Comparative study on the mutation spectrum of L-MYC and C-MYC genes of blood cfDNA in patients with ovarian cancer and healthy females

被引:1
|
作者
Shabir, Saba [1 ]
Asiaf, Asia [2 ]
机构
[1] Adesh Univ, Ctr Interdisciplinary Biomed Res, Bathinda, India
[2] Cluster Univ Srinagar, Govt Coll Women, Dept Clin Biochem, M A Rd, Srinagar, Kashmir, India
关键词
C-MYC; L-MYC; mutation; ovarian cancer; sanger sequencing; CELL-FREE DNA; AMPLIFICATION; THERAPY; FAMILY;
D O I
10.1111/jog.15808
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Background: This study aimed at detecting the mutations of L-MYC and C-MYC genes in ovarian cancer (OC) patients and healthy female volunteers using cell-free DNA (cfDNA).Methods: We evaluated cfDNA of 50 OC patients with different stages (I-IV) and 50 age-matched healthy female volunteers (controls) in order to access mutations in exon-1 of L-MYC (198 bp) and exon-3 of C-MYC (165 bp) genes using Sanger sequencing.Results: The total mutations reported were 43 and 7 in exon-1 of L-MYC and exon-3 of C-MYC genes, respective. The C-MYC and L-MYC gene mutational status recorded in both cases and controls were compared with the already available data on mutations in c-myc and L-myc databases viz SNP db-NCBI, ClinVar db, COSMIC, PubMed, and LitVar which suggested that the detected mutations in exon-1 of L-MYC and exon-3 of C-MYC genes are novel.Conclusion: Our study showed that cfDNA might be used for noninvasive detection of clinico-genomic profiles of OC patients and as a prognostic biomarker for the disease.
引用
收藏
页码:2894 / 2904
页数:11
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