Inhibition Mechanism of Acellular Dermal Matrix on Capsule Formation in Expander-Implant Breast Reconstruction After Postmastectomy Radiotherapy.

Annals of surgical oncology 2018 Vol.25(8) p. 2279-2287

Kim IK, Park SO, Chang H, Jin US

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Abstract

[BACKGROUND] Capsular contracture is one of the most common complications of expander-implant breast reconstruction. Recently, clinical reports have shown that use of an acellular dermal matrix (ADM) to cover breast implants decreases incidence of capsular contracture, but the underlying mechanism is unclear. Here, we examine how ADM reduces capsular formation in expander-implant breast reconstruction and identify cellular and molecular mechanisms of ADM-mediated reduction of capsular contracture in nonirradiated and irradiated patients.

[METHODS] Thirty patients who underwent immediate two-stage implant-based breast reconstruction were included; 15 received radiotherapy. While the tissue expander was changed to permanent silicone implant, biopsies of the subpectoral capsule and ADM capsule were performed. Capsule thickness, immunohistochemistry of α-smooth muscle actin (αSMA), vimentin, CD31, F4/80 expression, αSMA and CD31 coexpression, and relative gene expression levels of transforming growth factor (TGF)-β1 and platelet-derived growth factor (PDGF)-B were investigated.

[RESULTS] Irradiated submuscular capsules were thicker than nonirradiated submuscular capsules, but the thickness of ADM capsules did not significantly differ between nonirradiated and irradiated groups. Levels of myofibroblasts, fibroblasts, vascularity, EndoMT, and macrophages were significantly lower in ADM capsules than in submuscular capsules. With the exception of EndoMT, all others were increased in irradiated submuscular capsules compared with nonirradiated submuscular capsule, while none significantly differed between nonirradiated and irradiated ADM capsules.

[CONCLUSIONS] Use of ADM reduced myofibroblasts, vascularity, fibroblasts, and EndoMT in capsule tissues. Moreover, ADM use decreased macrophages, a key regulator of tissue fibrosis, as well as TGF-β1 and PDGF-B expression. We hope that these results provide basic concepts important for prevention of capsular contracture.

추출된 의학 개체 (NER)

유형영어 표현한국어 / 풀이UMLS CUI출처등장
재료 adm 무세포진피기질 dict 9
해부 breast 유방 dict 5
기법 submuscular 근막하 평면 dict 5
합병증 capsular contracture 피막구축 dict 4
재료 acellular dermal matrix 무세포진피기질 dict 2
해부 capsular scispacy 1
해부 cellular scispacy 1
해부 muscle actin scispacy 1
해부 myofibroblasts scispacy 1
해부 fibroblasts scispacy 1
해부 macrophages scispacy 1
해부 capsule tissues scispacy 1
해부 tissue scispacy 1
합병증 submuscular capsules scispacy 1
합병증 submuscular capsule scispacy 1
재료 silicone implant 실리콘 보형물 dict 1
약물 silicone C0037114
silicones
scispacy 1
약물 [BACKGROUND] Capsular scispacy 1
약물 [CONCLUSIONS] scispacy 1
기법 subpectoral 근막하 평면 dict 1
질환 breast implants decreases scispacy 1
질환 fibrosis C0016059
Fibrosis
scispacy 1
질환 Capsule scispacy 1
질환 expander-implant breast scispacy 1
질환 biopsies scispacy 1
질환 ADM capsule scispacy 1
기타 patients scispacy 1
기타 tissue expander scispacy 1
기타 vimentin scispacy 1
기타 CD31 scispacy 1
기타 F4/80 scispacy 1
기타 transforming growth factor scispacy 1
기타 platelet-derived growth factor scispacy 1
기타 submuscular capsules scispacy 1
기타 PDGF-B scispacy 1

MeSH Terms

Acellular Dermis; Breast Implantation; Breast Neoplasms; Combined Modality Therapy; Female; Fibrosis; Follow-Up Studies; Humans; Implant Capsular Contracture; Mammaplasty; Middle Aged; Postoperative Complications; Prognosis; Radiation Injuries; Radiotherapy, Adjuvant; Retrospective Studies; Tissue Expansion

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