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上皮—间质转化及其与头颈鳞状细胞癌的耐药性

Epithelial—mesenchymal transformation and association with chemoresistace in head and neck cancer
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摘要 上皮—间质转化(EMT)是对上皮来源的细胞发生表型转化过程的概括,主要参与胚胎发育和肿瘤进展,并在化学治疗耐药中发挥重要的作用。耐药是肿瘤化学治疗不能取得治愈性疗效的重要原因之一,明确化学治疗耐药机制,对于准确预测肿瘤细胞对化学治疗药物的敏感性以及如何逆转耐药以保证化学治疗持续有效,从而提高临床疗效和患者的长期生存率具有十分重要的意义。本文就EMT及其生物学意义、肿瘤化学治疗的耐药机制、EMT与化学治疗耐药的关系、EMT与头颈鳞状细胞癌的化学治疗耐药性等研究进展作一综述。 The differentiated epithelial cells could be transformed into mesenchymal cells through a cellular program named epithelial—mesenchymal transformation(EMT),which plays an important role in development,carcinoma invasion and also chemoresistance.Since chemoresistance always cause the failure of chemotherapy,to overcome chemoresistance is key to maintain the effectiveness of chemotherapy.This article reviews EMT and its biological significance,its association with chemoresistace,especially in head and neck cancer.
出处 《国际口腔医学杂志》 CAS 2011年第5期539-541,共3页 International Journal of Stomatology
关键词 上皮—间质转化 耐药机制 肿瘤 epithelial—mesenchymal transformation chemoresistance tumor
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参考文献20

  • 1Thomson S, Buck E, Pctti F, et al. Epithelial to mesen- chymal transition is a determinant of sensitivity of non- small-cell lung carcinoma cell lines and xenografts to epidermal growth factor receptor inhibition[J]. Cancer Rcs, 2005, 65 (20) : 9455-9462.
  • 2Greenburg G, Hay ED. Epithelia suspended in collagen gels can lose polarity and express characteristics of mi- grating mesenchymal cells[J]. J Cell Biol, 1982, 95 (1): 333-339.
  • 3Yang J, Weinberg RA. Epithelial--mesenchymal transi- tion: At the crossroads of development and tumor metas- tasis[J]. Dev Cell, 2008, 14(6) :818-829.
  • 4Acloque H, Adams MS, Fishwick K, et al. Epithelial-- mesenchymal transitions: The importance of changing cell state in development and disease[J]. J Clin Invest, 2009, 119(6) : 1438-1449.
  • 5Yah C, Grimm WA, Garner WL, et al. Epithelial to me- senchymal transition in human skin wound healing is in- duced by tumor necrosis factor-alpha through bone mor- phogenic protein-2[J]. Am J Pathol, 2010, 176(5):2247- 2258.
  • 6Lopez-Novoa JM, Nieto MA. Inflammation and EMT: An alliance towards organ fibrosis and cancer progression[J]. EMBO Mol Med, 2009, 1 (6/7) : 303-314.
  • 7Ma L, Teruya-Feldstein J, Weinberg RA. Ttanour inva- sion and metastasis initiated by microRNA-10b in breast cancer[J]. Nature, 2007, 449 (7163) : 682-688.
  • 8Chaffer CL Brennan JP, Slavin JL, et al. Mesenchymal- to-epithelial transition facilitates bladder cancer metas- tasis: Role of fihroblast growth factor receptor-2[J]. Can- cer Res, 2006, 66(23) : 11271-11278.
  • 9Lee TK, Man K, Poon RT, et al. Signal transducers and activators of transcription 5b activation enhances hepato- cellular carcinoma aggressiveness through induction of epithelial-mesenchymal transition[J]. Cancer Res, 2006, 66 (20) : 9948-9956.
  • 10Alonso SR, Tracey L, Ortiz P, et al. A high-throughput study in melanoma identifies epithelial--mesenchymal tra- nsition as a major determinant of metastasis[J]. Cancer Res, 2007, 67 (7) : 3450-3460.

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