Laminin N-terminus α31 is upregulated in invasive ductal breast cancer and changes the mode of tumour invasion



Troughton, Lee, Zech, Tobias ORCID: 0000-0001-8394-088X and Hamill, Kevin ORCID: 0000-0002-7852-1944
(2020) Laminin N-terminus α31 is upregulated in invasive ductal breast cancer and changes the mode of tumour invasion. bioRxiv. 2020.05.28.120964-.

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Abstract

Laminin N-terminus α31 (LaNt α31) is an alternative splice isoform derived from the laminin α3 gene. The LaNt α31 protein is enriched around the terminal duct lobular units in normal breast tissue. In the skin and cornea the protein influences epithelial cell migration and tissue remodelling. However, LaNt α31 has never been investigated in a tumour environment. Here we analysed LaNt α31 in invasive ductal carcinoma and determined its contribution to breast carcinoma invasion. LaNt α31 expression and distribution were analysed by immunohistochemistry in human breast tissue biopsy sections and tissue microarrays covering 232 breast cancer samples. This analysis revealed LaNt α31 to be upregulated in 56 % of invasive ductal carcinoma specimens compared with matched normal tissue, and further increased in nodal metastasis compared with the tumour mass in 45 % of samples. 65.8 % of triple negative cases displayed medium to high LaNt α31 expression. To study LaNt α31 function, an adenoviral system was used to induce expression in MCF-7 and MDA-MB-231 cells. Metabolic activity, 2D cell migration, and invasion into collagen hydrogels were not significantly different between LaNt α31 overexpressing cells and control treated cells. However, LaNt α31 overexpressing MDA-MB-231 cells displayed a striking change in their mode of invasion into laminin-containing Matrigel; changing from multicellular streaming to individual cellular-invasion. In agreement with these results, 66.7% of the tumours with the highest LaNt α31 expression were non-cohesive. Together these findings indicate that breast cancer-associated changes in LaNt α31 expression could directly contribute to tumour invasiveness, and that this little-studied protein may become a therapeutic target.

Item Type: Article
Uncontrolled Keywords: Breast Cancer, Cancer, Biotechnology, 2.1 Biological and endogenous factors, 2 Aetiology, Cancer
Divisions: Faculty of Health and Life Sciences
Faculty of Health and Life Sciences > Institute of Life Courses and Medical Sciences
Faculty of Health and Life Sciences > Institute of Systems, Molecular and Integrative Biology
Depositing User: Symplectic Admin
Date Deposited: 09 Mar 2022 11:03
Last Modified: 15 Mar 2024 04:23
DOI: 10.1101/2020.05.28.120964
Related URLs:
URI: https://livrepository.liverpool.ac.uk/id/eprint/3150280