Abstract

BackgroundBreast cancer (BC) is the most frequent female cancer and preferentially metastasizes to bone. The transcription factor TGFB-induced factor homeobox 1 (TGIF) is involved in bone metabolism. However, it is not yet known whether TGIF is associated with BC bone metastasis or patient outcome and thus of potential interest.MethodsTGIF expression was analyzed by immunohistochemistry in 1197 formalin-fixed, paraffin-embedded tissue samples from BC patients treated in the GAIN (German Adjuvant Intergroup Node-Positive) study with two adjuvant dose-dense schedules of chemotherapy with or without bisphosphonate ibandronate. TGIF expression was categorized into negative/low and moderate/strong staining. Endpoints were disease-free survival (DFS), overall survival (OS) and time to primary bone metastasis as first site of relapse (TTPBM).ResultsWe found associations of higher TGIF protein expression with smaller tumor size (p = 0.015), well differentiated phenotype (p < 0.001) and estrogen receptor (ER)-positive BC (p < 0.001). Patients with higher TGIF expression levels showed a significantly longer disease-free (DFS: HR 0.75 [95%CI 0.59–0.95], log-rank p = 0.019) and overall survival (OS: HR 0.69 [95%CI 0.50–0.94], log-rank p = 0.019), but no association with TTPBM (HR 0.77 [95%CI 0.51–1.16]; p = 0.213). Univariate analysis in molecular subgroups emphasized that elevated TGIF expression was prognostic for both DFS and OS in ER-positive BC patients (DFS: HR 0.68 [95%CI 0.51–0.91]; log-rank p = 0.009, interaction p = 0.130; OS: HR 0.60 [95%CI 0.41–0.88], log-rank p = 0.008, interaction p = 0.107) and in the HER2-negative subgroup (DFS:HR 0.67 [95%CI 0.50–0.88], log-rank p = 0.004, interaction p = 0.034; OS: HR 0.57 [95%CI 0.40–0.81], log-rank p = 0.002, interaction p = 0.015).ConclusionsOur results suggest that moderate to high TGIF expression is a common feature of breast cancer cells and that this is not associated with bone metastases as first site of relapse. However, a reduced expression is linked to tumor progression, especially in HER2-negative breast cancer.Trial registrationThis clinical trial has been registered with ClinicalTrials.gov; registration number: NCT00196872.

Highlights

  • Breast cancer (BC) is the most frequent female cancer and preferentially metastasizes to bone

  • Two hundred seventy-three patients had a recurrence, and 159 patients died within the observation period

  • In 90 cases bone metastasis was the first site of relapse

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Summary

Introduction

Breast cancer (BC) is the most frequent female cancer and preferentially metastasizes to bone. The transcription factor TGFB-induced factor homeobox 1 (TGIF) is involved in bone metabolism. It is not yet known whether TGIF is associated with BC bone metastasis or patient outcome and of potential interest. Breast cancer (BC) is the leading cancer among women in every European country but is the leading cause of death from cancer in women in Europe. The majority of deaths are not due to the primary tumor itself, but are the result of distant metastases to other organs in the body [2]. Bone metastases are largely incurable and associated with significant morbidity that negatively impacts the quality of life in metastatic BC patients. The development of BC bone metastases is a complex process involving crosstalk between disseminated BC cells and bone-derived molecules, leading to deregulation of signaling pathways critical for normal bone remodeling processes

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