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
143P - Ablation combined with tislelizumab in treating hepatocellular carcinoma: A phase II trial
Presenter: Yangxun Pan
Session: Poster Display
Resources:
Abstract
144P - Integrated clinical and genomic models using machine-learning methods to predict the efficacy of paclitaxel-based chemotherapy in patients with advanced gastric cancer from K-MASTER project
Presenter: Jwa Hoon Kim
Session: Poster Display
Resources:
Abstract
145P - Tislelizumab (TIS) + chemotherapy (Chemo)/chemoradiotherapy (CRT) as neoadjuvant treatment for resectable esophageal squamous cell carcinoma (R-ESCC)
Presenter: Longqi Chen
Session: Poster Display
Resources:
Abstract
146P - Phase (ph) Ib results of bemarituzumab (BEMA) added to capecitabine/oxaliplatin (CAPOX) or S-1/oxaliplatin (SOX) with or without nivolumab (NIVO) for previously untreated advanced gastric/gastroesophageal junction cancer (G/GEJC): FORTITUDE-103 study
Presenter: Keun-Wook Lee
Session: Poster Display
Resources:
Abstract
147P - Four-year overall survival (OS) update from the phase III HIMALAYA study of tremelimumab plus durvalumab in unresectable hepatocellular carcinoma (uHCC)
Presenter: Stephen Chan
Session: Poster Display
Resources:
Abstract
148P - Safety and efficacy of atezolizumab (Atezo) + bevacizumab (Bev) in Japanese patients (pts) with unresectable hepatocellular carcinoma (uHCC): Preliminary analysis of a prospective, multicenter, observational study (ELIXIR)
Presenter: Teiji Kuzuya
Session: Poster Display
Resources:
Abstract
149P - A prospective observational study of MSI screening in unresectable chemotherapy-naïve advanced gastric cancer/gastroesophageal junction cancer: WJOG13320GPS
Presenter: Yukiya Narita
Session: Poster Display
Resources:
Abstract
150P - Anlotinib plus chemotherapy as first-line therapy for gastrointestinal tumor patients with unresectable liver metastasis: Updated results from a multi-cohort, multi-center phase II trial ALTER-G-001-cohort C
Presenter: Junwei Wu
Session: Poster Display
Resources:
Abstract
151P - Relationship between depth of response and early tumor shrinkage with overall survival in advanced pancreatic cancer
Presenter: EMIKA KUROKI
Session: Poster Display
Resources:
Abstract
152P - Interim analysis of the NAPOLEON-2 study: Safety evaluation of nanoliposomal irinotecan with fluorouracil and folinic acid for unresectable pancreatic cancer patients with prior biliary drainage
Presenter: Futa Koga
Session: Poster Display
Resources:
Abstract