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3rd Edition of International Cancer & Immuno-Oncology Conference

March 15-17, 2027 | Singapore
March 15-17, 2027 | Singapore

Altered expression of endoplasmic reticulum stress response genes and circular RNAs in oral squamous cell carcinoma tumorigenesis

Vandana Tiwari, Conference Speaker
Dr. Ram Manohar Lohia Institute of Medical Sciences, India
Title : Altered expression of endoplasmic reticulum stress response genes and circular RNAs in oral squamous cell carcinoma tumorigenesis

Abstract:

Background: Oral squamous cell carcinoma (OSCC) is a leading malignancy with high mortality and poor prognosis. Dysregulation of endoplasmic reticulum stress response (ERSR) genes and circular RNAs (circRNAs) contributes to its tumorigenesis and progression.

Aim: This study aimed to evaluate the expression levels of ERSR-related genes and circRNAs in OSCC tissues and their role in disease pathogenesis.

Methods: A case-control study analyzed biopsy-confirmed OSCC tissues (n=25) and adjacent non-tumor tissues (n=25). Patient demographics, tumor location, histopathology, and TNM staging were recorded. Expression levels of ERSR genes (GRP78, CHOP, ATF6) and circ RNAs (CirRNA-CDR1S, CirRNA10036) were quantified using qRT-PCR. Relative fold changes were calculated using the 2?(ΔCT) method, with significance set at p < 0.05.

Results: The cohort included predominantly males (23:2), mean age 40±10.3 years. Risk factors included tobacco chewing (88%), smoking (64%), and alcohol consumption (36%). Tumors were located in the buccal mucosa (60%), tongue (28%), alveolus (8%), and lip (4%), with moderate (68%), well (28%), and poorly differentiated (4%) histopathology. Staging included T0 (8%), T1 (4%), T2 (40%), T3 (28%), and T4 (20%), with lymph node involvement in 36% (N+). Significant over expression was observed in OSCC tissues compared to non-tumor tissues: CirRNA-CDR1S (4.14-fold, p=0.048), CirRNA10036 (3.41-fold, p=0.034), ATF6 (4.71-fold, p=0.036), GRP78 (3.8-fold, p=0.03), and CHOP (1.63-fold, p=0.043).

Conclusion: ERSR genes and circRNAs are significantly up regulated in OSCC tissues, underscoring their role in tumorigenesis and progression. These findings warrant further validation in larger cohorts.

Keywords: OSCC, ERSR, Circular RNAs (Circ RNAs), Tumorigenesis, Gene expression.

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