Oral Squamous Cell Carcinoma Clinical Trial
Official title:
Validation of Assessment of Bmi-1 on Protein and Molecular Levels in Oral Dysplasia and Squamous Cell Carcinoma: A Diagnostic Study
The aim of the current study is to assess the validation of Bmi-1 detection at both protein and molecular levels in oral epithelial dysplasia and oral squamous cell carcinoma as a biomarker for early cancer detection versus biopsy embedded in paraffin blocks.
Head and neck squamous cell carcinoma (HNSCC) including oral squamous cell carcinoma (OSCC)
has been reported as the sixth most common cause of cancer mortality in the world and the
fifth most commonly occurring cancer. Thus a compelling need for investigation of the
underlying molecular events associated with OSCC tumorigenesis has emerged for better
understanding of such lesion. Moreover, identification of biomarkers for early detection and
prediction of prognosis became of extreme importance, as it was reported that early diagnosis
has been vital for effective treatment of OSCC and improved the survival rate of OSCC
patients.
OSCC may originate from malignant transformation of the normal oral mucosa, as well as from
oral potentially malignant lesions (OPMLs) with different degrees of oral epithelial
dysplasia (OED). The approach of a step-wise transition from OPMLs to OSCC was
well-established, but it could be difficult to predict if and when an OPML would undergo full
transformation and resulted in a tumor. Thus, using specific molecular biomarkers able to
identify OED lesions with higher potential for malignant transformation would be very
beneficial. Unfortunately, up to date there has been no tools available to monitor OED
lesions or HNSCC patients for early stages of local recurrences or distant metastases .
Among the recently introduced biomarkers, B-lymphoma Moloney murine leukemia virus insertion
region-1 (BMI1), a member of the polycomb group (PcG) genes, was considered to be pivotal in
regulating stemness-related genes involved in maintaining the self-renewal ability of stem
cells by promoting chromatin modifications. BMI1 was also known to be deregulated in various
human types of cancer. Previous studies have revealed the capability of BMI1 to be used as a
prognostic marker in gastric, esophageal, nasopharyngeal cancer, prostate, breast, cervical
and ovarian cancer, However, the role of BMI1 in maintaining self-renewal and tumorigenicity
in HNSCC or HNSCC-derived cancer stem cells (CSCs) remained to be clarified.
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