BIOCHEMISTRY, GENETICS & MOLECULAR BIOLOGY / REVIEW
 
HIGHLIGHTS
  • Gynecological tumors are important to women's health throughout the world.
  • This review focuses on the advances in biotechnology that have contributed to the management of gyneco-logical tumors.
  • Recent advances in biosensing technologies have significantly enhanced the detection of gynecological tumor markers.
KEYWORDS
TOPICS
ABSTRACT
Among oncological diseases of women, gynecological diseases deserve special attention. Gynecological tumors are important to women's health throughout the world. Notably, gynecologic malignancies represent a prevalent category of cancers affecting women globally. Single nucleotide polymorphisms have emerged as a promising source of genetic information to better understand complex diseases such as cancer, in terms of etiology, interindividual differences and treatment response. In this review, we summarize some selected gene single nucleotide polymorphisms’ implication in gynecological cancer susceptibility/predisposition, as well as the potential to use such genetic markers for improved diagnosis and individualized treatment of gynecological cancers. Furthermore, this review explores the advances in biotechnology that have contributed to the management of gynecological tumors, in particular endometrial tumors, with a focus on molecular diagnostics, therapeutic innovations, and personalized medicine. It is critical to investigate the single nucleotide gene polymorphisms as sociated with gynecologic cancer susceptibility/predisposition as some of them might be utilized as useful molecular markers for assessing gynecologic cancer predisposition and might be further used for diagnosis and treatment modalities in individuals with similar single nucleotide polymorphism profile. Moreover, recent advancements in biosensing technologies, particularly nano-biosensors and microfluidic biosensors, have significantly enhanced the detection of gynecological tumor markers. Taken together, the revolution in cancer research, diagnosis, and treatment has been made possible by advances in biotechnology in recent decades.
ABBREVIATIONS
APC: Adenomatous Polyposis Coli; BAX: BCL-2 Associated X protein; CIMP: CpG Island Methylator Phenotype; CHFR: Checkpoint with Forkhead-Associated and Ring Finger Domains; CASP8: Caspase 8; CD1: Cluster of Differentiation 1; COMT: Catechol-O-Methyltransferase; CIN: Cervical Intraepithelial Neoplasia; DACH1: Dachshund family transcription factor; GPR54: G Protein-Coupled Receptor 54; MLH1: MutL Homolog 1; HPSE: Heparanase; HOXA11: Homeobox A 11; IGF2R: Insulin like Growth Factor 2 Receptor; EC: Endometrial Cancer; ER: Estrogen Receptors; HPV: Human Papilloma Virus; MMR: Mismatch Repair; MSI: Micro-satellite Instability; PTEN: Phosphatase and tension homolog deleted on chromosome 10; P73: Tumor Protein P73; RASSF1A: Ras Association Domain Family Member 1A; RSK4: Ribosomal S6 Kinase 4; SNP: Single Nucleotide Polymorphism; SPRY2: Sprouty Homolog 2; TGFBR2: Transforming Growth Factor Beta Receptor 2
ACKNOWLEDGEMENTS
None.
FUNDING
None.
CONFLICT OF INTEREST
The authors declare no conflict of interest.
PEER REVIEW INFORMATION
Article has been screened for originality
Externally peer reviewed.
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