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Proliferating macrophages associated with high grade, hormone receptor negative breast cancer and poor clinical outcome
Authors:Michael J Campbell  Nathan Y Tonlaar  Elisabeth R Garwood  Dezheng Huo  Dan H Moore  Andrey I Khramtsov  Afred Au  Frederick Baehner  Yinghua Chen  David O Malaka  Amy Lin  Oyinlolu O Adeyanju  Shihong Li  Can Gong  Michael McGrath  Olufunmilayo I Olopade  Laura J Esserman
Institution:1. Department of Surgery, University of California, San Francisco, USA
2. Pritzker School of Medicine, University of Chicago, Chicago, USA
3. Department of Health Studies, University of Chicago, Chicago, USA
4. Department of Epidemiology and Biostatistics, University of California, San Francisco, USA
5. Department of Medicine, University of Chicago, Chicago, USA
6. Department of Pathology, University of California, San Francisco, USA
7. Department of Pathology, University of Chicago, Chicago, USA
8. Department of Laboratory Medicine and Medicine, San Francisco General Hospital, University of California, San Francisco, USA
9. Carol F. Buck Breast Care Center, 1600 Divisadero St, Box 1710, San Francisco, CA, 94115, USA
Abstract:Macrophages, a key cell in the inflammatory cascade, have been associated with poor prognosis in cancers, including breast cancer. In this study, we investigated the relationship of a subset of macrophages??proliferating macrophages (promacs)??with clinico-pathologic characteristics of breast cancer, including tumor size, grade, stage, lymph node metastases, hormone receptor status, subtype, as well as early recurrence, and survival. This study included a discovery and validation set that was conducted at two institutions and laboratories (University of California, San Francisco and University of Chicago) using two independent cohorts of patients with breast cancer. Formalin-fixed, paraffin-embedded sections and/or tissue microarrays were double-stained with anti-CD68 (a macrophage marker) and anti-PCNA (a proliferation marker) antibodies. The presence of intratumoral promacs was significantly correlated with high grade, hormone receptor negative tumors, and a basal-like subtype. In contrast, there was no correlation between promacs and tumor size, stage, or the number of the involved lymph nodes. These findings were consistent between the two study cohorts. Finally, promac numbers were a significant predictor of recurrence and survival. In the pooled analysis, elevated promac levels were associated with a 77% increased risk of dying (P?=?0.015). The presence of promacs in human breast cancer may serve as a prognostic indicator for poor outcomes and early recurrence and serve as a potential cellular target for novel therapeutic interventions.
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