Abstract 368P
Background
Oral Submucous Fibrosis (OSMF) is a chronic debilitating disease more frequently found in the South East Asian population. This disease poses a public health priority, as it is grouped under oral potentially malignant disorders, with malignant transformation rates of around 7 to 13%. Hence, early identification of high-risk OSMF patients is of the utmost importance to prevent malignant transformation. mRNA expression profiling is a promising method for identifying differentially expressed genes for disease prognosis in OSMF. The genetic profiling was performed using Tumor Signaling (TS) 360 Panel (Nanostring platform) to profile 780 humans across 40+ annotated pathways.
Methods
The RNA was initially isolated from patient tissue samples in different clinical stages of OSMF (n=8), OSMF transformed into oral squamous cell carcinoma (OSCC) (n=5) and healthy controls (HC) (n=5). The analysis of gene expression was conducted on the nCounter® TS 360™ Panel and NanoString platform. The raw transcriptome data were subjected to housekeeping-gene normalization using the geNorm algorithm in nCounter Advanced Analysis ver. 2.0.115. Normalized data were log2-transformed for analysis. A quality check of raw data was conducted using nSolver Analysis Software ver. 4.0 and NanoStringQCpro ver. 1.14.0.
Results
Among the 780 genes, AR, RPTOR and PRDX6 showed the highest differential expression between OSMF and OSCC (2.48, 1.1 and 0.76 fold change, respectively; p < 0.05). While, MLANA, WEE1 and MYB showed the highest differential expression between HC and OSCC (5.16, 2.61 and 2.11 fold change, respectively; p < 0.05). The upregulated genes were further validated using real time PCR which showed significant upregulation in OSMF and OSCC.
Conclusions
The present study is the first of its kind in India to the best of our knowledge, assessing the gene expression using the Nanostring platform in different clinical stages of OSMF. with validation in a large series of cases. The currenty study has evolved a panel of biomarkers, namely PRDX6, MLANA and AR to be potentially useful in identifying high-risk OSMF patients with an increased risk of OSCC development.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
C.V. Divyambika; R. Vijayalakshmi.
Funding
Indian Council of Medical Research (ICMR): 5/4/2-4/Oral Health/2021/NCD-II.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
415P - Initial experience in a real-world Asian cohort with a circulating tumor DNA (ctDNA) mutation-based multi-cancer early detection (MCED) assay
Presenter: Steven Tucker
Session: Poster Display
Resources:
Abstract
416P - Three-dimensional bioprinting model of ovarian cancer for identification of patient-specific therapy response
Presenter: Jiangang Zhang
Session: Poster Display
Resources:
Abstract
417P - Early experience in using plasma-only multi-omic minimal residual disease testing in early-stage colorectal cancer patients from Asia and the Middle East
Presenter: Shaheenah Dawood
Session: Poster Display
Resources:
Abstract
418P - Decoding the intricate cellular makeup of immune-related adverse events using single-cell and spatial analysis
Presenter: Dmitrii Shek
Session: Poster Display
Resources:
Abstract
420P - Combinatory genomic and transcriptomic sequencing of Chinese KRAS mutant non-small cell lung cancer revealed molecular and inflammatory heterogeneity in tumor microenvironment
Presenter: Xuchao Zhang
Session: Poster Display
Resources:
Abstract
421P - Comprehensive genomic profiling (CGP) unravels somatic BRCA (sBRCA) and homologous recombinant repair (HRR) gene alterations across multi-cancer spectrum
Presenter: Ramya Kodandapani
Session: Poster Display
Resources:
Abstract
422P - CD8Teff distinguished tumor immunotyping heterogeneity and enables precision immunotherapy
Presenter: luhui Mao
Session: Poster Display
Resources:
Abstract
423P - Insights into clinically actionable biomarkers in an Indian cancer cohort of 1000 patients using comprehensive genomic profiling (CGP)
Presenter: Mithua Ghosh
Session: Poster Display
Resources:
Abstract
424P - MD Anderson Cancer Center global precision oncology decision support (Glo-PODS) clinical trial genomic support: Pilot program at the Prince of Wales Hospital (Chinese University of Hong Kong - CUHK)
Presenter: Brigette Ma
Session: Poster Display
Resources:
Abstract
425P - Engineered <italic>Lactococcus lactis</italic> as a personalized cancer vaccine platform induces antitumour immunity via membrane-inserted peptide for neoantigens
Presenter: Meng Zhu
Session: Poster Display
Resources:
Abstract