Ontario Cancer Institute/Princess Margaret Hospital and The Campbell Family Institute for Cancer Research, Toronto, Ontario, Canada.
Cancer. 2012 Jun 15;118(12):3105-15. doi: 10.1002/cncr.26635. Epub 2011 Oct 25.
Hedgehog (Hh) signaling was assessed in patients with primary cervical carcinoma who were receiving chemoradiation. Because the up-regulation of Hh has been reported in response to hypoxia, the authors examined associations between Hh gene expression and measurements of HP5 (the percentage of oxygen pressure readings in each tumor <5 mm Hg) and interstitial fluid pressure (IFP).
Sonic hedgehog (SHH), Indian hedgehog (IHH), patched 1 and 2 (PTCH1 and PTCH2), smoothened (SMO), and glioma-associated oncogene family zinc finger 1 (Gli1) expression levels were determined using quantitative reverse transcriptase-polymerase chain reaction analysis on 85 frozen samples of primary cervical carcinoma and on 16 normal cervical samples. Clinicopathologic data were collected prospectively. Possible correlations between Hh expression and tumor hypoxia (HP5 and IFP) measured at the time of biopsy, the time to local recurrence, and disease-free survival (DFS) were examined.
At least 1 member of the Hh pathway was elevated in all but 1 tumor compared with normal tissue (P < .0001). Hh gene expression was heterogeneous with SHH, IHH, and GLI exhibiting bimodal distribution. Elevation of SHH expression (P = .04) and low SMO expression (P = .0007) were associated with HP5. The risk of local recurrence was associated with the up-regulation of SMO (hazard ratio [HR], 2.41; 95% confidence interval [CI], 1.00-5.82; P = .044), the up-regulation of >3 Hh genes (HR, 2.56; 95% CI, 1.09-6.00; P = .026), tumor size (HR, 1.41; 95% CI, 1.14-1.74; P = .0015), and lymph node-positive disease (HR, 2.82; 95% CI, 1.16-6.86; P = .022).
The proportion of tumors that expressed Hh genes in cervical cancer was very high. The current data support a role for the Hh pathway in repopulation after chemoradiation and suggest that SMO may be a valid therapeutic target. The authors concluded that further investigation into this pathway after radiation and Hh inhibition are warranted.
评估接受放化疗的原发性宫颈癌患者的 Hedgehog(Hh)信号。由于 Hh 的上调已被报道是对缺氧的反应,作者研究了 Hh 基因表达与 HP5(每个肿瘤中氧压力读数<5mmHg 的百分比)和间质液压力(IFP)测量值之间的关联。
使用定量逆转录聚合酶链反应分析对 85 例原发性宫颈癌冷冻样本和 16 例正常宫颈样本进行了 Sonic Hedgehog(SHH)、Indian Hedgehog(IHH)、patched 1 和 2(PTCH1 和 PTCH2)、smoothened(SMO)和 Glioma-associated oncogene family zinc finger 1(Gli1)表达水平的测定。前瞻性收集临床病理数据。检查 Hh 表达与活检时测量的肿瘤缺氧(HP5 和 IFP)、局部复发时间和无病生存(DFS)之间的可能相关性。
与正常组织相比,除 1 例肿瘤外,所有肿瘤中至少有一种 Hh 途径的成员升高(P<0.0001)。Hh 基因表达具有异质性,SHH、IHH 和 GLI 呈双峰分布。SHH 表达升高(P=0.04)和 SMO 表达降低(P=0.0007)与 HP5 相关。局部复发的风险与 SMO 的上调相关(危险比[HR],2.41;95%置信区间[CI],1.00-5.82;P=0.044),>3 个 Hh 基因的上调(HR,2.56;95%CI,1.09-6.00;P=0.026),肿瘤大小(HR,1.41;95%CI,1.14-1.74;P=0.0015)和淋巴结阳性疾病(HR,2.82;95%CI,1.16-6.86;P=0.022)。
宫颈癌中表达 Hh 基因的肿瘤比例非常高。目前的数据支持 Hh 途径在放化疗后再增殖中的作用,并表明 SMO 可能是一个有效的治疗靶点。作者得出结论,有必要在放疗后和 Hh 抑制后进一步研究该途径。