LASP1 interacts with N-WASP to activate the Arp2/3 complex and facilitate colorectal cancer metastasis by increasing tumour budding and worsening the pattern of invasion

• Published in: Oncogene Vol. 39; no. 35; pp. 5743 - 5755
• Main Authors: Yan, Pingping, Liu, Jian, Zhou, Rui, Lin, Chuang, Wu, Kunhe, Yang, Shibin, Yang, Shuai, Zhou, Jueyu, Xu, Lijun, Wang, Hui, Zhao, Liang
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 27.08.2020; Nature Publishing Group
• Subjects: 631/337/475; 631/67/1504/1885; 631/67/322; Actin; Adaptor Proteins, Signal Transducing - genetics; Apoptosis; Cell Biology; Colorectal cancer; Colorectal carcinoma; Colorectal Neoplasms - genetics; Colorectal Neoplasms - pathology; Cytoskeletal Proteins - genetics; Development and progression; Health aspects; Human Genetics; Humans; Internal Medicine; Invasiveness; LIM Domain Proteins - genetics; Medicine; Medicine & Public Health; Metastases; Metastasis; Muscle proteins; Neoplasm Metastasis; Oncology; Polymerization; Protein interaction; Protein-protein interactions; Proteins; Signal Transduction; Tumors; Wiskott-Aldrich Syndrome Protein - genetics; Wiskott-Aldrich Syndrome Protein - metabolism
• ISSN: 0950-9232; 1476-5594
• DOI: 10.1038/s41388-020-01397-7

LIM and SH3 protein 1 (LASP1) is a metastasis-related protein reported to enhance tumour progression in colorectal cancer (CRC). However, the underlying mechanism is still elusive. As the major biological and pathological functions of LASP1 are accomplished by its LIM and SH3 domains via protein–protein interactions, a yeast two-hybrid system was employed to screen novel LASP1-interacting proteins. N-WASP, a member of the Wiskott–Aldrich syndrome protein (WASP) family, was screened and identified as a LASP1-interacting protein overexpressed in CRC tissues. N-WASP could stimulate the migration and invasion of CRC cells in vitro and increase the formation of subcutaneous tumours, mesenteric implanted tumours and hepatic metastatic tumours. N-WASP could interact with and activate the Arp2/3 complex to stimulate actin polymerization, thus changing the migratory and invasive capabilities of CRC cells. The interaction of LASP1 with N-WASP did not influence the expression of N-WASP but recovered the reduced actin polymerization induced by N-WASP silencing. High N-WASP expression was detected in most clinical colorectal samples, and it was positively correlated with the expression of LASP1 and ARP3, as well as the tumour budding and pattern of invasion, but negatively correlated with host lymphocytic response. Our study suggests a new mechanism for LASP1-mediated CRC metastasis determined by exploring LASP1-interacting proteins and identifies N-WASP as a potential therapeutic target for CRC.