Department of Biomedical Sciences, Joan C. Edwards School of Medicine, Marshall University, Huntington, WV 25755, USA.
Cabell Huntington Hospital Laboratory, Department of Pathology, Joan C. Edwards School of Medicine, Marshall University, Huntington, WV 25701, USA.
Int J Mol Sci. 2024 Oct 1;25(19):10592. doi: 10.3390/ijms251910592.
Breast cancer is the most common cancer in women with multiple risk factors including smoking, genetics, environmental factors, and obesity. Smoking and obesity are the top two risk factors for the development of breast cancer. The effect of obesity on adipose tissue mediates the pathogenesis of breast cancer in the context of obesity. Triple-negative breast cancer (TNBC) is a breast cancer subtype within which the cells lack estrogen, progesterone, and HER2 receptors. TNBC is the deadliest breast cancer subtype. The 5-year survival rates for patients with TNBC are 8-16% lower than the 5-year survival rates for patients with estrogen-receptor-positive breast tumors. In addition, TNBC patients have early relapse rates (3-5 years after diagnosis). Obesity is associated with an increased risk for TNBC, larger TNBC tumors, and increased breast cancer metastasis compared with lean women. Thus, novel therapeutic approaches are warranted to treat TNBC in the context of obesity. In this paper, we show that peritumor breast adipose-derived secretome (ADS) from patients with a high (>30) BMI is a stronger inducer of TNBC cell invasiveness and JAG1 expression than peritumor breast ADS from patients with low (<30) BMI. These findings indicate that patient BMI-associated changes in peritumor AT induce changes in peritumor ADS, which in turn acts on TNBC cells to stimulate JAG1 expression and cancer cell invasiveness.
乳腺癌是女性最常见的癌症,其多种危险因素包括吸烟、遗传、环境因素和肥胖。吸烟和肥胖是乳腺癌发展的两个最大危险因素。肥胖对脂肪组织的影响介导了肥胖背景下乳腺癌的发病机制。三阴性乳腺癌(TNBC)是一种乳腺癌亚型,其细胞缺乏雌激素、孕激素和 HER2 受体。TNBC 是最致命的乳腺癌亚型。与雌激素受体阳性乳腺癌患者相比,TNBC 患者的 5 年生存率低 8-16%。此外,TNBC 患者的早期复发率(诊断后 3-5 年)较高。与瘦女性相比,肥胖与 TNBC 的风险增加、更大的 TNBC 肿瘤和更高的乳腺癌转移风险相关。因此,需要新的治疗方法来治疗肥胖背景下的 TNBC。在本文中,我们表明,来自 BMI 较高(>30)的患者的肿瘤周围乳腺脂肪组织衍生的分泌组(ADS)比来自 BMI 较低(<30)的患者的肿瘤周围乳腺 ADS 更强地诱导 TNBC 细胞侵袭和 JAG1 表达。这些发现表明,患者 BMI 相关的肿瘤周围 AT 变化诱导了肿瘤周围 ADS 的变化,进而作用于 TNBC 细胞,刺激 JAG1 表达和癌细胞侵袭。