国际口腔医学杂志 ›› 2018, Vol. 45 ›› Issue (2): 199-203.doi: 10.7518/gjkq.2018.02.013

• 综述 • 上一篇    下一篇

药物性牙龈增生与细胞增殖和凋亡相关性的研究进展

詹烨明, 张明珠   

  1. 昆明医科大学附属口腔医院牙周科 昆明 650000
  • 收稿日期:2017-09-25 修回日期:2017-12-20 出版日期:2018-03-01 发布日期:2018-03-01
  • 通讯作者: 张明珠,副教授,博士,Email:mingzhu_2070@qq.com
  • 作者简介:詹烨明,硕士,Email:258911196@qq.com
  • 基金资助:
    云南省科学技术厅-昆明医科大学应用基础研究联合项目(2- 014FZ039)

Research progress on the relevance between drug-induced gingival overgrowth and cell proliferation and apoptosis

Zhan Yeming, Zhang Mingzhu   

  1. Dept. of Periodontics, Stomatological Hospital, Kunming Medical University, Kunming 650000, China
  • Received:2017-09-25 Revised:2017-12-20 Online:2018-03-01 Published:2018-03-01
  • Supported by:
    This study was supported by Joint Project of Application Fundamental Research, Science and Technology Department, Yunnan Province and Kunming Medical University (2014FZ039).

摘要: 药物性牙龈增生是指长期服用某些药物(如钙通道阻滞剂、抗癫痫药物和免疫抑制剂)为主要因素而诱发的牙龈体积增大,其发病机制尚未完全明确。近年来研究发现,牙龈增生与细胞的增殖和凋亡有密切关系,本文就药物性牙龈增生与细胞增殖和凋亡的相关性研究进展进行综述。

关键词: 药物性牙龈增生, 细胞增殖, 凋亡, 炎症

Abstract: Patients who received a long-term drug therapy, including calcium channel blockers, antiepileptic and immunosuppressive drugs, often suffered from drug-induced gingival overgrowth (DIGO). However, the pathogenesis of DIGO remains unclear to date. A number of research found that DIGO is relevant to apoptosis and cell proliferation. Research progress on the relevance between drug-induced gingival overgrowth and the apoptosis and cell proliferation is summarised in this paper.

Key words: drug-induced gingival overgrowth, cell proliferation, apoptosis, inflammation

中图分类号: 

