MCP‐1 expression in breast cancer and its association with distant relapse

Author:

Mulholland Bridie S.12ORCID,Hofstee Pierre13ORCID,Millar Ewan K. A.456,Bliuc Dana7ORCID,O'Toole Sandra689,Forwood Mark R.10ORCID,McDonald Michelle M.711ORCID

Affiliation:

1. Graduate School of Medicine, Faculty of Science, Medicine and Health University of Wollongong Wollongong New South Wales Australia

2. Susan Wakil School of Nursing and Midwifery, Faculty of Medicine and Health University of Sydney Camperdown New South Wales Australia

3. The Tweed Hospital Northern New South Wales Local Health District Tweed Heads New South Wales Australia

4. St George and Sutherland Clinical Campuses, School of Clinical Medicine UNSW Medicine and Health, University of New South Wales Sydney New South Wales Australia

5. Department of Anatomical Pathology, NSW Health Pathology St George Hospital Kogarah Australia

6. Translational Breast Cancer Research Group, Cancer Ecosystems Program Garvan Institute of Medical Research Sydney New South Wales Australia

7. Bone Microenvironment Group, Skeletal Diseases Program Garvan Institute of Medical Research Sydney New South Wales Australia

8. Department of Tissue Pathology and Diagnostic Pathology Royal Prince Alfred Hospital Camperdown New South Wales Australia

9. Sydney Medical School, Faculty of Medicine and Health University of Sydney Camperdown New South Wales Australia

10. School of Pharmacy and Medical Sciences Menzies Health Institute Queensland, Griffith University Gold Coast Queensland Australia

11. School of Medical Sciences, Faculty of Medicine and Health University of Sydney Camperdown New South Wales Australia

Abstract

AbstractBackgroundDistant relapse of breast cancer complicates management of the disease and accounts for 90% of breast cancer‐related deaths. Monocyte chemoattractant protein‐1 (MCP‐1) has critical roles in breast cancer progression and is widely accepted as a pro‐metastatic chemokine.MethodsThis study explored MCP‐1 expression in the primary tumour of 251 breast cancer patients. A simplified ‘histoscore’ was used to determine if each tumour had high or low expression of MCP‐1. Patient breast cancers were retrospectively staged based on available patient data. p < 0.05 was used to determine significance and changes in hazard ratios between models were considered.ResultsLow MCP‐1 expression in the primary tumour was associated with breast cancer‐related death with distant relapse in ER− breast cancers (p < 0.01); however, this was likely a result of most low MCP‐1‐expressing ER− breast cancers being Stage III or Stage IV, with high MCP‐1 expression in the primary tumour significantly correlated with Stage I breast cancers (p < 0.05). Expression of MCP‐1 in the primary ER− tumours varied across Stage I, II, III and IV and we highlighted a switch in MCP‐1 expression from high in Stage I ER− cancers to low in Stage IV ER− cancers.ConclusionThis study has emphasised a critical need for further investigation into MCP‐1's role in breast cancer progression and improved characterisation of MCP‐1 in breast cancers, particularly in light of the development of anti‐MCP‐1, anti‐metastatic therapies.

Funder

Griffith Health Institute, Griffith University

Publisher

Wiley

Subject

Cancer Research,Radiology, Nuclear Medicine and imaging,Oncology

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