed that curcumin treatment significantly decreases the proliferation of fibroblasts and myofibroblasts, in a dose-dependent manner. This effect is more pronounced in myofibroblasts; the growth inhibitory rate for myofibroblasts incubated with curcumin was double of that for the similarly treated fibroblasts. Curcumin induces cell cycle arrest in myofibroblasts Cell cycle analysis shows that curcumin treatment results in a dose-dependent increase in the proportion of myofibroblast cells in G0/G1 phase. Curcumin induces cell apoptosis in myofibroblasts. The mechanism by which Curcumin mediates is pro-oxidant effects remain unclear. It has been suggested that mitochondria play a role in Curcumin-induced apoptosis. It is possible that Curcumin activates mitochondrial enzymes that lead to production of reactive oxygen species (ROS). This induction of ROS by Curcumin may occur through its interaction with thioredoxin reductase, thus altering it's activity to NADPH oxidase, which could then lead to the production of ROS. There have also been reports suggesting that Curcumin quenches ROS production and tugs acts as an antioxidant while others have reported that Curcumin quenches ROS production at low concentrations and induces ROS production at high concentrations. It also has been stated that micronutrients enhance the levels of vitamins A and C as well as selenium, in the supplemented groups, with a concomitant regression of precancerous lesions present on the palate. No side effects have been reported. VII. DISCUSSION Most of the treatment modalities for OSMF in practice are circumstantial and most of the studies that tested various treatment regimens lacked good design and follow up. Treatment of OSMF has largely been symptomatic. Though there are many therapeutic procedures available for OSMF, prevention is likely to be more effective then treatment. A study published in 2010 has suggested that mitochondria play a role in curcumin induced apoptosis.The FDA has approved curcumin as “generally regarded as safe”; It is widely used in food industry as a spice and coloring agent. The safety of curcumin, combined with its potential efficacy and low cost, makes it an ideal therapeutic drug for OSF, a disease prevalent mainly in the developing countries. H.K.E.S College of Pharmacy Gulbarga conducted a study in 2012 to determine the efficacy of mucoadhesive gel formulation of curcumin in treating OSF. The formulation was then planned for in-vivo studies using mice as model animal. In first phase of histopathological studies of OSMF induction in mice, a gross change of mucosa was observed and increased significance seen with the use of gutkha gel from 1 month application to 6 months applications. In second phase of treatment part of OSMF using prepared curcumin semi- solid preparation the encouraging results were observed. There was a marked reduction (more than 50%) of OSMF seen from the histopathological studies. Recently, studies have suggested the use of curcumin in treating OSF in humans. Curcumin inhibits proliferation, disrupts the cell cycle, induces apoptosis, and decreases the expression levels of type I and III collagen; and it clearly demonstrates curcumin’santifibrotic potential in vitro. Further studies need to be carried out to prove the efficiency of curcumin in treating OSMF. VIII. CONCLUSION Oral submucous fibrosis (OSF) is a chronic, insidious disease that is associated with significant functional morbidity and an increased risk for malignancy. It initially affects the lamina propria of the oral mucosa and as the disease progresses it involves the submucosa and the deeper tissues including muscles of the oral cavity with resulting loss of fibroelasticity. The clinical manifestations include blanching and stiffening of the oral mucosa leading to limitation in oral opening. the disease could be described as primarily as a collagen metabolic disorder with changes observed in the extracellular matrix of the lamina propria and in the deeper mucosal tissues of the oral cavity because of both increased collagen synthesis and/or reduced collagen degradation. Treatment aims at reversing the signs and symptoms and stopping the disease progression. Does not regress with habit cessation. Treatment includes Intralesional injection of corticosteroids, interferon-γand long term followup. There is a 19 times risk than normal for cancer development. Curcumin has been proven effective in the treatment of OSF in recent times.
  • 4. Oral Submucous fibrosis and the role of curcumin in its treatment: A review www.ijpsi.org 10 | Page REFERENCES [1] Antifibrotic Effect of Curcumin in TGF-β1-Induced Myofibroblasts from Human Oral Mucosa [2] Zhang, Shan-Shan; Gong, Zhao-Jian ; Li, Wen-Hui ; Wang, Xiao ; Ling, Tian-You ; Angadi PV, Kale AD, Hallikerimath S (2011). Evaluation of myofibroblasts in oral submucous Fibrosis: correlation with disease severity. J Oral Pathol Med, 40, 208-13. [3] Atsumi T, Tonosaki K, Fujisawa S (2006). Induction of early apoptosis and ROS generation activity in human gingival fibroblasts (HGF) and human submandibular gland carcinoma (HSG) cells treated with curcumin. Arch Oral Biol, 51, 913-21. [4] Boucher BJ, Mannan N (2002). Metabolic effects of the consumption of Areca catechu. Addict Biol, 7, 103-10. [5] Bruck R, Ashkenazi M, Weiss S, et al (2007). Prevention of liver cirrhosis in rats by curcumin. Liver Int, 27, 373-83. [6] Chen A, Xu J (2005). Activation of PPAR{gamma} by curcumin inhibits Moser cell growth and mediates suppression of gene expression of cyclin D1 and EGFR. Am J PhysiolGastrointest Liver Physiol, 288, G447-56. [7] Choudhuri T, Pal S, Das T, Sa G (2005). Curcumin selectively induces apoptosis in deregulated cyclin D1-expressed cells at G2 phase of cell cycle in a p53-dependent manner. J BiolChem, 280, 20059-68. [8] Divya CS, Pillai MR (2006). Antitumor action of curcumin in human papillomavirus associated cells involves downregulation of viral oncogenes, prevention of NFkB and AP-1 translocation, and modulation of apoptosis. MolCarcinog, 45, 320-32. [9] Elledge SJ (1996). Cell cycle checkpoints: preventing an identity crisis. Science, 274, 1664-72. [10] Fedorowicz Z, Chan Shih-Yen E, Dorri M, et al (2008). Interventions for the management of oral submucous fibrosis. Cochrane Database Syst Rev, 8, CD007156. [11] Gabbiani G (2003). The myofibroblast in wound healing and fibrocontractive diseases. J Pathol, 200, 500-3. [12] Goel A, Jhurani S, Aggarwal BB (2008). Multi-targeted therapy by curcumin: how spicy is it? MolNutr Food Res, 52, 1010-30. [13] Hinz B, Phan SH, Thannickal VJ, et al (2007). The myofibroblast: one function, multiple origins. Am J Pathol, 170, 1807-16. [14] International Agency for Research on Cancer (2005). WHO classification of tumors: pathology and genetics of head and neck tumors. IARC Press, Lyon. [15] Murti PR, Bhonsle RB, Pindborg JJ, Daftary DK, Gupta PC, Mehta FS. Malignant transformation rate in oral submucous fibrosis over a 17- year period. Community Dent Oral Epidemol. 1985;13: 340-1. [16] 1967;70(2):161-73 Subepithelial changes in oral submucous fibrosis., Sirsat SM, Pindborg JJ.