Signature of genetic associations in oral cancer

Oral cancer etiology is complex and controlled by multi-factorial events including genetic events. Candidate gene studies, genome-wide association studies, and next-generation sequencing identified various chromosomal loci to be associated with oral cancer. There is no available review that could gi...

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Bibliographic Details
Main Authors: Vishwas Sharma, Amrita Nandan, Amitesh Kumar Sharma, Harpreet Singh, Mausumi Bharadwaj, Dhirendra Narain Sinha, Ravi Mehrotra
Format: Article
Language:English
Published: IOS Press 2017-10-01
Series:Tumor Biology
Online Access:https://doi.org/10.1177/1010428317725923
Description
Summary:Oral cancer etiology is complex and controlled by multi-factorial events including genetic events. Candidate gene studies, genome-wide association studies, and next-generation sequencing identified various chromosomal loci to be associated with oral cancer. There is no available review that could give us the comprehensive picture of genetic loci identified to be associated with oral cancer by candidate gene studies–based, genome-wide association studies–based, and next-generation sequencing–based approaches. A systematic literature search was performed in the PubMed database to identify the loci associated with oral cancer by exclusive candidate gene studies–based, genome-wide association studies–based, and next-generation sequencing–based study approaches. The information of loci associated with oral cancer is made online through the resource “ORNATE.” Next, screening of the loci validated by candidate gene studies and next-generation sequencing approach or by two independent studies within candidate gene studies or next-generation sequencing approaches were performed. A total of 264 loci were identified to be associated with oral cancer by candidate gene studies, genome-wide association studies, and next-generation sequencing approaches. In total, 28 loci, that is, 14q32.33 (AKT1) , 5q22.2 (APC) , 11q22.3 (ATM) , 2q33.1 (CASP8) , 11q13.3 (CCND1) , 16q22.1 (CDH1) , 9p21.3 (CDKN2A) , 1q31.1 (COX-2) , 7p11.2 (EGFR) , 22q13.2 (EP300) , 4q35.2 (FAT1) , 4q31.3 (FBXW7) , 4p16.3 (FGFR3) , 1p13.3 (GSTM1-GSTT1) , 11q13.2 (GSTP1) , 11p15.5 (H-RAS) , 3p25.3 (hOGG1) , 1q32.1 (IL-10) , 4q13.3 (IL-8) , 12p12.1 (KRAS) , 12q15 (MDM2) , 12q13.12 (MLL2) , 9q34.3 (NOTCH1) , 17p13.1 (p53) , 3q26.32 (PIK3CA) , 10q23.31 (PTEN) , 13q14.2 (RB1) , and 5q14.2 (XRCC4) , were validated to be associated with oral cancer. “ORNATE” gives a snapshot of genetic loci associated with oral cancer. All 28 loci were validated to be linked to oral cancer for which further fine-mapping followed by gene-by-gene and gene–environment interaction studies is needed to confirm their involvement in modifying oral cancer.
ISSN:1423-0380