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缺氧以整合素αDβ1/血红蛋白δ依赖的方式促进结直肠癌的肿瘤生长。

Hypoxia favors tumor growth in colorectal cancer in an integrin αDβ1/hemoglobin δ-dependent manner.

作者信息

Koivunen Erkki, Madhavan Sudarrshan, Bermudez-Garrido Laura, Grönholm Mikaela, Kaprio Tuomas, Haglund Caj, Andersson Leif C, Gahmberg Carl G

机构信息

Programme in Molecular and Integrative Biosciences, Faculty of Biological and Environmental Sciences, University of Helsinki, Helsinki, Finland.

Drug Research Program, Division of Pharmaceutical Biosciences, Faculty of Pharmacy, University of Helsinki, Helsinki, Finland.

出版信息

Life Sci Alliance. 2024 Dec 3;8(2). doi: 10.26508/lsa.202402925. Print 2025 Feb.

Abstract

Low oxygen tension (PO), characterizes the tissue environment of tumors. The colorectal tumor line Colo205, grown under reduced oxygen tension expresses a novel αDβ1 integrin, which forms a cell surface complex with hemoglobin δ. This resulted in high local affinity for oxygen, which increased cell adhesion as compared with cells grown under normal oxygen tension. Staining with antibodies to the integrin αD polypeptide and hemoglobin δ, and transfection with cDNAs for GFP-hemoglobin δ and mCherry-αD, showed co-localization of αD and hemoglobin δ. Antibodies to αD and β1 integrins, an RGD peptide, and an αDβ1 binding peptide from hemoglobin δ, blocked the αDβ1-hemoglobin interaction and lowered oxygen consumption. Downregulation of integrin αD or hemoglobin δ expression inhibited cell proliferation in hypoxia. The very frequent expression of complexes between αDβ1 and hemoglobin δ on the cell surface offers potential diagnostic and therapeutic targets in colorectal cancer.

摘要

低氧张力(PO)是肿瘤组织环境的特征。在低氧张力条件下生长的结直肠肿瘤细胞系Colo205表达一种新型的αDβ1整合素,它与血红蛋白δ形成细胞表面复合物。这导致对氧气的高局部亲和力,与在正常氧张力下生长的细胞相比,增加了细胞黏附。用整合素αD多肽和血红蛋白δ的抗体染色,以及用GFP-血红蛋白δ和mCherry-αD的cDNA转染,显示αD和血红蛋白δ共定位。αD和β1整合素的抗体、RGD肽以及来自血红蛋白δ的αDβ1结合肽,阻断了αDβ1-血红蛋白的相互作用并降低了氧消耗。整合素αD或血红蛋白δ表达的下调抑制了缺氧条件下的细胞增殖。αDβ1与血红蛋白δ在细胞表面非常频繁地形成复合物,为结直肠癌提供了潜在的诊断和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d48a/11629678/aff1267ba556/LSA-2024-02925_FigS1.jpg

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