  • R781.4+1
[1] Kantarci A, Augustin P, Firatli E, et al.Apoptosis in gingival overgrowth tissues[J]. J Dent Res, 2007, 86(9):888-892.
[2] 黄雅玲, 李升, 杨明华. 药物性牙龈增生发病机制的研究进展[J]. 国际口腔医学杂志, 2008, 35(4): 414-417.
Huang YL, Li S, Yang MH.Progress in research on the pathogenesis of drug-induced gingival over-growth[J]. Int J Stomatol, 2008, 35(4):414-417.
[3] 刘培红, 马肃. 环孢素诱导牙龈上皮细胞增生的机制[J]. 国际口腔医学杂志, 2009, 36(1):81-83.
Liu PH, Ma S.Pathogenesis of ciclosporin-induced gingival epithelial hyperplasia[J]. Int J Stomatol, 2009, 36(1):81-83.
[4] Cetinkaya BO, Pamuk F, Keles GC, et al.The role of phosphatase and tensin homolog in drug-induced gingival overgrowth[J]. J Periodont Res, 2014, 49(3):307-313.
[5] Ponnaiyan D, Jegadeesan V.Cyclosporine A: novel concepts in its role in drug-induced gingival over-growth[J]. Dent Res J (Isfahan), 2015, 12(6):499-506.
[6] Chen J, Yang F, Yu X, et al.Cyclosporine A pro-motes cell proliferation, collagen and α-smooth muscle actin expressions in rat gingival fibroblasts by Smad3 activation and miR-29b suppression[J]. J Periodont Res, 2016, 51(6):735-747.
[7] Sobral LM, Aseredo F, Agostini M, et al.Molecular events associated with ciclosporin A-induced gin-gival overgrowth are attenuated by Smad7 overex-pression in fibroblasts[J]. J Periodont Res, 2012, 47(2):149-158.
[8] Chiang CY, Tu HP, Chen YT, et al.Up-regulation of retinoblastoma protein phosphorylation in gingiva after cyclosporine A treatment: an in vivo and in vitro study[J]. J Periodontal Res, 2011, 46(2):158-163.
[9] Takeuchi R, Matsumoto H, Akimoto Y, et al.Inhi-bition of G1 cell cycle arrest in human gingival fibro-blasts exposed to phenytoin[J]. Fundam Clin Phar-macol, 2012, 28(1):114-119.
[10] Tsai CH, Yu CC, Lee SS, et al.Upregulation of Slug expression by cyclosporine A contributes to the pathogenesis of gingival overgrowth[J]. J Formos Med Assoc, 2016, 115(8):602-608.
[11] Lin YH, Yu CC, Lee SS, et al.Elevated Snail ex-pression in human gingival fibroblasts by cyclos-porine A as the possible pathogenesis for gingival overgrowth[J]. J Formos Med Assoc, 2015, 114(12):1181-1186.
[12] 肖娟, 赵慧. 苯妥英钠性牙龈增生的病理机制[J]. 国际口腔医学杂志, 2012, 39(2):260-264.
Xiao J, Zhao H.Pathomechanism of phenytoin-in-duced gingival over-growth[J]. Int J Stomatol, 2012, 39(2):260-264.
[13] Takeuchi R.The effect of basic fibroblast growth factor on cell cycle in human gingival fibroblasts from nifedipine responder and non-responder[J]. J Oral Sci, 2004, 46(1):37-44.
[14] 顾奕, 于明琨, 吕立权, 等. p53、BCL-2、Caspase- 3等凋亡相关蛋白在大鼠脑损伤中的表达及意义[J]. 现代生物医学进展, 2011, 11(11):2030-2033.
Gu Y, Yu MK, Lü LQ, et al.Expression of p53, BCL-2 and caspase-3 in rats with brain injury[J]. Prog Modern Biomed, 2011, 11(11):2030-2033.
[15] Takeuchi R, Matsumoto H, Akimoto Y, et al.Reduc-tion in lipopolysaccharide-induced apoptosis of fi-broblasts obtained from a patient with gingival overgrowth during nifedipine-treatment[J]. Arch Oral Biol, 2011, 56(10):1073-1080.
[16] Ma S, Liu P, Li Y, et al.Cyclosporine a inhibits apo-ptosis of rat gingival epithelium[J]. J Periodontol, 2014, 85(8):1126-1134.
[17] Mitic K, Popovska M, Pandilova M, et al.The role of inflammation and apoptosis in cyclosporine A- induced gingival overgrowth[J]. Bosn J Basic Med Sci, 2013, 13(1):14-20.
[18] 王艳春. 低浓度硝苯地平诱导人牙龈上皮细胞Bcl-2, Bax及P53表达的实验研究[D]. 昆明: 昆明医科大学, 2014.
Wang YC.Experimental study on the expression of Bcl-2, Bax and P53 in human gingival epithelial cells induced by low concentration nifedipine[D]. Kunming: Kunming Medical University, 2014.
[19] 周洁, 潘亚萍. 牙龈卟啉单胞菌感染宿主细胞后对其凋亡调控研究进展[J]. 中国实用口腔科杂志, 2016, 9(5):308-311.
Zhou J, Pan YP.Research progress of Porphyro-monas gingivalis infection on mediation of apoptosis in host cells[J]. Chin J Pract Stomatol, 2016, 9(5): 308-311.
[20] Ogawa T, Ozaki A, Shimauchi H, et al.Hyporespon-siveness of inflamed human gingival fibroblasts from patients with chronic periodontal diseases against cell surface components of Porphyromonas gin-givalis[J]. FEMS Immunol Med Microbio, 1997, 18(1):17-30.
[21] Fujita T, Yoshimoto T, Matsuda S, et al.Interleukin- 8 induces DNA synthesis, migration and down-regula-tion of cleaved caspase-3 in cultured human gingival epithelial cells[J]. J Periodontal Res, 2015, 50(4):479-485.
[22] Gölz L, Memmert S, Rath-Deschner B, et al.Hypoxia and P. gingivalis synergistically induce HIF-1 and NF-κB activation in PDL cells and periodontal di-seases[J]. Mediators Inflamm, 2015, 2015: 438085.
[23] Schaumann T, Kraus D, Winter J, et al.Potential immune modularly role of glycine in oral gingival inflammation[J]. Clin Dev Immunol, 2013, 2013: 808367.
[24] Akiyama S, Amano A, Kato T, et al.Relationship of periodontal bacteria and Porphyromonas gingivalis fimA variations with phenytoin-induced gingival overgrowth[J]. Oral Dis, 2006, 12(1):51-56.
[25] Gong Y, Bi W, Cao L, et al.Association of CD14- 260 polymorphisms, red-complex periodontopatho-gens and gingival crevicular fluid cytokine levels with cyclosporine A-induced gingival overgrowth in renal transplant patients[J]. J Periodontal Res, 2013, 48(2):203-212.
[26] Trackman PC, Kantarci A.Molecular and clinical aspects of drug-induced gingival overgrowth[J]. J Dent Res, 2015, 94(4):540-546.
[27] 余方方, 叶新, 陈栋, 等. 苯妥英钠对内毒素作用下人牙周膜成纤维细胞增殖和表达TNF-α的影响[J]. 牙体牙髓牙周病学杂志, 2015, 25(7):396-399.
Yu FF, Ye X, Chen D, et al.Effects of phenytoin on the proliferation and tumor necrosis factor-α expre-ssion in LPS-treated human periodontal ligament fibroblasts[J]. Chin J Conserv Dent, 2015, 25(7):396-399.
[28] 韦艺,郭新程,周嫣,等. 环孢素A和肿瘤坏死因子α对人牙龈成纤维细胞增殖的影响[J]. 中华口腔医学杂志, 2012, 47(1):38-42.
Wei Y, Guo XC, Zhou Y, et al.Effect of cyclosporin A and tumor necrosis factor-α on cell proliferation of cultured human gingival fibroblasts[J]. Chin J Sto-matol, 2012, 47(1):38-42.
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