Arunkumar G, Murugan A K, Nagarajan M, Ajay C, Rajaraman R, Munirajan A K
Department of Genetics, Dr. ALM PG Institute of Basic Medical Sciences, University of Madras, Chennai, India.
Department of Molecular Oncology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.
Oral Dis. 2017 Jul;23(5):669-673. doi: 10.1111/odi.12655. Epub 2017 Mar 24.
Somatic mutations of the PIK3CA, CASP8, and NOTCH1 have been frequently detected in various human cancers. Our study aimed to analyze the mutational status of these genes in South Indian oral cancers.
We performed mutational analysis of the PIK3CA (exons 9 and 20), CASP8 (exon 9), and NOTCH1 (exons 5, 6, 7, 8, and 9) genes in 96, 48, and 44 oral cancer samples, respectively. All the specified exons were PCR (polymerase chain reaction)-amplified and directly sequenced by Sanger sequencing.
PIK3CA gene mutations were not found; however, a synonymous single nucleotide polymorphism (SNP) [rs17849079] was observed frequently [35/96 (36.4%)] in oral cancer samples. Further, no mutations were detected in the CASP8 gene, but observed a frequent [32/48 (66.6%)] SNP [rs1045487] in the oral cancer samples. We did not detect any mutation in the NOTCH1 gene (exons 5, 6, 7, 8, and 9) in all the [0/44] analyzed oral cancer samples.
This is the first study that reports the status of the PIK3CA, CASP8, and NOTCH1 mutations in South Indian oral cancer samples. Our study suggests that either mutations in these genes are uncommon in South Indian oral cancer samples or likely other genes in this pathway might be mutated.
PIK3CA、CASP8和NOTCH1的体细胞突变在多种人类癌症中经常被检测到。我们的研究旨在分析这些基因在南印度口腔癌中的突变状态。
我们分别对96份、48份和44份口腔癌样本中的PIK3CA(第9和20外显子)、CASP8(第9外显子)和NOTCH1(第5、6、7、8和9外显子)基因进行了突变分析。所有指定的外显子均通过聚合酶链反应(PCR)扩增,并通过桑格测序直接测序。
未发现PIK3CA基因突变;然而,在口腔癌样本中频繁观察到同义单核苷酸多态性(SNP)[rs17849079][35/96(36.4%)]。此外,在CASP8基因中未检测到突变,但在口腔癌样本中观察到频繁的[32/48(66.6%)]SNP[rs1045487]。在所有[0/44]分析的口腔癌样本中,我们未在NOTCH1基因(第5、6、7、8和9外显子)中检测到任何突变。
这是第一项报道南印度口腔癌样本中PIK3CA、CASP8和NOTCH1突变状态的研究。我们的研究表明,这些基因的突变在南印度口腔癌样本中并不常见,或者该通路中的其他基因可能发生了突变。