High-fat diet, but not duration of lactation, increases mammary gland lymphatic vessel function and subsequent growth of inflammatory breast cancer cells

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作者
Wintana Balema
Janelle Morton
Richard A. Larson
Li Li
Fred Christian Velasquez
Natalie W. Fowlkes
Savitri Krishnamurthy
Bisrat G. Debeb
Eva Sevick-Muraca
Wendy A. Woodward
机构
[1] MD Anderson UTHealth Houston Graduate School of Biomedical Sciences,Department of Experimental Radiation Oncology
[2] The University of Texas MD Anderson Cancer Center,The Morgan Welch IBC Clinic and Research Program
[3] The University of Texas MD Anderson Cancer Center,Department of Breast Medical Oncology
[4] The University of Texas Health Science Center,undefined
[5] Institute of Molecular Imaging,undefined
[6] Center for Molecular Imaging,undefined
[7] Department of Veterinary Medicine and Surgery,undefined
[8] UT MD Anderson Cancer Center,undefined
[9] Department of Pathology,undefined
[10] UT MD Anderson Cancer Center,undefined
[11] The University of Texas MD Anderson Cancer Center,undefined
[12] Department of Breast Radiation Oncology,undefined
[13] UT MD Anderson Cancer Center,undefined
关键词
High fat diet; IBC; Inflammatory breast cancer; Lymphatic pulsing; Podoplanin; Mammary gland; Weaning; Lactation; Pregnancy; Microenvironment; IBA1; CD163; PoEM;
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摘要
Inflammatory breast cancer (IBC) presents as rapid-onset swelling and breast skin changes caused by tumor emboli in the breast and breast skin lymphatics. IBC has been linked with obesity and duration of breastfeeding, but how these factors affect IBC tumor progression is not clear. We modeled the simultaneous effects of diet and weaning in mice on in vivo lymphatic function; on IBC tumor growth; and on aspects of the mammary gland microenvironment before and after IBC (SUM149) xenograft inoculation. We hypothesized that weaning status and diet would have synergistic effects on lymphatic function and the breast microenvironment to enhance IBC tumor growth. Changes in lymphatic structure and function were characterized with in vivo near-infrared fluorescence (NIRF) imaging. Mice were fed either a high-fat diet (HFD; 60 kcal%) or a normal/low-fat diet (LFD; 10 kcal%), bred twice, and subjected to either normal-duration nursing (NW) or forced weaning (FW). SUM149 IBC tumors were implanted at 14 months; images were obtained before and after implantation. Multiparous mice fed HFD showed increased pre-tumor lymphatic pulsing in both the FW and NW groups relative to mice fed LFD. HFD promoted tumor growth independent of weaning time (P = 0.04). Pre-tumor lymphatic pulsing was associated with tumor volume at 8 weeks (P = 0.02) and was significantly correlated with expression of the lymphatic tracking ligand CCL21 (P = 0.05, Table 1). HFD significantly increased the numbers of monocyte-derived IBA1+, CD163+, and CD11c+ cells (P < 0.0001, P < 0.0001, P = 0.0005) in the contralateral, non-tumor-bearing mammary gland. Numbers of lymphangiogenic podoplanin+/IBA1+ macrophages were increased in the ducts of HFD and FW mice (all P < 0.003). HFD in nulliparous mice had a similar increase in lymphatic pulsing at 14 weeks (P = 0.006), indicating that this functional change was independent of parity. We conclude that HFD induced increases in mammary gland lymphatic function, assessed as pulsing rate before tumor initiation, and correlated with inflammation in the mammary gland and increased SUM149 tumor growth. The relationship between diet, lymphatic pulsing, and tumor growth warrants further investigation.
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