Cancer Chemoprevention by Metformin Hydrochloride Compared to Placebo in Oral Potentially Malignant Lesions

Phase 4

Brief Summary: Evaluation of the metformin drug effect as a drug that found to improve the quality of tissues, decrease signs \& symptoms of cancer, and decrease histo-pathological criteria of dysplasia.

This will be done by the aid of measuring salivary Micro RNA 31 \& 210 in saliva in addition to measure cyclin A2 as an immuno-histochemical analysis.

Detailed Description: Oral squamous cell carcinomas (OSCCs) are among the most common types of head and neck cancers and are a major cause of significant morbidity. It was reported that 16- 62% of OSCCs develop from premalignant lesions, which often presents clinically as white or red mucosal patches known as leukoplakia and erythroplakia. The role of miRNA in cancer has been reiterated and established by many studies that have shown that miRNA signatures (i.e., mRNA expression profiles) can be useful for classifying human cancers. These studies have identified "cancer related miRNAs" through investigating expression profiles in matched normal and tumor tissues, as well as in body fluids. In addition, a vast number of studies have shown that miRNAs can play a role in regulating the expression of oncogenes and tumor suppressor genes, whereas others have shown that miRNA gene deletion or mutation can lead cancer initiation, progression and metastasis . Several potential mechanisms have been suggested for the ability of metformin to suppress cancer growth in vitro and vivo:

(1) Activation of LKB1/AMPK pathway, (2) Induction of cell cycle arrest and/or apoptosis, (3) Inhibition of protein synthesis, (4) Reduction in circulating insulin levels, (5) Inhibition of the unfolded protein response (UPR), (6) Activation of the immune system.

This study is performed to evaluate metformin effect on the patients premalignant lesion versus maintenace follow ups.

Recruitment & Eligibility

Inclusion Criteria

Both genders with age range from 20 to 70 years.
Patients able to return for the follow up visits and can perform oral hygiene measures.
Clinically diagnosed and histologically confirmed as having oral potentially malignant lesions.
Patients agreed to sign a written consent after understanding the nature of the study
Patients have diagnosed oral premalignant lesion/lesions and not yet turned into malignancy (atrophic lichen planus- leukoplakia-erythroplakia - oral submucous fibrosis)

Exclusion Criteria

- Diabetic patients (Diabetes Mellitus Type I & II)
Patients have cardiovascular, lung, Renal, Liver diseases
Patients on H2 blocker & proton pump inhibitors therapy as Ranitidine (affects metformin absorption and clearance)
Those with allergy or sensitivity to Metformin or Retinoids therapy or having any contraindication for their use.
Systemic and/or local systemic drug therapy within the last 3 months prior to the start of the study
Patients on steroidal or Non-steroidal anti-inflammatory drugs (NSAIDs) for at least the last 6 months
Patients on Antibiotics treatment for at least the last 2 months
Patients on Retinoid, green tea supplements or another natural products therapy
Patients with already diagnosed malignant lesion/lesions
Pregnant or Lactating females
Vulnerable groups as prisoners, mentally disabled, etc...

Arm && Interventions

Group	Intervention	Description
control	starch tablet	starch tablets
Metformin Hcl 500Mg 24Hr Sa Tab	Metformin Hcl 500Mg 24Hr Sa Tab	Metformin Hcl 500Mg 24Hr Sa Tab drug is given to the patient

Primary Outcome Measures

Name	Time	Method
Evaluate lesion size in millimeters	1 year	Evaluate lesion size in millimeters

Secondary Outcome Measures

Name	Time	Method
Measurement of salivary Micro RNA	1 year	measuring salivary markers 31\& 210 in saliva and also in tissue biopsy
Measuring immuno-histochemical marker	1 year	Measuring cyclin A2 marker in tissues

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