Department of Biomedical Engineering, College of Engineering, The Ohio State University, Columbus, Ohio, United States of America.
Department of Biochemistry and Molecular Biology, Hollings Cancer Center, Medical University of South Carolina, Charleston, South Carolina, United States of America.
PLoS One. 2021 Feb 3;16(2):e0245653. doi: 10.1371/journal.pone.0245653. eCollection 2021.
Collagen deposition contributes to both high mammographic density and breast cancer progression. Low stromal PTEN expression has been observed in as many as half of breast tumors and is associated with increases in collagen deposition, however the mechanism connecting PTEN loss to increased collagen deposition remains unclear. Here, we demonstrate that Pten knockout in fibroblasts using an Fsp-Cre;PtenloxP/loxP mouse model increases collagen fiber number and fiber size within the mammary gland. Pten knockout additionally upregulated Sparc transcription in fibroblasts and promoted collagen shuttling out of the cell. Interestingly, SPARC mRNA expression was observed to be significantly elevated in the tumor stroma as compared to the normal breast in several patient cohorts. While SPARC knockdown via shRNA did not affect collagen shuttling, it notably decreased assembly of exogenous collagen. In addition, SPARC knockdown decreased fibronectin assembly and alignment of the extracellular matrix in an in vitro fibroblast-derived matrix model. Overall, these data indicate upregulation of SPARC is a mechanism by which PTEN regulates collagen deposition in the mammary gland stroma.
胶原蛋白沉积既有助于提高乳房 X 光密度,也有助于促进乳腺癌的进展。多达一半的乳腺肿瘤中观察到基质中 PTEN 表达降低,并且与胶原蛋白沉积的增加有关,然而,将 PTEN 缺失与胶原蛋白沉积增加联系起来的机制尚不清楚。在这里,我们通过使用 Fsp-Cre;PtenloxP/loxP 小鼠模型证明,成纤维细胞中的 Pten 敲除会增加乳腺中胶原纤维的数量和纤维大小。此外,成纤维细胞中的 Pten 敲除还上调了 Sparc 的转录,并促进胶原蛋白从细胞内逸出。有趣的是,与正常乳腺相比,在几个患者队列中观察到肿瘤基质中的 SPARC mRNA 表达显著升高。虽然通过 shRNA 敲低 SPARC 并不影响胶原蛋白的逸出,但它显著降低了外源性胶原蛋白的组装。此外,SPARC 敲低还降低了体外成纤维细胞衍生基质模型中纤维连接蛋白的组装和细胞外基质的排列。总体而言,这些数据表明,SPARC 的上调是 PTEN 调节乳腺基质中胶原蛋白沉积的一种机制。