Pan-cancer analysis reveals the potential of hyaluronate synthase as therapeutic targets in human tumors.

Extracellular matrix Glioblastoma multiforme Hyaluronate synthase Immune Pan-cancer Prognosis Tumor microenvironment

Journal

Heliyon
ISSN: 2405-8440
Titre abrégé: Heliyon
Pays: England
ID NLM: 101672560

Informations de publication

Date de publication:
Aug 2023
Historique:
received: 28 05 2023
revised: 08 08 2023
accepted: 10 08 2023
medline: 28 8 2023
pubmed: 28 8 2023
entrez: 28 8 2023
Statut: epublish

Résumé

Hyaluronic acid (HA) is a crucial component of the extracellular matrix, and its level of accumulation is related to the progression of various malignant tumors. In this study, a pan-cancer analysis of the three enzymes called hyaluronan synthases (HAS1, HAS2, and HAS3) that produce HA was performed. The study comprehensively describes the characteristics of HAS1, HAS2, and HAS3 in cancers using public databases and tools, to identify the potential biological pathways involved at the molecular, protein, cellular, and clinical sample levels. The analysis showed that dysregulation of the three genes often occurs in cancer, contributing to cancer progression, metastasis, and prognosis. Overexpression of HAS2 promotes secretion of HA in GBM and enhances cell proliferation and migration. The common and specific functions of HAS in certain diseases have important research implications for the treatment and prognosis of tumors.

Identifiants

pubmed: 37636435
doi: 10.1016/j.heliyon.2023.e19112
pii: S2405-8440(23)06320-X
pmc: PMC10448108
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e19112

Informations de copyright

© 2023 The Authors.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

Xunxia Bao (X)

School of Life Sciences, Anhui Medical University, Hefei, 230032, China.

Juan Ran (J)

School of Life Sciences, Anhui Medical University, Hefei, 230032, China.

Chuifang Kong (C)

School of Life Sciences, Anhui Medical University, Hefei, 230032, China.

Zunxi Wan (Z)

School of Life Sciences, Northeast Normal University, Changchun, 130024, China.

Juling Wang (J)

School of Life Sciences, Anhui Medical University, Hefei, 230032, China.

Tengfei Yu (T)

School of Life Sciences, Anhui Medical University, Hefei, 230032, China.

Shengming Ruan (S)

School of Life Sciences, Anhui Medical University, Hefei, 230032, China.

Wenjing Ding (W)

School of Life Sciences, Anhui Medical University, Hefei, 230032, China.

Leiming Xia (L)

Department of Hematology, The First Affiliated Hospital of Anhui Medical University, Hefei, 230022, China.

Daoxiang Zhang (D)

School of Life Sciences, Anhui Medical University, Hefei, 230032, China.

Classifications MeSH