Effect of PECAM-1 and SMA on the prognosis of keloid after comprehensive treatment
YANG Yifei1,2, XU hui1,2, LONG Weiguo3, LI Yumei1,2
(1. Department of Dermatology, Affiliated Hospital of Jiangsu University, Zhenjiang Jiangsu 212001; 2. Jiangsu University Institute for Regenerative Medicine, Zhenjiang Jiangsu 212001; 3. Department of Pathology, Affiliated Hospital of Jiangsu University, Zhenjiang Jiangsu 212001, China)
Abstract: Objective: To explore the effect of the expression levels of platelet endothelial cell adhesion molecule-1 (PECAM-1) and smooth muscle actin (SMA) in the blood vessels of keloid on the prognosis of comprehensive treatment of keloid. Methods: From August 2020 to June 2022, a total of 61 patients with keloids diagnosed and treated in the Department of Dermatology, Affiliated Hospital of Jiangsu University were retrospectively analyzed, with a total of 69 keloids. All patients received comprehensive treatment of surgical resection and 90Sr isotope application. Immunohistochemical staining was used to detect the expression levels of PECAM-1 and SMA in blood vessels of surgically resected keloid specimens. All patients were followed up for 6 months by telephone and outpatient service. Results: A total of 19 (27.5%) keloids recurred within 6 months, and 11 (15.9%) had adverse reactions after 90Sr isotope application. The high expression rates of PECAM-1 and SMA in the recurrence group were higher than those in the non-relapse group (χ2=7.496, P=0.006; χ2=5.197, P=0.023); the incidence of adverse reactions after treatment had no significant association with the expression levels of PECAM-1 and SMA (χ2=0.172, P=0.935; χ2=1.110, P=0.484). Conclusion: The expression levels of PECAM-1 and SMA in keloid blood vessels were negatively correlated with the prognosis of comprehensive treatment, and they may be potential indicators for judging the prognosis of keloid.
羊逸飞1,2, 许辉1,2, 龙卫国3, 李遇梅1,2. 血小板内皮细胞黏附分子1和平滑肌肌动蛋白对瘢痕疙瘩综合治疗预后的影响[J]. 江苏大学学报:医学版, 2024, 24(01): 57-60.
YANG Yifei1,2, XU hui1,2, LONG Weiguo3, LI Yumei1,2. Effect of PECAM-1 and SMA on the prognosis of keloid after comprehensive treatment. Journal of Jiangsu University(Medicine Edition), 2024, 24(01): 57-60.
[1]Shim J, Oh SJ, Yeo E, et al. Integrated analysis of singlecell and spatial transcriptomics in keloids: highlights on fibrovascular interactions in keloid pathogenesis[J]. J Invest Dermatol, 2022, 142(8): 2128-2139.
[2]Liu X, Chen W, Zeng Q, et al. singlecell RNAsequencing reveals lineagespecific regulatory changes of fibroblasts and vascular endothelial cells in keloids[J]. J Invest Dermatol, 2022, 142(1): 124-135.
[4]Dey N, De P, Brian LJ. Evading antiangiogenic therapy: resistance to antiangiogenic therapy in solid tumors[J]. Am J Transl Res, 2015, 7(10): 1675-1698.
[5]Limandjaja GC, Niessen FB, Scheper RJ, et al. Hypertrophic scars and keloids: Overview of the evidence and practical guide for differentiating between these abnormal scars[J]. Exp Dermatol, 2021, 30(1): 146-161.
[7]Gastl G, Spizzo G, Obrist P, et al. EpCAM overexpression in breast cancer as a predictor of survival[J]. Lancet, 2000, 356(9246): 1981-1982.
[8]Mankowski P, Kanevsky J, Tomlinson J, et al. Optimizing radiotherapy for keloids: a metaanalysis systematic review comparing recurrence rates between different radiation modalities[J]. Ann Plast Surg, 2017, 78(4): 403-411.
[9]Renz P, Hasan S, Gresswell S, et al. Dose effect in adjuvant radiation therapy for the treatment of resected keloids[J]. Int J Radiat Oncol Biol Phys, 2018, 102(1): 149-154.
[11]Limandjaja GC, van den Broek LJ, Waaijman T, et al. Reconstructed human keloid models show heterogeneity within keloid scars[J]. Arch Dermatol Res, 2018, 310(10): 815-826.
[12]Suttho D, Mankhetkorn S, Binda D, et al. 3D modeling of keloid scars in vitro by cell and tissue engineering[J]. Arch Dermatol Res, 2017, 309(1): 55-62.
[13]Limandjaja GC, Belien JM, Scheper RJ, et al. Hypertrophic and keloid scars fail to progress from the CD34 /αsmooth muscle actin (αSMA)+immature scar phenotype and show gradient differences in αSMA and p16 expression[J]. Br J Dermatol, 2020, 182(4): 974-986.
[14]Rask L, Hgdall CK, Kjaer SK, et al. Association of CD31 and p53 with survival of ovarian cancer patients[J]. Anticancer Res, 2019, 39(2): 567-576.
[15]Wimmer I, Tietz S, Nishihara H, et al. PECAM1 stabilizes bloodbrain barrier integrity and favors paracellular TCell diapedesis across the bloodbrain barrier during neuroinflammation[J]. Front Immunol, 2019, 10: 711.
[16]Deng K, Xiao H, Liu X, et al. Strontium90 brachytherapy following intralesional triamcinolone and 5fluorouracil injections for keloid treatment: A randomized controlled trial[J]. PLoS One, 2021, 16(3): e0248799.