Current State of "Omics" Biomarkers in Pancreatic Cancer.

biomarker genomics glycomics metabolomics metagenomics omics pancreatic cancer personalized medicine proteomics systems biology transcriptomics

Journal

Journal of personalized medicine
ISSN: 2075-4426
Titre abrégé: J Pers Med
Pays: Switzerland
ID NLM: 101602269

Informations de publication

Date de publication:
14 Feb 2021
Historique:
received: 22 01 2021
revised: 08 02 2021
accepted: 11 02 2021
entrez: 6 3 2021
pubmed: 7 3 2021
medline: 7 3 2021
Statut: epublish

Résumé

Pancreatic cancer is one of the most fatal malignancies and the seventh leading cause of cancer-related deaths related to late diagnosis, poor survival rates, and high incidence of metastasis. Unfortunately, pancreatic cancer is predicted to become the third leading cause of cancer deaths in the future. Therefore, diagnosis at the early stages of pancreatic cancer for initial diagnosis or postoperative recurrence is a great challenge, as well as predicting prognosis precisely in the context of biomarker discovery. From the personalized medicine perspective, the lack of molecular biomarkers for patient selection confines tailored therapy options, including selecting drugs and their doses or even diet. Currently, there is no standardized pancreatic cancer screening strategy using molecular biomarkers, but CA19-9 is the most well known marker for the detection of pancreatic cancer. In contrast, recent innovations in high-throughput techniques have enabled the discovery of specific biomarkers of cancers using genomics, transcriptomics, proteomics, metabolomics, glycomics, and metagenomics. Panels combining CA19-9 with other novel biomarkers from different "omics" levels might represent an ideal strategy for the early detection of pancreatic cancer. The systems biology approach may shed a light on biomarker identification of pancreatic cancer by integrating multi-omics approaches. In this review, we provide background information on the current state of pancreatic cancer biomarkers from multi-omics stages. Furthermore, we conclude this review on how multi-omics data may reveal new biomarkers to be used for personalized medicine in the future.

Identifiants

pubmed: 33672926
pii: jpm11020127
doi: 10.3390/jpm11020127
pmc: PMC7918884
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

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Auteurs

Beste Turanli (B)

Department of Bioengineering, Marmara University, 34722 Istanbul, Turkey.

Esra Yildirim (E)

Department of Bioengineering, Marmara University, 34722 Istanbul, Turkey.

Gizem Gulfidan (G)

Department of Bioengineering, Marmara University, 34722 Istanbul, Turkey.

Kazim Yalcin Arga (KY)

Department of Bioengineering, Marmara University, 34722 Istanbul, Turkey.
Turkish Institute of Public Health and Chronic Diseases, 34718 Istanbul, Turkey.

Raghu Sinha (R)

Department of Biochemistry and Molecular Biology, Penn State College of Medicine, Hershey, PA 17033, USA.

Classifications MeSH