包膜挛缩
医学
植入
MMP3型
免疫染色
硅酮
乳房植入物
基因表达
假体周围
病理
基因
免疫组织化学
外科
内科学
生物
关节置换术
乳腺癌
乳房再造术
化学
有机化学
癌症
生物化学
作者
Giulia Daneshgaran,Daniel J. Gardner,Hsuan-Hsiu Annie Chen,Solmaz Niknam‐Bienia,Vinaya Soundarajan,Anjali C. Raghuram,Gene Kim,Paweł P. Łabaj,David P. Kreil,Charles Wang,Young‐Kwon Hong,Alex K. Wong
标识
DOI:10.1097/prs.0000000000009800
摘要
Purpose: Silicone breast implants with smooth outer shells are associated with higher rates of capsular contracture, while textured implants have been linked to the development of breast implant-associated ALCL. By assessing the gene expression profile of fibrous capsules formed in response to smooth and textured implants, we can gain insight into the development of breast implant-associated pathologies. Methods: Miniature smooth or textured silicone implants were surgically inserted into female rats (n=10) and harvested for the surrounding capsules on postoperative week 6. RNA sequencing and quantitative polymerase chain reaction were performed to identify genes differentially expressed between smooth and textured capsules. For clinical correlation, the expression of candidate genes was assayed in implant capsules harvested from human patients with and without capsular contracture. Results: Out of 18,555 differentially expressed transcripts identified, three candidate genes were selected: matrix metalloproteinase-3 (MMP3), troponin-T3 (TNNT3) and neuregulin-1 (NRG1). In textured capsules, relative gene expression and immunostaining of MMP3 and TNNT3 was upregulated while NRG1 was downregulated compared to smooth capsules (mean relative fold change: 8.79, p=0.0059; 4.81, p=0.0056; 0.40, p<0.0001, respectively). Immunostaining of human specimens with capsular contracture revealed similar gene expression patterns to those of animal-derived smooth capsules. Conclusion: An expression pattern of low MMP3/low TNNT3/high NRG1 is specifically associated with smooth implant capsules and human implant capsules with capsular contracture. Our clinically relevant breast implant rat model provides a strong foundation to further explore the molecular genetics of implant texture and its effect on breast implant-associated pathologies.
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