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

Low oxygen tension (PO<sub>2</sub>), 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.

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Publication Details

Journal
Life Science Alliance
Published
2024-12-03
DOI
https://doi.org/10.26508/lsa.202402925
Citations
3
Primary Topic
Cancer, Hypoxia, and Metabolism
Type
article
Field-Weighted Citation Impact
0.86

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article

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

Erkki Koivunen, Leif C. Andersson, Tuomas Kaprio, Carl G. Gahmberg et al.
3 citations
Life Science Alliance
Cancer, Hypoxia, and Metabolism
0.86
article

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

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

Abstract

Low oxygen tension (PO<sub>2</sub>), 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.

Life Science AllianceVol. 8(2)
University of Helsinki (FI), Helsinki University Hospital (FI)
Wilhelm och Else Stockmanns Stiftelse, Finska Läkaresällskapet, Magnus Ehrnroothin Säätiö
Good health and well-being
Openalex Percentile: Top 25%
Cancer, Hypoxia, and Metabolism
0.86
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