IL-8 and MCP-1/CCL2 regulate proteolytic activity in triple negative inflammatory breast cancer a mechanism that might be modulated by Src and Erk1/2

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dc.contributor.author Taha Mohamed, Hossam
dc.contributor.author El-Ghonaimy, Eslam A
dc.contributor.author El-Shinawi, Mohamed
dc.contributor.author Hosney, Mohamed
dc.contributor.author Götte, Martin
dc.contributor.author Woodward, Wendy A
dc.contributor.author El-Mamlouk, Tahani
dc.contributor.author Mostafa Mohamed, Mona
dc.date.accessioned 2020-06-20T08:32:26Z
dc.date.available 2020-06-20T08:32:26Z
dc.date.issued 8/15/2020
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dc.identifier.issn 0041008X
dc.identifier.other https://doi.org/10.1016/j.taap.2020.115092
dc.identifier.uri https://t.ly/KChk
dc.description Scopus en_US
dc.description.abstract Inflammatory breast cancer (IBC) is a highly metastatic and lethal breast cancer. As many as 25–30% of IBCs are triple negative (TN) and associated with low survival rates and poor prognosis. We found that the microenvironment of IBC is characterized by high infiltration of tumor associated macrophages (TAMs) and by over-expression of the cysteine protease cathepsin B (CTSB). TAMs in IBC secrete high levels of the cytokines interleukin-8 (IL-8) and monocyte chemoattractant protein-1 (MCP-1/CCL2) compared to non-IBC patients. Herein, we tested the roles of IL-8 and MCP-1/CCL2 in modulating proteolytic activity and invasiveness of TN-non-IBC as compared to TN-IBC and addressed the underlying molecular mechanism(s) for both cytokines. Quantitative real time PCR results showed that IL-8 and MCP-1/CCL2 were significantly overexpressed in tissues of TN-IBCs. IL-8 and MCP-1/CCL2 induced CTSB expression and activity of the p-Src and p-Erk1/2 signaling pathways relevant for invasion and metastasis in TN-non-IBC, HCC70 cells and TN-IBC, SUM149 cells. Dasatinib, an inhibitor of p-Src, and U0126, an inhibitor of p-Erk1/2, down-regulated invasion and expression of CTSB by HCC70 and SUM149 cells, a mechanism that is reversed by IL-8 and MCP-1/CCL2. Our study shows that targeting the cytokines IL-8 and MCP-1/CCL2 and associated signaling molecules may represent a promising therapeutic strategy in TN-IBC patients en_US
dc.language.iso en_US en_US
dc.publisher Academic Press Inc. en_US
dc.relation.ispartofseries Toxicology and Applied Pharmacology;Volume 401, 15 August 2020, Article number 115092
dc.subject Inflammatory Breast Cancer en_US
dc.subject Cathepsin B en_US
dc.subject IL-8 en_US
dc.subject MCP-1/CCL2 en_US
dc.subject Dasatinib en_US
dc.subject U0126 en_US
dc.title IL-8 and MCP-1/CCL2 regulate proteolytic activity in triple negative inflammatory breast cancer a mechanism that might be modulated by Src and Erk1/2 en_US
dc.type Article en_US
dc.identifier.doi https://doi.org/10.1016/j.taap.2020.115092
dc.Affiliation October University for modern sciences and Arts (MSA)


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