Laboratorio de Oncología Biomédica, Departamento de Enfermedades Crónico Degenerativas, Instituto Nacional de Enfermedades Respiratorias Ismael Cosio Villegas, México. ggonzalezavila @ yahoo.com
Respiration. 2013;85(4):281-8. doi: 10.1159/000336559. Epub 2012 Mar 22.
One of the risk factors associated with lung cancer in never-smoker patients is wood smoke exposure (WS). However, information about its clinical and molecular characteristics remains scant.
This was to analyze--in plasma from patients with tobacco- or wood-smoke-induced lung cancer--whether the enzymatic activity and concentration of matrix metalloproteinases (MMPs) and tissue inhibitors of matrix metalloproteinases (TIMPs) differ, and to determine whether there was a correlation between these indicators of the metastatic potential and the first-line chemotherapy response.
Patients were classified according to lung cancer associated with: the smoking of tobacco (T), WS and where no association with a known risk factor (N) could be established. The gelatinase activity of plasma MMP was analyzed by radiolabeled substrate degradation and zymography assay. Protein expression of MMPs and TIMPs was evaluated by Western blot densitometry analysis.
The 26.9% WS patients had a better response to therapy in comparison with the T group (OR = 4.9, 95% CI = 1.25-20.15; p = 0.019). The lowest gelatinase activity was observed in WS subjects, in comparison with T and N subjects (96.7 ± 15.9, 182.9 ± 31.5 and 163.3 ± 22.7 µg of degraded gelatin/mg of incubated plasma protein, respectively; p < 0.025); this enzymatic activity corresponded to MMP-2. The highest MMP-2, MMP-9, MT1-MMP and TIMP-1 plasma levels were observed in T subjects.
Tobacco and wood smoke have different effects on MMP and TIMP synthesis and gelatinase activity, directly influencing lung cancer metastatic potential and chemotherapy response.
不吸烟的肺癌患者的一个危险因素是木材烟雾暴露(WS)。然而,有关其临床和分子特征的信息仍然很少。
本研究旨在分析烟草或木材烟雾引起的肺癌患者血浆中基质金属蛋白酶(MMPs)和基质金属蛋白酶抑制剂(TIMPs)的酶活性和浓度是否存在差异,并确定这些转移潜能的指标与一线化疗反应之间是否存在相关性。
根据肺癌与吸烟(T)、WS 和与已知危险因素无关联(N)的关联,对患者进行分类。通过放射性标记底物降解和酶谱分析来分析血浆 MMP 的明胶酶活性。通过 Western blot 密度分析评估 MMPs 和 TIMPs 的蛋白表达。
26.9%的 WS 患者的治疗反应优于 T 组(OR=4.9,95%CI=1.25-20.15;p=0.019)。与 T 和 N 组相比,WS 组的明胶酶活性最低(96.7±15.9、182.9±31.5 和 163.3±22.7µg 降解明胶/mg 孵育血浆蛋白;p<0.025);这种酶活性与 MMP-2 相对应。T 组的 MMP-2、MMP-9、MT1-MMP 和 TIMP-1 血浆水平最高。
烟草和木材烟雾对 MMP 和 TIMP 的合成和明胶酶活性有不同的影响,直接影响肺癌的转移潜能和化疗反应。