Cohen Noam A, Lai Stephen Y, Ziober Amy F, Ziober Barry L
Department of Otorhinolaryngology-Head and Neck Surgery Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
Laryngoscope. 2004 Mar;114(3):418-23. doi: 10.1097/00005537-200403000-00006.
OBJECTIVES/HYPOTHESIS: Tumor hypoxia appears to be closely associated with tumor propagation, malignant progression, and resistance to radiotherapy. Hypoxia inducible factor-1alpha (HIF-1alpha) is a transcription factor that is upregulated under hypoxic conditions and activates hypoxic adaptation pathways which include neovascularization, erythropoiesis, and glycolysis. Hypoxia inducible factor-1alpha is under tight regulation with undetectable levels of expression in normoxia and robust expression in hypoxia. Mutations that activate oncogenes or inactivate tumor suppressor genes increase the expression of HIF-1alpha. Furthermore, it has been demonstrated that HIF-1alpha is overexpressed in head and neck squamous cell carcinoma and that the degree of expression has predictive and prognostic significance for patients undergoing radiotherapy. The study investigated whether overexpression of HIF-1alpha in head and neck squamous cell carcinoma results from a physiological response to local hypoxia or from oncogenic mutational progression.
Expression of HIF-1alpha under normoxic and hypoxic conditions was evaluated in cell lines derived from head and neck squamous cell carcinoma. Cell lines that were used displayed varying degrees of in vitro invasiveness.
Hypoxia inducible factor-1alpha expression was detected by Western blot analysis. Cells were treated for 3 hours in 1% oxygen, then re-exposed to normoxia for varying times before lysis and detection of HIF-1alpha.
Under normoxic conditions, HIF-1alpha expression was upregulated in invasive cells compared with noninvasive cells, and the degradation of HIF-1alpha following a hypoxic stimulus was blunted in invasive cells as compared with noninvasive cells.
The authors presented evidence that dysregulation of HIF-1alpha may play a role in the malignant progression of head and neck squamous cell carcinoma. It is likely that dysregulated expression of the transcription factor HIF-1alpha contributes to the invasive properties associated with hypoxia and advanced head and neck squamous cell carcinoma.
目的/假设:肿瘤缺氧似乎与肿瘤增殖、恶性进展及放疗抵抗密切相关。缺氧诱导因子-1α(HIF-1α)是一种转录因子,在缺氧条件下上调,并激活包括新血管生成、红细胞生成和糖酵解在内的缺氧适应途径。缺氧诱导因子-1α受到严格调控,在常氧条件下表达水平不可检测,而在缺氧时表达强烈。激活癌基因或使肿瘤抑制基因失活的突变会增加HIF-1α的表达。此外,已有研究表明HIF-1α在头颈部鳞状细胞癌中过表达,且表达程度对接受放疗的患者具有预测和预后意义。本研究调查了头颈部鳞状细胞癌中HIF-1α的过表达是对局部缺氧的生理反应还是致癌突变进展的结果。
在源自头颈部鳞状细胞癌的细胞系中评估常氧和缺氧条件下HIF-1α的表达。所使用的细胞系显示出不同程度的体外侵袭性。
通过蛋白质印迹分析检测缺氧诱导因子-1α的表达。细胞在1%氧气中处理3小时,然后在不同时间重新暴露于常氧,之后进行裂解并检测HIF-1α。
在常氧条件下,与非侵袭性细胞相比,侵袭性细胞中HIF-1α的表达上调,并且与非侵袭性细胞相比,缺氧刺激后侵袭性细胞中HIF-1α的降解减弱。
作者提供的证据表明,HIF-1α的失调可能在头颈部鳞状细胞癌的恶性进展中起作用。转录因子HIF-1α的失调表达可能导致与缺氧和晚期头颈部鳞状细胞癌相关的侵袭特性。