Treffer: Bioengineering and omics approaches for Type 1 diabetes practical research: advancements and constraints.

Title:
Bioengineering and omics approaches for Type 1 diabetes practical research: advancements and constraints.
Authors:
Peng X; Department of Endocrinology and Metabolism, Affiliated Hospital of North Sichuan Medical College, North Sichuan Medical College, Nanchong, Sichuan, China.; Department of Endocrinology and Metabolism, West China Hospital, Sichuan University, Chengdu, Sichuan, China., Li L; Department of Endocrinology and Metabolism, Affiliated Hospital of North Sichuan Medical College, North Sichuan Medical College, Nanchong, Sichuan, China., Peng Y; Department of Endocrinology and Metabolism, Affiliated Hospital of North Sichuan Medical College, North Sichuan Medical College, Nanchong, Sichuan, China., Zhou G; Department of Endocrinology and Metabolism, Affiliated Hospital of North Sichuan Medical College, North Sichuan Medical College, Nanchong, Sichuan, China., An Z; Department of Endocrinology and Metabolism, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Source:
Annals of medicine [Ann Med] 2025 Dec; Vol. 57 (1), pp. 2322047. Date of Electronic Publication: 2024 Dec 20.
Publication Type:
Journal Article; Review
Language:
English
Journal Info:
Publisher: Informa Healthcare Country of Publication: England NLM ID: 8906388 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1365-2060 (Electronic) Linking ISSN: 07853890 NLM ISO Abbreviation: Ann Med Subsets: MEDLINE
Imprint Name(s):
Publication: London : Informa Healthcare
Original Publication: Helsinki : Finnish Medical Society Duodecim, 1989-
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Contributed Indexing:
Keywords: Bioengineering; in vitro models; omics; type 1 diabetes
Substance Nomenclature:
0 (Insulin)
Entry Date(s):
Date Created: 20241220 Date Completed: 20241220 Latest Revision: 20250108
Update Code:
20250114
PubMed Central ID:
PMC11703378
DOI:
10.1080/07853890.2024.2322047
PMID:
39704022
Database:
MEDLINE

Weitere Informationen

Insulin dependency arises from autoimmunity that targets the β cells of the pancreas, resulting in Type 1 diabetes (T1D). Despite the fact that T1D patients require insulin for survival, insulin does not provide a cure for this disease or prevent its complications. Despite extensive genetic, molecular, and cellular research on T1D over the years, the translation of this understanding into effective clinical therapies continues to pose a significant obstacle. It is therefore difficult to develop effective clinical treatment strategies without a thorough understanding of disease pathophysiology. Pancreatic tissue bioengineering models of human T1D offer a valuable approach to examining and controlling islet function while tackling various facets of the condition. And in recent years, due to advances in high-throughput omics analysis, the genotypic and molecular profiles of T1D have become finer tuned. The present article will examine recent progress in these areas, along with their utilization and constraints in the realm of T1D.