Department of Pathology, Graduate School of Medicine, Kyung Hee University, Seoul, Korea.
Pathology. 2012 Oct;44(6):540-6. doi: 10.1097/PAT.0b013e32835803bc.
The MAPK pathway has been shown to contribute to the prognostic role and drug resistance in many cancers. In addition, the MAPK pathway was found to play a role in the aggressive behaviour of osteosarcoma (OS). We hypothesised that the expression of the MAPK pathway components may be of value in predicting the prognosis of patients with OS.
We evaluated the expression of pan-Ras, Raf-1, pMEK1/2 and pERK1/2 in 61 OS samples using immunohistochemistry and evaluated their effect on event free survival (EFS) and overall survival (OVS).
pan-Ras, Raf-1, pMEK1/2 and pERK1/2 were found to be expressed in seven (11%), 36 (59%), 36 (59%) and 30 (49%) of 61 samples, respectively. Patients groups whose tumours expressed Raf-1, pMEK1/2 or pERK1/2 had a poorer clinical outcome than the group whose tumours did not express those antibodies. In addition, positive pMEK1/2 expression was associated with shorter EFS and OVS, irrespective of other prognostic factors.
Our results further support the findings that aberrant expression of the MAPK pathway components may be the underlying mechanism behind OS, which results in more aggressive clinical behaviour. Furthermore, there may be a decrease in EFS and OVS in OS patients who have tumours that stain positively for pMEK.
MAPK 通路已被证明在许多癌症的预后作用和耐药性中发挥作用。此外,MAPK 通路被发现与骨肉瘤(OS)的侵袭性行为有关。我们假设 MAPK 通路成分的表达可能对预测 OS 患者的预后有价值。
我们使用免疫组织化学方法评估了 61 例 OS 样本中 pan-Ras、Raf-1、pMEK1/2 和 pERK1/2 的表达,并评估了它们对无事件生存(EFS)和总生存(OVS)的影响。
在 61 例样本中,pan-Ras、Raf-1、pMEK1/2 和 pERK1/2 的表达分别为 7(11%)、36(59%)、36(59%)和 30(49%)。与未表达这些抗体的肿瘤患者相比,表达 Raf-1、pMEK1/2 或 pERK1/2 的患者肿瘤具有更差的临床预后。此外,pMEK1/2 表达阳性与 EFS 和 OVS 较短有关,而与其他预后因素无关。
我们的结果进一步支持了 MAPK 通路成分的异常表达可能是 OS 的潜在机制,导致更具侵袭性的临床行为的发现。此外,pMEK 染色阳性的 OS 患者的 EFS 和 OVS 可能会降低。