Publikasi Scopus 2024 per tanggal 31 Mei 2024 (409 artikel)

Bestari M.B.; Joewono I.R.; Syam A.F.
Bestari, Muhammad Begawan (36098747800); Joewono, Ignatius Ronaldi (57211640542); Syam, Ari Fahrial (8443384400)
36098747800; 57211640542; 8443384400
A Quest for Survival: A Review of the Early Biomarkers of Pancreatic Cancer and the Most Effective Approaches at Present
2024
Biomolecules
14
3
364
0
Division of Gastroenterohepatology, Department of Internal Medicine, Hasan Sadikin General Hospital, Faculty of Medicine, University of Padjadjaran, Bandung, 40161, Indonesia; Mochtar Riady Comprehensive Cancer Center, Siloam Hospitals, Jakarta, 12930, Indonesia; Division of Gastroenterology, Department of Internal Medicine, Cipto Mangunkusumo National Central Hospital, Faculty of Medicine, University of Indonesia, Jakarta, 10430, Indonesia
Bestari M.B., Division of Gastroenterohepatology, Department of Internal Medicine, Hasan Sadikin General Hospital, Faculty of Medicine, University of Padjadjaran, Bandung, 40161, Indonesia; Joewono I.R., Mochtar Riady Comprehensive Cancer Center, Siloam Hospitals, Jakarta, 12930, Indonesia; Syam A.F., Division of Gastroenterology, Department of Internal Medicine, Cipto Mangunkusumo National Central Hospital, Faculty of Medicine, University of Indonesia, Jakarta, 10430, Indonesia
Pancreatic cancer (PC) is the most lethal type of cancer; it has the lowest 5-year survival rate among all other types of cancers. More than half of PC cases are diagnosed at an advanced stage due to PC’s insidious and non-specific symptoms. Surgery remains the most efficacious treatment option currently available, but only 10–20% of PC cases are resectable upon diagnosis. As of now, the sole biomarker approved by the United States Food and Drug Administration (US-FDA) for PC is carbohydrate antigen 19-9 (CA19-9); however, its use is limited for early diagnosis. An increasing number of studies have investigated a combination of biomarkers. Lately, there has been considerable interest in the application of a liquid biopsy, including the utilization of microRNAs (miRNAs), circulating tumor DNA (ctDNA), and circulating tumor cells (CTCs). Screening for PC is indicated for high-risk patients; studies on new diagnostic models combined with biomarkers for early detection have also shown promising results in terms of the ability of these models and biomarkers to aid clinicians in deciding on whether to start screening. This review seeks to provide a concise overview of the advancements in relation to existing biomarkers and explore novel strategies for the early detection of PC. © 2024 by the authors.
early biomarker; early diagnosis; pancreatic cancer
Biomarkers, Tumor; DNA, Neoplasm; Humans; Liquid Biopsy; MicroRNAs; Pancreatic Neoplasms; beta catenin; CA 19-9 antigen; carcinoembryonic antigen; circulating free DNA; circulating microRNA; circulating tumor DNA; collagen type 4; contrast medium; CXCL1 chemokine; epithelial cell adhesion molecule; gelatinase A; gelatinase B; glycoprotein; Leucine rich alpha 2 glycoprotein 1; microRNA; multi walled nanotube; nanoparticle; osteoprotegerin; stromal cell derived factor 1; tissue inhibitor of metalloproteinase; transthyretin; tumor marker; unclassified drug; vasculotropin C; DNA; microRNA; tumor marker; artificial intelligence; artificial neural network; blood group Lewis system; cancer growth; carcinogenesis; circulating tumor cell; droplet digital polymerase chain reaction; early diagnosis;
Multidisciplinary Digital Publishing Institute (MDPI)
2218273X
38540782
Review
Q1
1074
3733