4.4 Article

Therapeutic Targeting of Integrin αvβ6 in Breast Cancer

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OXFORD UNIV PRESS INC
DOI: 10.1093/jnci/dju169

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  1. Breast Cancer Campaign [BCC 2008 May PR32]
  2. Medical Research Council [MRC G0800825]
  3. Cancer Research UK [17764, 12008] Funding Source: researchfish
  4. Medical Research Council [G0800825] Funding Source: researchfish
  5. MRC [G0800825] Funding Source: UKRI

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Background Integrin alpha v beta 6 promotes migration, invasion, and survival of cancer cells; however, the relevance and role of alpha v beta 6 has yet to be elucidated in breast cancer. Methods Protein expression of integrin subunit beta6 (beta 6) was measured in breast cancers by immunohistochemistry (n > 2000) and ITGB6 mRNA expression measured in the Molecular Taxonomy of Breast Cancer International Consortium dataset. Overall survival was assessed using Kaplan Meier curves, and bioinformatics statistical analyses were performed (Cox proportional hazards model, Wald test, and Chi-square test of association). Using antibody (264RAD) blockade and siRNA knockdown of beta 6 in breast cell lines, the role of alpha v beta 6 in Human Epidermal Growth Factor Receptor 2 (HER2) biology (expression, proliferation, invasion, growth in vivo) was assessed by flow cytometry, MTT, Transwell invasion, proximity ligation assay, and xenografts (n = 3), respectively. A student's t-test was used for two variables; three-plus variables used one-way analysis of variance with Bonferroni's Multiple Comparison Test. Xenograft growth was analyzed using linear mixed model analysis, followed by Wald testing and survival, analyzed using the Log-Rank test. All statistical tests were two sided. Results High expression of either the mRNA or protein for the integrin subunit beta 6 was associated with very poor survival (HR = 1.60, 95% CI = 1.19 to 2.15, P = .002) and increased metastases to distant sites. Co-expression of beta 6 and HER2 was associated with worse prognosis (HR = 1.97, 95% CI = 1.16 to 3.35, P = .01). Monotherapy with 264RAD or trastuzumab slowed growth of MCF-7/HER2-18 and BT-474 xenografts similarly (P < .001), but combining 264RAD with trastuzumab effectively stopped tumor growth, even in trastuzumab-resistant MCF-7/HER2-18 xenografts. Conclusions Targeting alpha v beta 6 with 264RAD alone or in combination with trastuzumab may provide a novel therapy for treating high-risk and trastuzumab-resistant breast cancer patients.

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