MD Anderson UTHealth Houston Graduate School of Biomedical Sciences, Houston, TX, USA.
Department of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
J Mammary Gland Biol Neoplasia. 2023 Oct 6;28(1):21. doi: 10.1007/s10911-023-09548-8.
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.
炎性乳腺癌(IBC)表现为肿瘤栓子在乳腺和乳腺皮肤淋巴管中引起的快速发作肿胀和乳腺皮肤变化。IBC 与肥胖和母乳喂养持续时间有关,但这些因素如何影响 IBC 肿瘤的进展尚不清楚。我们模拟了饮食和断奶对体内淋巴管功能、IBC 肿瘤生长以及 IBC(SUM149)异种移植物接种前后乳腺微环境的影响。我们假设断奶状态和饮食会对淋巴管功能和乳腺微环境产生协同作用,从而增强 IBC 肿瘤的生长。通过体内近红外荧光(NIRF)成像来描述淋巴管结构和功能的变化。将小鼠分别喂食高脂肪饮食(HFD;60%卡路里)或正常/低脂肪饮食(LFD;10%卡路里),繁殖两次,并进行正常持续哺乳(NW)或强制断奶(FW)。在 14 个月时植入 SUM149 IBC 肿瘤;在植入前后获得图像。与喂食 LFD 的小鼠相比,喂食 HFD 的多胎小鼠在 FW 和 NW 组中表现出肿瘤前淋巴管脉冲增加。HFD 促进肿瘤生长,与断奶时间无关(P=0.04)。肿瘤前淋巴管脉冲与 8 周时的肿瘤体积相关(P=0.02),与淋巴管追踪配体 CCL21 的表达显著相关(P=0.05,表 1)。HFD 显著增加了非肿瘤侧乳腺中单核细胞衍生的 IBA1、CD163 和 CD11c 细胞的数量(P<0.0001,P<0.0001,P=0.0005)。HFD 和 FW 小鼠的乳腺导管中,淋巴管生成性 podoplanin/IBA1 巨噬细胞数量增加(均 P<0.003)。HFD 在未产小鼠中也在 14 周时引起淋巴管脉冲的类似增加(P=0.006),表明这种功能变化与产次无关。我们得出结论,HFD 诱导的乳腺淋巴管功能增加,以肿瘤起始前的脉冲率评估,并与乳腺炎症和 SUM149 肿瘤生长增加相关。饮食、淋巴管脉冲和肿瘤生长之间的关系值得进一步研究。